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. 2023 Apr 4;20(4):e1004205. doi: 10.1371/journal.pmed.1004205

Estimating health spending associated with chronic multimorbidity in 2018: An observational study among adults in the United States

Angela Y Chang 1,2,3,*, Dana Bryazka 4, Joseph L Dieleman 4
PMCID: PMC10072449  PMID: 37014826

Abstract

Background

The rise in health spending in the United States and the prevalence of multimorbidity—having more than one chronic condition—are interlinked but not well understood. Multimorbidity is believed to have an impact on an individual’s health spending, but how having one specific additional condition impacts spending is not well established. Moreover, most studies estimating spending for single diseases rarely adjust for multimorbidity. Having more accurate estimates of spending associated with each disease and different combinations could aid policymakers in designing prevention policies to more effectively reduce national health spending. This study explores the relationship between multimorbidity and spending from two distinct perspectives: (1) quantifying spending on different disease combinations; and (2) assessing how spending on a single diseases changes when we consider the contribution of multimorbidity (i.e., additional/reduced spending that could be attributed in the presence of other chronic conditions).

Methods and findings

We used data on private claims from Truven Health MarketScan Research Database, with 16,288,894 unique enrollees ages 18 to 64 from the US, and their annual inpatient and outpatient diagnoses and spending from 2018. We selected conditions that have an average duration of greater than one year among all Global Burden of Disease causes. We used penalized linear regression with stochastic gradient descent approach to assess relationship between spending and multimorbidity, including all possible disease combinations with two or three different conditions (dyads and triads) and for each condition after multimorbidity adjustment. We decomposed the change in multimorbidity-adjusted spending by the type of combination (single, dyads, and triads) and multimorbidity disease category.

We defined 63 chronic conditions and observed that 56.2% of the study population had at least two chronic conditions. Approximately 60.1% of disease combinations had super-additive spending (e.g., spending for the combination was significantly greater than the sum of the individual diseases), 15.7% had additive spending, and 23.6% had sub-additive spending (e.g., spending for the combination was significantly less than the sum of the individual diseases). Relatively frequent disease combinations (higher observed prevalence) with high estimated spending were combinations that included endocrine, metabolic, blood, and immune disorders (EMBI disorders), chronic kidney disease, anemias, and blood cancers. When looking at multimorbidity-adjusted spending for single diseases, the following had the highest spending per treated patient and were among those with high observed prevalence: chronic kidney disease ($14,376 [12,291,16,670]), cirrhosis ($6,465 [6,090,6,930]), ischemic heart disease (IHD)-related heart conditions ($6,029 [5,529,6,529]), and inflammatory bowel disease ($4,697 [4,594,4,813]). Relative to unadjusted single-disease spending estimates, 50 conditions had higher spending after adjusting for multimorbidity, 7 had less than 5% difference, and 6 had lower spending after adjustment.

Conclusions

We consistently found chronic kidney disease and IHD to be associated with high spending per treated case, high observed prevalence, and contributing the most to spending when in combination with other chronic conditions. In the midst of a surging health spending globally, and especially in the US, pinpointing high-prevalence, high-spending conditions and disease combinations, as especially conditions that are associated with larger super-additive spending, could help policymakers, insurers, and providers prioritize and design interventions to improve treatment effectiveness and reduce spending.


Using data from over 16 million people in the United States, Angela Y Chang and colleagues explore how multimorbidity, when considering 63 different conditions, influences health care expenditure.

Author summary

Why was this study done?

  • Many would agree that much health spending is directed towards complex cases that include a combination of multiple chronic conditions, but existing literature estimating disease-specific spending generally fail to systematically account for multimorbidity.

  • Few studies have explored whether different combinations of conditions lead to greater or less spending than the sum of having the diseases separately.

What did the researchers do and find?

  • We used a large claims dataset of over 16 million commercially insurance US working population in 2018 to study the relationship between annual health spending and multimorbidity.

  • We developed a novel approach to adjust spending for each disease for multimorbidity (i.e., estimating the additional/reduced spending that could be attributed in the presence of other conditions) and found that most diseases have higher estimated spending after adjustment.

  • We further found that chronic kidney disease, ischemic heart disease-related heart conditions, cirrhosis, and inflammatory bowel disease are associated with high spending per treated case, high observed prevalence, and contribute the most to spending when in combination with other chronic conditions.

What do these findings mean?

  • Multimorbidity adjustments should be performed for any health spending analysis, otherwise researchers will likely largely underestimate spending for most diseases while overestimating for the remaining diseases.

  • In the midst of a surging health spending globally, and especially in the United States, pinpointing high-prevalence, high-spending conditions and super-additive disease combinations could help policymakers design interventions to improve treatment effectiveness and reduce spending.

Introduction

There are many concerning trends in healthcare in the United States. One is the magnitude and rapid growth of health spending, estimated at nearly 20% of the US economy in 2020, which has more than doubled in the past two decades [1]. Another is the rise in the burden of multimorbidity, commonly defined as the coexistence of two or more chronic conditions [2,3]. These two trends are likely interrelated, yet there is lack of good understanding of the relationship between health spending and multimorbidity. For example, studies have found that having certain conditions may affect the treatment of other comorbidities, and it is possible that the disease combinations would lead to a higher or lower spending beyond the sum of the spending of single conditions [4,5]. Without considering the impact of multimorbidity on spending, we are likely missing the opportunity for synergistically and efficiently tackling these issues [6].

Better insights into how and why health spending is rapidly increasing could in turn help slow down its growth. With the rise in multimorbidity, however, it has become more difficult to accurately associate spending to single conditions. Upon reviewing previous literature of similar inquiries and recent systematic reviews on the cost of multimorbidity, we identified four main gaps in estimating spending in the context of multimorbidity [7,8]. First, most studies apply a simple definition of multimorbidity, commonly the count of conditions an individual has in addition to a base condition, and do not consider which additional diseases are being bundled [813]. For example, one study found that one additional chronic condition was associated with nearly double the annual health spending [14]. However, this information is not enough for policymaking. It is reasonable to hypothesize that a person with diabetes and hypertension would incur different levels of spending than another person with diabetes and depression, yet the relationship between spending and the types of disease combinations are rarely explored. Second, most studies only include a small set of chronic conditions, based on convenience sample or high prevalence [3,12,15,16]. This limitation is mostly due to data availability (data sources not reporting more conditions) or computational restrictions (inadequate methods or insufficient computational power to analyze larger sets of disease combinations) [17]. Third, studies like those published by the Centers for Medicare and Medicaid Services (CMS) estimated per capita spending for dyads and triads of 20 chronic conditions, but they did not estimate spending for each disease after adjusting for multimorbidity (i.e., how spending for combinations can be attributed back to single conditions) [18]. This was also presented in a recent systematic review and meta-analysis, in which the authors were able to calculate the mean cost data of only 11 common dyads, and none of the reviewed studies reported whether the combinations have additive, sub-, or super-additive spending [7]. Finally, some studies focus on a single condition and estimate effects of comorbidities on spending of this particular condition, but it is difficult to combine the results of these studies to compare across diseases due to vastly different study designs [11,1921]. The most similar study design is by Dieleman and colleagues, which includes a comprehensive set of conditions and estimate spending after reallocating resources based for comorbidities, but it still retains focus on individual health conditions rather than the spending associated with multimorbidity [22].

This study attempts to fill these literature gaps and propose a novel approach to understanding this topic. First, instead of merely counting the number of chronic conditions an individual has, we are interested in how different types of multimorbidity combinations—for example, cardiovascular diseases + mental disorders or dementia + musculoskeletal disorders—lead to different spending outcomes. Previous studies found that multimorbidity leads to higher spending, but whether having one additional chronic condition (and the type of additional condition) leads to a super-additive rather than simply additive effect on health spending is unclear. Furthermore, to our knowledge, no study in the US has shown a synergistic effect between chronic conditions—where health spending among adults with two conditions is less than the simple addition of spending associated with the single conditions. We also estimated spending associated with single chronic conditions by considering the contribution of multimorbidity, i.e., additional spending that could be attributed in the presence of other chronic conditions. From here onwards, we call this the “multimorbidity-adjusted spending.” Second, we used the comprehensive list of conditions from the Global Burden of Disease (GBD) 2019 study to create all possible two- and three-way combinations [23]. The use of a comprehensive list of chronic conditions gave us a more accurate set of spending estimates that is also comparable across conditions.

Methods

This study is reported following the REporting of studies Conducted using Observational Routinely collected health Data (RECORD) guideline.

Data source

The Truven Health MarketScan Commercial Claims and Encounters Database provides claim-level healthcare information on millions of commercially insured enrollees below age 65 [24,25]. We used claims data from the 2018 inpatient services, outpatient services, and inpatient admissions tables. We restricted the study sample to adults between ages 18 and 64 with unique enrollee identification numbers. To our knowledge, the differences in patients’ sociodemographic characteristics and the universe of all privately insured individuals has not been assessed. For example, Truven stated that the data mostly come from large employers, and thus individuals employed in medium and small firms may be underrepresented [26]. We excluded enrollees with mismatching demographic data, such as people who had two birth years or were assigned both male and female in different claim records. We further excluded enrollees whose spending data were missing or were negative; enrollees with claim records that had zero spending were not excluded.

Defining and assigning chronic condition diagnoses

The GBD 2019 cause hierarchy includes 297 most-detailed diseases and injuries [23]. First, to identify chronic conditions, we selected with an average duration of greater than one year, and injuries were excluded from this analysis [27]. Second, to allow mapping between the database and GBD causes, we collected all International Classification of Diseases, 10th Revision, Clinical Modification codes (ICD-10) associated with each chronic cause previously conducted by the Institute for Health Metrics and Evaluation (IHME) US Disease Expenditure Project (DEX) [1]. Third, to improve data efficiency by reducing the number of covariates in the regression model, we combined a subset of more-detailed conditions with lower observed prevalence into larger disease categories (see Table A2 in S1 Appendix). For example, all alcohol and drug use-related mental disorders (such as opioid, cocaine, amphetamine, cannabis, and other drug use) were grouped into one; esophageal and stomach cancers were combined and renamed as upper gastrointestinal cancers. Fourth, we applied the algorithm set by the CMS Chronic Conditions Data Warehouse, which qualifies an ICD code to be associated with a chronic condition if it is present in at least one inpatient or two outpatient claims [28,29]. Finally, we ran through all claims and considered an individual to have the chronic condition if the criteria described above were met. We included all diagnoses code associated with all claims records and did not restrict the analysis to only primary diagnosis or a small subset of diagnoses codes.

For comprehensiveness, GBD and DEX have assigned residual “other” categories, such as “other chronic respiratory diseases” and “other neoplasms,” although these categories are generally poorly defined. In this study, we included these “other” conditions in the statistical analysis but did not present the results in the main paper. The full results, including these “other” categories, are reported in Table A5 in S1 Appendix.

Estimating annual spending per enrollee

We estimated annual insurance spending for each enrollee by adding all net payments reported in 2018. The net payment for each claim, as defined by the data source, is the payment to a provider for a service, calculated by removing deductibles, coinsurance, and coordination of benefits and other savings from gross covered payment [24]. We included spending on all claims assigned to the person, regardless of whether the claim was associated with a chronic condition. Including both chronic and non-chronic spending is necessary to be able to capture the potential effects of having chronic conditions on the individual’s overall health outcomes, health seeking behaviors, and ultimately, health spending. Spending was transformed on a natural logarithmic scale. All estimates are presented in 2018 US dollars.

Estimating super-additive, additive, and sub-additive effects of chronic conditions on annual health spending

This study took a person-based regression approach—regressing a person’s total 2018 health spending on health conditions indicators—in estimating spending per treated case [30,31]. We applied the following linear regression model:

spendi=β0i+j=1Jβijdxij+k=1Kβikdyadik+l=1Lβiltriadil+agei+sexi+regiondummiesi+εi (1)

where i is enrollee, dxj is each chronic condition, dyadk and triadl represent the interaction terms for all possible chronic condition dyads and triads, respectively, agei, sexi, and regioni represent the enrollee’s age group (10-year age groups), sex, region of residence (Northeast, North Central, South, West, and Unknown), and εi is the error term [14]. This equation estimates the spending associated with single conditions and different combinations. For example, an estimated positive and statistically significant βik^ suggests that the combination has a super-additive effect on spending, which is greater than the sum of the spending associated with having these conditions separately. If βik^ is not statistically different from zero, it would suggest that the combination has an additive effect, and a statistically significant negative coefficient suggests that the combination has a synergistic, negative effect, meaning that spending is less than the sum of the spending associated with having the conditions separately.

Given the large size of the dataset (6.7+ billion claims), over 40,000 covariates representing all possible dyads and triads of chronic conditions, and the need for strong computational power, we applied a regression framework using the stochastic gradient descent (SGD) approach, a commonly used method in solving large machine learning problems. SGD updates the regression coefficients iteratively to minimize the objective function for the regression model of interest (minimize mean squared error), using a smaller batch of data for each iteration. The general concept and objective of this approach is close to that of a typical ordinary least squares regressions [32]. To prevent having too many variables in the model that have small contributions, we applied a lasso penalized regression model to shrink the coefficient values of these covariates. To ensure stability of the model results, we conducted 50 SGD model runs and bootstrapped the results across runs for 10,000 times to get the estimates for all coefficients. Details on the model and parameter setting can be found in Section 3A of S1 Appendix.

Estimates of total spending associated with any combination were derived by adding the coefficients for the single conditions independently and the coefficients from the interaction terms (from the combinations). For example, total spending for diabetes + osteoarthritis was calculated as the sum of the coefficient for diabetes, coefficient for osteoarthritis, and coefficient for the interaction term diabetes * osteoarthritis. For triads, we further added the three dyads to the sum.

Estimating spending associated with each individual health condition, adjusting for multimorbidity (“multimorbidity-adjusted spending”)

For the second outcome of interest, we are interested in estimating the proportion of spending for the combination that could be attributed back to single conditions. For example, we would have a more accurate spending on diabetes because we would have not only the diabetes-specific spending but also the additional or reduced amount of spending diabetes incurs when in combination with other conditions. More specifically, the coefficient of the interaction term for the diabetes–osteoarthritis combination needs to be split into one part associated with diabetes and another with osteoarthritis. A four-step process was implemented to do so:

First, we ran a linear regression model among study population with diabetes to estimate the effect of having osteoarthritis on annual health spending:

spendj=β0j+k=1K1βjkdxjk+agej+sexj+regionj+εj (2)

where j is the enrollee with the disease (diabetes in this example), and dxk is each additional chronic condition beyond diabetes. With this equation, we derive βosteoarthritis|diabetes, the coefficient representing the effect of having osteoarthritis on spending among people with diabetes. We ran the same model for people with osteoarthritis to derive βdiabetes|osteoarthritis, the coefficient representing the effect of having diabetes on spending among people with osteoarthritis.

Second, we took the coefficient of the interaction term for diabetes and osteoarthritis, βdiabetes,osteoarthritis (derived from Eq 1), and split the coefficient into two parts:

βdiabetes,osteoarthritis=βdiabetes|combination+βosteoarthritis|combination (3)
=βdiabetes,osteoarthritis×βdiabetes|osteoarthritisβdiabetes|osteoarthritis+βosteoarthritis|diabetes
+βdiabetes,osteoarthritis×βosteoarthritis|diabetesβdiabetes|osteoarthritis+βosteoarthritis|diabetes

where βdiabetes|combination is the estimated part of the interaction coefficient that is attributed to diabetes, and βosteoarthritis|combination is the part attributed to osteoarthritis. βdiabetes|osteoarthritis is the coefficient from Eq (2) on the indicator variable of whether those with osteoarthritis also have diabetes as a comorbidity, and βosteoarthritis|diabetes is the coefficient on the indicator variable of whether those with diabetes also have osteoarthritis as a comorbidity. To estimate spending among all interaction coefficients that should be attributed to having diabetes, we repeated the previous steps for all conditions that co-occurred with diabetes.

Third, we calculated prevalence, i.e., the probability of the disease combinations occurring among people with diabetes (for example, the probability of someone with diabetes also having osteoarthritis). This is needed for the next step, in which we adjusted each spending estimates based on its prevalence, such that more common combinations of diabetes and another disease receives a higher weight than combinations that are less common. This was done by multiplying the spending associated with the combination with its prevalence from step 3 and summed across disease combinations. This final figure is the part of the spending associated with dyads that should be attributed to diabetes. The same approach was extended to combinations of three, in which we ran the model among people with two conditions and took the coefficient on the indicator variable of having the third condition (explained in more detail in Section 2 in S1 Appendix).

For the purpose of comparison, we estimated the non-adjusted spending for each condition by using the same regression model in Eq (1) but without the disease interaction terms (k=1Kβikdyadik and l=1Lβiltriadil). The results from this simple model (referred in the results as “non-adjusted spending”) was then used to compare against the main results (multimorbidity-adjusted spending).

We decomposed the change in multimorbidity-adjusted spending by the type of combination (single, dyads, and triads) and the multimorbidity disease categories (e.g., cardiovascular, neoplasms).

For the purpose of reporting, we present estimates of health spending for a 35- to 44-year-old female from the South region, which reflects the most common age, sex, and regional characteristics of the study population. We also report the coefficients for all demographic covariates in Table A4 in S1 Appendix. For estimates for disease combinations, only those with observed prevalence greater than 50 per 100,000 people are listed in the figures and tables.

Quantifying uncertainty

First, to generate 95% uncertainty interval (UI) for spending associated with disease combinations, we bootstrapped the means from all the model runs for 10,000 times. Second, to generate UI for multimorbidity-adjusted spending for each single condition, we ran Monte Carlo simulations (n = 1,000 draws) while varying the estimates associated with the combination and the proportion of combination attributed to each single condition.

Analyses were performed using R, version 4.0.5 (R Foundation for Statistical Computing, Vienna, Austria), and Python 3.8.1 (Python Software Foundation, Hampton, New Hampshire, USA).

Results

Selected chronic conditions

A total of 166 most-detailed GBD causes were determined as chronic (listed in Table A1 in S1 Appendix), of which we reduced down to 63 by combining them into larger disease categories to improve data efficiency (Table 1).

Table 1. Observed prevalence, proportion of multimorbidity, multimorbidity-adjusted annual per capita spending, and the comorbidities with the highest attributable spending for all chronic conditions.

Chronic condition Observed prevalence rate (per 100,000) Proportion with additional chronic condition Multimorbidity-adjusted annual spending per treated case Ratio of multimorbidity-adjusted spending and non-adjusted spending
Neoplasms
Bladder and kidney cancers 173.7 95.1% $1,536 [1,421–1,672] 1.6
Blood cancers 218.7 94.8% $9,387 [8,627–10,071] 2.8
Brain and nervous system cancer 40.2 95.9% $6,298 [5,334–7,386] 3.7
Breast cancer 5,169.2 92.2% $579 [516–655] 0.6
Colon and rectum cancer 3,145.2 95.3% $1,132 [949–1,285] 1.4
Ear, nose, throat cancers 32.7 97.2% $1,406 [1,223–1,567] 2.4
Reproductive organ cancers 3,945.4 87.9% $837 [723–960] 1.8
Gastrointestinal gland cancers 41.4 98.6% $3,462 [3,078–3,904] 2.6
Hodgkin lymphoma 34.9 91.4% $1,191 [1,086–1,316 1.8
Lip and oral cavity cancers 31.1 97.0% $1,536 [1,374–1,680] 2.3
Skin cancers 790.5 98.2% $806 [644–946] 1.2
Thyroid cancer 202.0 93.7% $534 [460–592] 1.2
Tracheal, bronchus, and lung cancer 94.6 98.4% $5,422 [4,874–6,085] 2.9
Upper gastrointestinal cancers 21.2 97.7% $1,917 [1,788–2,056] 2.2
Cardiovascular diseases
Atrial fibrillation and flutter 642.2 96.9% $5,147 [4,864–5,475] 3.1
IHD-related heart conditions 2,228.2 97.7% $6,029 [5,529–6,529] 1.9
Peripheral vascular disease 457.8 98.4% $1,265 [1,175–1,338] 1.3
Rheumatic heart disease 137.1 98.6% $4,268 [4,17–4,472] 2.9
Stroke 698.8 98.7% $5,395 [4,564–6,326] 2.3
Chronic respiratory diseases
Asthma 3,020.4 93.3% $1,277 [1,238–1,323] 0.9
COPD 723.3 97.8% $1,496 [1,399–1,601] 1.0
Interstitial lung disease and pulmonary sarcoidosis 170.2 97.7% $1,024 [950–1,113] 0.8
Digestive diseases
Cirrhosis 1,536.8 96.7% $6,465 [6,090–6,930] 2.3
Gallbladder and biliary diseases 801.8 93.7% $7,509 [6,825–8,124] 2.3
Gastritis and duodenitis, peptic ulcer disease 5,890.0 95.4% $2,550 [2,484–2,612] 1.4
Inflammatory bowel disease 1,030.6 89.0% $4,697 [4,594–4,813] 1.8
Inguinal, femoral, and abdominal hernia 977.5 93.6% $2,608 [2,608–2,608] 1.2
Neurological disorders
Alzheimer’s disease and other dementias 106.6 98.0% $896 [785–1,19] 1.2
Epilepsy 430.7 89.5% $1,882 [1,765–2,19] 1.1
Headache disorders 2,797.6 94.6% $563 [489–624] 0.7
Multiple sclerosis 226.9 91.9% $1,532 [1,403–1,669] 1.1
Parkinson’s disease 49.4 94.8% $307 [257–364] 1.1
Mental disorders
Anxiety disorders 10,574.6 89.9% $1,087 [996–1,163] 3.0
Attention-deficit/hyperactivity disorder 2,059.2 84.9% $137 [127–145] 1.1
Bipolar disorder 779.5 93.2% $1,008 [914–1,087] 1.6
Depressive disorders 5,853.0 94.0% $963 [804–1,138] 1.3
Schizophrenia 98.7 91.2% $911 [809–1,26] 1.4
Substance use disorders 1,847.5 92.4% $3,325 [3,36–3,568] 1.2
Diabetes and kidney diseases
CKD 1,456.1 97.6% $14,376 [12,291–16,670] 4.4
Diabetes 9,086.4 95.2% $910 [790–1,44] 2.0
Skin and subcutaneous diseases 21,662.3 86.2% $303 [252–364] 1.0
Sense organ diseases 6,909.4 87.7% $1,020 [907–1,116] 1.0
Musculoskeletal disorders
Gout 758.9 93.6% $409 [334–498] 2.0
Low back and neck pain 14,952.6 94.1% $861 [747–987] 1.1
Osteoarthritis 3,664.1 98.1% $3,239 [2,714–3,848] 1.7
Rheumatoid arthritis 306.8 95.7% $424 [359–480] 0.9
Other non-communicable diseases
Congenital birth defects 835.0 94.0% $4,150 [3,748–4,577] 1.9
EMBI disorders 11,813.9 93.2% $2,386 [2,071–2,742] 1.5
Gynecological diseases 15,033.3 83.2% $2,318 [2,082–2,578] 1.2
Hemoglobinopathies and hemolytic anemias 5,307.4 92.5% $3,371 [2,862–3,803] 1.7
Oral disorders 657.6 85.7% $1,589 [1,384–1,819] 1.2
Communicable diseases
HIV/AIDS 329.9 81.4% $623 [543–694] 1.2
Risk factors
Hyperlipidemia 13,465.3 96.4% $204 [176–234] 0.6
Hypertension 17,727.3 93.7% $563 [501–635] 1.1
Obesity 9,915.2 94.1% $1,491 [1,346–1,613] 1.0
Tobacco use 2,580.4 94.4% $2,516 [2,267–2,810] 1.0

*Top three excluding the disease itself and all the “other” categories (7 others).

CKD, chronic kidney disease; COPD, chronic obstructive pulmonary disease; EMBI disorders, endocrine, metabolic, blood, and immune disorders; IHD, ischemic heart disease.

Study population

A total of 16,288,894 enrollees and their 6,726,532,451 claims were included in the analysis. Population characteristics are presented in Table 2: 56.2% were female, mean age was 42.3 years, the number of chronic conditions for an individual ranged from 0 to 32, with a mean of 2.6 conditions. Approximately 23.6% enrollees had no chronic conditions, 20.2% had one condition, and the remaining 56.2% had two or more chronic conditions, of which 94.0% of them had more than three conditions. Looking at single chronic conditions, skin and subcutaneous diseases (21,662 per 100,000; 21.7% of all study population), hypertension (17,727; 17.7%), gynecological diseases (15,033, 15.0%), musculoskeletal pain (14,953; 15.0%), and hyperlipidemia (13,465; 13.5%) had the highest observed prevalence rates. Looking at combinations of chronic conditions, the most common health condition dyads were hyperlipidemia + hypertension (7,177; 7.2%), diabetes + hypertension (5,044; 5.0%), hypertension + skin and subcutaneous diseases (4739; 4.7%), diabetes + hyperlipidemia (4,625; 4.6%), and gynecological diseases + skin and subcutaneous diseases (4,589; 4.6%); the most frequent health condition triads included two high-prevalence risk factors (hyperlipidemia + hypertension) plus one of the following chronic conditions: diabetes (3,069; 3.1%), skin and subcutaneous diseases (2,065; 2.1%), obesity (1,914; 1.9%), endocrine, metabolic, blood, and immune disorders (EMBI disorders) (1,888; 1.9%), and diabetes + hypertension + obesity (1,571; 1.6%). The mean and median annual health spending of the study population were $6,388 and $633, respectively.

Table 2. Summary statistics of study population.

Characteristic Statistic
Total 16,288,894
Sex 56.2% Female
Age 42.3 (SD 13.5)
Region
    Northeast 19.0%
    North Central 20.5%
    South 44.2%
    West 16.2%
    Unknown 0.3%
Mean (median) annual spending Mean 6,388.0
Median 633.3
SD 36,561.7
Mean (median) number of chronic conditions Mean 2.6
Median 2.0
SD 2.7

Spending for combinations of chronic conditions

Out of 41,664 possible health condition combinations (dyads or triads), regression coefficients for 25,277 (60.1%) were positive (super-additive), 6,553 (15.7%) were nearly zero (additive; between −1 and 1), and 9,834 (23.6%) were negative (sub-additive). Among health condition combinations with observed prevalence rate greater than 50 per 100,000, the five largest super-additive spending were found in combinations of blood cancers + hemoglobinopathies and hemolytic anemias (henceforth anemias) (+$3,227, 95% UI [2,541,3,905]), chronic kidney disease + EMBI disorders + anemias (+$3,111 [2,679,3,535]), chronic kidney disease + anemias (+$3,074 [2,718,3,431]), blood cancers + EMBI disorders (+$3,017 [2,427,3,591]), chronic kidney disease + EMBI disorders (+$2,887 [2,617,3,148]). The five largest sub-additive spending were found in EMBI disorders + hyperlipidemia (−$733 [−851,−620]), hyperlipidemia + anemias (−$702 [−885,−516]), cirrhosis + hyperlipidemia (−$610 [−838,−370]), hyperlipidemia + anemias + skin and subcutaneous diseases (−$558 [−692,−416]), and chronic kidney disease + low back and neck pain + hyperlipidemia (−$545 [−727,−363]). More details are provided in Table A6 in S1 Appendix.

When we consider the total spending associated with combinations (i.e., including the coefficients of the intercept, covariates, single conditions, and three dyads in the case of triads), the top five highest spending with observed prevalence greater than 50 per 100,000 were combinations of EMBI disorders + anemias + skin and subcutaneous diseases ($7,120 [6,899,7,319]), chronic kidney disease + EMBI disorders ($6,730 [6,387,7,29]), EMBI disorders + anemias + hypertension ($6,325 [5,762,6,950]), cirrhosis + EMBI disorders ($5,370 [5,236,5,528]), ischemic heart disease (IHD)-related conditions + hypertension + hyperlipidemia ($5,339 [5,115,5,574]). Note that while these have the highest estimated spending, they do not have the highest observed prevalence. Instead, when we further focus on combinations with at least 1% prevalence, we found the following combinations with the highest spending: IHD + hyperlipidemia + hypertension ($5,234 [4,538,5,826]), EMBI disorders + anemias ($4,961 [4,381,5,483]), gynecological diseases + anemias ($3,243 [3,126,3,350]), gastritis and duodenitis, peptic ulcer disease + obesity ($3,064 [2,978,3,158]), IHD + hyperlipidemia ($3,038 [2,759,3,295]).

Multimorbidity-adjusted spending for single chronic conditions

The majority of individuals with one of the 63 chronic conditions had at least one or more of the remaining 62 conditions. The highest proportions were recorded among individuals with stroke (98.7%), gastrointestinal gland cancers (98.6%), rheumatic heart disease (98.6%), tracheal, bronchus, and lung cancer (98.4%), and peripheral vascular disease (98.4%); the lowest proportions included HIV/AIDS (81.4%), gynecological diseases (83.2%), attention-deficit and hyperactivity disorder (84.9%), oral disorders (85.7%), and skin and subcutaneous diseases (86.2%). The average across all conditions was 93.9%.

With multimorbidity adjustment, the following 10 chronic conditions had the highest multimorbidity-adjusted spending per treated case: chronic kidney disease ($14,376 [12,291,16,670]), blood cancers ($9,387 [8,627,10,071]), gallbladder and biliary diseases ($7,509 [6,825,8,124]), cirrhosis ($6,465 [6,090,6,930]), brain and nervous system cancer ($6,298 [5,334,7,386]), IHD ($6,029 [5,529,6,529]), tracheal, bronchus, and lung cancer ($5,422 [4,874,6,085]), stroke ($5,395 [4,564,6,326]), atrial fibrillation and flutter ($5,147 [4,864,5,475]), and inflammatory bowel disease ($4,697 [4,594,4,813]). Among these, chronic kidney disease, cirrhosis, IHD, and inflammatory bowel disease had observed prevalence rates greater than 1,000 per 100,000 people (Fig 1).

Fig 1. Multimorbidity-adjusted spending per treated case and observed prevalence for 63 chronic conditions.

Fig 1

Abbreviations: ADHD, attention-deficit/hyperactivity disorder; COPD, chronic obstructive pulmonary disease; EMBI, endocrine, metabolic, blood, and immune disorders; ENT, ear, nose, throat; GERD, gastroesophageal reflux disease; GI, gastrointestinal; hernia, inguinal, femoral, and abdominal hernia; IHD, ischemic heart disease; PHD, peripheral vascular disease; PUD, peptic ulcer disease; sarcoidosis, interstitial lung disease and pulmonary sarcoidosis; sense, sense organ diseases; skin, skin and subcutaneous diseases.

Comparing the multimorbidity-adjusted spending estimates to non-adjusted spending, we found that 50 conditions (among 63) had higher spending after adjustments, 7 had less than 5% difference, and 6 had lower spending (Table 1). The top five conditions with the largest increase in spending after multimorbidity adjustment include chronic kidney disease (4.4 times increase), brain and nervous system cancer (3.7 times), atrial fibrillation and flutter (3.1), anxiety disorders (3.0), and rheumatic heart disease (2.9). The top five conditions with the largest decrease in spending after adjustment include breast cancer (0.6), hyperlipidemia (0.6), headache disorders (0.7), interstitial lung disease (0.8), and rheumatoid arthritis (0.9).

Decomposition of the multimorbidity-adjusted spending by the type of combination (single, dyads, and triads) for conditions with the highest spending per treated case is in Fig 2. The sizes of the contribution of dyads and triads are a function of the estimated spending associated with the disease combination as well as the observed prevalence of the combination among people with the condition. For example, for chronic kidney disease, less than 25% (in gray) is attributed to people having just chronic kidney disease, while approximately 50% (in yellow) is the increase due being in combination with a second condition, and the remaining 25% (in purple) is the increase due to being in a triad. Conditions such as chronic kidney disease and brain and nervous system cancer have higher contribution of spending from dyads and triads not only because spending on its combinations are high, but also because people with these conditions have higher probabilities of having multimorbidity (see Table 1, 97.6 and 95.9%, respectively) (Fig 2).

Fig 2. Decomposition of multimorbidity-adjusted spending by the type of combination (single, dyads, triads) for chronic conditions with the top 10 highest spending per treated case.

Fig 2

Finally, for conditions with the highest spending per treated case, we further decomposed the contribution of dyads and triads (the yellow and purple bars in Fig 2) by the type of coexisting disease categories (Fig 3). This graph shows how other condition contribute to the increase in spending for the index condition. For the purpose of comparison, we present stacked bar plots capped at 100%, but the actual spending estimates for each disease can be found in Table 1. First, spending associated with having only the index condition itself is presented in gray, ranging from less than 25% in chronic kidney disease to over 50% in inflammatory bowel disease and IHD, consistent with what was shown in Fig 2. Second, each color represents one major disease category, and the size of the bars represent the prevalence-weighted sum of the multimorbidity-adjusted spending associated with the coexisting disease category in combination with the index condition. For example, for chronic kidney disease (the first bar in Fig 3), we estimated overall multimorbidity-adjusted spending as approximately $14,300 (Table 1). In the figure, we see that the largest contributions to spending increase come from being in combination with “other non-communicable disease” (such as EMBI disorders), followed by cardiovascular and respiratory diseases, contributing to approximately 20%, 15%, and 10% of the total estimate, respectively. In other words, in the multimorbidity-adjusted estimates for chronic kidney disease, close to half (approximately $7,000) is due to being in combination with these disease categories. For the two cancers included in this figure, we see that other neoplasms account for the largest share of increases, and specifically for brain and nervous system cancer, we also see a large contribution from neurological disorders.

Fig 3. Decomposition of multimorbidity-adjusted spending by multimorbidity disease categories, for chronic conditions with the top 10 highest spending per treated case.

Fig 3

Discussion

The relationship between multimorbidity and health spending has been listed as one of the research priorities proposed by the Academy of Medical Sciences [33]. This paper takes two perspectives—assessing spending on combinations of chronic conditions and assessing spending on a single chronic conditions with a multimorbidity adjustment—to provide different interpretation of a large dataset and more accurate spending estimates on a comprehensive list of conditions. Below, we highlight four key takeaways from this study.

First, across different sets of analyses, we consistently found chronic kidney disease, blood cancers, cirrhosis, and IHD to be associated with high spending per treated case, high observed prevalence, and contributing the most to spending when in combination with other chronic conditions. Preventing these conditions from occurring could mean large savings not only from its own treatment spending but also from its effect on spending on other conditions. While this study does not allow us to explain why, our results could guide further research designs, such as, for example, the distribution of spending by outpatient and inpatient services, and whether each have different additive/super-additive patterns. Reasons for super-additive spending could include greater utilization frequency, more complex disease trajectories due to disease and/or medication interactions, and lack of coordination between services [34]. Some have suggested that most clinical trials focus on treatments for single conditions and exclude participants with multimorbidity; therefore, even if the clinical guidelines are tailored for people with multimorbidity, the treatments may not be the most appropriate for this population [10]. Interventions such as care coordination, improvements in patient–provider communication, or targeting common risk factors have been proposed as means to reducing multimorbidity spending [34]. On the other hand, previous studies have pointed to how treatment for concordant conditions, defined as conditions similar in risk profile and management, could benefit from synergistic effects because services for chronic conditions that are treated by the same specialty (such as cardiology or internal medicine) may be more coordinated or are under more favorable payment schemes, leading to lower total spending than the spending for single conditions combined [3539].

Second, contrary to common belief, multimorbidity does not always lead to greater spending than the sum of the spending associated with having these conditions separately: 40% of combinations did not have super-additive spending. In this study, the sub-additive spending was commonly found among people with hyperlipidemia or breast cancer alongside another chronic condition (i.e., conditions with lower spending post-adjustment; see Table 1). Sub-additive spending could mean that there may either be synergistic or harmful effects in how these patients are seeking or receiving care. Blakeley and colleagues hypothesized that sub-additive spending could also be due to down-prioritization of treatment for the comorbidities [17]. Compared to concordant diseases, discordant diseases, defined as those not directly related in pathogenesis or management, were found previously to either have zero or negative effects on one another [3539].

Third, decomposition of spending associated with the type of combination (single/dyads/triads) and categories of multimorbidity (e.g., cardiovascular, neoplasms) allows us to more clearly identify and target common patterns of multimorbidity associated with high spending. For example, a large increase in spending associated with stroke, atrial fibrillation and flutter, and chronic kidney disease come from triads (Fig 2), which are likely more complicated, and a more concerted management effort to reduce the prevalence and/or spending associated with these single conditions could yield highly cost-effective results.

Fourth, a large proportion of our study population has multimorbidity, even among our study population who are under age 65. A previous study found that much of the recent growth in health spending in the Medicare population is due to increasing number of people with multimorbidity [40]. While this study focused on adults not eligible for Medicare, it is reasonable to assume that the increasing prevalence of multimorbidity in this population also is contributing to the substantial increase in spending. Consistent with previous studies, the highest observed prevalence rates were found among combinations of hyperlipidemia, hypertension, diabetes, skin and subcutaneous diseases, gynecological diseases, low back and neck pain, and EMBI disorders [2,12,18].

It is difficult to benchmark our results because no other study had a similar scope. We chose five studies that are quite different but relevant for triangulation. Dieleman and colleagues estimated population-level spending for a comprehensive set of conditions, and among chronic conditions in all ages, including ages 15 to 64, they found the largest positive increases in chronic kidney diseases, alcohol disorders, diabetes mellitus, chronic obstructive pulmonary disease (COPD), and skin and subcutaneous diseases, and largest decreases in atrial fibrillation and flutter, urinary diseases, gynecological diseases, bipolar disorders, and depressive disorders [22]. While not the main focus of this study, among these conditions, we observed the same directional changes in only half of those listed above. Possible explanations include the difference in estimating spending for a population (instead of per treated case in our study), the assumption of assessing multiplicative (instead of additive) effects, its focus on inpatient and nursing facility spending (instead of inpatient and outpatient), and the inclusion of more conditions and combinations. Second, DEX, which looks at spending at the population level for all ages and types of payers, also identified IHD, hypertension, and urinary diseases among conditions with the highest spending [1]. Though, note that the reason for high population-level spending could either be because of high individual-level spending, high prevalence, or a mix of both (e.g., medium-level spending times medium-level prevalence could lead to relatively high overall spending). Third, Tran and colleagues performed a meta-analysis based on 15 studies for 11 most frequently reported dyads, and estimated mean costs to be between $13,270 (hypertension + musculoskeletal disorder) and $85,820 (cancer first year after diagnosis + mental health conditions) (2021 International Dollars). These numbers are larger than our estimates; however, they are not comparable due to differences in study population, age, study design, among other factors. Among the studies reported by the review and used similar data sources, we found qualitatively similar results reported for rheumatoid arthritis, chronic kidney disease, and diabetes [4143]. Fourth, compared to Rezaee and Pollock who estimated total outpatient spending for conditions in a large US health system between 2008 and 2013, we reached a similar conclusion that hyperlipidemia, hypertension, and combinations of these two conditions along with other conditions are prevalent and costly [12]. They estimated that one additional chronic condition was associated with increased spending of approximately $600 but did not report further on the types of combinations nor did they distinguish between super- or sub-additive spending [12]. Finally, the study by Blakely and colleagues estimates individual-level spending estimates from New Zealand [17]. Using higher-level disease categories, they found the highest single-condition spending in chronic lung, liver, and kidney diseases, and the highest spending in combinations of cancer + neurological disorders, cardiovascular diseases + chronic lung, liver, and kidney diseases.

This study has several strengths and limitations. One key strength is the application of a large and comprehensive set of 63 chronic conditions (which are composed of 166 most-detailed GBD causes), overcoming limitations faced by existing studies due to lack of data availability or computational limitations. Moreover, we were able to study combinations of up to three conditions per individual, not limited to a small set or combinations of only two conditions [17,44]. Second, this study is based on a comprehensive administrative claims database that encompasses a large population of over 16 million adults in the US, providing sufficient information on the diagnoses and spending of enrollees. Compared to other datasets such as self-reported data, administrative data are often more reliable and allows for easier comparisons across studies [45]. However, the data do not include information on functional limitations and disease duration, which could provide more insights into the relationship between conditions and spending [46]. Due to the structure of administrative claims data, this paper takes a healthcare payer’s perspective, which likely underestimate the true cost of multimorbidity because we do not account for out-of-pocket payments or indirect costs. Third, we analyzed the relationship between multimorbidity and spending from two perspectives—single and combination of conditions. Instead of classifying combinations into one as primary diagnosis and the others as comorbidities as done in other studies, we took a multimorbidity perspective and distributed the spending across all conditions based on weights provided by a set of separate regression models [21,22].

The limitations of this study include the following. First, MarketScan data are a convenience sample—it is not representative of the commercially insured US adult population. For example, MarketScan data draw disproportionately from the southern region of the US [47]. We lack data on income but we assume this population has higher income than the general population since this is an employment-based claims database. We therefore cannot conclude that our results are generalizable at the national level. Similarly, this study focused on adults younger than 65 and the results thus should not be generalized to the Medicare population, who have the highest prevalence of chronic conditions. This is also a cross-sectional analysis focusing on 2018, with a gap of four years from the time of this writing in 2022. Ideally, we would study multiple years to identify time of diagnose as well as minimize the impact of random variations in health spending between years, but due to data access and financial restrictions at the time of writing, we are unable to do so. This has been found as a common limitation across studies on this topic [8]. The COVID-19 pandemic also significantly delayed our ability to analyze data. We also only have data on spending associated with a diagnosis, but we do not know about disease severity beyond what is represented in the ICD codes. Second, our spending variable only considers expenses incurred during inpatient or outpatient visits and does not include spending on pharmaceuticals or medical products incurred outside of these visits, nursing facility spending, nor indirect costs such as opportunity costs, transportation costs, and costs due to lost productivity—which are likely substantially higher among people with certain combinations than others. While the dataset has information on pharmaceutical spending for enrollees outside of visits (such as retail settings), we did not include it because of the difficulty in mapping pharmaceuticals to exact diagnoses (since drugs may be prescribed for multiple purposes). It is possible that individuals may have chosen pharmaceutical products over seeking provider services, which would lead to an underestimation of inpatient/outpatient spending for certain diseases. Third, the model structure implicitly assumes that the contributions of additional conditions on spending are additive and not multiplicative [46]. Related, the study design only allows for non-causal interpretation of the results. Fourth, while our list of chronic conditions, as well as the approach of diagnosing chronic conditions, follow the approach set by the CMS [2,43], there may be a more precise definition of categorizing diseases as chronic that are more suitable. We also do not include injuries and non-chronic conditions, some of which might have large impacts on spending. Fifth, due to computational limitations, we were only able to estimate spending for dyads and triads, though we speculate that combinations beyond three conditions do not contribute much to the multimorbidity adjustment.

This paper offers several insights into how the economic and health burden of multimorbidity could be better understood and provides a systematic method for measuring spending on multiple chronic health conditions that could be replicated elsewhere. In the midst of a surging health spending globally, and especially in the US, pinpointing high-prevalence, high-spending conditions and disease combinations, as especially conditions that are associated with larger super-additive spending, could help policymakers, insurers, and providers prioritize and design cost-effective interventions to improve treatment effectiveness and reduce spending.

Supporting information

S1 RECORD Checklist. RECORD checklist.

(DOCX)

S1 Appendix. Technical appendix.

Table A1. List of most-detailed GBD causes determined as chronic conditions. Table A2. Chronic conditions and its most-detailed GBD causes. Table A3. Summary statistics of 50 SGD model runs. Table A4. Summary statistics of study population. Table A5. Covariates and their regression coefficients. Table A6. Observed prevalence and estimated multimorbidity-adjusted annual spending per treated case for the “other” conditions. Table A7. Regression coefficients for disease combinations with prevalence rate of greater than 100 per 100,000 (ordered by spending).

(DOCX)

Abbreviations

CMS

Centers for Medicare and Medicaid Services

COPD

chronic obstructive pulmonary disease

DEX

Disease Expenditure Project

EMBI

endocrine, metabolic

blood

and immune

GBD

Global Burden of Disease

ICD-10

International Classification of Diseases, 10th Revision

IHD

ischemic heart disease

IHME

Institute for Health Metrics and Evaluation

SGD

stochastic gradient descent

UI

uncertainty interval

Data Availability

Data used in this paper cannot be made available due to contractual restrictions but can be purchased from IBM MarketScan Research Database. It provides claim-level health care information on millions of commercially insured enrollees below age 65. Contact can be made through this website: https://www.merative.com/contact.

Funding Statement

Research reported in this publication was supported by the National Institute on Aging of the National Institutes of Health (Award Number P30AG047845 to JLD and AYC). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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Decision Letter 0

Philippa Dodd

19 Aug 2022

Dear Dr Chang,

Thank you for submitting your manuscript entitled "Estimating health spending associated with chronic multimorbidity in 2018: an observational study among adults in the United States" for consideration by PLOS Medicine.

Your manuscript has now been evaluated by the PLOS Medicine editorial staff as well as by an academic editor with relevant expertise and I am writing to let you know that we would like to send your submission out for external peer review.

However, before we can send your manuscript to reviewers, we need you to complete your submission by providing the metadata that is required for full assessment. To this end, please login to Editorial Manager where you will find the paper in the 'Submissions Needing Revisions' folder on your homepage. Please click 'Revise Submission' from the Action Links and complete all additional questions in the submission questionnaire.

Please re-submit your manuscript within two working days, i.e. by Aug 23 2022 11:59PM.

Login to Editorial Manager here: https://www.editorialmanager.com/pmedicine

Once your full submission is complete, your paper will undergo a series of checks in preparation for peer review. Once your manuscript has passed all checks it will be sent out for review.

Feel free to email us at plosmedicine@plos.org if you have any queries relating to your submission.

Kind regards,

Dr. Philippa Dodd, MBBS MRCP PhD

Senior Editor

PLOS Medicine

Decision Letter 1

Philippa Dodd

13 Dec 2022

Dear Dr. Chang,

Thank you very much for submitting your manuscript "Estimating health spending associated with chronic multimorbidity in 2018: an observational study among adults in the United States" (PMEDICINE-D-22-02788R1) for consideration at PLOS Medicine.

Your paper was evaluated by a senior editor and discussed among all the editors here. It was also discussed with an academic editor with relevant expertise, and sent to independent reviewers, including a statistical reviewer. The reviews are appended at the bottom of this email and any accompanying reviewer attachments can be seen via the link below:

[LINK]

In light of these reviews, I am afraid that we will not be able to accept the manuscript for publication in the journal in its current form, but we would like to consider a revised version that addresses the reviewers' and editors' comments. Obviously we cannot make any decision about publication until we have seen the revised manuscript and your response, and we plan to seek re-review by one or more of the reviewers.

In revising the manuscript for further consideration, your revisions should address the specific points made by each reviewer and the editors. Please also check the guidelines for revised papers at http://journals.plos.org/plosmedicine/s/revising-your-manuscript for any that apply to your paper. In your rebuttal letter you should indicate your response to the reviewers' and editors' comments, the changes you have made in the manuscript, and include either an excerpt of the revised text or the location (eg: page and line number) where each change can be found. Please submit a clean version of the paper as the main article file; a version with changes marked should be uploaded as a marked up manuscript.

In addition, we request that you upload any figures associated with your paper as individual TIF or EPS files with 300dpi resolution at resubmission; please read our figure guidelines for more information on our requirements: http://journals.plos.org/plosmedicine/s/figures. While revising your submission, please upload your figure files to the PACE digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email us at PLOSMedicine@plos.org.

We expect to receive your revised manuscript by Jan 03 2023 11:59PM. Please email us (plosmedicine@plos.org) if you have any questions or concerns.

***Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.***

We ask every co-author listed on the manuscript to fill in a contributing author statement, making sure to declare all competing interests. If any of the co-authors have not filled in the statement, we will remind them to do so when the paper is revised. If all statements are not completed in a timely fashion this could hold up the re-review process. If new competing interests are declared later in the revision process, this may also hold up the submission. Should there be a problem getting one of your co-authors to fill in a statement we will be in contact. YOU MUST NOT ADD OR REMOVE AUTHORS UNLESS YOU HAVE ALERTED THE EDITOR HANDLING THE MANUSCRIPT TO THE CHANGE AND THEY SPECIFICALLY HAVE AGREED TO IT. You can see our competing interests policy here: http://journals.plos.org/plosmedicine/s/competing-interests.

Please use the following link to submit the revised manuscript:

https://www.editorialmanager.com/pmedicine/

Your article can be found in the "Submissions Needing Revision" folder.

To enhance the reproducibility of your results, we recommend that you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. Additionally, PLOS ONE offers an option to publish peer-reviewed clinical study protocols. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols

Please ensure that the paper adheres to the PLOS Data Availability Policy (see http://journals.plos.org/plosmedicine/s/data-availability), which requires that all data underlying the study's findings be provided in a repository or as Supporting Information. For data residing with a third party, authors are required to provide instructions with contact information for obtaining the data. PLOS journals do not allow statements supported by "data not shown" or "unpublished results." For such statements, authors must provide supporting data or cite public sources that include it.

We look forward to receiving your revised manuscript.

Sincerely,

Philippa Dodd, MBBS MRCP PhD

PLOS Medicine

plosmedicine.org

-----------------------------------------------------------

Requests from the editors:

GENERAL

Please respond to all editor and reviewer comments detailed below, in full.

Please note reviewer comments below requiring the use of language which clearly clarifies your descriptions and definitions/categorizations

Please address the conceptualization issues identified

Thank you for reporting (we think!) according to RECORD – see below, please clarify.

Please review the guidance using the link below regarding reporting of studies:

http://www.equator-network.org/?post_type=eq_guidelines&eq_guidelines_study_design=economic-evaluations&eq_guidelines_clinical_specialty=0&eq_guidelines_report_section=0&s=

We suggest you report in line with RECORD (CHEERS is targeted to economic evaluations of interventions and STROBE is epidemiological reporting). Please provide the relevant completed checklist. In the checklist, please include sufficient text excerpted from the manuscript to explain how you accomplished all applicable items.

Please include the relevant associated checklist and indicate in your statement in the methods section where it can be located

DATA AVAILABLIITY STATEMENT

The Data Availability Statement (DAS) requires revision. For each data source used in your study:

a) If the data are freely or publicly available, note this and state the location of the data: within the paper, in Supporting Information files, or in a public repository (include the DOI or accession number).

b) If the data are owned by a third party but freely available upon request, please note this and state the owner of the data set and contact information for data requests (web or email address). Note that a study author cannot be the contact person for the data.

c) If the data are not freely available, please describe briefly the ethical, legal, or contractual restriction that prevents you from sharing it. Please also include an appropriate contact (web or email address) for inquiries (again, this cannot be a study author).

ABSTRACT

Please structure your abstract using the PLOS Medicine headings (Background, Methods and Findings, Conclusions).

Please combine the Methods and Findings sections into one section, “Methods and findings”.

Abstract Background: Provide the context of why the study is important. The final sentence should clearly state the study question.

Abstract Methods and Findings:

Please ensure that all numbers presented in the abstract are present and identical to numbers presented in the main manuscript text.

Please include the years during which the study took place, length of follow up, and clearly define the main outcome measures.

Please include the actual amounts and/or absolute risk(s) of relevant outcomes (including NNT or NNH where appropriate), not just relative risks or correlation coefficients. (Example for absolute risks: PMID: 28399126).

Please define the numerical values contained within square parentheses (UIs as per your main methods/results).

Please also quantify the main results with p values (as well as UIs)

Please include any important dependent variables that are adjusted for in the analyses.

In the last sentence of the Abstract Methods and Findings section, please describe the main limitation(s) of the study's methodology.

Abstract Conclusions:

Please address the study implications without overreaching what can be concluded from the data; the phrase "In this study, we observed ..." may be useful.

Please interpret the study based on the results presented in the abstract, emphasizing what is new without overstating your conclusions.

Please avoid vague statements such as "these results have major implications for policy/clinical care". Mention only specific implications substantiated by the results.

Please avoid assertions of primacy ("We report for the first time....")

AUTHOR SUMMARY

Thank you for including an author summary

Line 79: “Few studies have explored whether the combinations….” suggest “whether different combinations of conditions…” or something similar

Line 83: “16+ million…” suggest over 16 million

Line 95: “Multimorbidity adjustments should be done…” suggest performed in place of done

Please remove the data availability statement form the end of the author summary and include only in the manuscript submission form

INTRODUCTION

If there has been a systematic review of the evidence related to your study (or you have conducted one), please refer to and reference that review and indicate whether it supports the need for your study.

METHODS

Line 167: “…Strengthening the Reporting of Observational Studies in 168 Epidemiology (RECORD) guideline.” Should read, “REporting of studies Conducted using Observational Routinely collected health Data (RECORD) guideline.”

Please remove role of the funding source from the end of the methods section and include only in the manuscript submission form

FIGURES and TABLES

To improve accessibility to those with color blindness, please consider avoiding the use of green and/or red

Please provide an appropriate caption/legend for all figures and tables such that its contents are clearly described without the need to refer to the text.

Please provide a table showing the baseline characteristics of the study population

Table 1 (and throughout) where you report adjusted analyses, please also provide the unadjusted analyses for comparison, and please indicate in an appropriate caption or footnote which factors are adjusted for

Figures 1 and 2: are not very accessible to the reader – text overlies other text and makes it unreadable. The legend refers to sub-categories which the specific conditions presented in the graph fall into, this can be confusing to the reader. Please revise accordingly

Figure 3: in isolation, it is difficult to interpret what this figure shows. Is combination 1, 2, 3 (as referred to in the legend) the equivalent of single, dyads and triads (as referred to in the title)? Please revise to improve accessibility in-line with previous comments

Figure 4: please see reviewer comments which we agree with, and revise accordingly

DISCUSSION

Please remove the sub-heading conclusion such that the discussion reads as a continuous piece of prose

Please remove statements at line 602 and 603 and include only in the masncuript submission form

SUPPORTING INFORMATION

Please provide appropriate captions for all tables

Please provide p-values where 95% UIs are reported

Please provide unadjusted analyses where relevant and in the caption/footnote indicate which factors are adjusted for

Table A1 and A2: Please define GBD

Comments from the reviewers:

Reviewer #1: I enjoyed reading this paper, which is well-written and clearly organised. The study aims to (1) assess if disease combinations are super-additive, additive, or sub-additive in regard to health spending, and (2) estimate disease-specific health spending that accounts for multimorbidity. The first research aim is particularly relevant to policy and clinical practice as it may inform prioritization of disease combinations most likely to result in the highest healthcare spending. Using private insurance claims of 16m enrollees, the paper finds that 60% of them (pairs or triads) are super-additive. The chronic conditions with the highest multimorbidity-adjusted spending include CKD, cirrhosis, IHD, and inflammatory bowel disease. The authors claim that prioritizing interventions to reduce the prevalence and/or spending of these conditions could yield to cost-effective results. Below I provide some comments that the authors may consider to potentially improve the paper:

1. Conceptualisation of the health expenditure model:

* The paper offers no rationale for the specification of the health spending equation (equation 1, page 7). How did the authors choose the independent variables? Some sort of conceptual framework, specific to multimorbidity such as the one by Zulman et al 2014 on multimorbidity interrelatedness, could have guided this piece. How do the authors think that important variables such as disease severity, time since diagnosis, or total number of conditions may be confounding existing results?

* Why did the authors limit themselves to disease dyads and triads? Based on the characteristics of the study population this may be particularly relevant (94% of those with multimorbidity had more than three conditions). Did the authors at some point consider the possibility of characterising the actual disease combinations in the sample using cluster analysis?

2. Estimation of the health expenditure model:

* Which estimator was used in the stochastic gradient descent approach? How does this estimation approach account for the skewed (non-normal) distribution of health expenditures?

* How was goodness of fit of the model assessed? What percentage of the variability in individual health expenditures is this model able to explain?

3. Limitations of the sample used:

* The authors used a cross-sectional sample. Without adjusting for time since diagnosis or disease severity, the disease stage that the estimated expenditures pertain to is unclear.

* How is the study sample different from a US nationally representative sample? On page 5, the authors state that differences have not been assessed before but I wonder if they could be at least approximated by comparisons to publicly available sources. How could the disease prevalence of a subsample of commercially insured enrolled differ from a nationally representative sample? I think this is an important point to understand the usability and generalisability of study findings.

4. Consideration on study definitions:

* What is the rationale behind not restricting claims to primary diagnosis to generate a more accurate estimate of the cost of a chronic condition? (page 6, lines 205-206). Does that mean that under the cost of CKD, costs of acute events are also included?

5. Other conceptualisation issues:

* In my opinion, how generating multimorbidity-adjusted health expenditure estimates for *individual* chronic conditions helps understanding the economic burden of multimorbidity could be more clearly articulated. The paper seems focused on multimorbidity, yet its conclusions apply to individual conditions. How do the conclusions of this paper then relate to the design of interventions to improve health outcomes of individuals with multimorbidity?

* The authors only considered costs but not health outcomes, so the conclusion on cost-effectiveness towards the end is hard to follow and unclear how it can be drawn from the study results.

Other comments:

* From what perspective was annual spending computed? It seems to include provider payments but exclude out-of-pocket expenditures incurred by the beneficiary? What is the rationale behind this choice and how does that affect your disease-specific expenditure estimates?

* How could spending data be negative (line 184, page 6)?

Reviewer #2: Reviewer's comments

1. Summary of the research and general comment:

This is an interesting and topical multimorbidity study, which estimated the costs of disease combinations and explored the interaction of co-existing conditions within an individual and their impact on costs. The study is very well structured, with a large sample size and number of disease combinations.

The main limitations are that the study did not capture cost components beyond outpatient and inpatient services and unable to account for changes through time; however these are well acknowledged in the limitation. The methods section relating to the decomposition of the change in multimorbidity-adjusted spending can be more elaborative.

In general, writing up a paper on the topic of (the cost of) multimorbidity is challenging. It is easy for readers to get lost and confuse themselves amidst the myriads of jargons, the overwhelming number of ways diseases are combined, and all the different ways of expressing the same term (e.g. when referring to the cost of a condition, it is important to emphasize whether the author is referring to a condition as part of a disease combination or a single condition by itself; etc.)

In light of such complexities, phrasing should be as accurate and consistent as possible and details on methodology, terminologies should be elaborated as much as possible, to enable readers (who are not experts on multimorbidity) to easily follow. It is commendable that the author gave various examples of specific conditions/dyads throughout the paper. It would be helpful to be a bit more elaborative in places (see points below), and to be consistent with the choice of terms.

2. Discussion of specific areas for improvement:

A. Major comments:

1. Line 190-192: Can the author explain why injuries were excluded from the list of chronic conditions? For example, hip fracture rates in the US are amongst the highest in the world and links to long-term disability outcomes, similar to stroke.

2. Line 301-305, the author described the third and fourth step in estimating spending associated with each individual health condition, adjusting for multimorbidity. It will be beneficial to the readers if the author explains the reasons for undertaking these steps. Perhaps, the author can also demonstrate this using an equation.

3. Can the author elaborate more in the method section what they specifically did to arrive at the estimates for the total spending associated with combinations?

4. Did the author log-transform cost, or how did the author address non-linearity/non-normality/unequal variance in the data?

5. Line 420-427: "Decomposition of the change in multimorbidity-adjusted spending by the type of combination (single, dyads, and triads) for conditions with the highest spending per treated case". To the reviewer's understanding, this is the spending on single conditions, when taking into account other co-morbidities. For example in the case of CKD, is the below the correct interpretation of this finding?

* For MM-adjusted spending for CKD, less than 25% is attributed to the base cost itself (in the case of an individual with only 1 condition, i.e. CKD). The yellow stripe (which represents around 50% of the total), is the increase in cost of CKD due to the interaction with the second condition - in the case of dyad. The red (which represents over 25% of the total), is the increase in cost of CKD due to the interaction with a third condition - in the case of triad.

* Does it imply that individuals with only 1 condition (CKD only) will incur lower cost than the adjusted estimate above and proportionate to the green stripe in the graph?

* Is this the increase 'on average'? For example, if CKD is comorbid with 2 other conditions (triad), the increase in CKD cost is the same on average and not particular to any specific conditions?

The reviewer advises that the author describes more in this section, to help readers understand what is being explored. If the above bullet points are the correct way to interpret this result, perhaps the author can consider elaborating it in such a way - citing the specific breakdowns (25%, 50%,…) as an example.

6. Line 429: "Comparing pre- and post-multimorbidity adjustment spending estimates, we found that 50 conditions (among 63) had higher spending after adjustments, 7 had less than 5% difference, and 6 had lower spending (Table 1)."

The author mentions pre-adjusted costs but has not presented these anywhere, or how it was calculated. The reviewer deems this necessary, especially for the latter (to be included in the method section).

7. Line 442: "In other words, among these diseases, estimated multimorbidity-adjusted spending are at least twice higher than the non-adjusted spending estimates."

- By "non-adjusted", is the author referring to the average cost of this specific condition among those with only 1 condition (base cost)?

- By "twice higher", does the author mean "double"? The reviewer suggests that the author rephrases "twice higher" to "double" for more accuracy and clarity.

- The author may also consider revising Line 442-443 as follow, so as to clearly distinguish between the spending for individual conditions and the spending for combinations.

"In other words, the estimated multimorbidity-adjusted spending for these individual diseases are at least, double that of their respective non-adjusted estimates."

8. Similarly, for Line 443: "For chronic kidney disease, we observe an increase of more than three times", while the reviewer understands the point, it may be a bit ambiguous to others. The author may consider revising this sentence to:

"For chronic kidney disease, spending increased fourfold after MM-adjustment."

(This is a safe way to phrase and unlikely to be misinterpreted.)

9. Line 438-448:

For this section, the reviewer would also like to clarify for enhanced understanding:

* In the example of CKD, the different colors show the increase in cost for CKD when CKD is comorbid with other conditions. For example, when comorbid with "other NCD" (bright green), the cost of CKD doubles that of the base cost (the base cost is the cost of CKD in the case of an individual with only 1 condition, i.e. CKD). Is this the correct way to understand?

* Is the change in CKD cost different when it is comorbid with 2 other conditions simultaneously instead of 1 (in the case of triads)? For example, when CKD is comorbid with both CVD and 'other NCD' at the same time, is the increase in cost of CKD simply additive of the thickness of their respective stripes?

10. Line 446: "For cancers, we see that other cancers account for the largest share of increases, and specifically for brain and nervous system cancer we also see a large contribution from neurological disorders."

- By 'other cancers', the reviewer assumes the author is referring to 'neoplasms' in Figure 3, however 'neoplasms' may be benign (not cancer) or malignant (cancer). The author should refrain from using the term 'other cancers'.

11. It would be useful if the author also presented in the Appendix the estimated spending for all disease combinations with a prevalence rate greater than 100 per 100,000 (or a higher threshold, in case the number of combinations is too high).

12. The estimated spending for disease combinations reported in the paper are on average much lower than those reported in other studies from the US (see 10.1186/s12916-022-02427-9), some of which also analyzed MarketScan data. Does the author have more thoughts on why that is?

13. Exploring the distribution of cost components (i.e., outpatient vs inpatient) of costly disease combinations would also be useful in identifying the driver of high costs. This is particularly relevant in the discussion, where the author discusses the potential reasons for super-additive spending.

14. The strengthening of the integrated primary care system is an important intervention to target as the burden of multimorbidity increases. It would be relevant to mention this alongside prioritizing prevention, in the Author Summary (Line 94-99). The author has mentioned service coordination, patient-provider communication in the discussion, and these are aspects of integrated care. In addition, provider-provider communication and self-management are important aspects to also consider. Provider financing models (fee-for-service vs capitation) may also affect the level of service utilization/cost.

15. Line 481-483: Here it would be useful to give an example of triads or dyads that had sub-additive spending.

B. Minor comments:

1. Line 167-168: Please cite the RECORD guideline.

2. Line 198: Please remove "to".

3. The "==" in equation 3 should just be "=".

4. Line 377-380: Are the reported costs in brackets total or incremental? If they are indeed incremental (i.e. the overall increase in cost due to the interaction of the component diseases), then perhaps the author should clearly specify that, and also add a "+" before each Dollar sign.

E.g. blood cancers + hemoglobinopathies and hemolytic anemias (henceforth anemias) (+$3227, 95%UI [2541-3905]).

5. Line 382: Please add '$' to "cirrhosis + hyperlipidemia (-610 [-838- -370])" for consistency.

6. Line 384: Please revise '$-' to '-$' in "hyperlipidemia ($-545 [-727- -363])" for consistency.

7. Line 422: Consider changing "size" to "sizes".

8. Line 473: Please revise "point to" to "have pointed to".

9. The reviewer finds the style of visualization in Figure 1 a bit difficult to follow.

10. For Figure 4, please name the ten graphs from A to J for ease of referencing.

11. Figure 4:

* Each graph gives the false impression that it represents the proportions of cost of various conditions co-existing in the same individual. Readers may have to refer to the main text to understand. In theory, graphs and charts should be self-explanatory; readers should be able to infer from them immediately without having to read the main text. If this is the most optimal way to visualize the result, the author may want to be more descriptive in the main text (as suggested in the points made above) as well as add a short sentence on what is going on in the graphs/what was done to get there (also for Figure 3).

* The bright red and/or dark orange stripe are often small and shadowed by the dark red bar (due to the color palette, and as these stripes tend to be very thin), the author may consider changing the bright red/dark orange to other distinctive colors or change the orders of the colors so that distinctive colors are next to each other.

* In the legend, dark orange refers to both diabetes and CKD merged together. In the first graph for CKD, is it correct that there is a thin dark orange stripe that represents both Diabetes and CKD? If yes, would there be an overlap here? If that stripe is actually not dark orange, but a bright red stripe (these two colors cannot be distinguished by the reviewer, as it is thin and shadowed by the dark red color of CVD), then is Diabetes missing from this graph? Where in fact, does the Diabetes and CKD stripe (dark orange) appear across the 10 graphs?

Reviewer #3: This study explores the relationship between multimorbidity and spending on inpatient and outpatient care among adults in the US.

Comments:

"This study is reported following the Strengthening the Reporting of Observational Studies in 168 Epidemiology (RECORD) guideline."

Can the authors please clarify if they followed STROBE or RECORD guidelines here?

Can the authors also please supply the associated checklist in the supplementary material?

"This study took a person-based regression approach - regressing a person's total 2018 health spending on health conditions indicators - in estimating spending per treated case [28,29]. We applied the following linear regression model:... "

and

"we applied a regression framework using the stochastic gradient descent (SGD) approach... we applied a lasso penalized regression model to shrink the coefficient values of these covariates"

and

"To ensure stability of the model results, we conducted 50 SGD model runs and bootstrapped the results across runs for 10,000 times to get the estimates for all coefficients"

The authors have applied technically appropriate methods, which they describe clearly within the article.

Similarly, the authors have conducted rigorous and comprehensive models for "Estimating spending associated with each individual health condition, adjusting for multimorbidity".

"First, to generate 95% uncertainty interval (UI) for spending associated with disease combinations, we bootstrapped the means from all the model runs for 10,000 times. Second, to generate UI for spending associated with single conditions, we ran Monte Carlo simulations (n=1,000 draws) while varying the estimates associated with the combination and the proportion of combination attributed to each single condition."

The authors have conducted suitable analyses to help demonstrate the uncertainty and robustness of the study findings.

Overall, the authors have communicated the study Results accurately and the main study limitations have been suitably addressed in the Discussion.

Furthermore, the authors provide satisfactorily detailed methods and results in the supplementary material.

Any attachments provided with reviews can be seen via the following link:

[LINK]

Decision Letter 2

Philippa Dodd

9 Feb 2023

Dear Dr. Chang,

Thank you very much for re-submitting your manuscript "Estimating health spending associated with chronic multimorbidity in 2018: an observational study among adults in the United States" (PMEDICINE-D-22-02788R2) for review by PLOS Medicine.

I have discussed the paper with my colleagues and the academic editor and it was also seen again by 2 reviewers. I am pleased to say that provided the remaining editorial and production issues are dealt with we are planning to accept the paper for publication in the journal.

The remaining issues that need to be addressed are listed at the end of this email. Any accompanying reviewer attachments can be seen via the link below. Please take these into account before resubmitting your manuscript:

[LINK]

***Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.***

In revising the manuscript for further consideration here, please ensure you address the specific points made by each reviewer and the editors. In your rebuttal letter you should indicate your response to the reviewers' and editors' comments and the changes you have made in the manuscript. Please submit a clean version of the paper as the main article file. A version with changes marked must also be uploaded as a marked up manuscript file.

Please also check the guidelines for revised papers at http://journals.plos.org/plosmedicine/s/revising-your-manuscript for any that apply to your paper. If you haven't already, we ask that you provide a short, non-technical Author Summary of your research to make findings accessible to a wide audience that includes both scientists and non-scientists. The Author Summary should immediately follow the Abstract in your revised manuscript. This text is subject to editorial change and should be distinct from the scientific abstract.

We expect to receive your revised manuscript within 1 week. Please email us (plosmedicine@plos.org) if you have any questions or concerns.

We ask every co-author listed on the manuscript to fill in a contributing author statement. If any of the co-authors have not filled in the statement, we will remind them to do so when the paper is revised. If all statements are not completed in a timely fashion this could hold up the re-review process. Should there be a problem getting one of your co-authors to fill in a statement we will be in contact. YOU MUST NOT ADD OR REMOVE AUTHORS UNLESS YOU HAVE ALERTED THE EDITOR HANDLING THE MANUSCRIPT TO THE CHANGE AND THEY SPECIFICALLY HAVE AGREED TO IT.

Please ensure that the paper adheres to the PLOS Data Availability Policy (see http://journals.plos.org/plosmedicine/s/data-availability), which requires that all data underlying the study's findings be provided in a repository or as Supporting Information. For data residing with a third party, authors are required to provide instructions with contact information for obtaining the data. PLOS journals do not allow statements supported by "data not shown" or "unpublished results." For such statements, authors must provide supporting data or cite public sources that include it.

To enhance the reproducibility of your results, we recommend that you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. Additionally, PLOS ONE offers an option to publish peer-reviewed clinical study protocols. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols

Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript.

Please note, when your manuscript is accepted, an uncorrected proof of your manuscript will be published online ahead of the final version, unless you've already opted out via the online submission form. If, for any reason, you do not want an earlier version of your manuscript published online or are unsure if you have already indicated as such, please let the journal staff know immediately at plosmedicine@plos.org.

If you have any questions in the meantime, please contact me or the journal staff on plosmedicine@plos.org.  

We look forward to receiving the revised manuscript by Feb 16 2023 11:59PM.   

Sincerely,

Philippa Dodd, MBBS MRCP PhD

PLOS Medicine

plosmedicine.org

------------------------------------------------------------

Requests from Editors:

GENERAL

Thank you for your considerate and detailed responses to previous editor and reviewer requests. Please see below for further revisions which we require you address in full.

ABSTRACT

Line 72: please remove this statement and include only in the manuscript submission form

AUTHOR SUMMARY

Line 79: we would advise against the use of the word “anecdotally” perhaps, “Many would agree…” or something similar. Please revise. In addition, perhaps “…directed towards…” instead of “…focused on…”

Line 86: Please revise this statement for clarity and improved accessibility to the reader

INTRODUCTION

Line 156: “…to date, no study…” suggest the addition of “to our knowledge” as claims of supremacy can be risky

Line 162: “For example, we would have a more accurate spending on stroke because we would have not only the stroke-specific spending but also the additional or reduced amount of spending stroke incurs when in combination with other conditions.” Suggest moving this statement to an appropriate part of the methods section as it justifies/explains the benefit of the adjustment, as we understand things.

STATISTICAL REPORTING

Line 390: “…anemias (+$3111 [2679-3535])…” and line 393: “…hyperlipidemia (-$733 [-851- -620])…” I note the use of hyphens as well as the reporting of negative values which could be confusing to the reader. Suggest the use of commas instead

REFERENCES

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Comments from Reviewers:

Reviewer #2: The author has acknowledged, addressed and/or responded well to issues highlighted by the reviewer. The reviewer has no further comments/suggestions and congratulates the authors on this important study.

Reviewer #3: Many thanks to the authors for responding to each comment in turn.

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Decision Letter 3

Philippa Dodd

20 Feb 2023

Dear Dr Chang, 

On behalf of my colleagues and the Academic Editor, Professor Aaron Kesselheim, I am pleased to inform you that we have agreed to publish your manuscript "Estimating health spending associated with chronic multimorbidity in 2018: an observational study among adults in the United States" (PMEDICINE-D-22-02788R3) in PLOS Medicine.

Before we can publish your manuscript, we require that you make the following amendment:

* Line 403 "($4961 [4381-5483])" please replace the hyphen with a comma.

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Thank you again for submitting to PLOS Medicine. We look forward to publishing your paper. 

Best wishes,

Pippa 

Philippa Dodd, MBBS MRCP PhD 

PLOS Medicine

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 RECORD Checklist. RECORD checklist.

    (DOCX)

    S1 Appendix. Technical appendix.

    Table A1. List of most-detailed GBD causes determined as chronic conditions. Table A2. Chronic conditions and its most-detailed GBD causes. Table A3. Summary statistics of 50 SGD model runs. Table A4. Summary statistics of study population. Table A5. Covariates and their regression coefficients. Table A6. Observed prevalence and estimated multimorbidity-adjusted annual spending per treated case for the “other” conditions. Table A7. Regression coefficients for disease combinations with prevalence rate of greater than 100 per 100,000 (ordered by spending).

    (DOCX)

    Attachment

    Submitted filename: plosmed_RR_dec2022.docx

    Data Availability Statement

    Data used in this paper cannot be made available due to contractual restrictions but can be purchased from IBM MarketScan Research Database. It provides claim-level health care information on millions of commercially insured enrollees below age 65. Contact can be made through this website: https://www.merative.com/contact.


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