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. 2016 Dec;138(6):e20161809. doi: 10.1542/peds.2016-1809

Use of Low-Value Pediatric Services Among the Commercially Insured

Kao-Ping Chua a,b,, Aaron L Schwartz c, Anna Volerman a,d, Rena M Conti b,e, Elbert S Huang d
PMCID: PMC5127068  PMID: 27940698

Abstract

BACKGROUND:

Claims-based measures of “low-value” pediatric services could facilitate the implementation of interventions to reduce the provision of potentially harmful services to children. However, few such measures have been developed.

METHODS:

We developed claims-based measures of 20 services that typically do not improve child health according to evidence-based guidelines (eg, cough and cold medicines). Using these measures and claims from 4.4 million commercially insured US children in the 2014 Truven MarketScan Commercial Claims and Encounters database, we calculated the proportion of children who received at least 1 low-value pediatric service during the year, as well as total and out-of-pocket spending on these services. We report estimates based on "narrow" measures designed to only capture instances of service use that were low-value. To assess the sensitivity of results to measure specification, we also reported estimates based on "broad measures" designed to capture most instances of service use that were low-value.

RESULTS:

According to the narrow measures, 9.6% of children in our sample received at least 1 of the 20 low-value services during the year, resulting in $27.0 million in spending, of which $9.2 million was paid out-of-pocket (33.9%). According to the broad measures, 14.0% of children in our sample received at least 1 of the 20 low-value services during the year.

CONCLUSIONS:

According to a novel set of claims-based measures, at least 1 in 10 children in our sample received low-value pediatric services during 2014. Estimates of low-value pediatric service use may vary substantially with measure specification.


What’s Known on This Subject:

Claims-based measures of “low-value” pediatric services could facilitate the implementation of interventions to reduce the provision of unnecessary care to children. Few such measures have been developed. The extent and financial burden of low-value pediatric service use are unknown.

What This Study Adds:

Using novel claims-based measures of 20 low-value pediatric services and claims from 4.4 million commercially insured children, at least 1 in 10 children in our sample received a low-value pediatric service during 2014.

Recent high-profile initiatives such as Choosing Wisely have highlighted the importance of avoiding “low-value” pediatric health care services that typically do not improve child health.1 Reducing the use of these services could prevent iatrogenic harm (eg, radiation exposure from imaging tests)2 while decreasing unnecessary financial burden on families and the health care system.311 Improving the efficiency of pediatric care is an increasingly important policy goal given the rapid rise in pediatric health care expenditures12 as well as the proliferation of alternative payment models such as pediatric accountable care organizations (ACOs), which incentivize providers to judiciously use resources and enhance the quality of care.1318

Large-scale analyses of overuse can be facilitated by measures that directly assess low-value pediatric service use in insurance claims databases.48 These measures exploit the relative strengths of claims data, including their large sample sizes, longitudinal nature, widespread availability, and inclusion of utilization across multiple providers and care settings.3,4 Using 1 such set of measures, for example, Schwartz et al4 found that 25% to 42% of elderly Medicare beneficiaries received at least 1 of 26 low-value services in 2009, resulting in $1.9 billion to $8.5 billion in spending. A subsequent study used these measures to report reduced use of certain low-value services after implementation of the Medicare Pioneer ACO model.6

To date, however, few claims-based measures of low-value pediatric services have been developed. Furthermore, the extent and financial burden of low-value pediatric service use are unknown. To address these gaps, we developed a novel set of claims-based measures for 20 low-value pediatric services that occur across a variety of conditions and settings. We used these measures and a large claims database to estimate use of and spending on the 20 services among 4.4 million commercially insured US children in 2014.

Methods

Construction of Low-Value Service Measures

In fall 2015, members of our research team of pediatricians and health services researchers compiled a candidate list of low-value pediatric services by reviewing >400 recommendations from the Choosing Wisely initiative, recommendations from the US Preventive Services Task Force and the United Kingdom’s National Institute for Health and Care Excellence, child-focused evidence reports from the Cochrane Collaboration, clinical practice guidelines published by US medical specialty societies such as the Infectious Diseases Society of America, and peer-reviewed literature.1956 Based on this review, we identified several hundred low-value pediatric services, including services that cause more harm than benefit (eg, cough and cold medicines for young children) and services that typically do not improve child health (eg, Papanicolaou tests). From this list, we excluded services that could not be easily identified as low-value in claims due to the lack of necessary clinical information (eg, head imaging for minor head trauma), as well as services that were likely to be infrequent among children (eg, electroencephalograms for headache).

We ultimately selected 20 pediatric services that could be identified as low-value in claims data, including 6 diagnostic tests, 5 imaging tests, and 9 prescription drugs. We constructed claims-based measures of these 20 services based on data elements that are typically contained in US insurance claims data, including: International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) diagnosis and procedure codes; Current Procedural Terminology codes; and demographic information. Our measures assessed low-value service use in primary care offices, hospital outpatient departments, urgent care centers, retail clinics, emergency departments, community hospitals, and academic children’s hospitals.

For the main analysis, we constructed “narrow measures” that included multiple restrictions to only capture instances of service use that were low-value, potentially at the expense of missing some instances of low-value service use. For many of the narrow measures, we employed a modified version of a widely used administrative algorithm to exclude services received by children with a “complex chronic condition” (eg, congenital anomalies, dependence on technology, cancer).57 These children are excluded from many clinical practice guidelines, and assessment of care appropriateness for these children may be difficult without detailed clinical information. Other restrictions were based on relevant studies, guidelines, and reports identifying each service as low-value (Table 1).1956 The codes used in each measure are presented in Supplemental Information.

TABLE 1.

Claims-Based Measures of 20 Low-Value Pediatric Services

Service No. Service Source Justification Broad Measure Definition Narrow Measure Definition (Additional Exclusions) Denominator
1 Population-based screening for vitamin D deficiency CW Because vitamin D deficiency is common, healthy patients at risk should take supplements instead of being tested. Screening is useful for very high-risk patients when laboratory values will be used to determine the aggressiveness of supplementation24,25 25-hydroxy vitamin D blood test (1) No diagnosis potentially warranting testing on day of test or prior claimsa (osteomalacia, rickets, hyperparathyroidism, osteoporosis, pathologic fracture, obesity, sarcoidosis, hepatic failure, chronic kidney disease, inflammatory bowel disease, cystic fibrosis, celiac disease, failure to thrive, malnutrition, eating disorder, developmental motor delay, long-term glucocorticoid use) All children
(2) No diagnosis of vitamin D deficiency in prior claimsa
(3) No diagnosis indicating pregnancy on day of test
(4) Exclude children with complex chronic conditionsb (eg, children with risk factors for severe vitamin D deficiency such as malabsorption or poor nutrition)
2 Skin prick test or IgE blood tests in children with atopic dermatitis CW Patch testing is more useful for evaluating atopic dermatitis than skin prick tests or IgE blood tests26,27 Skin prick test or allergen-specific IgE blood test and diagnosis of atopic dermatitis on day of test (1) No other diagnoses potentially warranting testing on day of test (food allergy, anaphylaxis, asthma, allergic or chronic rhinitis, allergic conjunctivitis, allergic colitis/gastroenteritis, history of penicillin allergy) Children with a diagnosis of atopic dermatitis during the year
3 Testing for RSV in children with bronchiolitis AAP Testing is only indicated in the rare situation in which knowledge of the etiologic agent would change clinical management28 Test for RSV (eg, rapid RSV test) or respiratory viral panel and diagnosis of bronchiolitis on day of test (1) Exclude infants aged <90 d (may be part of a sepsis evaluation) Children with a diagnosis of bronchiolitis during the year
(2) Exclude testing associated with hospitalizationc (may be required for cohorting patients per hospital policy)
(3) Exclude children who received Synagis prophylaxis in the prior 30 d (breakthrough RSV infection may prompt discontinuation of prophylaxis)
(4) Exclude children with complex chronic conditionsb (could influence decision to initiate influenza therapy in these high-risk patients)
4 Blood tests in children with a simple febrile seizure AAP Electrolyte levels are often abnormal in children with simple febrile seizures; incidence of bacteremia is not increased in children with simple febrile seizures29 Blood cell count or electrolytes and diagnosis of simple febrile seizure on day of test (1) Exclude infants aged <1 y (blood cell count may be part of an evaluation for central nervous system infections in this age group) Children with a diagnosis of simple febrile seizure during the year
(2) No diagnosis for complex febrile seizure, vomiting/diarrhea, or dehydration on day of test (could warrant blood or electrolyte testing)
(3) Exclude testing associated with hospitalizationc
(4) Exclude children with complex chronic conditionsb (eg, children with epilepsy or congenital neurologic anomalies)
5 Cervical cancer screening with human papillomavirus test or Papanicolaou test in children CW Evidence does not support cervical cancer screening before age 21 y in most cases30,31 Human papillomavirus test or Papanicolaou test (1) No diagnosis potentially warranting testing on day of test or prior claima (abnormal Papanicolaou test result, dysplasia, or malignancy of cervix/vagina/vulva) Female children aged ≥14 y
USPTF (2) Exclude children with complex chronic conditionsb (eg, children with HIV or other immunodeficiency)
6 Testing for group A streptococcal pharyngitis in children aged <3 y IDSA Streptococcal pharyngitis (and therefore acute rheumatic fever) are rare before age 3 y32 Test for group A streptococcal pharyngitis (eg, rapid streptococcal test or throat culture) in children aged <3 y (1) Exclude testing associated with hospitalizationc Children aged <3 y
(2) No diagnosis indicating exposure to communicable diseases on day of test (eg, sick contact with strep throat)
(3) Exclude children with complex chronic conditionsb (eg, children with immunodeficiency)
7 Face or nose radiograph in children with head or face trauma CW Radiographs are not sensitive for the detection of facial or nasal fractures in children; CT scans are preferred3335 Radiographs of face or nose and diagnosis of head or face trauma on same day of test No additional restrictions Children with a diagnosis of head or face trauma during the year
8 Ultrasound in children with cryptorchidism CW Ultrasound is neither sensitive nor specific for localizing nonpalpable testes3638 Ultrasound of scrotum, pelvis, abdomen, or retroperitoneum and diagnosis of cryptorchidism on day of test (1) Exclude imaging in neonates aged ≤28 d (ultrasound may be part of an evaluation for a disorder of sex development in neonatal period) Children with a diagnosis of cryptorchidism during the year
(2) No diagnosis potentially warranting imaging on day of test or prior claima (eg, indeterminate sex, adrenogenital disorder, hypospadias, obesity)
9 Sinus imaging in children with acute sinusitis CW Sinus imaging is not routinely necessary to diagnose acute sinusitis39 Paranasal sinus radiograph, maxillofacial CT scan, or face MRI and diagnosis of acute sinusitis on day of test (1) No diagnosis of acute sinusitis between 180 and 30 d before imaging Children with a diagnosis of acute sinusitis during the year
(2) No diagnosis of chronic sinusitis on day of imaging or prior 180 d
(3) No other diagnosis potentially warranting imaging on day of test (orbital cellulitis, cranial nerve palsy, meningismus, seizures, visual disturbances, exophthalmos, altered mental status, nasal polyps)
(4) Exclude imaging associated with hospitalizationc
(5) Exclude children with complex chronic conditionsb (eg, children with cystic fibrosis or immunodeficiency)
10 Neuroimaging in children with a simple febrile seizure AAP Evidence does not support need to routinely obtain neuroimaging in children with simple febrile seizures; neuroimaging may involve risks of radiation exposure or procedural sedation29 Head CT or brain MRI and diagnosis of simple febrile seizure on day of test (1) No other diagnosis potentially warranting imaging on day of test (complex febrile seizure, focal neurologic examination abnormalities, head/face trauma) Children with a diagnosis of simple febrile seizure during the year
(2) Exclude imaging associated with hospitalizationc
(3) Exclude children with complex chronic conditionsb (eg, children with epilepsy, congenital neurologic anomalies, ventriculoperitoneal shunt)
11 Neuroimaging in children with headache CW Results of neuroimaging are typically negative in the absence of risk factors for structural disease4244 Head CT or brain MRI scan and diagnosis of headache on day of test (1) No diagnosis potentially warranting imaging on day of test (convulsions, syncope, head/face trauma, posttraumatic headache, complicated headache syndromes, bleeding disorders, history of stroke, focal neurologic examination abnormalities) Children aged ≥12 y with a diagnosis of headache during the year
(2) Exclude imaging associated with hospitalizationc
(3) Exclude children with complex chronic conditionsb (eg, children with cancer or hydrocephalus)
12 Cough and cold medications in children aged <6 y CW Evidence does not support efficacy; concerns about side effects45,46 Drug claim for cough or cold medicationd in children aged <6 y No additional exclusions Children aged <6 y
CC
13 Oral antibiotics for acute upper respiratory infections CW Evidence does not support efficacy; concerns about side effects and antibiotic resistance47 Drug claim for oral antibiotics within 3 d of a diagnosis of acute upper respiratory infection No other diagnosis potentially warranting oral antibiotics on the same day of the index diagnosis of acute upper respiratory infection or in the following 3 de Children with a diagnosis of acute upper respiratory infection during the year
CC
NICE
14 Oral antibiotics for acute OME CW Evidence does not support efficacy; concerns about side effects and antibiotic resistance48,49 Drug claim for oral antibiotic within 3 d of a diagnosis of acute OME (1) No other diagnosis potentially warranting oral antibiotics on the same day of the index diagnosis of acute OME or in the following 3 de Children with a diagnosis of acute OME during the year
CC (2) No diagnosis of acute OME between 180 and 90 d before the index diagnosis
NICE (3) No diagnosis of chronic OME on the day of the index diagnosis or in the prior 180 d
15 Oral antibiotics for acute otitis externa CW Otic antibiotics are the first-line therapy for acute otitis externa50 Drug claim for oral antibiotic within 3 d of a diagnosis of acute otitis externa (1) No other diagnosis potentially warranting oral antibiotics on the same day of the index diagnosis of acute otitis externa or in the following 3 de Children with a diagnosis of acute otitis externa during the year
(2) No diagnosis of acute otitis externa during the 30 d before the index diagnosis
(3) No diagnosis of chronic or malignant otitis externa on the same day of the index diagnosis or during the prior 180 d
(4) Exclude children with complex chronic conditionsb (eg, children with immunodeficiency)
16 Oral antibiotics after tonsillectomy CW Evidence does not support efficacy; concerns about side effects and antibiotic resistance51,52 Drug claim for oral antibiotic within 3 d of tonsillectomy (1) No other diagnosis potentially warranting oral antibiotics on the same day of the tonsillectomy or in the following 3 de Children undergoing tonsillectomy during the year
CC (2) Exclude children with complex chronic conditionsb (eg, children requiring endocarditis prophylaxis due to heart disease or implants)
17 Oral antibiotics for bronchiolitis AAP Evidence does not support efficacy; concerns about side effects and antibiotic resistance53 Drug claim for oral antibiotic within 3 d of a diagnosis of bronchiolitis (1) No other diagnosis potentially warranting oral antibiotics on the same day of the index diagnosis of bronchiolitis or in the following 3 de Children with a diagnosis of bronchiolitis during the year
NICE
18 Oral corticosteroids for bronchiolitis CW Evidence does not support efficacy; concerns about side effects28 Drug claim for oral corticosteroid within 3 d of a diagnosis of bronchiolitis (1) Exclude children with complex chronic conditionsb (eg, children taking steroids for other conditions) Children with a diagnosis of bronchiolitis during the year
AAP
CC
NICE
19 Short-acting β-agonists for bronchiolitis CW Evidence does not support efficacy; concerns about side effects28,53 Drug claim for inhaled short-acting β-agonist within 3 d of a diagnosis of bronchiolitis (1) Limit to first-time wheezing (defined as no diagnosis of wheezing, bronchiolitis, or asthma before the index diagnosis of bronchiolitis) Children with a diagnosis of bronchiolitis during the year
CC (2) Exclude children with complex chronic conditionsb (eg, patients with chronic lung disease)
NICE
20 Acid blockers for infants with uncomplicated gastroesophageal reflux CW Reflux in infancy is most often physiologic and does not require treatment; little is known about safety of proton pump inhibitors, particularly in infants5456 Drug claim for oral histamine2-blocker or oral proton pump inhibitor in infants aged <1 y (1) No diagnosis potentially warranting acid blockade on the same day of drug claim or in prior claima (failure to thrive, weight loss, underweight, irritability, excessive crying, apnea, apparently life-threatening event, gastritis, peptic ulcer, gastrointestinal bleed) Infants aged <1 y
NICE (2) Exclude children with complex chronic conditionsb (eg, children with risk factors for severe gastroesophageal reflux disease such as neurologic impairment)

AAP, American Academy of Pediatrics; CC, Cochrane Collaboration; CT, computed tomography; CW, Choosing Wisely; IDSA, Infectious Diseases Society of America; IgE, immunoglobulin E; NICE, National Institute for Health and Care Excellence; OME, otitis media with effusion; RSV, respiratory syncytial virus; USPTF, US Preventive Task Force.

a

Refers to all claims from January 1, 2013, until the day before the service.

b

Defined as children with an ICD-9 diagnosis or procedure code indicating a complex chronic condition on any claim from January 1, 2013, until the day of the service; codes were based on a widely used algorithm (see Feudtner et al57).

c

Defined as a test occurring on or between the admission and discharge dates for a hospitalization.

d

Defined as medications containing pseudoephedrine, phenylephrine, guaifenesin, dextromethorphan, brompheniramine, chlorpheniramine, homatropine/hydrocodone, codeine/promethazine, and codeine/pyrilamine. Diphenhydramine was excluded because it is commonly used for indications other than cough and cold.

e

Bacterial infections such as acute suppurative otitis media, urinary tract infection, pneumonia, and cellulitis.

To assess whether the amount of detected low-value service use varies with measure specification, we also created broad versions of our 20 measures, following previously published studies in the adult population.4 These “broad measures” contained minimal restrictions and were designed to capture most instances of service use that were low-value, potentially at the expense of misclassifying some instances of appropriate service use as low-value.

For each measure, we defined a denominator population of children who could potentially receive the service (eg, children with a diagnosis of bronchiolitis for the low-value bronchiolitis measures). For denominator populations based on age cutoffs (eg, children aged <3 years), we used age as of January 1, 2014. In a sensitivity analysis, results were not substantially altered when using age as of December 31, 2014 (Supplemental Information).

Data Source and Study Design

We conducted a cross-sectional analysis of the 2014 Truven MarketScan Commercial Claims and Encounters database, a convenience sample of claims data from >47 million US residents aged 0 to 64 years with employer-sponsored private health insurance. Because many measures excluded children with specific diagnosis or procedure codes in previous claims, we used the 2013 MarketScan database as a “look-back period” for the 2014 analyses.

Study Population

There were 12.2 million children aged 0 to 18 years in the 2014 MarketScan database. To ensure a sufficiently long look-back period for each instance of service use, we limited the sample to children who were born before 2013 and continuously enrolled for 365 days in 2013 and 2014, or born in 2013 or 2014 and continuously enrolled until the end of 2014. Of the resulting 6 374 551 million children, we excluded 1 336 938 million children whose prescription drug claims were not included in the MarketScan database and an additional 632 843 children who were enrolled in capitated plans in any month during 2014 (because claims submitted by these plans may not reliably report payment).5860 The final sample included 4 404 770 children, representing 5.6% of the 78.1 million US children in 2014 and 11.9% of the 36.9 million US children with employer-sponsored private insurance in 2014.61

Statistical Analyses

Summary statistics were calculated by using the demographic information available in the MarketScan enrollment file. Using the narrow and broad measures, we calculated the percentage of eligible children in the denominator population who received each service at least once during the year, the number of services received per 100 eligible children, and the percentage of children in the overall sample who received at least 1 of the 20 low-value services during the year. For each service and across all services, we also calculated out-of-pocket spending (the sum of coinsurance, copays, and deductibles) and total spending (allowed charges). To provide context for spending estimates, we limited the sample to children who received each service at least once in 2014, then calculated the proportion of annual health care spending among these individuals that was due to the service.

A single instance of service use can be represented by multiple claims in the MarketScan database due to separate billing of facility and professional components, claims adjustment, or billing error.58 For analyses of service use, we considered multiple instances of a service on the same day for a given individual to represent a single instance of service use. For spending analyses, we summed payment variables across all claims for a service on the same day for a given individual. This method of collapsing payment to the “claim-day” has been used in previous MarketScan analyses, including an Institute of Medicine report on geographic variation in spending among the privately insured US population.59,60

Analyses were performed by using SAS version 9.4 (SAS Institute, Inc, Cary, NC). The institutional review board of the University of Chicago exempted this study from review.

Results

Of the 4.4 million children in the sample, 29.3% were aged 0 to 5 years, 35.6% were aged 6 to 12 years, and 35.1% were aged 13 to 18 years; 51.1% were male; and 85.2% lived in an urban area. Our sample included children from all US states, Washington, DC, and Puerto Rico.

Table 2 and Fig 1 report the percentage of overall service counts, out-of-pocket spending, and total spending constituted by each category of low-value service use (diagnostic tests, imaging tests, and prescription drugs). Table 2 also reports the percentage of children in the sample who received at least 1 service in these categories during the year.

TABLE 2.

Use of and Spending on Low-Value Diagnostic Tests, Imaging Tests, and Prescription Drugs

Variable Diagnostic Tests (Measures 1–6) Imaging Tests (Measures 7–11) Prescription Drugs (Measures 12–20) Total
Narrow measures
 Service counts 286 066 19 470 419 957 707 493
 % of total low-value service count in sample 37.9% 2.8% 59.4% NA
 Out-of-pocket spending $2 394 690 $2 448 950 $4 312 215 $9 155 855
 % of total out-of-pocket spending on low-value services in sample 26.2% 26.7% 47.1% NA
 Total spending $6 951 671 $9 103 717 $10 934 306 $26 989 694
 % of total spending on low-value services in sample 25.8% 33.7% 40.5% NA
 % of sample receiving at least 1 service during the year 3.9% 0.4% 6.1% 9.6%a
Broad measures
 Service counts 357 161 36 196 726 789 1 120 146
 % of total low-value service count in sample 31.9% 3.2% 64.9% NA
 Out-of-pocket spending $3 760 452 $4 847 918 $7 678 528 $16 286 898
 % of total out-of-pocket spending on low-value services in sample 23.1% 29.8% 47.1% NA
 Total spending $12 338 221 $20 009 840 $20 608 710 $52 956 771
 % of total spending on low-value services in sample 23.3% 37.8% 38.9% NA
 % of sample receiving at least 1 service during the year 5.1% 0.7% 9.7% 14.0%a

NA, not applicable.

a

Represents the percentage of the sample receiving at least 1 of the 20 low-value pediatric services during the year. This number does not equal the sum of the first 3 columns because some children were affected by >1 category of low-value service during the year.

FIGURE 1.

FIGURE 1

Distribution of: A, low-value service counts, B, out-of-pocket spending on low-value services, and C, total spending on low-value services. Estimates are based on the narrow measures and represent the proportion of sample totals accounted for by low-value diagnostic tests, imaging tests, and prescription drugs.

According to the narrow measures, 37.9%, 2.8%, and 59.4% of all low-value services in our sample were for diagnostic tests, imaging tests, and prescription drugs, respectively (Table 2). Low-value imaging occurred relatively infrequently but accounted for 26.7% of all out-of-pocket spending and 33.7% of all spending on low-value services detected by using our measures. During the year, 3.9%, 0.4%, and 6.1% of children in the sample received at least 1 low-value diagnostic test, imaging test, and prescription drug. Overall, 9.6% of children in the sample received at least 1 of the 20 low-value services during the year. Total spending across all 20 services was $27.0 million, of which $9.2 million was paid out-of-pocket (33.9%).

According to the broad measures, 14.0% of children in the sample received at least 1 of the 20 low-value services during the year (Table 2). Total spending was $53.0 million, of which $16.3 million was paid out-of-pocket (30.8%).

Table 3 displays use and spending estimates for each of the 20 low-value pediatric services. Some services were received by a low percentage of eligible children but a large number of children overall due to the size of the denominator (eg, vitamin D testing), whereas other services were received by a high percentage of eligible children but a small number of children overall because the condition is rare (eg, ultrasound for cryptorchidism). Estimates of low-value service use varied significantly between the narrow and broad measures for some measures (eg, allergy testing for eczema) but not for others (eg, cervical cancer screening). Among the major categories of low-value pediatric services, we observed the highest rates of use for prescription drugs. Spending on each low-value service represented small proportions of annual health care spending among children who received the service during the year (median among 20 services, 0.7% for broad measures and 0.5% for narrow measures).

TABLE 3.

Use of and Spending on 20 Low-Value Pediatric Services

Service No. Service Narrow Measures Broad Measures
No. of Children in Denominator No. Receiving Service at Least Once During Year % of Denominator Receiving Service at Least Once During Year No. of Services per 100 Children in Denominator Out-of-Pocket Spending($ Million) Total Spending ($ Million) No. Receiving Service at Least Once During Year % of Denominator Receiving Service at Least Once During Year No. of Services Per 100 Children in Denominator Out-of-Pocket Spending ($ Million) Total Spending ($ Million)
1 Vitamin D screening 4 404 770 54 125 1.2 1.3 0.8 2.5 87 279 2.0 2.3 1.4 5.1
2 Allergy testing for atopic dermatitis 96 642 2314 2.4 2.6 0.1 0.4 10 657 11.0 12.7 0.7 2.3
3 Respiratory syncytial virus testing for bronchiolitis 60 459 10 857 18.0 19.7 0.2 0.5 14 561 24.1 27.0 0.2 0.7
4 Bloodwork for febrile seizures 4825 782 16.2 31.5 0.0 0.1 1279 26.5 55.6 0.0 0.2
5 Cervical cancer screening 635 766 11 480 1.8 2.4 0.0 0.5 14 696 2.3 3.6 0.1 0.7
6 Testing for group A streptococcal pharyngitis in children aged <3 y 735 958 94 890 12.9 24.4 1.2 3.0 105 142 14.3 27.4 1.3 3.3
7 Radiographs of face or nose for trauma 195126 6821 3.5 3.7 0.3 0.7 6821 3.5 3.7 0.3 0.7
8 Ultrasound for cryptorchidism 5161 894 17.3 19.1 0.1 0.3 1184 22.9 25.9 0.1 0.3
9 Sinus imaging for sinusitis 329 054 1603 0.5 0.5 0.1 0.2 3205 1.0 1.1 0.2 0.6
10 Neuroimaging for febrile seizures 4825 186 3.9 4.1 0.0 0.2 391 8.1 8.7 0.1 0.3
11 Neuroimaging for headache 110 941 8909 8.0 8.5 1.9 7.7 21 470 19.4 21.4 4.2 18.1
12 Cough and cold medications 1 290 473 42 129 3.3 4.5 0.6 1.1 42 129 3.3 4.5 0.6 1.1
13 Oral antibiotics for upper respiratory tract infections 785 199 142 660 18.2 20.7 1.4 3.4 271 022 34.5 42.5 3.0 7.8
14 Oral antibiotics for otitis media with effusion 127 245 50 930 40.0 45.5 0.6 1.5 69 728 54.8 66.6 0.9 2.4
15 Oral antibiotics for acute otitis externa 78 758 8526 10.8 11.0 0.1 0.2 25 316 32.1 34.5 0.3 0.7
16 Oral antibiotics after tonsillectomy 20 567 5294 25.7 26.0 0.0 0.1 6552 31.9 32.3 0.0 0.1
17 Oral antibiotics for bronchiolitis 60 459 9710 16.1 17.4 0.1 0.2 24 238 40.1 46.0 0.3 0.7
18 Oral steroids for bronchiolitis 60 459 10 686 17.7 19.6 0.1 0.1 12 040 19.9 22.2 0.1 0.1
19 Short-acting β-agonists for bronchiolitis 60 459 16 827 27.8 28.4 0.2 0.6 26 053 43.1 48.5 0.3 1.0
20 Acid blockers for infants with reflux 569 022 30 639 5.4 15.5 1.3 3.6 45 284 8.0 25.6 2.2 6.7

Due to the large sample size of our study, our estimates had very small 95% confidence intervals.62 For example, estimates of the percentage of children who received at least 1 low-value pediatric service during the year had 95% confidence intervals with a width <0.08 percentage point.

Discussion

Even though most children are healthy and have a limited number of interactions with the health care system, at least 9.6% of children in our sample received at least 1 of 20 low-value pediatric services during 2014, consistent with the notion that waste in pediatrics may be widespread. Although previous literature has documented significant underuse of high-value pediatric services such as immunizations,63 our findings suggest that overuse of low-value services may be an equally pressing deficiency in pediatric care quality. Our findings are similar to those of previous studies showing frequent use of low-value services among adults,311 which suggests that interventions to improve care efficiency should include patients across the entire age spectrum.

This study highlights the clinical and policy importance of reducing the use of low-value pediatric services. Most importantly, the services assessed in our study can directly harm children both in the short term (eg, side effects from antibiotics) and the long term (eg, increased lifetime incidence of cancer from unnecessary imaging). Furthermore, one-third of all spending on low-value pediatric services in our study was paid out-of-pocket, suggesting that use of these services could lead to unnecessary financial burden for families exposed to cost-sharing. Finally, our findings suggest that reducing use of low-value pediatric services could substantially decrease health care spending.10 Annual spending on low-value pediatric services totaled $27.0 million in our sample, which included 11.9% of all commercially insured children in the United States.61 Under the strong assumption that our sample is representative of this population, total annual spending on the 20 low-value pediatric services is roughly $227 million just for commercially insured children alone.

Our use of direct claims-based measures differs from the approach of previous pediatric overuse studies, most of which have indirectly assessed waste by documenting unexplained variation in care patterns between regions and hospitals.6466 This variation-based approach is useful for setting target rates of utilization based on a percentile rate, or “achievable benchmark of care.”66 However, it is difficult to determine appropriateness based on relative rates of utilization, especially if case mix differences between comparison groups cannot be adjusted for with available data or if waste frequently occurs even among providers with the lowest utilization rates.3,4 In contrast, direct approaches produce estimates of the absolute level of low-value service use, a quantity that is easier to interpret in isolation.

Conversely, a potential challenge of using claims-based measures to assess overuse may be the sensitivity of estimates to measure specification. In our study, we frequently observed a wide range of estimates when using narrow and broad versions of measures, illustrating a fundamental tradeoff when measuring overuse in claims: overly narrow measures may only capture a small fraction of all service use that is low-value, whereas overly broad measures may capture a significant amount of service use that is high-value.4 This scenario suggests that for each application of claims-based measures of low-value services, organizations and researchers must carefully tailor the measures to their measurement goals.

Despite this challenge, claims-based measures of low-value services could be essential tools in several types of pediatric quality improvement efforts,3 including pay-for-performance initiatives. For example, Massachusetts provider groups participating in the Alternative Quality Contract received a global budget and additional financial payments based on improvements in performance on several claims-based quality measures, including 1 measure assessing low-value antibiotic prescriptions.14 However, although payment could be carefully linked to aggregate performance on claims-based measures at the level of large provider groups, we would caution against using these measures to summarily deny payment for individual instances of apparent low-value service use, as claims may be unable to fully account for the heterogeneous and idiosyncratic clinical circumstances leading to service use in each health care encounter.67

Our study has a number of limitations. First, as with any administrative data analysis, we did not have access to potentially important clinical information that might influence assessments of appropriateness, which could lead to potential misclassification of services as low-value even when using the narrow measures. Although future efforts such as chart reviews may help quantify the reliability of claims-based measures, we also note that in many research settings, the impact of any misclassification bias can be attenuated by including additional restrictions or by using strong study designs. For example, 1 study used a difference-in-differences design and claims-based measures to evaluate the impact of the Medicare Pioneer ACO model on low-value service use.6 In this study, any significant differential changes in low-value service use were unlikely to be driven by misclassification bias unless the change in this bias before and after implementation of the ACO model differed in magnitude between the non-ACO and ACO groups. Analyses of trends in low-value pediatric service use will also not be affected by any misclassification bias unless the magnitude of this bias changes over time.

Second, it is unclear whether our results generalize to other pediatric populations, including publicly insured children. It is possible that publicly insured children receive fewer low-value services due to access barriers that result in less care overall; however, it is also possible that these children receive more low-value services because of systematic disparities in the quality of their care. Third, condition-based measures that use diagnosis codes as inclusion criteria may miss instances of low-value service use if the condition was not appropriately coded in claims (eg, if acute otitis media with effusion was coded as acute otitis media, not otherwise specified). Fourth, although we relied on recommendations from several high-profile organizations to classify a service as low-value, we acknowledge that some providers may have different perceptions of the utility of some of the services we assessed.

Finally, we only assessed 20 services, which we carefully selected from a large list of candidates primarily on the basis of whether they could be identified as low-value in claims. As such, our findings undoubtedly underestimate use of and spending on low-value pediatric services, including other services that could potentially be measured with additional claims-based measures as well as services that cannot be easily classified as low value by using claims data. We also note that our spending estimates do not account for any downstream events associated with low-value service use, including immediate events (eg, follow-up testing for false-positive initial results) and events that may occur much later (eg, use of broad-spectrum antibiotics due to antimicrobial resistance from antibiotic overuse).6870 To more fully capture the scope of low-value service use in pediatrics, future studies should quantify these downstream costs, identify costly low-value interventions for children with complex chronic conditions,57 and assess low-value applications of lucrative elective procedures that may not have been included by medical specialty societies participating in Choosing Wisely.71

Conclusions

Overuse of low-value services may be widespread in pediatrics. As health care systems increasingly incorporate payment and delivery models that prioritize value, claims-based measures of low-value pediatric services could facilitate the implementation of interventions to reduce the provision of potentially harmful services to children.

Acknowledgment

The authors thank Mona Sharifi, MD, MPH, for her helpful comments on the manuscript.

Glossary

ACO

accountable care organization

ICD-9

International Classification of Diseases, Ninth Revision

Footnotes

Dr Chua conceptualized and designed the study, acquired the data, conducted the initial analyses, drafted the initial manuscript, and revised the manuscript for important intellectual content; Dr Schwartz conceptualized and designed the study, interpreted the data, and revised the manuscript for important intellectual content; Drs Volerman and Conti interpreted the data and reviewed and revised the manuscript for important intellectual content; and Dr Huang interpreted the data, reviewed and revised the manuscript for important intellectual content, and supervised the study; all authors approved the final manuscript as submitted and agree to be accountable for all aspects of the work.

FINANCIAL DISCLOSURE: The authors have indicated they have no financial relationships relevant to this article to disclose.

FUNDING: Dr Schwartz is supported by a training grant from the National Institute on Aging (F30 AG044106). Dr Huang is supported by a grant from the National Institute of Diabetes and Digestive and Kidney Diseases (K24 DK105340). Supported by the National Institutes of Health (NIH).

POTENTIAL CONFLICT OF INTEREST: Dr Schwartz reports consulting on quality measurement for Nuna Inc; the other authors have indicated they have no potential conflicts of interest to disclose.

COMPANION PAPER: A companion to this article can be found online at www.pediatrics.org/cgi/doi/10.1542/peds.2016-3228.

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