Skip to main content
Journal of Clinical Medicine logoLink to Journal of Clinical Medicine
. 2021 Nov 12;10(22):5269. doi: 10.3390/jcm10225269

Differences in Hospitalization Outcomes of Kidney Disease between Patients Who Received Care by Nephrologists and Non-Nephrologist Physicians: A Propensity-Score-Matched Study

Chien-Wun Wang 1,2, Yu Yang 3, Chun-Chieh Yeh 4,5, Yih-Giun Cherng 1,2, Ta-Liang Chen 2,6,7,, Chien-Chang Liao 2,7,8,9,10,*,
Editor: Magdi Yaqoob
PMCID: PMC8623768  PMID: 34830549

Abstract

The influence of physician specialty on the outcomes of kidney diseases (KDs) remains underexplored. We aimed to compare the complications and mortality of patients with admissions for KD who received care by nephrologists and non-nephrologist (NN) physicians. We used health insurance research data in Taiwan to conduct a propensity-score matched study that included 17,055 patients with admissions for KD who received care by nephrologists and 17,055 patients with admissions for KD who received care by NN physicians. Multivariable logistic regressions were conducted to calculate adjusted odds ratios (ORs) with 95% confidence intervals (CIs) for 30-day mortality and major complications associated with physician specialty. Compared with NN physicians, care by nephrologists was associated with a reduced risk of 30-day mortality (OR 0.29, 95% CI 0.25–0.35), pneumonia (OR 0.82, 95% CI 0.76–0.89), acute myocardial infarction (OR 0.68, 95% CI 0.54–0.87), and intensive care unit stay (OR 0.78, 95% CI 0.73–0.84). The association between nephrologist care and reduced admission adverse events was significant in every age category, for both sexes and various subgroups. Patients with admissions for KD who received care by nephrologists had fewer adverse events than those who received care by NN physicians. We suggest that regular nephrologist consultations or referrals may improve medical care and clinical outcomes in this vulnerable population.

Keywords: complications, hospitalization, kidney disease, mortality, nephrologists

1. Introduction

Kidney disease led to 1.2 million deaths in 2017 and is also one of the leading causes of years lived with disability [1,2]. Kidney diseases increase the risk of cardiovascular events, stroke, cognitive impairment, anemia, and electrolyte and bone disorders, accounting for substantial medical costs [3]. Subclinical chronic kidney diseases and acute kidney injury are commonly overlooked and regarded as harmless or reversible. However, there is accumulating evidence that changes in absolute serum creatinine are linked to greater mortality, development of chronic kidney disease, and increased healthcare expenditures [4,5]. Awareness, prevention, and early intervention are crucial to halt the progression of kidney diseases.

Physician specialty has an impact on patient outcomes and has been reported among cardiologists [6,7], gastroenterologists [8], neurologists [9], pulmonologists [10], and intensivists [11,12]. To date, only a few studies have examined the influence of physician specialty on the outcomes of kidney diseases [13,14,15]. Prior studies have demonstrated that early nephrologist consultation reduces the risk of 30-day mortality [14,16], lengths of intensive care unit and hospital stays [13], dialysis dependence at hospital discharge [14], and all-cause mortality at 6 months [14]. However, there are some study limitations in interpreting these findings, including relatively small sample sizes [13,15], restrictions to patients with acute kidney injury [13,14,15], and inadequate control for confounding factors [13,14]. In addition, whether nephrologists, as primary care providers, improve the outcomes of patients with kidney diseases remains unclear.

Accordingly, we used medical insurance claims data in Taiwan and conducted a population-based study to evaluate patients hospitalized for kidney diseases. Our purpose is to compare the in-hospital outcomes of kidney diseases between medical care from nephrologists and non-nephrologist (NN) physicians.

2. Methods

2.1. Source of Data

We used research data from the reimbursement claims of Taiwan’s National Health Insurance, which contain information on inpatient and outpatient medical services. Demographic characteristics, physicians’ primary and secondary diagnoses, treatment procedures, prescriptions, and medical expenditures were collected in the database. The insurance program covered more than 99% of people in Taiwan, and many scientific articles based on this database have been published in outstanding journals worldwide.

2.2. Ethical Approval

To protect patient privacy, the electronic database used in this study was decoded with patient identification scrambled for further academic access for research. Although the Ministry of Health and Welfare, Taiwan, exempts such uses from informed consent, the guidelines of the Declaration of Helsinki were obeyed during the execution of this study. This study was also approved by the Institutional Review Board of Taipei Medical University (TMU-JIRB-201509050).

2.3. Study Design

From the reimbursement claims of Taiwan’s National Health Insurance, we identified 67,246 patients with non-surgical admissions due to KD in 2008–2013, with 35,950 of them receiving inpatient care by nephrologists. For appropriate comparison and obtaining eligible study subjects, we used a propensity-score matching technique to select 17,055 patients receiving inpatient care by nephrologists and 6264 patients receiving inpatient care by NN physicians. Factors in the propensity-score matching included sociodemographic information (such as age, sex, and low income), types of KD, and history of disease (such as hypertension, diabetes, hyperlipidemia, mental disorders, ischemic heart disease, heart failure, liver cirrhosis, and chronic obstructive pulmonary disease). We compared the complications, mortality, intensity of care, length of hospital stay, and medical expenditures during admission due to KD between patients receiving inpatient care by nephrologists and those receiving inpatient care by NN physicians.

2.4. Measures and Definition

Based on previous studies, we defined the status of low income according to the regulations of the Ministry of Health and Welfare, Taiwan. In this study, the NN physicians included physicians with medical specialties in general medicine, family medicine, neurology, cardiology, gastroenterology, thoracic medicine, endocrinology, and infectious disease. The physician’s diagnosis and the International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) were used to identify coexisting medical conditions within the 24-month pre-admission period, including hypertension (codes 401–405), diabetes (code 250), hyperlipidemia, mental disorders (codes 290–319), ischemic heart disease (codes 410–414), heart failure (code 428), liver cirrhosis (codes 571.2, 571.5, and 571.6), and chronic obstructive pulmonary disease (codes 491, 492, and 496). Types of KD included acute glomerulonephritis, nephrotic syndrome, chronic glomerulonephritis, nephropathy, unspecified acute kidney failure, chronic kidney disease, renal failure, unspecified renal sclerosis, unspecified disorders from nephropathy, kidney infections, and hydronephrosis. During the index admission for KD, pneumonia (codes 480–486), septicemia (codes 038 and 998.5), urinary tract infection (code 599.0), mortality, length of hospital stay, and medical expenditures were considered study outcomes.

2.5. Statistical Analysis

To select appropriate study subjects for comparison, a propensity-score matched pair analysis was used to identify patients with admissions for KD who received care by NN physicians and nephrologists. A non-parsimonious multivariable logistic regression model was used to estimate a propensity score for patients receiving or not receiving care by nephrologists. In this model, the covariates included age, sex, low income, types of KD, hypertension, diabetes, hyperlipidemia, mental disorders, ischemic heart disease, heart failure, liver cirrhosis, and chronic obstructive pulmonary disease. We matched the patients who received care by nephrologists to the patients who received care by NN physicians using a greedy matching algorithm (without replacement), with a caliper width of 0.2 SDs of the log odds of the estimated propensity score. Categorical variables between patients who received cared by nephrologists and patients who received care by NN physicians were analyzed by using frequencies (percentages) and chi-square tests. The t-tests and means ± standard deviations were used to compare continuous variables between patients who received care by nephrologists and those who received care by NN physicians. We calculated the adjusted odds ratios (ORs) and 95% confidence intervals (CIs) of the outcomes of admissions for KD associated with physician specialty by using multiple logistic regressions. A subgroup analysis was also performed to examine the association between KD outcomes and physician specialty in the subgroups according to age, sex, number of medical conditions, and types of KD.

3. Results

Because propensity-score matching was used (Table 1), the standardized mean difference of every factor is <0.001, such as age, sex, and low income, hypertension, diabetes, hyperlipidemia, mental disorders, ischemic heart disease, heart failure, liver cirrhosis, and chronic obstructive pulmonary disease, and types of KD.

Table 1.

Characteristics of patients hospitalized due to kidney diseases received care by nephrologists and non-nephrologist physicians (after matching) *.

NN Physicians
(N = 17,055)
Nephrologists
(N = 17,055)
SMD
Sex n (%) n (%)
Female 10,114 (59.3) 10,114 (59.3) <0.001
Male 6941 (40.7) 6941 (40.7) <0.001
Age, years
 20–29 169 (1.0) 169 (1.0) <0.001
 30–39 275 (1.6) 275 (1.6) <0.001
 40–49 809 (4.7) 809 (4.7) <0.001
 50–59 1868 (11.0) 1868 (11.0) <0.001
 60–69 3725 (21.8) 3725 (21.8) <0.001
 70–79 5969 (35.0) 5969 (35.0) <0.001
 ≥80 4240 (24.9) 4240 (24.9) <0.001
Low income
 No 16,040 (94.1) 16,040 (94.1) <0.001
 Yes 1015 (5.9) 1015 (5.9) <0.001
Types of kidney diseases
 Acute glomerulonephritis 90 (0.5) 90 (0.5) <0.001
 Nephrotic syndrome 201 (1.2) 201 (1.2) <0.001
 Chronic glomerulonephritis 453 (2.7) 453 (2.7) <0.001
 Nephropathy, unspecified 115 (0.7) 115 (0.7) <0.001
 Acute kidney failure 4249 (24.9) 4249 (24.9) <0.001
 Chronic kidney disease 3964 (23.2) 3964 (23.2) <0.001
 Renal failure, unspecified 476 (2.8) 476 (2.8) <0.001
 Renal sclerosis, unspecified 4 (0.02) 4 (0.02) <0.001
Disorders from nephropathy 70 (0.4) 70 (0.4) <0.001
 Infections of kidney 7260 (42.6) 7260 (42.6) <0.001
 Hydronephrosis 173 (1.0) 173 (1.0) <0.001
Medical conditions
 Hypertension 8938 (52.4) 8938 (52.4) <0.001
 Diabetes 6714 (39.4) 6714 (39.4) <0.001
 Hyperlipidemia 542 (3.2) 542 (3.2) <0.001
 Mental disorders 3936 (23.1) 3936 (23.1) <0.001
 Ischemic heart disease 3491 (20.5) 3491 (20.5) <0.001
 Heart failure 1981 (11.6) 1981 (11.6) <0.001
 Liver cirrhosis 359 (2.1) 359 (2.1) <0.001
 COPD 2897 (17.0) 2897 (17.0) <0.001

COPD: chronic obstructive pulmonary disease; NN, non-nephrologist; SMD, standardized mean difference. * After matching by propensity score, the standardized mean difference between nephrologists and NN physicians in every factor is <0.001.

Compared with patients with KD who received care by NN physicians (Table 2), those with KD who received care by nephrologists had lower risks of in-hospital complications, including pneumonia (OR 0.82, 95% CI 0.76–0.89), acute myocardial infarction (OR 0.68, 95% CI 0.54–0.87), intensive care (OR 0.78, 95% CI 0.73–0.84), and 30-day mortality (OR 0.29, 95% CI 0.25–0.35). A shorter length of hospital stay (10.7 ± 12.2 days vs. 12.6 ± 32.2 days, p < 0.0001) and lower medical expenditure (1717 ± 2623 US dollars vs. 1929 ± 3525 US dollars, p < 0.0001) were found in patients who received care by nephrologists as compared to those who received care by NN physicians.

Table 2.

The comparison of outcomes after admissions due to kidney diseases in patients received care by nephrologists and non-nephrologist physicians.

NN Physicians
(N = 17,055)
Nephrologists
(N = 17,055)
Risk of Outcomes
Outcomes after Admission Events % Event % OR (95% CI) †
30-day mortality 621 3.6 192 1.1 0.29 (0.25–0.35)
In-hospital complications
 Pneumonia 1633 9.6 1372 8.0 0.82 (0.76–0.89)
 Septicemia 2105 12.3 2080 12.2 0.99 (0.92–1.05)
 Pulmonary embolism 23 0.1 24 0.1 1.04 (0.59–1.85)
 Urinary tract infection 3452 20.2 4058 23.8 1.24 (1.18–1.31)
 Deep wound infection 33 0.2 29 0.2 0.88 (0.53–1.45)
 Acute myocardial infarction 162 1.0 111 0.7 0.68 (0.54–0.87)
Intensive care unit stay 2011 11.8 1632 9.6 0.78 (0.73–0.84)
Medical expenditure, USD ‡ 1929 ± 3525 1717 ± 2623 p < 0.0001
Length of hospital stay, days ‡ 12.6 ± 32.2 10.7 ± 12.2 p < 0.0001

CI, confidence interval; NN, non-nephrologist; OR, odds ratio. † Adjusted for all covariates listed in Table 1. ‡ Mean ± SD.

In the stratified analysis (Table 3), we found that care by nephrologists was associated with reduced adverse events during admissions for KD in the subgroups of females (OR 0.78, 95% CI 0.73–0.85); males (OR 0.70, 95% CI 0.65–0.76); and people aged 20–49 years (OR 0.70, 95% CI 0.53–0.93), 50–59 years (OR 0.70, 95% CI 0.58–0.86), 60–69 years (OR 0.73, 95% CI 0.64–0.83), 70–79 years (OR 0.72, 95% CI 0.66–0.79), and ≥80 years (OR 0.79, 95% CI 0.72–0.88). The association between care by nephrologists and reduced adverse events during admissions for KD was also significant in people with (OR 0.76, 95% CI 0.60–0.97) or without low income (OR 0.74, 95% CI 0.70–0.79), acute kidney failure (OR 0.61, 95% CI 0.56–0.67), and chronic kidney disease (OR 0.72, 95% CI 0.65–0.80). The adjusted ORs of adverse events during admissions for KD patients with 0, 1, 2 and 3 or more medical conditions were 0.83 (95% CI 0.71–0.96), 0.76 (95% CI 0.69–0.84), 0.71 (95% CI 0.64–0.79), and 0.72 (95% CI 0.64–0.80), respectively.

Table 3.

The stratified analysis for the adverse events after the admission due to kidney diseases associated with physician specialty.

Adverse Events *
n Events Rate, % OR (95% CI) †
 Female NN physicians 10,114 1792 17.7 1.00 (reference)
Nephrologists 10,114 1488 14.7 0.78 (0.73–0.85)
 Male NN physicians 6941 1838 26.5 1.00 (reference)
Nephrologists 6941 1418 20.4 0.70 (0.65–0.76)
 Age 20–49 years NN physicians 1253 143 11.4 1.00 (reference)
Nephrologists 1253 107 8.5 0.70 (0.53–0.93)
 Age 50–59 years NN physicians 1868 288 15.4 1.00 (reference)
Nephrologists 1868 217 11.6 0.70 (0.58–0.86)
 Age 60–69 years NN physicians 3725 673 18.1 1.00 (reference)
Nephrologists 3725 525 14.1 0.73 (0.64–0.83)
 Age 70–79 years NN physicians 5969 1344 22.5 1.00 (reference)
Nephrologists 5969 1054 17.7 0.72 (0.66–0.79)
 Age ≥80 years NN physicians 4240 1182 27.9 1.00 (reference)
Nephrologists 4240 1003 23.7 0.79 (0.72–0.88)
 No low income NN physicians 16,040 3437 21.4 1.00 (reference)
Nephrologists 16,040 2749 17.1 0.74 (0.70–0.79)
 Low income NN physicians 1015 193 19.0 1.00 (reference)
Nephrologists 1015 157 15.5 0.76 (0.60–0.97)
 Acute kidney failure NN physicians 4249 1627 38.3 1.00 (reference)
Nephrologists 4249 1168 27.5 0.61 (0.56–0.67)
 Chronic kidney disease NN physicians 3964 1078 27.2 1.00 (reference)
Nephrologists 3964 842 21.2 0.72 (0.65–0.80)
 Infections of kidney NN physicians 7260 665 9.2 1.00 (reference)
Nephrologists 7260 651 9.0 0.98 (0.87–1.10
 Others NN physicians 1582 260 16.4 1.00 (reference)
Nephrologists 1582 245 15.5 0.93 (0.77–1.13)
 0 medical condition ‡ NN physicians 2620 503 19.2 1.00 (reference)
Nephrologists 2620 438 16.7 0.83 (0.71–0.96)
 1 medical condition ‡ NN physicians 5581 1112 19.9 1.00 (reference)
Nephrologists 5581 907 16.3 0.76 (0.69–0.84)
 2 medical conditions ‡ NN physicians 4900 1052 21.5 1.00 (reference)
Nephrologists 4900 809 16.5 0.71 (0.64–0.79)
 ≥3 medical conditions ‡ NN physicians 3954 963 24.4 1.00 (reference)
Nephrologists 3954 752 19.0 0.72 (0.64–0.80)

CI, confidence interval; NN, non-nephrologist; OR, odds ratio. * Adverse events included with 30-day mortality, pneumonia, acute myocardial infarction, intensive care unit stay. † Adjusted for all covariates listed in Table 1. ‡ Included hypertension diabetes, hyperlipidemia, mental disorders, ischemic heart disease, heart failure liver cirrhosis, and chronic obstructive pulmonary disease within the 24-month pre-admission period.

Table 4 showed the stratified analysis by specific medical conditions for the association between physician specialty and adverse events after the admission due to kidney diseases.

Table 4.

The stratified analysis by specific medical conditions for the association between physician specialty and adverse events after the admission due to kidney diseases.

Adverse Events *
n Events Rate, % OR (95% CI) †
No hypertension NN physicians 8117 1739 21.4 1.00 (reference)
Nephrologists 8117 1390 17.1 0.74 (0.68–0.80)
Hypertension NN physicians 8938 1891 21.2 1.00 (reference)
Nephrologists 8938 1516 17.0 0.75 (0.69–0.81)
No diabetes NN physicians 10,341 2186 21.1 1.00 (reference)
Nephrologists 10,341 1802 17.4 0.77 (0.72–0.83)
Diabetes NN physicians 6714 1444 21.5 1.00 (reference)
Nephrologists 6714 1104 16.4 0.70 (0.64–0.77)
No hyperlipidemia NN physicians 16,513 3531 21.4 1.00 (reference)
Nephrologists 16,513 2851 17.3 0.76 (0.72–0.81)
Hyperlipidemia NN physicians 542 99 18.3 1.00 (reference)
Nephrologists 542 55 10.2 0.50 (0.35–0.72)
No mental disorders NN physicians 13,119 2762 21.1 1.00 (reference)
Nephrologists 13,119 2230 17.0 0.75 (0.71–0.80)
Mental disorders NN physicians 3936 868 22.1 1.00 (reference)
Nephrologists 3936 676 17.2 0.71 (0.64–0.80)
No ischemic heart disease NN physicians 13,564 2839 20.9 1.00 (reference)
Nephrologists 13,564 2295 16.9 0.75 (0.71–0.80)
Ischemic heart disease NN physicians 3491 791 22.7 1.00 (reference)
Nephrologists 3491 611 17.5 0.71 (0.63–0.80)
No heart failure NN physicians 15,074 3080 20.4 1.00 (reference)
Nephrologists 15,074 2465 16.4 0.75 (0.70–0.79)
Heart failure NN physicians 1981 550 27.8 1.00 (reference)
Nephrologists 1981 441 22.3 0.74 (0.64–0.85)
No liver cirrhosis NN physicians 16,696 3553 21.3 1.00 (reference)
Nephrologists 16,696 2836 17.0 0.74 (0.70–0.79)
Liver cirrhosis NN physicians 359 77 21.5 1.00 (reference)
Nephrologists 359 70 19.5 0.88 (0.60–1.28)
No COPD NN physicians 14,158 2822 19.9 1.00 (reference)
Nephrologists 14,158 2279 16.1 0.76 (0.71–0.80)
COPD NN physicians 2897 808 27.9 1.00 (reference)
Nephrologists 2897 627 21.6 0.70 (0.62–0.79)

CI, confidence interval; COPD, chronic obstructive pulmonary disease; NN, non-nephrologist; OR, odds ratio. * Adverse events included with 30-day mortality, pneumonia, acute myocardial infarction, intensive care unit stay. † Adjusted for all covariates listed in Table 1.

4. Discussion

In this study, we utilized a large patient sample and conducted meticulous analyses using propensity-score matching procedures to evaluate the association of care by nephrologists with the outcomes of kidney diseases. Our analyses showed that patients admitted for kidney diseases had better outcomes when receiving primary care from nephrologists, including lower risks of 30-day mortality, pneumonia, acute myocardial infarction, and intensive care, as well as shorter lengths of hospital stay and lower medical expenditures. These findings provide valuable implications for optimal care in patients with kidney diseases.

This study showed the better outcomes of patients admitted for kidney diseases with care by nephrologists, which is consistent with prior studies [13,14,15,16,17,18,19]. Of note, our study has several strengths compared to previous studies in evaluating the benefits of involvement of nephrologists in kidney diseases. First, our study included not only patients diagnosed with acute kidney injury [13,14,15,16,17,18,19] or admitted to the intensive care unit [13,15,16] but also those with chronic kidney diseases and glomerulonephritis, which increases the external validity of our results. In addition, the large patient sample of our cohort allows for the implementation of propensity-score matching to multiple covariates, which helps minimize potential confounding biases. Third, most prior studies focused on the effect of nephrologist consultations [13,14,15,16,18,19], which may be hardly generalizable to nephrologists as primary care providers. Fourth, the nationwide coverage of our dataset included patients receiving wide-ranging levels of hospital care, which was lacking in previous studies [14,15,16,17,18,19].

We proposed some possible explanations for the superior prognosis of medical care by nephrologists. First, nephrologists are more familiar with the courses of kidney diseases and are able to avoid preventable kidney injuries in the early stage of renal diseases, resulting in better renal functional reserve at discharge [17] and a lower overall mortality rate [14,15,18,19]. Second, nephrologists have better adherence to evidence-based practices to examine ideal candidates requiring renal replacement therapy and to initiate dialysis in a timely manner, which might better preserve renal function and reduce mortality due to uremia [16,20,21]. Third, nephrologists are knowledgeable about the latest guidelines for kidney disease therapies and have better adherence to evidence-based practices [20,21]. The vigilance of evidence-based practice has a positive effect on patient outcomes, including preserved renal function [20,21]. Fourth, patients with decreased renal function have impaired immunity and higher vulnerability to infections [22]. Nephrologists may change modifiable risk factors for nosocomial pneumonia, such as improving nutrition and controlling organ failure [23]. Fifth, chronic kidney disease is associated with an exceedingly high risk of coronary artery disease and causes a worse prognosis after myocardial infarction [24]. A study has shown that early and frequent care by nephrologists before the initiation of dialysis may reduce the post-dialysis occurrence of major cardiovascular outcomes through better control of anemia, fluid overload, and potassium homeostasis [25].

Our study showed that care by nephrologists was associated with a higher risk of urinary tract infection than care by general physicians. There are some possible explanations for this result. First, previous studies have demonstrated that specialists achieved a higher diagnostic accuracy for diseases within their specialty areas compared to that in general physicians and family physicians [26]. Nephrologists may have a higher level of awareness and familiarity regarding the manifestation and diagnosis of urinary tract infection, which results in a higher diagnostic rate [27]. Second, specialists are prone to pull cases toward their specialty [28], which may cause more frequent diagnoses of urinary tract infections while under the care of a nephrologist, namely, “ascertainment bias”. Third, patients referred to nephrologists may have more rapidly progressive and severe kidney diseases, which was associated with a higher incidence of urinary tract infection [29]. However, our research database lacked information about disease progression and severity.

The disparity in the in-hospital outcomes between nephrologists and general physicians may also result from patient factors. A large-scale survey showed that approximately 13.4% of patients did not comply with referrals to medical specialist care, which may reflect differences in demographic and socioeconomic attributes [30]. Lower socioeconomic status was linked to a higher risk of acute kidney injury and death from renal causes [31]. Second, among Taiwanese patients, there are obstacles to accessing the resources of renal supportive care due to the lack of structured and practical pathways, which may contribute to underrecognition and undertreatment of renal diseases [32]. Patients overcoming the barriers to specialist care have a higher level of support from family members and social networks [33], which may improve outcomes by ameliorating depressive affects, enhancing patient perception of quality of life, and improving patient compliance [34]. Third, patients seeking specialty services may have better health literacy and knowledge of common chronic diseases and receive timely renal care, which subsequently improved the outcome after admission [35].

The national prospective cohort study in the United States indicated that the incidence of hospitalizations for sepsis was 110/1000 patient-years in patients with renal dialysis [36]. Among 8937 patients with renal dialysis who received non-cardiac surgeries in Taiwan, 11% of them had postoperative septicemia [37]. In contrast, among 8803 patients who were admitted to the intensive care unit with sepsis, 730 (8.3%) patients had end-stage renal disease [38]. Septicemia was considered as one of common complications for patients with kidney disease, particularly in dialysis patients [39,40]. The results of our study provided similar phenomenon showing that about 12% of patients with renal hospitalization had septicemia.

Our stratified analyses showed that the reduced adverse events associated with care by nephrologists were consistent across various subgroups, except for patients with kidney infections. We considered that patients with more severe renal infections might be more likely to be referred to nephrologists, which could lead to a higher rate of in-hospital adverse events in the group who received care by nephrologists. In addition, kidney infection (acute pyelonephritis) represents the most severe form of urinary tract infection and is associated with a high risk of both morbidity and mortality [41]. This might override the benefit of nephrologist care in patient outcomes.

There are some limitations to this study. First, we have no information regarding lifestyle, laboratory measures (such as estimated glomerular filtration rate, serum creatinine and electrolytes), and medications for kidney diseases. Second, we did not have data with respect to hospital volume. General physicians and nephrologists in high-volume hospitals may have more resources to better diagnose and treat kidney diseases, which could improve patient outcomes [42]. Third, there were no data concerning physician experience, which may affect the quality of health care, patient behavior, and clinical outcomes [43]. Fourth, our analyses did not consider the severity of renal diseases or the level of renal functional reserve. This could cause selection bias, as patients with more severe kidney diseases may be transferred to medical centers or to care by nephrologists. Fifth, our dataset did not include people with subclinical renal diseases, because they may not seek standard medical care. In addition, residual confounding bias was always possible, although we adjusted for many potential confounders. Finally, we could not fully determine whether a patient had real kidney disease or myocardial infarction because there is no laboratory and detailed prescription items in this study, it is impossible to determine whether a patient had real kidney disease or myocardial infarction. The validity of diagnosis codes has been evaluated, such as chronic kidney disease [44], acute myocardial infarction [45], and pneumonia [46]. The positive predictive value of health claims data for chronic kidney disease defined as an estimated glomerular filtration rate <60 mL/min/1.73 m2 ranged from 60 to 89% [44]. Regarding acute myocardial infarction, the use of ICD-9-CM 410 yields a positive predictive value of 92% and a sensitivity of 88% based on the research database of Taiwan’s National Health Insurance [45].

In conclusion, patients admitted for kidney diseases had better in-hospital outcomes when they received medical care from nephrologists rather than NN physicians. Regular nephrologist consultations or referrals may improve medical care and clinical outcomes in this vulnerable population. This warrants future studies to better clarify the benefits of active and timely nephrologist care in clinical outcomes.

Author Contributions

Conceptualization: C.-W.W., Y.Y., C.-C.Y., Y.-G.C., T.-L.C., and C.-C.L.; formal analysis: C.-C.L.; investigation: C.-W.W., Y.Y., C.-C.Y., Y.-G.C., T.-L.C., and C.-C.L.; methodology: C.-W.W., Y.Y., C.-C.Y., Y.-G.C., T.-L.C., and C.-C.L.; writing—original draft: C.-W.W. and C.-C.L.; writing—review and editing: C.-W.W., Y.Y., C.-C.Y., Y.-G.C., T.-L.C., and C.-C.L. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Taiwan’s Ministry of Science and Technology (MOST106-2314-B-038-036-MY3; MOST110-2314-B-038-108-MY2).

Institutional Review Board Statement

This study was also approved by the Institutional Review Board of Taipei Medical University (TMU-JIRB-201509050).

Informed Consent Statement

Informed consent was not required because the analysis used preexisting deidentified data.

Data Availability Statement

The data underlying this study is from the Health and Welfare Data Science Center. Interested researchers can obtain the data through formal application to the Health and Welfare Data Science Center, Department of Statistics, Ministry of Health and Welfare, Taiwan (http://dep.mohw.gov.tw/DOS/np-2497-113.html (accessed on 8 November 2021)). Under the regulations from the Health and Welfare Data Science Center, we have made the formal application (included application documents, study proposals, and ethics approval of the institutional review board) of the current insurance data. The authors of the present study had no special access privileges in accessing the data which other interested researchers would not have.

Conflicts of Interest

The authors declare no conflict of interest.

Footnotes

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.GBD Chronic Kidney Disease Collaboration Global, regional, and national burden of chronic kidney disease, 1990–2017: A systematic analysis for the Global Burden of Disease Study 2017. Lancet. 2020;395:709–733. doi: 10.1016/S0140-6736(20)30045-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.GBD 2017 DALYs and HALE Collaborators Global, regional, and national disability-adjusted life-years (DALYs) for 359 diseases and injuries and healthy life expectancy (HALE) for 195 countries and territories, 1990–2017: A systematic analysis for the Global Burden of Disease Study 2017. Lancet. 2018;392:1859–1922. doi: 10.1016/S0140-6736(18)32335-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Jha V., Garcia-Garcia G., Iseki K., Li Z., Naicker S., Plattner B., Saran R., Wang A.Y.M., Yang C.W. Chronic kidney disease: Global dimension and perspectives. Lancet. 2013;382:260–272. doi: 10.1016/S0140-6736(13)60687-X. [DOI] [PubMed] [Google Scholar]
  • 4.Kao S.S., Kim S.W., Horwood C.M., Hakendorf P., Li J.Y., Thompson C.H. Variability in inpatient serum creatinine: Its impact upon short- and long-term mortality. QJM Int. J. Med. 2015;108:781–787. doi: 10.1093/qjmed/hcv020. [DOI] [PubMed] [Google Scholar]
  • 5.Lameire N.H., Bagga A., Cruz D., Maeseneer J.D., Endre Z., Kellum J.A., Liu K.D., Mehta R.L., Pannu N., Biesen W.V., et al. Acute kidney injury: An increasing global concern. Lancet. 2013;382:170–179. doi: 10.1016/S0140-6736(13)60647-9. [DOI] [PubMed] [Google Scholar]
  • 6.Perino A.C., Fan J., Schmitt S.K., Askari M., Kaiser D.W., Deshmukh A., Heidenreich P.A., Swan C., Narayan S.M., Wang P.J., et al. Treating Specialty and Outcomes in Newly Diagnosed Atrial Fibrillation: From the TREAT-AF Study. J. Am. Coll. Cardiol. 2017;70:78–86. doi: 10.1016/j.jacc.2017.04.054. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Kulkarni V.T., Ross J.S., Wang Y., Nallamothu B.K., Spertus J.A., Normand S.L.T., Masoudi F.A., Krumholz H.M. Regional density of cardiologists and rates of mortality for acute myocardial infarction and heart failure. Circ. Cardiovasc. Qual. Outcomes. 2013;6:352–359. doi: 10.1161/CIRCOUTCOMES.113.000214. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Mellinger J.L., Moser S., Welsh D.E., Yosef M.T., Van T., McCurdy H., Rakoski M.O., Moseley R.H., Glass L., Waljee A.K., et al. Access to Subspecialty Care And Survival Among Patients With Liver Disease. Am. J. Gastroenterol. 2016;111:838–844. doi: 10.1038/ajg.2016.96. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Kim A.S., Sidney S., Bernstein A.L., Douglas V.C., Johnston S.C. Urgent neurology consultation from the ED for transient ischemic attack. Am. J. Emerg. Med. 2011;29:601–608. doi: 10.1016/j.ajem.2009.12.025. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Shannon H., Stocks J., Gregson R.K., Dunne C., Peters M.J., Main E. Clinical effects of specialist and on-call respiratory physiotherapy treatments in mechanically ventilated children: A randomised crossover trial. Physiotherapy. 2015;101:349–356. doi: 10.1016/j.physio.2014.12.004. [DOI] [PubMed] [Google Scholar]
  • 11.Billington E.O., Zygun D.A., Stelfox H.T., Peets A.D. Intensivists’ base specialty of training is associated with variations in mortality and practice patterns. Crit. Care. 2009;13:R209. doi: 10.1186/cc8227. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Pronovost P.J., Angus D.C., Dorman T., Robinson K.A., Dremsizov T.T., Young T.L. Physician staffing patterns and clinical outcomes in critically ill patients: A systematic review. JAMA. 2002;288:2151–2162. doi: 10.1001/jama.288.17.2151. [DOI] [PubMed] [Google Scholar]
  • 13.Mehta R.L., McDonald B., Gabbai F., Pahl M., Farkas A., Pascual M.T.A., Zhuang S., Kaplan R.M., Chertow G.M. Nephrology consultation in acute renal failure: Does timing matter? Am. J. Med. 2002;113:456–461. doi: 10.1016/S0002-9343(02)01230-5. [DOI] [PubMed] [Google Scholar]
  • 14.Perez-Valdivieso J.R., Bes-Rastrollo M., Monedero P., de Irala J., Lavilla F.J. Prognosis and serum creatinine levels in acute renal failure at the time of nephrology consultation: An observational cohort study. BMC Nephrol. 2007;8:14. doi: 10.1186/1471-2369-8-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Ponce D., Zorzenon Cde P., dos Santos N.Y., Balbi A.L. Early nephrology consultation can have an impact on outcome of acute kidney injury patients. Nephrol. Dial. Transplant. 2011;26:3202–3206. doi: 10.1093/ndt/gfr359. [DOI] [PubMed] [Google Scholar]
  • 16.Flores-Gama C., Merino M., Baranda F., Cruz D.N., Ronco C., Vazquez-Rangel A. The impact of integrating nephrologists into the postoperative cardiac intensive care unit: A cohort study. Cardiorenal. Med. 2013;3:79–88. doi: 10.1159/000350545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Balasubramanian G., Al-Aly Z., Moiz A., Rauchman M., Zhang Z., Gopalakrishnan R., Balasubramanian S., El-Achkar T.M. Early nephrologist involvement in hospital-acquired acute kidney injury: A pilot study. Am. J. Kidney Dis. 2011;57:228–234. doi: 10.1053/j.ajkd.2010.08.026. [DOI] [PubMed] [Google Scholar]
  • 18.Costa e Silva V.T., Liaño F., Muriel A., Díez R., de Castro I., Yu L. Nephrology referral and outcomes in critically ill acute kidney injury patients. PLoS ONE. 2013;8:e70482. doi: 10.1371/journal.pone.0070482. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Nascimento G.V.R.D., Silva M.D.N., Carvalho Neto J.D., Feitosa Filho L.R., Antão J.D. Outcomes in acute kidney injury in noncritically ill patients lately referred to nephrologist in a developing country: A comparison of AKIN and KDIGO criteria. BMC Nephrol. 2020;21:94. doi: 10.1186/s12882-020-01751-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Fürthauer J., Flamm M., Sönnichsen A. Patient and physician related factors of adherence to evidence based guidelines in diabetes mellitus type 2, cardiovascular disease and prevention: A cross sectional study. BMC Fam. Pract. 2013;14:47. doi: 10.1186/1471-2296-14-47. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Liu K.D., Matthay M.A., Chertow G.M. Evolving practices in critical care and potential implications for management of acute kidney injury. Clin. J. Am. Soc. Nephrol. 2006;1:869–873. doi: 10.2215/CJN.00450206. [DOI] [PubMed] [Google Scholar]
  • 22.Kurts C., Panzer U., Anders H.J., Rees A.J. The immune system and kidney disease: Basic concepts and clinical implications. Nat. Rev. Immunol. 2013;13:738–753. doi: 10.1038/nri3523. [DOI] [PubMed] [Google Scholar]
  • 23.Zuo M., Tang J., Xiang M., Long Q., Dai J., Hu X. Characteristics and factors associated with nosocomial pneumonia among patients undergoing continuous renal replacement therapy (CRRT): A case-control study. Int. J. Infect. Dis. 2018;68:115–121. doi: 10.1016/j.ijid.2018.01.008. [DOI] [PubMed] [Google Scholar]
  • 24.Sarnak M.J., Amann K., Bangalore S., Cavalcante J.L., Charytan D.M., Craig J.C., Gill J.S., Hlatky M.A., Jardine A.G., Landmesser U., et al. Chronic Kidney Disease and Coronary Artery Disease: JACC State-of-the-Art Review. J. Am. Coll. Cardiol. 2019;74:1823–1838. doi: 10.1016/j.jacc.2019.08.1017. [DOI] [PubMed] [Google Scholar]
  • 25.Yang J.Y., Huang J.W., Chen L., Chen Y.Y., Pai M.F., Tung K.T., Peng Y.S., Hung K.Y. Frequency of Early Predialysis Nephrology Care and Postdialysis Cardiovascular Events. Am. J. Kidney Dis. 2017;70:164–172. doi: 10.1053/j.ajkd.2016.12.018. [DOI] [PubMed] [Google Scholar]
  • 26.Hughes A.J., Daniel S.E., Ben-Shlomo Y., Lees A.J. The accuracy of diagnosis of parkinsonian syndromes in a specialist movement disorder service. Brain. 2002;125:861–870. doi: 10.1093/brain/awf080. [DOI] [PubMed] [Google Scholar]
  • 27.Harrold L.R., Field T.S., Gurwitz J.H. Knowledge, patterns of care, and outcomes of care for generalists and specialists. J. Gen. Intern. Med. 1999;14:499–511. doi: 10.1046/j.1525-1497.1999.08168.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Hashem A., Chi M.T., Friedman C.P. Medical errors as a result of specialization. J. Biomed. Inform. 2003;36:61–69. doi: 10.1016/S1532-0464(03)00057-1. [DOI] [PubMed] [Google Scholar]
  • 29.Ahmed H., Farewell D., Francis N.A., Paranjothy S., Butler C.C. Risk of adverse outcomes following urinary tract infection in older people with renal impairment: Retrospective cohort study using linked health record data. PLoS Med. 2018;15:e1002652. doi: 10.1371/journal.pmed.1002652. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Van Dijk C.E., de Jong J.D., Verheij R.A., Jansen T., Korevaar J.C., de Bakker D.H. Compliance with referrals to medical specialist care: Patient and general practice determinants: A cross-sectional study. BMC Fam. Pract. 2016;17:11. doi: 10.1186/s12875-016-0401-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Hounkpatin H.O., Fraser S.D.S., Johnson M.J., Harris S., Uniacke M., Roderick P.J. The association of socioeconomic status with incidence and outcomes of acute kidney injury. Clin. Kidney J. 2019;13:245–252. doi: 10.1093/ckj/sfz113. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Chao C.T., Tsai H.B., Shih C.Y., Hsu S.H., Hung Y.C., Lai C.F., Ueng R.H., Chan D.C., Hwang J.J., Huang S.J. Establishment of a renal supportive care program: Experience from a rural community hospital in Taiwan. J. Formos. Med. Assoc. 2016;115:490–500. doi: 10.1016/j.jfma.2015.12.009. [DOI] [PubMed] [Google Scholar]
  • 33.Legido-Quigley H., Lopez P.A.C., Balabanova D., Perel P., Lopez-Jaramillo P., Nieuwlaat R., Schwalm J.-D., McCready T., Yusuf S., McKee M. Patients’ knowledge, attitudes, behaviour and health care experiences on the prevention, detection, management and control of hypertension in Colombia: A qualitative study. PLoS ONE. 2015;10:e0122112. doi: 10.1371/journal.pone.0122112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Cohen S.D., Sharma T., Acquaviva K., Peterson R.A., Patel S.S., Kimmel P.L. Social support and chronic kidney disease: An update. Adv. Chronic. Kidney Dis. 2007;14:335–344. doi: 10.1053/j.ackd.2007.04.007. [DOI] [PubMed] [Google Scholar]
  • 35.Taylor D.M., Fraser S., Dudley C., Oniscu G.C., Tomson C., Ravanan R., Roderick P., ATTOM investigators Health literacy and patient outcomes in chronic kidney disease: A systematic review. Nephrol. Dial. Transplant. 2018;33:1545–1558. doi: 10.1093/ndt/gfx293. [DOI] [PubMed] [Google Scholar]
  • 36.Gupta R., Plantinga L.C., Fink N.E., Melamed M.L., Coresh J., Fox C.S., Levin N.W., Powe N.R. Statin use and sepsis events in patients with chronic kidney disease. JAMA. 2007;297:1455–1464. doi: 10.1001/jama.297.13.1455. [DOI] [PubMed] [Google Scholar]
  • 37.Cherng Y.G., Liao C.C., Chen T.H., Xiao D., Wu C.H., Chen T.L. Are non-cardiac surgeries safe for dialysis patients? A population-based retrospective cohort study. PLoS ONE. 2013;8:e58942. doi: 10.1371/journal.pone.0058942. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Bou Chebl R., Tamim H., Abou Dagher G., Sadat M., Ghamdi G., Itani A., Saeedi A., Arabi Y.M. Sepsis in end-stage renal disease patients: Are they at an increased risk of mortality? Ann. Med. 2021;53:1737–1743. doi: 10.1080/07853890.2021.1987511. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Powe N.R., Jaar B., Furth S.L., Hermann J., Briggs W. Septicemia in dialysis patients: Incidence, risk factors, and prognosis. Kidney Int. 1999;55:1081–1090. doi: 10.1046/j.1523-1755.1999.0550031081.x. [DOI] [PubMed] [Google Scholar]
  • 40.Foley R.N., Guo H., Snyder J.J., Gilbertson D.T., Collins A.J. Septicemia in the United States dialysis population, 1991 to 1999. J. Am. Soc. Nephrol. 2004;15:1038–1045. doi: 10.1097/01.ASN.0000119144.95922.C4. [DOI] [PubMed] [Google Scholar]
  • 41.Eliakim-Raz N., Babitch T., Shaw E., Addy I., Wiegand I., Vank C., Torre-Vallejo L., Joan-Miquel V., Steve M., Grier S., et al. Risk factors for treatment failure and mortality among hospitalized patients with complicated urinary tract infection: A multicenter retrospective cohort study (RESCUING Study Group) Clin. Infect. Dis. 2019;68:29–36. doi: 10.1093/cid/ciy418. [DOI] [PubMed] [Google Scholar]
  • 42.Ross J.S., Normand S.-L.T., Wang Y., Ko D.T., Chen J., Drye E.E., Keenan P.S., Lichtman J.H., Bueno H., Schreiner G.C., et al. Hospital volume and 30-day mortality for three common medical conditions. N. Engl. J. Med. 2010;362:1110–1118. doi: 10.1056/NEJMsa0907130. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Joynt K.E., Orav E.J., Jha A.K. Physician volume, specialty, and outcomes of care for patients with heart failure. Circ. Heart Fail. 2013;6:890–897. doi: 10.1161/CIRCHEARTFAILURE.112.000064. [DOI] [PubMed] [Google Scholar]
  • 44.Van Oosten M.J.M., Logtenberg S.J.J., Edens M.A., Hemmelder M.H., Jager K.J., Bilo H.J.G., Stel V.S. Health claims databases used for kidney research around the world. Clin Kidney J. 2020;14:84–97. doi: 10.1093/ckj/sfaa076. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Cheng C.L., Lee C.H., Chen P.S., Li Y.H., Lin S.J., Yang Y.H. Validation of acute myocardial infarction cases in the national health insurance research database in taiwan. J. Epidemiol. 2014;24:500–507. doi: 10.2188/jea.JE20140076. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Su V.Y., Liu C.J., Wang H.K., Wu L.A., Chang S.C., Perng D.W., Su W.J., Chen Y.M., Lin E.Y., Chen T.J., et al. Sleep apnea and risk of pneumonia: A nationwide population-based study. CMA J. 2014;186:415–421. doi: 10.1503/cmaj.131547. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

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

Data Availability Statement

The data underlying this study is from the Health and Welfare Data Science Center. Interested researchers can obtain the data through formal application to the Health and Welfare Data Science Center, Department of Statistics, Ministry of Health and Welfare, Taiwan (http://dep.mohw.gov.tw/DOS/np-2497-113.html (accessed on 8 November 2021)). Under the regulations from the Health and Welfare Data Science Center, we have made the formal application (included application documents, study proposals, and ethics approval of the institutional review board) of the current insurance data. The authors of the present study had no special access privileges in accessing the data which other interested researchers would not have.


Articles from Journal of Clinical Medicine are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

RESOURCES