SYSTEMATIC REVIEW article

Front. Med., 04 November 2022

Sec. Nephrology

Volume 9 - 2022 | https://doi.org/10.3389/fmed.2022.1038315

Incidence, predictors, and outcomes of early hospital readmissions after kidney transplantation: Systemic review and meta-analysis

  • 1. Department of Internal Medicine, Dow University of Health Sciences, Karachi, Pakistan

  • 2. Department of Internal Medicine, Dr. Sampurnanand Medical College, Jodhpur, Rajasthan, India

  • 3. Department of Internal Medicine, Mayo Clinic Health System, Mankato, MN, United States

  • 4. Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, United States

  • 5. Department of Pulmonology, Texas A&M University College of Medicine, Bryan, TX, United States

  • 6. Department of Anesthesiology, Mayo Clinic, Rochester, MN, United States

Article metrics

View details

12

Citations

3,7k

Views

1,3k

Downloads

Abstract

Background:

Early hospital readmission (EHR) within 30 days after kidney transplantation is a significant quality indicator of transplant centers and patient care. This meta-analysis aims to evaluate the incidence, predictors, and outcomes of EHR after kidney transplantation.

Methods:

We comprehensively searched the databases, including PubMed, Cochrane CENTRAL, and Embase, from inception until December 2021 to identify studies that assessed incidence, risk factors, and outcome of EHR. The outcomes included death-censored graft failure and mortality. Data from each study were combined using the random effect to calculate the pooled incidence, mean difference (MD), odds ratio (OR), and hazard ratio (HR) with 95% confidence interval (CI).

Results:

A total of 17 studies were included. The pooled EHR incidence after kidney transplant was 24.4% (95% CI 21.7–27.3). Meta-analysis showed that recipient characteristics, including older recipient age (MD 2.05; 95% CI 0.90–3.20), Black race (OR 1.31; 95% CI 1.11, 1.55), diabetes (OR 1.32; 95% CI 1.22–1.43), and longer dialysis duration (MD 0.85; 95% CI 0.41, 1.29), donor characteristics, including older donor age (MD 2.02; 95% CI 0.93–3.11), and transplant characteristics, including delayed graft function (OR 1.75; 95% CI 1.42–2.16) and longer length of hospital stay during transplantation (MD 1.93; 95% CI 0.59–3.27), were significantly associated with the increased risk of EHR. EHR was significantly associated with the increased risk of death-censored graft failure (HR 1.70; 95% CI 1.43–2.02) and mortality (HR 1.46; 95% CI 1.27–1.67) within the first year after transplantation.

Conclusion:

Almost one-fourth of kidney transplant recipients had EHR within 30 days after transplant, and they had worse post-transplant outcomes. Several risk factors for EHR were identified. This calls for future research to develop and implement for management strategies to reduce EHR in high-risk patients.

Introduction

Kidney transplantation is the best renal replacement therapy option for end-stage kidney disease patients. Kidney transplant recipients have a higher long-term survival and quality of life than those who remains on dialysis (1, 2). Despite the advances in kidney transplantation and post-transplant care, hospital readmission is still frequent. Kidney transplant recipients are at higher risk of readmission given more comorbidity burden and vulnerability to complications (3, 4).

Early hospital readmission (EHR), defined as any hospitalization within 30 days of discharge following kidney transplantation, is a significant quality indicator of transplant centers and patient care (5). EHR is related to an increased morbidity, decreased quality of life, and higher medical expenditure and resource utilization (6). Reduced reimbursements from Medicare for hospitals with higher-than-expected readmission rates have been implemented due to recent policy changes aimed to reduce avoidable hospital readmissions and to improve health outcomes while reducing medical expenditure (6, 7). The incidence of EHR after kidney transplantation reported in the literature is variable. Different risk factors for EHR after kidney transplantation have been described (5, 810). Recognizing the risk factors for EHR is critical for identifying kidney transplant recipients who may benefit from additional post-transplant surveillance and the development of new strategies to reduce EHR.

The objective of this meta-analysis was to determine the incidence of EHR, identify the risks factors for EHR, and assess the impact of EHR on post-transplant outcomes in kidney transplant recipients.

Materials and methods

This article has been reported in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines (11).

Data sources and search strategy

We conducted a systematic literature search for relevant articles in the databases, including Pubmed, Embase, and Cochrane CENTRAL, using a comprehensive search strategy from inception until December 20th, 2021. The combination of the following MeSH keywords was used: “renal transplant,” “kidney transplant,” “readmission,” “early hospital readmission,” “30-day readmission,” “incidence,” “rate,” “predictor,” “risk factors,” and “association.” The detailed search strategy is presented in Supplementary Table 1.

Study selection and inclusion criteria

We included studies that reported the incidence, predictors, or outcomes of EHR after kidney transplantation. EHR was defined as 30-day readmission to any institution, due to any cause, after kidney transplantation. We excluded studies with (1) readmission >30 days after kidney transplantation, (2) combined kidney transplantations with other organs, (3) no outcomes of interest, and (4) reviews and letters. Duplicated studies retrieved from the systemic search were identified and eliminated using Endnote (Clarivate Analytics, Thomson Reuters Corporation, Philadelphia, Pennsylvania). The articles were screened based on titles and abstracts by two independent researchers (KI, AI) and subsequently assessed for relevance by reviewing full-text articles. References of the articles were also screened to identify additional studies.

The potential of sample dependence arises when multiple papers included in the review report findings from analyses on the same cohort of patients. When the studies had overlapping periods, the potential for sample dependence was minimized by the selection of studies with the longest period of data collection as the representative study for that cohort, for each variable. However, when two or more studies had the same period of data collection, the study with higher methodological quality was selected as the representative study.

Data extraction and outcomes

Two independent researchers (KI and AI) extracted data from the eligible articles. The following information was extracted: name of the first author, year of publication, study design, country of origin, sample size, subject demographics, comorbidities, and incidence of EHR. Data regarding the risk factors for EHR included the following recipient characteristics: age, gender, black race, body mass index (BMI), diabetes, prior dialysis, and dialysis duration; donor characteristics: age, donor type, and expanded donor criteria; and transplant characteristics: delayed graft function (DGF) and length of hospital stay during transplantation. The outcomes of EHR included death-censored graft failure and mortality within 1 year after kidney transplant. Raw data and adjusted estimates were extracted.

For studies that provided medians and ranges instead of means and standard deviations or provided only means in the absence of standard deviations, the means and/or standard deviations were calculated using the formula described by Hozo et al. (12). Some studies reported readmissions within 30 days of the procedure and others reported those within 30 days of discharge, readmissions data were extracted according to either definition, and the definition used by each study was recorded.

Statistical analysis and quality assessment

We utilized Review Manager v.5.3 (The Nordic Cochrane Center, The Cochrane Collaboration, 2014) and MedCalc v 20.027 to perform all the analyses. A random-effects model was used to calculate the Mantel Haenszel odds ratios (OR) for dichotomous variables and mean difference (MD) for continuous variables. Adjusted estimates were reported using inverse variance adjusted Hazard ratios (aHR). All estimates were reported with a confidence interval (CI) of 95% and a p-value < 0.05 was considered significant in all cases. We examined the correlation between the risk factors and EHR; risk factors reported in 3 or more studies were statistically analyzed. When available, risk factors based on multivariate analysis were also collected. To rule out the possibility of any single study disproportionately affecting the results, a leave-one-out sensitivity analysis was carried out by removing one study at a time. The quality appraisal of the included studies was performed by using the Newcastle–Ottawa Quality Assessment Scale (13). Each study was graded as: low bias risk (8–9 points), moderate bias risk (5–7 points), or significant bias risk (0–4 points).

Results

Literature search and baseline characteristics

The initial search strategy identified a total of 700 potentially relevant articles. After excluding the duplicates, 408 articles were screened for relevance based on their titles and abstracts. Out of these, 52 full-text articles that aligned with the objective of the manuscript were reviewed. Ultimately, 17 studies were included in the final analysis, out of which twelve were cohort studies (10 retrospective, 1 prospective, and 1 ambispective) and one was a case-control study (5, 810, 1425). Supplementary Figure 1 presents the PRISMA flowchart outlining the search process. Table 1 summarizes the study characteristics of the included articles and the causes of EHR. The results of the meta-analysis of potential risk factors for EHR are presented in Table 2. Figure 1 illustrates the results of all pooled analyses, while Supplementary Figures 2–19 present the individual plots of each potential risk factor of EHR.

Table 1

Study Country Study design Total participants No. of readmitted patients No. of non-readmitted patients within 30 days Readmission rate Definition of readmission Age [mean (SD)] Male gender (%) Causes of 30-day readmission
Bergman et al. (8) Canada Retrospective cohort; single-center 213 41 172 19.20% 30-days readmission rate 67.6 Renal (36.6%), infectious (29.3%), and gastrointestinal issues (21.9%)
Chu et al. (9) China Retrospective chart review; single-center 518 9 509 1.74% 30-days readmission rate 33.75 71
Covert et al. (14) US Retrospective case-control; single-center 384 64 320 16.70% 30-days readmission rates in kidney transplant recipients. 54.4 Infection (19%), surgical (18%), surgical complications (18%), Others (15%)
Dols et al. (15) US Retrospective, observational study 315 70 245 22.20% Hospital readmissions within 30 days following kidney transplantation Graft dysfunction (46%), nausea/vomiting (18%), infection (18%), volume overload or depletion (15%), and surgical complications (13%).
Famure et al. (16) US Ambispective observational cohort; single-center 1,093 212 881 19.40% First re-admission occurring within 30 days after discharge from the transplant hospitalization. 49.9 (13.2) 61.1 Infection (21), renal and genitourinary (20.5), rejection (14.9), drug toxicity (8.3), surgical complication (7.4), cardiovascular (5.2), gastrointestinal (1.8), endocrine (0.9), other (18.3)
Hogan et al. (17) US Retrospective cohort; multi-center 40,461 12,985 27,476 31.80% Hospital readmission within 30 days of discharge from transplant hospitalization 53.12 (13.68) 61.99
Kang et al. (18) Korea Retrospective, observational study; single-center 103 32 71 31.10% 1 or more readmissions within 30 days 62.1 Electrolyte imbalance (46.9%), acute rejection (18.6%), surgical complications (9.4%), infection
Kim et al. (5) UK Prospective cohort; single-center 269 56 213 20.82% ≥1 hospital readmission within 30 days of discharge from transplant hospitalization Median 55 (41–64) 59.11 Surgical reasons (25%): lymphocele, urinoma, hematoma, hernia, and infected incision site; infectious (18%): transplant pyelonephritis, neutropenic fever, pneumonia, cellulitis, gastroenteritis; metabolic (18%): electrolyte abnormalities, altered mental status; renal (14%): acute kidney injury (AKI) due to acute tubular necrosis (ATN) or acute rejection; gastrointestinal (12.5%); cardiovascular (9%); and miscellaneous (3.5%): anxiety, autonomic dysfunction.
Lichvar et al. (19) US Retrospective cohort study; single-center 216 71 145 32.80% 30-day readmission rate 50.5 (SD 13.9) 60.7 Electrolyte abnormalities (18.3%), allograft dysfunction (12.0.7)
Luan et al. (20) US Retrospective cohort study; single-center 1,064 286 778 26.90% Hospital readmissions within 30 days following kidney transplantation 49.3 (13.2) 62.8 Surgical complications (32.4%), infection (20.1%), acute kidney injuries/acute rejection (13.0%), Cardiovascular (11.0%), fluid and electrolyte issues (11.5%), gastrointestinal complaints (5.7%), deep vein thrombosis (1.3%), and others (5.0%).
Lubetzky et al. (21) US Retrospective cohort study; single-center 462 145 317 31.40% ≥1 hospital readmission within 30 days of discharge from transplant hospitalization 60.2 Surgical (20.7%), infection (21.7%), graft dysfunction (20.9%), gastrointestinal (21.7%), metabolic (21.7%), and others (13.9%)
McAdams-Demarco et al. (10) US National study of longitudinal Medicare claims data; multicenter 32,961 10,052 22,909 31% ≥1 hospital readmission within 30 days of discharge from transplant hospitalization 47.5 41 Renal (36), infection (12), endocrine (11), gastrointestinal (7), circulatory (6), allergy or drug effects (3), trauma (3), rehabilitation (3), renal failure (2), and others (17)
Naylor et al. (22) Canada Population-based cohort; multi-center 5,437 1,128 4,309 20.70% Hospital readmission within 30 days of discharge from transplant hospitalization 36.6 Rejection (18.7%); complications of procedures, not elsewhere classified (13.6%); acute renal failure (5.7%); other disorders of urinary system (4.3%); and post-procedural disorders of genitourinary system, not elsewhere classified (2.6%)
Nguyen et al. (23) US Retrospective cohort study; single-center 2,371 749 1,622 32% ≥1 hospital readmission within 30 days of discharge from transplant hospitalization median 50 60 Graft dysfunction (26.9%), gastrointestinal (16.3%), infection (11.2%), fluid and electrolyte abnormalities (9.3%), fever evaluation (8.7%), and hematologic (4.8%), pulmonary (4.1%), cardiovascular (4.6%), urologic (3.3%), surgical (3%)
Schucht et al. (24) US Retrospective chart review; single-center 141 37 104 26.20% 30-day readmission rate 54.8 (13.7) 55
Tavares et al. (25) Brazil Retrospective cohort study; single-center 1,175 313 862 26.60% Hospital readmission within 30 d following kidney transplantation 45.9 (35.2–54.5) 62.6 Infection (67%), surgical complications (14%), metabolic disturbances (11%), acute rejection (4.8%), cardiovascular events (2.2%), and renal artery stenosis (1%)
Whitlock et al., (26) US Retrospective chart review; single-center 325 99 226 30.46% Hospital readmission within 30 days of discharge from transplant hospitalization 52.3 (42.8, 61.1) 60.9

Baseline characteristics of included studies.

SD: standard deviation.

Table 2

Potential associations No. of studies No. of participants Pooled estimates Lower limit 95% CI Upper limit 95% CI p-value Heterogeneity I2 (%)
Recipient characteristics
Age 9 43,774 MD: 2.05 0.90 3.20 0.0005* 97
Gender 9 43,774 OR: 1.00 0.89 1.12 0.98 56
Black race 7 42,494 OR: 1.31 1.11 1.55 0.001* 64
Body mass index 4 36,232 MD: 0.53 −0.08 1.14 0.09 77
Diabetes 8 41,894 OR: 1.32 1.22 1.43 < 0.00001* 14
Prior dialysis 5 8,962 OR: 1.32 0.98 1.78 0.07 57
Number of years on dialysis 7 42,544 MD: 0.85 0.41 1.29 0.0001* 99
Donor characteristics
Age 5 41,099 MD: 2.02 0.93 3.11 0.0003* 96
Status of the donor (alive/dead) 9 43,764 OR: 1.64 0.71 3.79 0.24 99
Expanded donor criteria 5 36,046 OR: 1.35 0.81 2.25 0.25 93
Transplant characteristics
Delayed graft function 7 41,794 OR: 1.75 1.42 2.16 < 0.00001* 82
Length of hospital stay during transplantation 5 37,367 MD: 1.93 0.59 3.27 0.005* 99
Outcomes associated with EHR
Death-censored graft failure within the first year after transplantation. 3 6,754 HR: 1.70 1.43 2.02 < 0.00001* 2
Mortality within the first year of renal transplant 3 6,754 HR: 1.46 1.27 1.67 < 0.00001* 0

Meta-analysis of the risk factors and outcomes associated with early hospital readmission (30-day) after kidney transplantation.

OR, odds ratio; MD, mean difference; HR, hazard ratio; CI, confidence interval; p-value: probability value,

*

significant.

Figure 1

Figure 1

Forest plot summarizing the pooled analyses of all potential factors associated with early hospital readmission (30-day) after kidney transplantation. IV, inverse variance; SE, standard error; CI, confidence interval; HER, early hospital readmission.

Quality assessment and publication bias

The methodological quality assessment of included studies (Supplementary Table 2) showed that seven studies had low risk of bias, while 10 had moderate risk of bias. Therefore, all the studies were eligible for quantitative analysis. The funnel plots of publication bias are illustrated in Supplementary Figures 20, 21. There was no significant publication bias among all the outcomes, and the individual p-values of Begg-Mazumdar's rank correlation test and Egger's regression test are presented in Supplementary Table 3.

Results of meta-analysis

Incidence of early hospital readmission

A total of 16 studies reported the incidence of EHR after kidney transplantation in 26,285 out of total 87,124 transplant recipients. The pooled incidence of EHR in kidney transplant recipients was 24.4% [95% CI = 21.7–27.3 %; I2 = 98.26%; Figure 2).

Figure 2

Figure 2

The pooled incidence of 30-day readmission after kidney transplantation.

Predictors

Recipient characteristics

Recipient characteristics assessed across included studies were age, gender, black race, body mass index, diabetes, prior dialysis, and number of years on dialysis. Meta-analysis revealed that recipient's older age (MD = 2.05 [95% CI 0.90, 3.20]; p = 0.0005; I2 = 97%), black race (OR = 1.31 [95% CI 1.11, 1.55]; p = 0.001; I2 = 64%), diabetes (OR = 1.32 [95% CI 1.22, 1.43]; p < 0.00001; I2 = 14%), and longer dialysis duration (MD = 0.85 [95% CI 0.41, 1.29]; p = 0.0001; I2 = 99%) were significantly associated with increased EHR (Figure 1, Supplementary Figures 2–5). However, no significant association of EHR was found with recipient's gender (OR = 1.00 [95% CI 0.89, 1.12]; p = 0.98; I2 = 56%), body mass index (MD = 0.53 [95% CI −0.08, 1.14]; p = 0.09; I2 = 77%), and prior dialysis (OR = 1.32 [95% CI 0.98, 1.78]; p = 0.07; I2 = 57%) (Figure 1, Supplementary Figures 6–8).

On pooling studies that reported adjusted data, we observed that recipient's older age (MD = 1.16 [95% CI 1.00, 1.35]; p = 0.05; I2 = 89%) and longer dialysis duration (MD = 1.01 [95% CI 1.00, 1.02]; p = 0.04; I2 = 76%) remained significantly associated with EHR (Supplementary Figures 9, 10).

Donor characteristics and transplant characteristics

The meta-analyzed donor characteristics included older age, donor type, and expanded donor criteria. Older donor age was significantly associated with increased EHR (MD = 2.02 [95% CI 0.93, 3.11]; p = 0.0003; I2 = 96%) (Figure 1, Supplementary Figure 11). However, deceased donor (OR = 1.64 [95% CI 0.71, 3.79]; p = 0.24; I2 = 99%) and expanded donor criteria (OR = 1.35 [95% CI 0.81, 2.25]; p = 0.25; I2 = 93%) were not significantly associated with EHR (Figure 1, Supplementary Figures 12, 13).

Transplant characteristics, including delayed graft function (OR = 1.75 [95% CI 1.42, 2.16]; p < 0.00001; I2 = 82%) and longer length of hospital stay during transplantation (MD = 1.93 [95% CI 0.59, 3.27]; p = 0.0003; I2 = 99%), were significantly associated with increased EHR (Figure 1, Supplementary Figures 14, 15). On adjusted analysis, delayed graft function (aOR = 1.43 [95% CI 1.11, 1.85]; p = 0.006; I2 = 74%) and longer length of hospital stay (aOR = 1.20 [95% CI 1.07, 1.36]; p = 0.002; I2 = 91%) and remained significantly associated with increased EHR (Supplementary Figures 16, 17).

The results of leave-one-out sensitivity analysis and studies that caused a significant drop in heterogeneity are shown in Supplementary Table 4. Deceased donor (OR = 1.35 [0.81, 2.25]; p = 0.0010; I2 = 68%) and expanded donor criteria (OR = 1.60 [1.11, 2.32]; p = 0.01; I2 = 66%) became significant predictors of EHR on performing leave-one-out sensitivity analysis.

Outcomes

Overall, three studies with a total of 1,460 kidney transplant recipients with EHR and 5,294 recipients without EHR documented the association of EHR with death-censored graft failure and mortality within 1 year after kidney transplant. EHR was significantly associated with increased risk of death-censored graft failure within the first year after transplantation (aHR = 1.70 [95% CI 1.43, 2.02]; p < 0.00001; I2 = 2%) (Supplementary Figure 18). EHR was significantly associated with increased mortality (aHR = 1.46 [95% CI 1.27, 1.67]; p < 0.00001; I2 = 0%) (Supplementary Figure 19).

Discussion

In the current meta-analysis, we have summarized pertinent evidence on the incidence, risk factors, and outcomes of EHR in kidney transplantation. Significant recipient-related risk factors of EHR after kidney transplantation included age, gender, black race, BMI, diabetes, and a higher number of years on dialysis. Similarly, older donor age and deceased donor were significant donor-related predictors of EHR. Delayed graft function (DGF) and a longer length of hospital stay during transplantation were significant transplant characteristics that increased the odds of EHR. Moreover, EHR was significantly associated with incident death-censored graft failure and mortality within the first year of transplantation.

Our study showed a pooled incidence of 30-day readmission of 24.4% [95% CI = 21.7–27.3 %). This is higher than the incidence of readmission previously reported in patients undergoing orthopedic procedures (5.4%), colectomy (14.7%), and pancreatic resection (19.1%) (2729). However, other organ transplantation studies on liver (30.6%) and lung transplantation (45.4%) have reported higher incidence of EHR (30, 31).

We found an increased risk of EHR in black recipients. This finding is consistent with a greater risk of readmission in black recipients in conditions such as congestive heart failure, myocardial infarction, and pneumonia (32). Moreover, a longer time on dialysis was observed to be a significant risk factor for EHR in kidney transplantation. This could be explained by the immunological modifications, associated comorbidity burden, and physiological reserve decline (17, 33). An increase in risk of EHR and mortality due to infections have been shown in both hemodilaysis and peritoneal dialysis patients (34). Meier-Kriesche et al. reported that a longer duration of dialysis pre-transplant was associated with an increased risk of death censored graft loss (p < 0.001). Dialysis treatment of 6–12, 12, and 12–24 months was associated with a 37, 55, and 68% greater risk for death-censored graft loss, respectively (35).

In our analysis diabetes increased the risk of EHR. A previous retrospective study of 366 kidney transplant, transplant due to diabetic nephropathy was significantly associated with more and earlier post-transplant readmissions compared with patients who underwent transplants due to non-diabetic end-stage kidney disease (36). Diabetes is one of the most important factors for recurrent urinary tract infection after the transplant, and these types of infections are the most frequent in renal transplant patients (37). Moreover, Enomoto et al. (38) reported that diabetic patients were more likely to be readmitted (adjusted OR = 1.17, 95% CI 1.15–1.19; p < 0.001) compared to non-diabetics. Factors associated with readmissions included infections (9.4 vs. 7.7%), heart failure (6.0 vs. 3.1%), and chest pain/myocardial infarction (5.5 vs. 3.3%) (39).

DGF leads to an increased risk of EHR and short-term as well as long-term graft loss (39). Dialysis-dependent states and various other comorbidities are also linked with a longer length of hospital stay. Prolonged hospital stay could lead to higher chances of contracting infections. A shorter length of stay may indicate a low-risk recipient receiving a kidney from a low-risk donor (19). EHR was also significantly associated with death-censored graft failure and mortality within the first year of kidney transplant. Heldal et al. showed that DGF was an independent risk factor for death-censored graft loss in patients aged 60 years or more, while Faravardeh et al. reported that DGF and acute rejection were predictors for graft failure in younger recipients as well (40, 41). Mortality is associated with infectious, cardiovascular, and cerebrovascular complications but also depends on transplant center practices and the quality of post-transplant follow-up (5).

Our systematic review suggests patients at high risk of EHR can be identified through relevant risk factors. Patients are likely to have more than one of the above-mentioned risk factors and, therefore, predictive models should be developed to identify patients at high risk of EHR at the time of discharge. It may provide the basis of a robust risk predictive model given the number of studies included. Such patients could be selected in clinical trials to experiment with interventions to prevent early readmissions. A systematic review by Leppin et al. observed that tested interventions prevented 30-day readmissions in patients admitted to an inpatient ward for a minimum of 24 h for any medical or surgical reason. They reported that multidisciplinary strategies which increase patients' easy access to post-discharge care were the most successful (42). Quality improvement initiatives decreased the risk of readmissions by 23.7, 12.1, and 6.3% in chronic obstructive pulmonary disease, congestive heart failure patients and the general population, respectively (43, 44). Taber et al. implemented a multi-faceted strategy to improve health care value for kidney transplant patients, particularly those who developed DGF. They reported that the length of hospital stay during transplantation in DGF patients decreased from 8 to 4 days at the start of the intervention, while the national length of hospital stay during this time was 10 days (45). Moreover, focus on patient education, improved discharge planning, post-discharge phone calls, patient hotlines, and follow-up home visits also yielded positive results (46).

There are several limitations in our meta-analysis. First, most of the included articles were single-center observational studies, which limits cohort size and generalization of data. Most studies were retrospective in nature; therefore, the inherent confounding of the study type was inevitable. Second, some included articles defined EHR as readmission within 30 days from the date of the transplant procedure, while others measured EHR from the date of discharge after transplantation. Third, our study reported significant heterogeneity across various risk factors. Heterogeneity in our meta-analysis could be due to various factors that lead to effect size variability. The high I-squared values in the incidence of EHR and other risk factors in our study could be attributed to differences in sex, age, surgeon training, and time from enrollment in the included studies. Last, there was insufficient data to assess the role of type of immunosuppression on EHR after kidney transplantation.

Conclusion

This meta-analysis reported a high incidence of EHR in kidney transplant patients and summarized the evidence available on the risk factors associated with it. The most prominent risk factors include recipient's black race, diabetes, a higher number of years on dialysis, delayed graft function (DGF), and a longer length of hospital stay during transplantation. EHR is associated with death censored graft failure and mortality within the first year of transplantation. Hence, future research should aim to develop and implement predictive models for patient identification and novel management strategies to reduce EHR in patients at risk.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Statements

Data availability statement

Publicly available datasets were analyzed in this study. This data can be found here: Data is available upon reasonable request from the authors.

Author contributions

KI and SSR: concept/design. AI and SKK: data analysis/interpretation. MH, KI, AI, and SKK: drafting article. FY, TK, CT, and SS: critical revision of the article. TK, CT, and SS: approval of the article. FY: statistics. AI and SSR: data collection. All authors contributed to the article and approved the submitted version.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmed.2022.1038315/full#supplementary-material

    Abbreviations

  • EHR

    early hospital readmission

  • DGF

    delayed graft function.

References

  • 1.

    Suthanthiran M Strom TB . Renal transplantation. N Engl J Med. (1994) 331:36576. 10.1056/NEJM199408113310606

  • 2.

    Wolfe RA Ashby VB Milford EL Ojo AO Ettenger RE Agodoa LYC et al . Comparison of mortality in all patients on dialysis, patients on dialysis awaiting transplantation, and recipients of a first cadaveric transplant. N Engl J Med. (1999) 341:172530. 10.1056/NEJM199912023412303

  • 3.

    Weinhandl ED Snyder JJ Israni AK Kasiske BL . Effect of comorbidity adjustment on CMS criteria for kidney transplant center performance. Am J Transpl. (2009) 9:50616. 10.1111/j.1600-6143.2008.02527.x

  • 4.

    Harhay MN Hill AS Wang W Even-Shoshan O Mussell AS Bloom RD et al . Measures of global health status on dialysis signal early rehospitalization risk after kidney transplantation. PLoS ONE. (2016) 11:e0156532. 10.1371/journal.pone.0156532

  • 5.

    Kim SH Baird GL Bayliss G Merhi B Osband A Gohh R et al . single-center analysis of early readmission after renal transplantation. Clin Transpl. (2019) 33:e13520. 10.1111/ctr.13520

  • 6.

    Jencks SF Williams M V Coleman EA . Rehospitalizations among patients in the medicare fee-for-service program. N Engl J Med. (2009) 360:141828. 10.1056/NEJMsa0803563

  • 7.

    Epstein AM . Revisiting readmissions—changing the incentives for shared accountability. N Engl J Med. (2009) 360:14579. 10.1056/NEJMe0901006

  • 8.

    Bergman J Tennankore K Vinson A . Early and recurrent hospitalization after kidney transplantation: analysis of a contemporary Canadian cohort of kidney transplant recipients. Clin Transpl. (2020) 34:e14007. 10.1111/ctr.14007

  • 9.

    Chu A Zhang T Fang Y Yuan L Guan X Zhang H . Unplanned hospital readmissions after kidney transplantation among patients in Hefei, China: incidence, causes and risk factors. Int J Nurs Sci. (2020) 7:2916. 10.1016/j.ijnss.2020.05.002

  • 10.

    McAdams-Demarco MA Grams ME Hall EC Coresh J Segev DL . Early hospital readmission after kidney transplantation: patient and center-level associations. Am J Transpl. (2012) 12:32838. 10.1111/j.1600-6143.2012.04285.x

  • 11.

    Page MJ McKenzie JE Bossuyt PM Boutron I Hoffmann TC Mulrow CD et al . The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. J Clin Epidemiol. (2021) 134:17889. 10.1016/j.jclinepi.2021.02.003

  • 12.

    Hozo SP Djulbegovic B Hozo I . Estimating the mean and variance from the median, range, and the size of a sample. BMC Med Res Methodol. (2005) 5:110. 10.1186/1471-2288-5-13

  • 13.

    Luchini C Stubbs B Solmi M Veronese N . Assessing the quality of studies in meta-analyses: advantages and limitations of the Newcastle Ottawa scale. World J Meta-Anal. (2017) 5:804. 10.13105/wjma.v5.i4.80

  • 14.

    Covert KL Fleming JN Staino C Casale JP Boyle KM Pilch NA et al . Predicting and preventing readmissions in kidney transplant recipients. Clin Transpl. (2016) 30:77986. 10.1111/ctr.12748

  • 15.

    Dols JD Chargualaf KA Spence AI Flagmeier M Morrison ML . Impact of population differences: post-kidney transplant readmissions. Nephrol Nurs J. (2018) 45:27380.

  • 16.

    Famure O Kim ED Au M Zyla RE Huang JW Chen PX Li Y et al . What are the burden, causes, and costs of early hospital readmissions after kidney transplantation?Prog Transpl. (2021) 31:1607. 10.1177/15269248211003563

  • 17.

    Hogan J Arenson MD Adhikary SM Li K Zhang X Zhang R Valdez JN et al . Assessing predictors of early and late hospital readmission after kidney transplantation. Transpl Direct. (2019) 5:918. 10.1097/TXD.0000000000000918

  • 18.

    Kang IC Kim IK Son S Ju MK . Impact of early hospital readmissions after kidney transplantation on graft function. Transpl Proc. (2018) 50:235962. 10.1016/j.transproceed.2017.12.062

  • 19.

    Lichvar AB Patel A Pierce D Gimbar RP Tzvetanov I Benedetti E et al . Factors influencing emergency department utilization and hospital re-admissions in a predominantly obese, racially diverse urban renal transplant population. Prog Transpl. (2021) 31:729. 10.1177/1526924820978596

  • 20.

    Luan FL Barrantes F Roth RS Samaniego M . Early hospital readmissions post-kidney transplantation are associated with inferior clinical outcomes. Clin Transpl. (2014) 28:48793. 10.1111/ctr.12347

  • 21.

    Lubetzky M Yaffe H Chen C Ali H Kayler LK . Early readmission after kidney transplantation: examination of discharge-level factors. Transplantation. (2016) 100:107985. 10.1097/TP.0000000000001089

  • 22.

    Naylor KL Knoll GA Slater J McArthur E Garg AX Lam NN et al . Risk factors and outcomes of early hospital readmission in Canadian kidney transplant recipients: a population-based multi-center cohort study. Can J Kidney Health Dis. (2021) 8:20543581211060926. 10.1177/20543581211060926

  • 23.

    Nguyen MC Avila CL Brock GN Benedict JA James I El-Hinnawi A et al . “Early” and “Late” hospital readmissions in the first year after kidney transplant at a single center. Clin Transpl. (2020) 34:e13822. 10.1111/ctr.13822

  • 24.

    Schucht J Davis EG Jones CM Cannon RM . Incidence of and risk factors for multiple readmissions after kidney transplantation. Am Surg. (2020) 86:11620. 10.1177/000313482008600230

  • 25.

    Tavares MG Cristelli MP Ivani de Paula M Viana L Felipe CR Proença H et al . Early hospital readmission after kidney transplantation under a public health care system. Clin Transpl. (2019) 33:e13467. 10.1111/ctr.13467

  • 26.

    Whitlock RS Seals S Seawright A Wynn JJ Anderson C Earl TM . Socioeconomic factors associated with readmission after deceased donor renal transplantation. Am Surg. (2017) 83:75560.

  • 27.

    Bernatz JT Tueting JL Anderson PA . Thirty-day readmission rates in orthopedics: a systematic review and meta-analysis. PLoS ONE. (2015) 10:e0123593. 10.1371/journal.pone.0123593

  • 28.

    Fisher A V Fernandes-Taylor S Campbell-Flohr SA Clarkson SJ Winslow ER Abbott DE et al . 30-day readmission after pancreatic resection: a systematic review of the literature and meta-analysis. Ann Surg. (2017) 266:24250. 10.1097/SLA.0000000000002230

  • 29.

    Bliss LA Maguire LH Chau Z Yang CJ Nagle DA Chan AT et al . Readmission after resections of the colon and rectum: predictors of a costly and common outcome. Dis Colon Rectum. (2015) 58:116473. 10.1097/DCR.0000000000000433

  • 30.

    Mumtaz K Lee-Allen J Porter K Kelly S Hanje J Conteh LF et al . Thirty-day readmission rates, trends and its impact on liver transplantation recipients: a national analysis. Sci Rep. (2020) 10:111. 10.1038/s41598-020-76396-5

  • 31.

    Osho AA Castleberry AW Yerokun BA Mulvihill MS Rucker J Snyder LD et al . Clinical predictors and outcome implications of early readmission in lung transplant recipients. J Heart Lung Transpl. (2017) 36:54653. 10.1016/j.healun.2016.11.001

  • 32.

    Joynt KE Orav EJ Jha AK . Thirty-day readmission rates for Medicare beneficiaries by race and site of care. JAMA. (2011) 305:67581. 10.1001/jama.2011.123

  • 33.

    Chopra B Sureshkumar KK . Kidney transplantation in older recipients: Preemptive high KDPI kidney vs. lower KDPI kidney after varying dialysis vintage. World J Transpl. (2018) 8:1029. 10.5500/wjt.v8.i4.102

  • 34.

    Laurin LP Harrak H Elftouh N Ouimet D Vallée M Lafrance JP . Outcomes of infection-related hospitalization according to dialysis modality. Clin J Am Soc Nephrol. (2015) 10:81724. 10.2215/CJN.09210914

  • 35.

    Meier-Kriesche HU Port FK Ojo AO Rudich SM Hanson JA Cibrik DM et al . Effect of waiting time on renal transplant outcome. Kidney Int. (2000) 58:13117. 10.1046/j.1523-1755.2000.00287.x

  • 36.

    Ramezani M Ghoddousi K Hashemi M Khoddami-Vishte HR Fatemi-Zadeh S Saadat SH et al . Diabetes as the cause of end-stage renal disease affects the pattern of post kidney transplant rehospitalizations. Transpl Proc. (2007) 39:9669. 10.1016/j.transproceed.2007.03.074

  • 37.

    Schachtner T Stein M Reinke P . Diabetic kidney transplant recipients: Impaired infection control and increased alloreactivity. Clin Transpl. (2017) 31:e12986. 10.1111/ctr.12986

  • 38.

    Enomoto LM Shrestha DP Rosenthal MB Hollenbeak CS Gabbay RA . Risk factors associated with 30-day readmission and length of stay in patients with type 2 diabetes. J Diabetes Compl. (2017) 31:1227. 10.1016/j.jdiacomp.2016.10.021

  • 39.

    Ojo AO Wolfe RA Held PJ Port FK Schmouder RL . Delayed graft function: risk factors and implications for renal allograft survival. Transplantation. (1997) 63:96874. 10.1097/00007890-199704150-00011

  • 40.

    Heldal K Hartmann A Leivestad T Svendsen M V Foss A Lien B et al . Clinical outcomes in elderly kidney transplant recipients are related to acute rejection episodes rather than pretransplant comorbidity. Transplantation. (2009) 87:104551. 10.1097/TP.0b013e31819cdddd

  • 41.

    Faravardeh A Eickhoff M Jackson S Spong R KGBRla A Issa N et al . Predictors of graft failure and death in elderly kidney transplant recipients. Transplantation. (2013) 96:108996. 10.1097/TP.0b013e3182a688e5

  • 42.

    Leppin AL Gionfriddo MR Kessler M Brito JP Mair FS Gallacher K et al . Preventing 30-day hospital readmissions: a systematic review and meta-analysis of randomized trials. JAMA Intern Med. (2014) 174:1095107. 10.1001/jamainternmed.2014.1608

  • 43.

    Nuckols TK Keeler E Morton S Anderson L Doyle BJ Pevnick J et al . Economic evaluation of quality improvement interventions designed to prevent hospital readmission: a systematic review and meta-analysis. JAMA Intern Med. (2017) 177:975. 10.1001/jamainternmed.2017.1136

  • 44.

    Rohde J Joseph A Tambedou B Jain NK Khan SA Surani S et al . Reducing 30-day all-cause acute exacerbation of chronic obstructive pulmonary disease readmission rate with a multidisciplinary quality improvement project. Cureus. (2021) 13:19917. 10.7759/cureus.19917

  • 45.

    Taber DJ Pilch NA McGillicuddy JW Bratton CF Lin A Chavin KD et al . Improving the perioperative value of care for vulnerable kidney transplant recipients. J Am Coll Surg. (2013) 216:66878. 10.1016/j.jamcollsurg.2012.12.023

  • 46.

    Hoyer EH Needham DM Atanelov L Knox B Friedman M Brotman DJ . Association of impaired functional status at hospital discharge and subsequent rehospitalization. J Hosp Med. (2014) 9:27782. 10.1002/jhm.2152

Summary

Keywords

readmission, early hospital readmission, kidney transplant, incidence, predictors

Citation

Iqbal K, Hasanain M, Rathore SS, Iqbal A, Kazmi SK, Yasmin F, Koritala T, Thongprayoon C and Surani S (2022) Incidence, predictors, and outcomes of early hospital readmissions after kidney transplantation: Systemic review and meta-analysis. Front. Med. 9:1038315. doi: 10.3389/fmed.2022.1038315

Received

06 September 2022

Accepted

17 October 2022

Published

04 November 2022

Volume

9 - 2022

Edited by

Vivek Jha, Imperial College London, United Kingdom

Reviewed by

Woo Yeong Park, Keimyung University Dongsan Medical Center, South Korea; Eva Gavela Martínez, Doctor Peset University Hospital, Spain

Updates

Copyright

*Correspondence: Farah Yasmin Kinza Iqbal

This article was submitted to Nephrology, a section of the journal Frontiers in Medicine

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Outline

Figures

Cite article

Copy to clipboard


Export citation file


Share article

Article metrics