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. Author manuscript; available in PMC: 2014 Nov 1.
Published in final edited form as: Am J Kidney Dis. 2013 May 29;62(5):10.1053/j.ajkd.2013.03.022. doi: 10.1053/j.ajkd.2013.03.022

Comparison of Life Participation Activities Among Adults Treated by Hemodialysis, Peritoneal Dialysis, and Kidney Transplantation: A Systematic Review

Tanjala S Purnell 1,2, Priscilla Auguste 2, Deidra C Crews 2,3, Julio Lamprea-Montealegre 2,4, Temitope Olufade 2,4, Raquel Greer 1,2, Patti Ephraim 2,4, Johanna Sheu 5, Daniel Kostecki 2, Neil R Powe 6, Hamid Rabb 3, Bernard Jaar 2,3, L Ebony Boulware 1,2,4
PMCID: PMC3809150  NIHMSID: NIHMS486330  PMID: 23725972

Abstract

Background

A comprehensive assessment of the association of patients’ renal replacement therapy (RRT) modality on their participation in life activities (physical function, travel, recreation, freedom, work) is needed.

Study Design

Systematic review of peer-reviewed published studies.

Setting & Population

Adults undergoing RRT (hemodialysis, peritoneal dialysis, or transplantation).

Selection Criteria for Studies

We searched PubMed, Cochrane Library, and EMBASE from January 1980 through April 2012 for English-language articles that compared participation in life activities among patients receiving 1) hemodialysis compared with peritoneal dialysis, 2) hemodialysis compared with kidney transplantation, or 3) peritoneal dialysis compared with kidney transplantation.

Predictor

RRT modality.

Outcomes

Reported rates of physical function, travel, recreation, freedom, and work-related activities by RRT modality.

Results

A total of 46 studies (6 prospective cohort, 38 cross-sectional, and 2 pre-post transplantation) provided relevant comparisons of life participation activities among patients treated with hemodialysis, peritoneal dialysis, and kidney transplantation. Studies were conducted from 1985 to 2011 among diverse patient populations in 16 distinct locations. A majority of studies reported greater life participation rates among patients with kidney transplants compared to patients receiving either hemodialysis or peritoneal dialysis. In contrast, a majority of studies reported no differences in outcomes between patients receiving hemodialysis and patients receiving peritoneal dialysis. These results were consistent throughout the study period, across diverse populations, and among the subset of studies that performed appropriate adjustments for potential confounding factors.

Limitations

Many studies included in the review had significant design weaknesses.

Conclusions

Evidence suggests patients with kidney transplants may experience better rates of life participation compared to patients receiving dialysis, while patients receiving hemodialysis and patients receiving peritoneal dialysis may experience similar rates of life participation. Rigorously performed studies are needed to better inform patients about the association of RRT on these important patient reported outcomes.

Keywords: dialysis, ESRD treatment, kidney transplantation, physical functioning, quality of life, social participation


Patients initiating renal replacement therapy (RRT) for end-stage renal disease (ESRD) experience significant morbidity and limitations in quality of life1,2. Limitations include often-substantial decrements in patients’ involvement in social and recreational activities, freedom, and abilities to work and travel, which have been associated with poorer overall health status and survival17. While their declining involvement in life activities may be attributed, in part, to patients’ significant ESRD-associated morbidity8, the extent to which patients’ mode of RRT might independently influence their life participation has not been well-quantified.

The various RRT modalities (hemodialysis, peritoneal dialysis and kidney transplantation) have distinct characteristics, including different delivery methods (e.g., treatment in a center versus at home), requirements for self-care (e.g., clinician directed versus self-directed), levels of physical invasiveness (e.g., need for catheters or surgery), and associated symptoms (e.g., fatigue with dialysis or transplantation medication side effects). Each of these RRT characteristics could substantially influence patients’ abilities to engage in social and recreational activities912, and they are frequently presented to patients as important factors they should consider while approaching decisions regarding initiating or switching RRT modalities1317.

Prior studies suggested patients who undergo transplantation generally experience better quality of life than dialysis patients1820, while there may be no significant differences for patients on hemodialysis compared with peritoneal dialysis21,22. However, these studies broadly examined quality of life without a specific focus on systematically examining the independent association of RRT modality with patients’ physical activity, freedom, and their abilities to participate in key activities of daily living, such as their abilities to work, travel, and participate in social and recreational activities, all important but distinct aspects which contribute to patients’ global quality of life. Patients with ESRD and their families view information about the influence of RRT selection on these life activities as important to include in educational material informing patients’ RRT selection decisions23. Systematic reviews summarizing evidence of associations between RRT modality choice and patients’ abilities to participate in these important life activities could therefore greatly enhance informed decisions about RRT selection.

We performed a systematic literature review to provide an evidence-based summary of the association of patients’ RRT modality with their rates of life participation activities across a variety of outcomes measures, settings, and patient populations.

Methods

Study Design

We performed a systematic review of published, peer-reviewed studies describing differences in rates of five types of activities reflecting various aspects of life participation (i.e., physical function, travel, recreation, freedom, and work outcomes) reported by adults with ESRD receiving different RRTs. We assessed factors that could influence the validity of study findings, and we quantified the direction and magnitude of differences in life participation outcomes among patients receiving different RRTs.

Populations Studied

Eligible articles reported on adults receiving RRT (hemodialysis, peritoneal dialysis, and kidney transplantation). Hemodialysis modalities considered eligible in our study included both in-center hemodialysis and ‘non-specific’ hemodialysis (i.e., patients on in-center hemodialysis plus one or more alternative modes of hemodialysis, such as satellite hemodialysis, home hemodialysis, nocturnal dialysis, etc.). We included both deceased donor and living donor kidney transplantation.

Data Sources and Literature Search Strategy

We identified studies potentially eligible for inclusion in our review through a search of all studies in PubMed, EMBASE, and the Cochrane Library (trials only) from January 1980 through April 2012. An expert methodologist and content experts within our team developed comprehensive search strategies to identify relevant studies. Our search terms consisted of key words for each treatment modality and terms for each of the five life participation outcomes. We hand-searched bibliographies of all potentially-relevant studies to identify additional articles that our electronic search might have missed. Our initial hand search of bibliographies revealed that there were missed studies reporting primarily on ‘quality of life’ outcomes but also reporting relevant life participation outcomes as secondary outcomes. Thus, we repeated our electronic search with additional terms consisting of key words to identify studies primarily reporting on ‘quality of life’ outcomes. We conducted this expanded search in all three databases and screened all studies for their potential inclusion in our review. The detailed search strategies are included within Table S1 (provided as online supplementary material).

We identified studies as reporting on physical function outcomes if they reported data on patients’ limitations in performing activities of daily living, patients’ self-reported physical functioning assessed via quality of life sub-scales (e.g., in SF-36), or other measures of physical activity. We identified studies as reporting on travel outcomes if they reported on patients’ travel abilities or restrictions. We identified studies as reporting on recreation outcomes if they reported on patients’ abilities to engage in recreational or social activities (e.g., in SF-36). We identified studies as reporting on freedom outcomes if they reported on patients’ perceived independence, ability to perform usual tasks, or intrusiveness. We identified studies as reporting on work outcomes if they reported on employment status or working capacity.

Study Inclusion and Exclusion Criteria, Data Extraction

We reviewed titles and abstracts of identified citations for potential inclusion. We then reviewed the full text of any citation deemed potentially relevant. We included studies if they reported on relevant outcomes (physical function, travel, recreation, freedom, and work) as a primary or secondary outcome, and if they compared relevant outcomes for participants on at least two different ESRD treatment modalities (i.e., hemodialysis, peritoneal dialysis, or kidney transplantation). We excluded articles if they 1) were not written in English, 2) did not include relevant outcomes, 3) included only participants younger than 18 years old, 4) contained no original data (i.e. review, commentary, editorial, meeting abstract, or letter) 5) were case reports, or 6) did not compare differences in relevant outcomes among patients receiving different RRT modalities. We also excluded studies of special populations (e.g., studies including only home hemodialysis patients but not in-center hemodialysis patients) to prevent expected small study size bias. For each article that met our inclusion criteria, two reviewers independently extracted data, including information on study design, follow-up, RRT modalities compared, locations, sample sizes, participant characteristics, and outcomes. Reviewers resolved disagreements by discussion and adjudication with a third party.

Classification of Study Designs

We classified eligible studies into one of four main design types: randomized controlled trial (RCT), longitudinal cohort (prospective/retrospective), cross sectional, and pre-post transplantation24. We classified a study as RCT if it contained two or more groups receiving different RRT modalities, and patients were randomly allocated to RRT modality as indicated by investigators. We classified a study as cohort if there were at least two groups receiving different RRT modalities (without random allocation), and investigators reported repeated assessments of relevant outcomes. Such studies could be prospective or retrospective in nature. We classified a study as cross-sectional if there were at least two groups receiving different RRT modalities (without random allocation), and investigators assessed relevant outcomes at only one point in time. Finally, we classified a study as pre-post transplantation if there was only a single group of kidney transplant recipients, and investigators reported relevant outcomes for patients both prior to and after receiving kidney transplants (i.e., at least two assessments of relevant outcomes with participants serving as their own controls). For this design, we only included studies where investigators explicitly described which RRT modality patients received prior to transplantation.

Assessment of Studies’ External and Internal Validity for Relevant Outcomes

Two reviewers used a modified version (Item S1) of a previously published instrument25 to independently assess studies’ reporting on factors which could influence the validity of findings, including studies’ external validity (i.e., inclusion and exclusion criteria, recruitment response rate) and factors influencing studies’ internal validity (i.e., potential for selection bias, validity and appropriateness of outcome assessment, and rigor of statistical analyses to account for potential confounding). We considered studies to have described the inclusion and exclusion criteria well if they clearly reported their criteria or if they specified that all consecutive subjects were enrolled. We also categorized studies’ response rates (<45%, 45%–59%, 60%–79%, or ≥80%), and we considered adequate response rates to be present if they reported 60% or greater response. We considered studies to have minimal potential for selection bias if investigators reported no significant or only minor differences in participant characteristics that could influence relevant outcomes. We considered assessments of relevant outcomes to be valid if studies clearly defined ascertainment of relevant outcomes using standard and previously validated instruments. We considered studies’ statistical analyses to have been appropriately conducted if analyses attempted to account for factors potentially confounding the association between participants’ RRT modality and relevant outcomes (e.g., using multivariable adjustment within regression models), or if important confounding was unlikely within studies. Two reviewers independently assessed study quality, and reviewers resolved disagreements with the aid of a third party.

Data Synthesis and Analysis

We decided a priori not to statistically combine results in a meta-analysis because we expected studies to be methodologically and clinically diverse. For instance, some studies reported outcomes as means on scales (e.g. SF-36 physical function score) while others reported the percentage of participants achieving a particular physical activity threshold or percentage of patients who were employed. Therefore, we qualitatively synthesized results for individual studies within summary evidence tables to help clarify the similarities and differences among studies that appear to address similar research questions across a variety of measures and patient populations.

In an effort to assess the magnitude and direction of reported associations in a standard manner across studies reporting these heterogeneous outcomes, we calculated Cohen’s d effect size indices and 95% confidence intervals (CIs) for each treatment comparison using Microsoft Excel spreadsheets containing published formulas for calculations26,27. Cohen’s d is an index commonly used in research synthesis that represents the sample estimate of the standardized mean difference in outcomes between groups reported within studies26. We classified statistically significant Cohen’s d effect sizes as small (0.2–0.49), moderate (0.5–0.79), or large (≥ 0.8) using standard criteria28. We considered a two-sided p-value of <0.05 to be statistically significant for studies that reported p-values for results of analyses testing differences in relevant outcomes. We used the calculated 95% CI of the Cohen’s d effect size to determine statistical significance for studies that did not report p-values for results29. We considered 95% CIs that did not contain zero to be statistically significant. We considered non-statistically significant results to indicate that RRT modalities were no different with respect to life participation outcomes.

Results

Search Results

Our electronic search of potentially relevant citations identified 2,247 in PubMed, 2,662 in EMBASE, and 356 (trials) in the Cochrane Library. After reviewing a total of 5,265 titles and abstracts identified through our electronic searches, 189 articles were eligible for full text review. We retained 36 articles that met our inclusion criteria. Our hand-search of bibliographies yielded an additional 10 articles. We included a total of 46 studies in the final review2,7,9,19,20,3070. (Figure 1)

Figure 1.

Figure 1

Summary of Literature Search and Article Review Process

Studies’ Characteristics

Eligible studies were conducted over a period of some 3 decades (1985–2011), with greater than half published since 2000. The studies were heterogeneous in design (6 cohort, 38 cross-sectional, and 2 pre-post transplantation), their sample sizes (ranging from 46 to 18,015 total participants), and their participants’ demographic characteristics. Approximately one third of studies were performed in the United States, while the remaining studies were from the United Kingdom, Malaysia, Thailand, Iran, Greece, Japan, The Netherlands, Turkey, Denmark, Taiwan, Poland, Italy, Spain, Australia, and Germany. (Table 1) We also collected data on additional patient characteristics, such as mean treatment time, primary ESRD cause, employment status, and education. Unfortunately, these data were not systematically reported within the articles, and thus we included these data within Table S2.

Table 1.

Study Characteristics and Outcome Domains Addressed

Study Earliest Year of Study Data Location Study Design (Follow Up) Treatment Modality Sample Size Patient Demographics Outcome Domains
Age (y) Female Sex US Racial/Ethnic Minority Married* Physical Travel Rec Freedom Work
2011 Ibrahim 2011 Malaysia; Multi-Site Cross-Sectional HD 183 37.6% aged 51–60 y 48.5% N/A 75.9% X X
PD 91
2010 Johansen 2005 US; Multi-Site Cross-Sectional HD 161 M:60.7 ±14.6; F:59.8 ±13.8 45% M: 28%; F: 36% N/R X
PD 1,386
2009 Aiyasanon 2005 Thailand; Single-Site Cross-Sectional HD 87 54.05 49.4% N/A 66.7% X X X X X
PD 23 61.39 47.8% N/A 69.6%
2009 Alavi 2007 Iran; Single-Site Cross-Sectional HD 63 55.3 ± 14.5 55.6% N/A 81% X
TX 100 40.6 ± 14 41% N/A 77%
2009 Borowiak 2009 Poland; Multi-site Cross-Sectional HD 50 59.6 ± 13.4 56% N/A N/R X X
PD 50 58.9 ± 13.2 48%
2009 Kontodimoloulos N/R Greece; Multi-Site Cross-Sectional HD 642 58.1 ± 14.9 38.7% N/A 65.7% X X
PD 65 58.7 ± 12.9 49.2% N/A 75.4%
TX 167 43.7 ± 12.5 39.5% N/A 63.6%
2009 Masuda 2009 Japan; Single-Site Cross-Sectional HD 35 58.3 ± 14.7 31.4% N/A N/R X
PD 26 47.5 ± 14.2 46.2%
2009 Panagopoulou 2009 Greece; Single-Site Pre-Post Tx HD 40 57 ± 25 50% N/A 67.5% X
PD 36 59 ± 25 41.6% N/A 72.2%
TX 48 39 ± 20 33% N/A 47.9%
2009 Thong 1997 Netherlands; Multi-Site Cross-Sectional HD 1010 63.2 ± 13.8 43.3% N/A 65% X
PD 543 53.3 ± 14.6 36.1% N/A 73.5%
2009 Basok N/R Turkey; Single-Site Cross-Sectional HD 24 43.08 ± 12.44 100% N/A N/R X X
PD 21 45.19 ± 8.92
TX 20 36.45 ± 8.55
2007 Apostolou 2007 Greece; Single-Site Cross-Sectional PD 26 53.6 ± 12.7 42.3% N/A 65% X X
TX 20 49.2 ± 11.4 50% N/A 89%
2007 Molsted N/R Denmark; Single-Site Cross-Sectional HD 71 59 ± 16 24% N/A N/R X
PD 59 59 ± 13 44%
2007 Sayin 2007 Turkey; Single-Site Cross-Sectional HD 75 46.91 ± 15.77 28% N/A 74.7% X X
PD 41 46.15 ± 15.29 61% N/A 70.7%
TX 20 33.15 ± 10.61 65% N/A 45.0%
2006 Juergensen N/R US; Multi-Site Cross-Sectional HD 84 69.6 ± 13.3 N/R 20% 60% X
PD 62 55 ± 14 N/R 17% 57%
2006 Ogutmen 2003 Turkey; Multi-Site Cross-Sectional HD 64 48.14 ± 15.5 42.2% N/A 70% X X
PD 207 46.00 ± 13.88
TX 302 38.22 ± 11.52
2005 Barendse N/R UK; Single-Site Cross-Sectional HD 35 52.8 ± 14.3 39% N/A 76% X
PD 57
TX 46
2005 Kutner 1996 US; Multi-Site Prospective Cohort (1 y) HD 455 61.2 ± 15.6 43.3% 29.9% 53.4% X
PD 413 56.1 ± 14.7 47.2 % 19.9% 65.6%
2005 Lee 2002 UK; Single-Site Cross-Sectional HD 99 M: 62.4 ± 14.5; F: 64.0 ± 13.8 39% N/A N/R X X X X
PD 74 M: 63.5 ± 13.6; F: 53.7 ± 15.5 49%
TX 209 M: 53.6 ± 13.8; F: 51.6 ± 14.1 40%
2005 Niu 2002 Taiwan; Multi-Site Cross-Sectional HD 80 54.7 ± 13.5 57.9% N/A 72.5% X
PD 80 50.8 ± 12.2
TX 80 43.3 ± 8.8
2005 Van de Ham N/R Netherlands; Multi-Site Cross-Sectional HD 16 49.0 ± 11.9 48.57% N/A N/R X
TX 35 52.3 ± 10.4 37.5%
2004 Wu 1995 US; Multi-Site Prospective Cohort (1 y) HD 698 54 48% 37% 51% X X X X X
PD 230 59 46% 20% 67%
2003 Manns 1999 UK; Single-Site Prospective Cohort (1 y) HD 151 62.2 13% N/A 64% X X
PD 41 56.1 80% N/A 70%
2003 Tomasz N/R Poland; Single-Site Cross-Sectional HD 61 57.84 ± 11.85 39.34% N/A 14.75% X X X
TX 83 43.3 ± 11.73 48.19% N/A 71.08%
2002 Baiardi 1997 Italy; Single-Site Prospective Cohort (16+ mo) HD 171 61.9 ± 13.4 37.4% N/A N/R X
PD 30 64.0 ± 15.7 36.7%
TX 34 44.0 ± 12.0 35.3%
2002 Harris 2002 UK; Multi-Site Prospective Cohort (1 y) HD 96 77.0 ± 4.4 38% N/A N/R X
PD 78 76.8 ± 4.0 30%
2000 Carmichael N/R UK; Single-Site Cross-Sectional HD 49 57.8 ± 13 34.7% N/A 71.4% X X
PD 97 57 ± 15 40.2% N/A 70.1%
2000 Diaz-Buxo 1996 US; Multi-Site Cross-Sectional HD 16,755 59.44 ± 15.28 48.22% 47.07% N/R X X
PD 1,260 53.45 ± 15.31 49.52% 31.03%
2000 Fujisawa N/R Japan; Multi-Site Cross-Sectional HD (awaiting TX) 114 45.8 ± 11.9 24% N/A N/R X
HD (not awaiting TX) 45.7 ± 6.8 31%
TX 117 43.9 ± 9.1 57%
1999 Merkus 1993 Netherlands; Multi-Site Cross-Sectional HD 120 59 ± 16 43% N/A N/R X X
PD 106 52 ± 14 35%
1998 Jofre 1993 Spain; Multi-Site Pre-Post Tx Pre-TX (HD) 93 45 ± 13.2 45% N/A N/R X
Post-TX
1997 Merkus 1997 Netherlands; Multi-Site Cross-Sectional HD 120 59.3 ± 15.5 43% N/A 68% X X
PD 106 52.3 ± 14.0 35% N/A 79%
1996 Curtin 1996 US; Multi-Site Cross-Sectional HD 238 43 ± 10.6 50.1% 49.6% N/R X
PD 30
1996 Lok N/R Australia; Single-Site Cross-Sectional HD 56 42.5 37.5% N/A N/R X
PD 8
1995 Khan N/R UK; Single-Site Cross-Sectional HD 43 48.8 41.6% N/A N/R X
PD 27
TX 102
1995 Tell N/R US; Single-Site Cross-Sectional HD (in-center) 186 54.9 ± 15.3 52% 51% M: 70%;
F: 49%
X
HD (home) 12
PD 58
1994 Holley 1993 US; Single-Site Cross-Sectional HD 46 N/R 53% 48% N/R X
PD 31
1992 Pietrabissa 1982 Italy; Single-Site Cross-Sectional HD 172 N/R N/R N/A N/R X
TX 71
1991 Tucker N/R US; Single-Site Cross-Sectional HD 22 50.4 ± 13.8 62% 72% 62% X
PD 29 47.1 ± 13.9 45% 27% 73%
1990 Devins N/R Canada; Single-Site Prospective Cohort** (6 wk) HD (in-center) 39 41 42% N/A 63% X X
HD (home) 15
PD 11
TX 34
1990 Koch N/R Germany; Multi-Site Cross-Sectional HD 290 50.1 43% N/A 68% X
PD 68 51.8 32% N/A 79%
TX 761 43.5 41% N/A 70%
1990 Simmons 1970 US; Multi-Site Cross-Sectional HD 83 Range, 19-–56 N/R N/R N/R X X X X
PD 510
TX (current) 91
TX (historical) 82
1989 Bremer N/R US; Multi-Site Cross-Sectional HD (in-center) 105 57.1 ± 13.4 49% 38% N/R X
HD (self-care) 41 54.5 ± 11.4 46% 37%
HD (home) 47 53.2 ± 12.9 49% 19%
PD 79 54.9 ± 13.7 35% 13%
TX (first) 166 37.6 ± 11.4 42% 15%
TX (failed) 30 36.3 ± 10.3 60% 20%
TX (>1) 21 31.2 ± 8.3 38% 10%
1989 Julius 1984 US; Multi-Site Cross-Sectional HD 95 60% >44 y 41.1% 49.5% 61.1% X
PD 119 60.5% >44 y 48.7% 23.3% 63.0%
1988 Wolcott N/R US; Multi-Site Cross-Sectional HD 33 47.4 ± 15.1 30% 39% 49% X
PD 33 46.2 ± 14.4 30% 33% 64%
1987 Hart N/R US; Multi-Site Cross-Sectional HD (in-center) 347 51.9 50% 46.5% N/R X X
HD (home) 287 47.0 35.9% 13.6%
PD 81 49.8 54.3% 16.1%
TX 144 37.2 43.8% 16.6%
1985 Evans N/R US; Multi-Site Cross-Sectional HD (in-center) 347 47.6 44.5% 27.2% NR X
HD (home) 287 75%
PD 81 75%
TX 44 66.7%

Note: Unless otherwise indicated, age is given as mean or mean ± standard deviation; other patient demographics given as percentage.

HD = hemodialysis; PD = peritoneal dialysis; Tx = transplant; M=Male; F=Female; NR = not reported; NA = not applicable; US, United States; UK, United Kingdom; Physical, physical functioning; Rec, recreation;

*

Or Living with a Partner.

Factors Influencing Studies’ Internal and External Validity

Most studies described their inclusion and exclusion criteria well (Table S3). A majority of studies reported response rates of 60% or greater and conducted valid outcome assessments. However, many studies were influenced by potential selection bias. Also, the comparative groups of participants within many studies were deemed to be different enough in aspects other than selection of RRT modality such that observed associations between RRT modality and life participation activities could be confounded by group differences. Few studies were judged to have performed appropriate statistical analyses to account for these differences, which could potentially confound observed associations between study participants’ RRT modalities and life participation outcomes. (Table 2)

Table 2.

Summary of Study Quality Assessment for Relevant Outcomes

Outcome Domain Total Articles Well-Described Criteria* Response Rate >60% Minimal Risk of Bias** Valid Outcome Assessment Appropriate Adjustment^
Physical Function 35 25 (71%) 18 (51%) 6 (17%) 34 (97%) 13 (37%)
Travel 2 2 (100%) 1 (50%) 2 (100%) 2 (100%) 1 (50%)
Recreation 20 15 (75%) 13 (65%) 5 (25%) 19 (95%) 5 (25%)
Freedom 7 6 (86%) 3 (43%) 3 (43%) 7 (100%) 1 (14%)
Work 13 8 (61%) 8 (61%) 2 (15%) 13 (100%) 4 (31%)

Note: Quality Assessment: number of articles that met criteria (% of total articles)

*

Inclusion and exclusion criteria

**

Selection bias.

^

For potential confounders. Total articles.

Measures Used to Assess Associations between RRT Modality and Life Participation Outcomes

Studies used a variety of measures to capture life participation outcomes. Physical function was measured using several tools, including the SF-36 physical functioning and role physical measures, author-developed difficulties in activities of daily living and physical well-being scales, and Karnofsky self-reported scores2,7,9,20,3032,3538,40,4349,5158,6069. Travel was measured using the CHOICE (Choices for Healthy Outcomes in Caring for ESRD) Health Experience Questionnaire (CHEQ), and the Thai version of the CHEQ2,30. Recreation was measured using several tools, including the SF-36 social functioning measure, Thai CHEQ, Intrusiveness Ratings Scale, Sickness Impact Profile, and author-developed patient questionnaires 2,9,20,30,33,35,36,38,41,42,45,48,49,52,55,58,59,6467. Freedom was measured using several tools, including the CHEQ, Thai CHEQ, Renal Treatment Satisfaction Questionnaire, Index of Well-Being and author-developed social well-being scale2,20,30,32,34,41,55,62. Work was also measured using several tools, including the CHEQ, Thai CHEQ, Sickness Impact Profile, Intrusiveness Ratings Scale, and patient-reported work status2,9,19,20,30,38,39,42,53,55,58,70. We provide a detailed description of the included outcome measures (i.e., whether the measure is validated, outcome type, range of scores, and whether a higher score indicates a better outcome) within Table S4.

Comparison of Life Participation Activities

Patients Receiving Hemodialysis Versus Peritoneal Dialysis

A total of 39 studies evaluated life participation activities between patients receiving hemodialysis compared to patients receiving peritoneal dialysis2,9,16,19,20,30,3236,38,41,42,4453,5557,59,6163,6570. Most studies reported on multiple outcomes, thus providing 41 physical function, 2 travel, 18 recreation, 8 freedom, and 13 work-related comparisons. The majority of comparisons demonstrated no significant differences in physical function outcomes (76%), recreation outcomes (78%), freedom outcomes (75%), and work outcomes (69%). (Table 3) These findings of no differences in outcomes were consistent across study designs, location, and quality ratings with 100% of comparisons from cohort studies, 81% of comparisons from US-based studies, 83% of comparisons from studies that properly adjusted for potential confounders, and 70% of comparisons from studies published after 2000 favoring neither RRT modality. (Table 4)

Table 3.

Physical Function and Life Participation Outcome Measures and Study Results: HD versus PD

Study; Design Outcome Measure HD PD Statistical Results Treatment Favored
N Estimate@ N Estimate@ Reported P** Effect Size^ Calculated CI****
Physical Function
Aiyasanon; 2009; CS Thai SF-36 Physical Functioning 87 52 23 29 0.001 0.79 ---- HD
Aiyasanon; 2009 (CS) Thai SF-36 Role Physical 87 37 23 17 <0.05 0.46 ---- HD
Aiyasanon; 2009 (CS) CHEQ (Thai) Role Physical 87 77 23 59 0.001 0.79 ---- HD
Tell; 1995 (CS) Karnofsky self-report 186 72.9 58 78 0.02 −0.34 ---- PD
Masuda; 2009 (CS) Average no. steps/d 35 3,391 26 6,336 <0.05 −0.83 (−4784.1, −1105.9) PD
Merkus; 1997 (CS) SF-36 Physical Functioning 120 50.7 120 60.9 <0.05 −0.37 (−17.3, −3.1) PD
Merkus; 1999 (CS) SF-36 Physical Functioning 120 50.7 106 60.9 <0.05 −0.36 ---- PD
Ogutmen; 2006 (CS) SF-36 Role Physical 64 35.71 207 55.10 <0.05 −0.43 (−32.1, −6.7) PD
Thong; 2009 (CS) SF-36 Physical Functioning 1,010 48.3 543 61.2 <0.05 −0.47 (−15.8, −10.0) PD
Thong; 2009 (CS) SF-36 Role Physical 1,010 25.9 543 35.7 <0.05 −0.26 (−13.7, −5.9) PD
Harris; 2002 (Cohort) UK-version SF-36 PCS 96 31.6 78 32.0 0.2 −0.03 ---- ----
Kutner; 2005 (Cohort) SF-36 Physical Functioning 32 N/R 141 N/R 0.3 −3.48 --- ---
Kutner; 2005 (Cohort) SF-36 Role Physical 32 N/R 141 N/R 0.3 −2.90 --- ---
Wu; 2004 (Cohort) SF-36 Physical Functioning 452 1.0# 133 0.72# 0.1 --- ---- ---
Wu; 2004 (Cohort) SF-36 Role Physical 452 1.0# 133 0.84# 0.7 --- ---- ---
Baiardi; 2002 (CS)*** SF-36 Physical Functioning 171 59.3 30 59.7 N/R −0.01 (−11.2, 10.4) ----
Basok; 2009 (CS) SF-36 Physical Functioning 24 62.27 21 56.61 N/R 0.25 (−7.9, 19.2) ----
Basok; 2009 (CS) SF-36 Role Physical 24 58.83 21 39.29 N/R 0.46 (−6.1, 45.2) ----
Borowiak; 2009 (CS) EQ 5D (mobility) 50 38## 50 44## NS −0.14 (−0.6, 0.3) ----
Carmichael;2000 (CS) SF-36 Physical Functioning 49 44.4 97 40.3 NS 0.13 (−6.4, 14.6) ---
Carmichael;2000 (CS) SF-36 Role Physical 49 21.4 97 19.7 NS 0.05 (−9.8, 13.2) ---
Devins; 1990 (CS)*** Author-developed difficulties in ADL scale 39 2 11 2.6 NS −0.40 (−1.6, 0.4) ---
Diaz-Buxo; 2000 (CS) SF-36 Physical Functioning 16,755 41.4 1,260 42.1 N/R −0.11 (−2.4, 1.0) ---
Diaz-Buxo; 2000 (CS) SF-36 Role Physical 16,755 33.1 1,260 33 N/R −0.01 (−2.4, 2.1) ---
Ibrahim; 2011 (CS) SF-36 Physical Functioning 183 72.568 91 75.275 N/R −0.15 (−7.2, 1.8) ----
Ibrahim; 2011 (CS) SF-36 Role Physical 183 68.443 91 76.786 N/R −0.41 (13.5, −3.2) ----
Koch; 1990 (CS) Satisfaction with physical function 290 0.51 68 0.47 N/R 0.09 (−0.2, 0.4) ---
Kontodimopoulos; 2008 (CS) Greek SF-36 Physical Functioning 642 49.2 65 49.2 0.9 0.00 (−7.8, 7.8) ---
Kontodimopoulos; 2008 (CS) Greek SF-36 Role Physical 642 40.3 65 30.9 0.08 0.21 (−1.8, 20.6) ---
Lee; 2005 (CS) SF-36 Physical Functioning 99 26.5 74 30.9 NS −0.16 (−12.9, 4.1) ---
Lee; 2005 (CS) SF-36 Role Physical 99 60.4 74 60.6 NS 0.00 (−13.4, 12.9) ---
Lok; 1996 (CS) HD Stressor Scale 56 3.76 8 3.43 NS 0.32 (−0.4, 1.1) ---
Manns; 2003 (CS) SF-36 Physical Functioning 151 46.2 41 40 0.2 0.22 ---- ---
Manns; 2003 (CS) SF-36 Role Physical 151 27 41 29.3 0.7 −0.06 ---- ---
Merkus; 1997 (CS) SF-36 Role Physical 106 28.6 106 31.7 NS −0.08 (−13.3, 7.1) ----
Ogutmen; 2006 (CS) SF-36 Physical Functioning 64 56.99 207 57.06 N/R −0.83 (−46.9, −23.8) ---
Niu; 2005 (CS) WHOQOL-BREF (Taiwan) 80 11.96 80 11.61 N/R −0.99 (−0.4, 1.1) ---
Sayin; 2007 (CS) SF-36 Physical Functioning 75 55.90 41 55.76 0.1 0.00 (−10.8, 11.1) ----
Sayin; 2007 (CS) SF-36 Role Physical 75 40.69 41 39.10 0.9 0.04 (−13.7, 16.9) ----
Simmons; 1990 (CS) Author developed physical well-being scale (summary score) 83 14.04 510 14.64 N/R −1.00 (−1.5, 0.3) ---
Wolcott; 1988 (CS) Karnofsky (clinical performance) 33 72.5 33 72.9 NS --- --- ---
Travel
Aiyasanon; 2009 (CS) CHEQ (Thai) (travel restrictions) 87 68 23 51 <0.05 0.46 ---- HD
Wu; 2004 (Cohort) CHEQ-Travel 452 1.0 133 1.07 0.8 −0.03 ---- ---
Recreation
Carmichael;2000(CS) SF-36 Social Functioning 49 44.9 97 53.2 <0.05 −0.29 (−18.2, 1.6) PD
Ibrahim; 2011 (CS) SF-36 Social Functioning 183 77.322 91 83.516 N/R −0.31 (−11.3, −1.1) PD
Lee; 2005 (CS) SF-36 Social Functioning 99 36.7 74 46.5 <0.05 −0.33 (−18.8, 1.6) PD
Tucker; 1991 (CS) Quality of Life Assessment Battery (mean recreation/wk) 29 5.1 22 7.3 <0.05 −0.34 (−5.9, 1.5) PD
Wu; 2004 (Cohort) CHEQ (limitations to recreation) 452 1.0 133 0.85 0.5 0.06 ---- ---
Aiyasanon; 2009(CS) CHEQ (Thai) (recreation) 87 65 23 62 NS 0.46 ---- ---
Basok; 2009 (CS) SF-36 Social Functioning 24 68.75 21 63.69 0.1 0.19 (−10.8, 20.9) ---
Devins; 1990 (CS)*** Intrusiveness Ratings Scale 39 2.5 11 3.2 NS −0.51 (−1.6, 0.2) ---
Diaz-Buxo; 2000 (CS) SF-36 Social Functioning 16,755 64 1,260 66.1 NS −0.04 (−2.8, 0.6) ---
Hart; 1987 (CS) Sickness Impact Profile 343 23.7 77 24 NS −0.25 ---- ---
Juergensen; 2006 (CS) Author developed questions (recreation) 84 4.95 52 5.12 NS −0.09 (−0.8, 0.5) ---
Kontodimopoulos 2008 (CS) Greek SF-36 Social Functioning 642 58.1 65 54.9 0.4 0.11 (−4.5, 10.9) ---
Manns; 2003 (CS) SF-36 Social Functioning 151 60.7 41 62.2 0.8 −0.06 ---- ---
Merkus; 1997 (CS) SF-36 Social Functioning 120 63.1 120 68.9 NS −0.21 (−12.9, 1.3) ----
Merkus; 1999 (CS) SF-36 Social Functioning 120 63.1 106 68.9 NS −0.26 ---- ---
Ogutmen; 2006 (CS) SF-36 Social Functioning 64 66 207 71.9 NS −0.27 (−11.9, 0.3) ---
Sayin; 2007 (CS) SF-36 Social Functioning 75 62.62 41 56.32 0.5 0.22 (−4.6, 17.2) ----
Simmons; 1990 (CS) Author-developed scale 83 2.24 510 2.21 NS 0.03 (−0.2, 0.3) ---
Freedom
Aiyasanon;2009 (CS) CHEQ (Thai) (freedom) 87 57 23 42 <0.05 0.46 ---- HD
Juergensen; 2006 (CS) Author-developed scale (independence) 84 5.14 52 6.18 0.02 −0.41 ---- PD
Wu; 2004 (Cohort) CHEQ (freedom) 452 1.0 133 1.03 0.9 −0.01 ---- ---
Borowiak; 2009 (CS) EQ-5D (usual activity) 50 40 50 46 NS −0.13 (−0.6, 0.3) ----
Barendse; 2005 (CS) Renal Treatment Satisfaction Questions 35 4.3 57 4.3 NS 0.00 (−0.7, 0.7) ---
Bremer; 1989 (CS) Index of Well-Being (tied-down, free) 105 4.9 79 4.5 NS −0.55 (−0.2, 1.0) ---
Lee; 2005 (CS) EQ-5D (usual activities) 99 18.09 74 20.55 NS −0.20 (−0.5, 0.1) ---
Simmons; 1990 (CS) Author-developed social well-being scale 83 5.17 510 5.29 NS −0.14 (−0.3, 0.1) ---
Work
Evans; 1985 (CS) Reported ability to work 347 44.8## 81 27.8## N/R 0.41 (0.1, 0.7) HD
Hart; 1987 (CS) Sickness Impact Profile (work) 338 45 81 51 <0.01 −0.32 ---- HD
Julius; 1989 (CS) Reported working or looking 95 0.096## 119 0.227## <0.05 −0.56 (−1.0, −0.1) PD
Molsted; 2007 (CS) KDQOL (work status) 71 17.9 59 33.6 <0.05 −0.42 (−28.8, −2.6) PD
Wu; 2004 (Cohort) CHEQ (work) 452 1.0 133 1.17 0.5 −0.07 ---- ---
Aiyasanon; 2009 (CS) CHEQ (Thai) (limitations to work) 87 67 23 57 NS 0.46 ---- ---
Curtin; 1996 (CS) Percent of employed pts 311 23.4 42 28.6 0.2 −0.14 (−0.5, 0.2) ---
Devins; 1990 (CS)*** Intrusiveness Ratings Scale 39 4 11 3.6 NS 0.19 (−1.0, 1.8) ---
Hart; 1987 (CS) Pt-reported work 46 0.37## 31 0.52## NS −0.34 (−0.8, 0.2) ---
Lee; 2005 (CS) KDQOL (work status) 99 20 74 28.2 NS −0.23 (−18.8, 2.4) ---
Panagopoulou2009 (CS)*** Pt-reported full time employment 40 0.05## 36 0.138## N/R −0.61 (−1.6, 0.3) ---
Panagopoulou2009 (CS)*** Pt-reported part-time employment 40 0.15## 36 0.17## N/R −0.08 (−0.8, 0.6) ---
Simmons; 1990 (CS) Author developed scale (job) 83 2.18 510 2.38 NS −0.17 (−0.5, 0.1) ---
@

Estimates are means unless otherwise noted.

**

Author-reported p-values.

^

Calculated Cohen’s d.

#

Odds ratio.

##

Percentage.

***

denotes studies were originally designed as longitudinal cohort but authors only reported cross-sectional assessments of relevant outcomes

****

We calculated the CI for the Cohen’s d effect size difference for studies that reported all of the needed estimates (e.g., means plus standard deviations) We reported ‘---‘ for studies that we could not calculate the CIs for due to missing estimates.

Abbreviations and definitions: ADL, activities of daily living; CS, cross sectional study design; NS, not statistically significantly different at P>0.05 level; NR, not reported within the article; Pt, patient; Pts, patients; CI, confidence interval; HD, hemodialysis; PD, peritoneal dialysis; CHEQ, CHOICE (Choices for Healthy Outcomes in Caring for ESRD) Health Experience Questionnaire; SF-36, 36-Item Short-Form Health Survey; PCS, physical component summary; UK, United Kingdom; KDQOL, Kidney Disease Quality of Life scale; WHOQOL-BREF, World Health Organization Quality of Life instrument, short version,

Table 4.

Summary of Published Evidence Comparing Life Participation Outcomes by RRT Modality and Study Characteristics

HD vs. PD HD vs. Tx PD vs. Tx

No. of outcomes that No. of outcomes that No. of outcomes that

Favors HD Favors Neither Favors PD Favors HD Favors Neither Favors Tx Favors PD Favors Neither Favors Tx

Physical Function Domain
Study Design
 Randomized Trial
 Prospective Cohort 5
 Cross-Sectional 3 26 6 8 17 7 14
 Pre-Post Transplant 1

Location
 US 8 1 1
 Non-US 3 23 7 8 17 7 13

Study Quality
 Appropriate Adjustment* 12 2 2 3 3 2
 No/Minimal Adjustment* 3 19 5 6 15 4 12

Publication Year
 1980–1990 4 1 2 1 2
 1991–2000 6 3 1 4 2
 2001–2012 3 21 4 6 12 6 10

Outcome Measures
 SF-36 (Thai/UK/Greek) 2 24 5 5 10 5 10
 CHEQ (Thai) 1
 Karnofsky 1 1
 EQ-5D 1
 WHOQOL 1 2 1
 Sickness Impact Profile 1
 Nottingham 1
 HD Stressor Scale 1
 Author-developed scales 2 2 1 1 1
 Other patient reports 1 1 2 1 2
 Physical assessments 1 1

Travel Domain
Study Design
 Randomized Trial
 Prospective Cohort 1
 Cross-Sectional 1
 Pre-Post Transplant

Location
 US 1
 Non-US 1

Study Quality
 Appropriate Adjustment* 1
 No/Minimal Adjustment* 1

Publication Year
 1980–1990
 1991–2000
 2001–2012 1 1

Outcome Measures
 CHEQ (Thai) 1 1

Recreation Domain
Study Design
 Randomized Trial
 Prospective Cohort 1
 Cross-Sectional 13 4 4 3 2 5
 Pre-Post Transplant

Location
 US 5 1 2 2
 Non-US 9 3 4 1 2 3

Study Quality
 Appropriate Adjustment* 4 1 1 1
 No/Minimal Adjustment* 10 4 3 3 1 4

Publication Year
 1980–1990 1 2 3
 1991–2000 2
 2001–2012 2 3 1 2 2

Outcome Measures
 SF-36 (Greek) 3 2 1 2 2
 Sickness Impact Profile 1 1
 Intrusiveness Ratings Scale 1 1
 WHOQOL-100 1
 Quality of Life Assessment Battery 1
 Author-developed scales 1 1

Freedom Domain
Study Design
 Randomized Trial
 Prospective Cohort 1
 Cross-Sectional 1 5 1 4 4
 Pre-Post Transplant

Location
 US 3 1 2 2
 Non-US 1 3 2 2

Study Quality
 Appropriate Adjustment* 1
 No/Minimal Adjustment* 1 5 1 4 4

Publication Year
 1980–1990 2 2 2
 1991–2000
 2001–2012 1 4 1 2 2

Outcome Measures
 CHEQ (Thai) 1 1
 EQ 5D 2 1 1
 Renal Treatment Satisfaction 1 1 1
 Index of Well-Being 1 1 1
 Author-developed scales 1 1 1 1

Work Domain
Study Design
 Randomized Trial
 Prospective Cohort 1
 Cross-Sectional 2 8 2 6 5
 Pre-Post Transplant

Location
 US 2 4 1 3 3
 Non-US 5 1 3 2

Study Quality:
 Appropriate Adjustment* 1 2 1 1 1
 No/Minimal Adjustment* 1 7 1 5 4

Publication Year
 1980–1990 2 3 1 4 4
 1991–2000 1
 2001–2012 5 1 2 1

Outcome Measures
 CHEQ (Thai) 2
 Sickness Impact Profile 1 1 1
 KDQOL 1 1 1 1
 Intrusiveness Ratings Scale 1 1 1
 WHOQOL-100 1
 Author-developed scales 1 1 1
 Other patient reports 1 4 1 1 1

RRT, renal replacement therapy; HD, hemodialysis; PD, peritoneal dialysis; Tx, transplantation; US, United States; SF-36, 36-Item Short-Form Health Survey; CHEQ, CHOICE (Choices for Healthy Outcomes in Caring for ESRD) Health Experience Questionnaire; WHOQOL, World Health Organization Quality of Life instrument; UK, United Kingdom; KDQOL, Kidney Disease Quality of Life scale;

*

For confounders.

Patients Receiving Hemodialysis Versus Transplant Recipients

A total of 22 studies evaluated life participation activities between patients receiving hemodialysis compared to patients with kidney transplants9,19,20,3134,37,38,40,4345,5155,58,60,63,66. Most studies reported on multiple outcomes, thus providing 26 physical function, 7 recreation, 4 freedom, and 6 work-related comparisons. The majority of comparisons demonstrated small to large differences in activities among patients with kidney transplants compared to patients receiving hemodialysis, with transplant patients having better physical function (90%), freedom (100%), and work outcomes (100%). (Table 5) These findings of better outcomes in transplant patients were observed among 71% of comparisons from cross-sectional studies, 100% of comparisons from US-based studies, 57% of comparisons from studies that properly adjusted for potential confounders, and 65% of comparisons from studies published after 2000 favoring kidney transplantation. (Table 4)

Table 5.

Physical Function and Life Participation Outcome Measures and Study Results: HD versus Tx

Study; Design Outcome Measure HD Tx Statistical Results Treatment Favored
N Estimate* N Estimate* Reported P** Effect Size^ Calculated CI****
Physical Function
Alavi; 2009; CS Nottingham Extended ADL 63 31.7 100 51.4 0.00 −1.62 (−23.6, −15.8) TX
Basok; 2009 (CS) SF-36 Physical Functioning 24 62.27 20 77.78 N/R −0.73 (−28.4, −2.6) TX
Fujisawa; 2000 (CS) SF-36 Physical Functioning 114 81.6 117 86.2 <0.05 −0.29 (−8.7, −0.5) TX
Khan; 1995 (CS) SF-36 Physical Functioning 43 46.35 102 67.51 <0.05 −0.36 ---- TX
Khan; 1995 (CS) SF-36 Role Physical 43 51.09 102 63.22 <0.05 −0.36 ---- TX
Koch; 1990 (CS) Satisfaction with life questions 290 0.51## 761 0.18## N/R 0.86 (0.7, 1.0) TX
Kontodimopoulos; 2008 (CS) SF-36 (Greek) Physical Functioning 642 49.2 167 72.9 <0.001 −0.83 (−28.6, −18.8) TX
Kontodimopoulos 2008 (CS) SF-36 (Greek) Role Physical 642 40.3 167 62.6 <0.001 −0.51 (−29.8, −14.8) TX
Lee; 2005 (CS) SF-36 Physical Functioning 99 26.5 209 56.4 <0.05 −0.99 (−37.1, −22.7) TX
Lee; 2005 (CS) SF-36 Role Physical 99 60.4 209 86.7 <0.05 −0.76 (−34.6, −18.0) TX
Niu; 2005 (CS) WHOQOL-BREF (Taiwan; physical health) 80 11.96 80 14.34 <0.05 −0.99 (−3.1, −1.6) TX
Ogutmen; 2006 (CS) SF-36 Role Physical 64 35.71 302 71.09 <0.05 −0.83 (−47.0, −23.8) TX
Panagopoulou 2009 (CS)*** Pt-reported full time employment 40 0.05# 48 0.375# N/R −1.34 (−2.2, −0.5) TX
Sayin; 2007 (CS) SF-36 Physical Functioning 75 55.90 20 68.75 N/R −0.51 (−25.5, −0.2) TX
Simmons; 1990 (CS) Author-scale physical well-being score 83 14.04 91 17.55 <0.01 −0.99 (−4.6, −2.4) TX
Tomasz; 2003 (CS) WHOQOL-100 61 12.28 83 13.3 <0.05 −0.37 (−1.9, −0.1) TX
Van den Ham; 2005 (CS) Symptom-limited graded cycle-ergometry test (ie, exercise test) 16 6.2 35 7.2 <0.05 −0.67 (−1.9, −0.1) TX
Jofre; 1998; (Pre-Post) Sickness Impact Profile 93 5.5 93 3.6 <0.01 0.29 (0.0, 3.8) TX
Baiardi; 2002(CS)*** SF-36 Physical Functioning 171 59.3 34 64.6 N/R −0.19 (−15.7, 5.1) ----
Basok; 2009 (CS) SF-36 Role Physical 24 58.83 20 60 N/R −0.04 (−26.6, 23.3) ---
Devins; 1990 (CS)** Author-scale (difficulties daily living) 39 2 34 1.7 NS 0.17 (−0.5, 1.1) ---
Fujisawa; 2000 (CS) SF-36 Role Physical 114 68 117 77.6 NS −0.26 (−19.2, 0.0) ---
Ogutmen; 2006 (CS) SF-36 Physical Functioning 64 56.99 302 59.92 NS −0.11 (−10.2, 4.4) ---
Panagopoulou; 2009 (CS)*** Pt-reported part time employment 40 0.15# 48 0.19# N/R −0.16 (−0.8, 0.5) ---
Pietrabissa; 1992 (CS) Physical well-being scale developed by Simmons et al. (summary score) 172 12.38 71 11.81 NS 0.28 ---- ---
Sayin; 2007 (CS) SF-36 Role Physical 75 40.69 20 42.50 N/R −0.05 (−20.7, 17.1) ----
Recreation
Hart; 1987 (CS) Sickness Impact Profile (recreation/pastimes) 343 23.7 146 9 N/R ---- ---- TX
Kontodimopoulos 2008 (CS) SF-36 (Greek) Social Functioning 642 58.1 167 72.4 <0.001 −0.49 (−19.3, −9.3) TX
Simmons; 1990 (CS) Author-developed scale (recreation) 83 2.24 91 2.86 <0.05 −0.67 (−0.9, −0.3) TX
Basok; 2009 (CS) SF-36 Social Functioning 24 68.75 20 64.38 0.1 0.14 (−14.6, 23.3) ---
Devins; 1990 (CS)*** Intrusiveness Ratings Scale (recreation/social) 39 2.5 34 2 NS 0.32 (−0.2, 1.0) ---
Sayin; 2007 (CS) SF-36 Social Functioning 75 62.62 20 57.93 0.5 0.18 (−8.5, 17.9) ----
Tomasz; 2003 (CS) WHOQOL-100 (environment) 61 11.93 83 12.43 NS −0.26 (−1.1, 0.1) ---
Freedom
Barendse; 2005(CS) Renal Treatment Satisfaction Questionnaire 35 4.3 46 5.7 <0.05 −1.12 (−2.0, −0.8) TX
Bremer; 1989 (CS) Index of Well-Being (tied-down, free) 105 4.2 166 5.3 <0.05 −0.55 (−1.6, −0.6) TX
Lee; 2005 (CS) EQ-5D (usual activities) 99 18.09 209 54.95 <0.05 −0.94 (−1.3, −0.6) TX
Simmons; 1990 (CS) Author-developed scale (doing most things) 83 5.17 91 5.78 <0.05 −0.83 (−0.8, −0.4) TX
Work
Devins; 1990 (CS)*** Intrusiveness Ratings Scale (work/finances) 39 4 34 2.1 <0.05 1.03 (1.0, 2.8) TX
Evans; 1985 (CS) Patient reported ability to work 347 44.8# 144 62.3# N/R −0.39 (−0.6, −0.2) TX
Hart; 1987 (CS) Sickness Impact Profile (work) 338 45 144 28.4 N/R ---- ---- TX
Tomasz; 2003 (CS) WHOQOL-100 (working capacity) 61 10.4 83 12.18 <0.05 −0.46 (−3.1, −0.5) TX
Lee; 2005 (CS) KDQOL (work status) 99 20 209 46.8 <0.05 −0.65 (−36.7, −16.9) TX
Simmons; 1990 (CS) Author-developed scale (job satisfaction) 83 2.18 91 2.66 <0.01 −0.44 (−0.8, −0.1) TX
^

Calculated Cohen’s d.

*

Estimates are means unless otherwise noted.

**

Author-reported p-values.

#

Percentage.

##

Percentage with low satisfaction with physical performance.

***

denotes studies were originally designed as longitudinal cohort but authors only reported cross-sectional assessments of relevant outcomes

****

We calculated the confidence interval for the Cohen’s d effect size difference for studies that reported all of the needed estimates (e.g., means plus standard deviations) We reported ‘---‘ for studies that we could not calculate the confidence intervals for due to missing estimates.

Abbreviations and definitions: ADL, activities of daily living; CS, cross sectional study design; Pre-Post, pre-post transplantation; NS, not statistically significantly different at P>0.05 level; NR, not reported within article; Pt, patient; Pts, patients; CI, confidence interval; HD, hemodialysis; KDQOL, Kidney Disease Quality of Life scale; SF-36, 36-Item Short-Form Health Survey; WHOQOL, World Health Organization Quality of Life instrument; BREF, short version, Tx, transplantation

Patients Receiving Peritoneal Dialysis Versus Transplant Recipients

A total of 17 studies evaluated life participation activities between patients receiving peritoneal dialysis compared to patients with kidney transplants9,19,20,3234,38,4345,5153,55,63,64,66. Most studies reported on multiple outcomes, thus providing 21 physical function, 7 recreation, 4 freedom, and 5 work-related comparisons. The majority of comparisons demonstrated small to large differences in activities among patients with kidney transplants compared to patients receiving peritoneal dialysis, with transplant patients having better physical function (90%), freedom (100%), and work outcomes (100%). (Table 6) These findings of better outcomes in transplant patients were observed among 76% of comparisons from cross-sectional studies, 100% of comparisons from US-based studies, 50% of comparisons from studies that properly adjusted for potential confounders, and 65% of comparisons from studies published after 2000 favoring kidney transplantation. (Table 4)

Table 6.

Physical Function and Life Participation Outcome Measures and Study Results: PD versus Tx

Study; Design Outcome Measure PD Tx Statistical Results Treatment Favored
N Estimate* N Estimate* Reported P** Effect Size^ Calculated CI****
Physical Function
Apostolou; 2007; CS SF-36 Physical Functioning 26 36 20 51.5 0.01 −2.77 (−18.9, −12.1) TX
Apostolou; 2007 (CS) SF-36 Role Physical 26 12 20 47.5 0.001 −4.95 (−39.8, −31.2) TX
Basok; 2009 (CS) SF-36 Physical Functioning 21 56.61 20 77.78 N/R −1.09 (−33.4, −8.9) TX
Khan; 1995 (CS) SF-36 Physical Functioning 27 38.99 102 67.51 <0.05 −0.43 ---- TX
Khan; 1995 (CS) SF-36 Role Physical 27 29.7 102 63.22 <0.05 −0.43 ---- TX
Koch; 1990 (CS) Pt-reported low satisfaction with physical performance 68 0.47# 761 0.18# N/R 0.80 (0.49, 1.0) TX
Kontodimopoulos; 2008 (CS) SF-36 (Greek) Physical Functioning 65 49.2 167 72.9 <0.001 −1.04 (−30.3, −17.1) TX
Kontodimopoulos; 2008 (CS) SF-36 (Greek) Role Physical 65 30.9 167 62.6 <0.001 −0.76 (−43.7, −19.7) TX
Lee; 2005 (CS) SF-36 Physical Functioning 74 30.9 209 56.4 <0.05 −0.83 (−33.6, −17.1) TX
Lee; 2005 (CS) SF-36 Role Physical 74 60.6 209 86.7 <0.05 −0.79 (−34.8, −17.3) TX
Niu; 2005 (CS) WHOQOL-BREF (Taiwan; Scale physical health) 80 11.61 80 14.34 <0.05 −1.17 (−3.5, −2.0) TX
Ogutmen; 2006 (CS) SF-36 Role Physical 207 55.1 302 71.09 <0.05 −0.36 (−23.8, −8.1) TX
Panagopoulou; 2009 (CS)*** Pt-reported full time employment 36 0.14 48 0.375 N/R −0.71 (−1.3, −0.1) TX
Simmons; 1990 (CS) Author-scale physical well-being score 510 14.64 91 17.55 <0.01 −0.72 (−3.8, −2.0) TX
Baiardi; 2002 (CS)*** SF-36 Physical Functioning 30 59.7 34 64.6 N/R −0.17 (−19.4, 9.6) ----
Basok; 2009 (CS) SF-36 Role Physical 21 45.81 20 60 N/R −0.47 (−48.6, 7.2) ---
Devins; 1990 (CS)*** Author-developed difficulties in ADL scale 11 2.6 34 1.7 NS 0.49 (−0.4, 2.2) ---
Ogutmen; 2006 (CS) SF-36 Physical Functioning 207 57.06 302 59.92 N/R −0.12 (−7.1, 1.4) ---
Panagopoulou; 2009 (CS)*** Pt-reported employment 36 0.17# 48 0.19# N/R −0.07 (−0.7, 0.5) ---
Sayin; 2007 (CS) SF-36 Physical Functioning 41 55.76 20 68.75 0.1 −0.47 (−27.9, 2.0) ----
Sayin; 2007 (CS) SF-36 Role Physical 41 39.10 20 42.50 0.9 −0.08 (−25.3, 18.5) ----
Recreation
Apostolou; 2007 (CS) SF-36 Social Functioning 26 49.3 20 76.7 0.001 −5.67 (−30.3, −24.5) TX
Devins; 1990 (CS)*** Intrusiveness Ratings Scale (recreation/social activities) 11 3.2 34 2 <0.05 0.82 (0.2, 2.0) TX
Hart; 1987 (CS) Sickness Impact Profile (recreation) 77 24 146 9 <0.05 ---- ---- TX
Kontodimopoulos; 2008 (CS) SF-36 (Greek) Social Functioning 65 54.9 167 72.4 <0.001 −0.67 (−25.0, −10.0) TX
Simmons; 1990 (CS) Author-scale (recreation satisfaction) 510 2.21 91 2.86 <0.05 −0.66 (−0.9, −0.4) TX
Basok; 2009 (CS) SF-36 Social Functioning 21 63.39 20 64.38 NS −0.03 (−16.3, 14.9) ---
Sayin; 2007 (CS) SF-36 Social Functioning 41 56.32 20 57.93 0.5 −0.05 (−18.5, 15.3) ----
Freedom
Barendse; 2005 (CS) Renal Treatment Satisfaction 57 4.3 46 5.7 <0.05 −1.05 (−1.9, −0.9) TX
Bremer; 1989 (CS) Index of Well-Being (tied-down, free) 79 4.5 166 5.3 <0.05 −0.44 (−1.3, −0.3) TX
Lee; 2005 (CS) EQ-5D (usual activities) 74 20.55 209 54.95 <0.05 −0.85 (−1.2, −0.5) TX
Simmons; 1990 (CS) Author-scale (doing most things) 510 5.29 91 5.78 <0.05 −0.59 (−0.7, −0.3) TX
Work
Devins; 1990 (CS)*** Intrusiveness Ratings Scale (work) 11 3.6 34 2.1 <0.05 1.01 (0.5, 2.5) TX
Evans; 1985 (CS) Pt-reported ability to work 81 27.8# 144 62.3# N/R −0.80 (−1.1, −0.5) TX
Hart; 1987 (CS) Sickness Impact Profile (work) 81 51 144 28.4 <0.01 ---- ---- TX
Lee; 2005 (CS) KDQOL (work status) 74 28.2 209 46.8 <0.05 −0.43 (−30.2, −7.0) TX
Simmons; 1990 (CS) Author-scale (job satisfaction) 510 2.38 91 2.66 N/R −0.23 (−0.5, −0.01) TX
^

Calculated Cohen’s d.

*

Estimates are means unless otherwise noted.

#

Percentage.

**

Author-reported p-values.

***

denotes studies were originally designed as longitudinal cohort but authors only reported cross-sectional assessments of relevant outcomes

****

We calculated the CI for the Cohen’s d effect size difference for studies that reported all of the needed estimates (e.g., means plus standard deviations) We reported ‘---‘ for studies that we could not calculate the CIs for due to missing estimates.

Abbreviations and definitions: ADL, activities of daily living; CS, cross sectional study design; Pre-Post, pre-post transplantation; NS, not statistically significantly different at P>0.05 level; NR, not reported within article; Pt, patient; Pts, patients; CI, confidence interval; PD, peritoneal dialysis; KDQOL, Kidney Disease Quality of Life scale; SF-36, 36-Item Short-Form Health Survey; WHOQOL, World Health Organization Quality of Life instrument; BREF, short version, Tx, transplantation

Discussion

In this systematic review, a majority of studies consistently reported better physical functioning, greater engagement in social and recreational activities, greater independence, and better ability to work among patients with kidney transplants compared to patients receiving dialysis. Included studies did not report significant differences in outcomes between patients receiving hemodialysis and patients receiving peritoneal dialysis. Studies used a variety of measures to assess outcomes and were conducted among patients from diverse demographic backgrounds and clinical settings.

To our knowledge, this is the most comprehensive and recent systematic review to explore differences in rates of life participation activities among patients receiving various RRT modalities. With a carefully designed literature search and rigorous methods, we synthesized the results of 46 studies published over nearly three decades. Our findings, which summarize evidence on a broad range of life participation outcomes, should help patients and physicians better understand the quality and quantity of evidence available to inform their RRT selection choices. Outcomes were assessed both objectively (e.g. symptom-limited graded cycle ergometry tests) and subjectively reported by patients themselves (e.g. patient-reported questionnaires). We found that the magnitude and direction of associations we observed were similar for subjective patient-reported outcomes and objective clinical outcome measures. This may provide evidence of the importance and intrinsic similarity of both subjective and objective measurements, which attempt to comprehensively capture the extent to which patients are able to assimilate normal activities after initiating therapies.

As with every systematic review, the strength of our conclusions depends on the quality of available studies. Substantial limitations in the studies we identified indicate the evidence should be interpreted with caution. First, a majority of the studies reported outcomes at a single time point among patients often being observed for other (i.e. non-life participation) primary outcomes. Thus, we were only able to assess potential associations (versus true causal links) between RRT modality and outcomes of interest. It is possible that other important clinical characteristics influencing patients’ initial selection of RRT modalities (e.g., comorbid disease burden and medical eligibility for certain RRT modalities) could have also influenced their rates of life participation. For instance, patients enrolled in these studies who had received kidney transplants could have been healthier than those who may not have received kidney transplants. Studies variably accounted for these and other related factors, such as the presence or absence of diabetes or peripheral vascular disease, which could influence observed associations between RRT modality and rates of life participation. Ideally, randomized controlled trials would be performed to quantify differences in life participation among patients randomly selected to receive different RRTs. However, the feasibility of performing such trials is low, particularly since choice of RRT is influenced by a variety of factors, including patient and provider preferences, patients’ families’ capacities to support certain RRTs (e.g., managing peritoneal dialysis supplies and equipment at home), and patients’ medical suitability for transplants. One randomized trial conducted to compare mean quality-adjusted life-year (QALY) and survival among patients receiving hemodialysis compared to peritoneal dialysis reported statistically-equivalent QALY scores between the two groups of patients; however, the trial was prematurely stopped due to low inclusion rate71.

Additional potential limitations deserve consideration. First, we excluded non-English articles, which could introduce potential language bias. However, only 15% of potential articles were not published in English, and our included studies were conducted among a heterogeneous patient population representing 16 distinct locations worldwide. Therefore, we anticipate that the exclusion of these non-English articles will not significantly change our observed findings. Second, our review did not fully assess some potential treatment characteristics that might influence life participation outcomes, such as treatment intensity. Third, several of our included studies were identified from our hand-search of bibliographies but were not retrieved through our initial search of electronic databases. Although our electronic search yielded 5,265 citations that were potentially content-relevant, many of these studies were excluded due to a lack of comparative reporting of outcomes. We encountered difficulties devising electronic search terms to explicitly distinguish studies that are both content-relevant and inherently comparative in nature (i.e., reported relevant outcomes by RRT modality). Further, we speculate that some missed articles may have also been indexed prior to the inclusion of key search terms (e.g., MeSH headings and subheadings in PubMed) for our outcomes of interest72. Finally, we did not seek unpublished data from investigators who may have studied life participation among patients on RRT. It is possible studies reporting better outcomes among patients with transplants were more likely to be published. Notwithstanding these limitations, we believe our review provides a comprehensive summary of the most recent evidence regarding rates of life participation among patients receiving various RRTs and could serve as a valuable resource to patients and clinicians seeking to understand the current state of evidence informing this area.

In summary, a majority of studies reported better rates of life participation among patients with kidney transplants compared to patients receiving dialysis. Studies reported no significant differences in activities among patients receiving hemodialysis and patients receiving peritoneal dialysis. Many studies featured significant weaknesses in their design, limiting inferences. Rigorously performed studies incorporating randomized or longitudinal designs allowing for causal inferences and appropriately accounting for factors which could confound observed differences in outcomes among patients on different RRTs could better guide patients’ and nephrologists’ selection decisions.

Supplementary Material

01

Table S1: Search strategy and terms.

02

Table S2: Additional study participant characteristics.

03

Table S3: Assessment of individual study quality for relevant outcomes of interest.

04

Table S4: Description of outcome measures.

05

Item S1: Structured quality assessment questions.

Acknowledgments

The authors sincerely thank Blair Anton, MLIS, MS (Associate Director, Clinical Informationist Services, Johns Hopkins Welch Medical Library) and Victoria Goode, MLIS (Clinical Informationist, Johns Hopkins Welch Medical Library) for their methodological expertise in helping to develop the search terms.

Support: Dr Purnell was supported by grant F31DK084840 from the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) of the National Institutes of Health (NIH). Dr Crews was supported by the Harold Amos Medical Faculty Development Program of the Robert Wood Johnson Foundation, Princeton, NJ. Dr Greer was supported by the National Center for Research Resources of the NIH and grant 5KL2RR025006 from the NIH Roadmap for Medical Research. Dr Powe was supported, in part, by grants R01DK079682 and K24DK02643 from the NIH-NIDDK. Dr Rabb was supported by grant R01DK079682 from the NIH-NIDDK. Dr Boulware was supported by grants R01DK079682 and K23DK070757 from the NIH-NIDDK.

Footnotes

Financial Disclosure: The authors declare that they have no other relevant financial interests.

Note: The supplementary material accompanying this article (doi:_______) is available at www.ajkd.org

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Associated Data

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

Supplementary Materials

01

Table S1: Search strategy and terms.

02

Table S2: Additional study participant characteristics.

03

Table S3: Assessment of individual study quality for relevant outcomes of interest.

04

Table S4: Description of outcome measures.

05

Item S1: Structured quality assessment questions.

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