Volume 48, Issue 5, Supplement , Pages S34-S47, November 2008
Autogenous versus prosthetic vascular access for hemodialysis: A systematic review and meta-analysis
Article Outline
Objectives
The autogenous arteriovenous access for chronic hemodialysis is recommended over the prosthetic access because of its longer lifespan. However, more than half of the United States dialysis patients receive a prosthetic access. We conducted a systematic review to summarize the best available evidence comparing the two accesses types in terms of patient-important outcomes.
Methods
We searched electronic databases (MEDLINE, EMBASE, Cochrane CENTRAL, Web of Science and SCOPUS) and included randomized controlled trials and controlled cohort studies. We pooled data for each outcome using a random effects model to estimate the relative risk (RR) and its associated 95% confidence interval (CI). We estimated inconsistency caused by true differences between studies using the I2 statistic.
Results
Eighty-three studies, of which 80 were nonrandomized, met eligibility criteria. Compared with the prosthetic access, the autogenous access was associated with a significant reduction in the risk of death (RR, 0.76; 95% CI, 0.67-0.86; I2 = 48%, 27 studies) and access infection (RR, 0.18; 95% CI, 0.11-0.31; I2 = 93%, 43 studies), and a nonsignificant reduction in the risk of postoperative complications (hematoma, bleeding, pseudoaneurysm and steal syndrome, RR 0.73; 95% CI, 0.48-1.16; I2 = 65%, 31 studies) and length of hospitalization (pooled weighted mean difference –3.8 days; 95% CI, –7.8 to 0.2; P = .06). The autogenous access also had better primary and secondary patency at 12 and 36 months.
Conclusion
Low-quality evidence from inconsistent studies with limited protection against bias shows that autogenous access for chronic hemodialysis is superior to prosthetic access.
Several studies have demonstrated that autogenous arteriovenous access for chronic hemodialysis has longer patency compared with prosthetic access.1, 2 The National Kidney Foundation Dialysis Outcomes Quality Initiative (NKF KDOQI) advocates the use of autogenous access if possible in all clinical scenarios.3
Nevertheless, the prosthetic access is widely used in the United States, to the extent that in 2002, it represented 80% of accesses used in prevalent dialysis patients compared with 24% in Europe.4 The increased use of prosthetic access may be attributed to putative benefits in some patients such as women and the elderly,5, 6, 7 the availability of off-the-shelf conduit for placement, the higher reimbursement associated with prosthetic access placement, the ability to cannulate and use the prosthetic access without waiting for maturation, more amenability of the prosthetic access to thrombectomy, and the high nonmaturity rate of the autogenous access.8, 9, 10 To our knowledge, no published systematic reviews have evaluated the two types of accesses in terms of patient-important outcomes other than patency, such as death and sepsis.
To aid physicians and patients in making informed choices about the placement and management of hemodialysis access, the Society for Vascular Surgery created a multispecialty committee to produce clinical practice guidelines based on the best available evidence. The aim of this review is to inform the development of these guidelines and compare the two types of accesses in terms of patient-important outcomes.
Methods
The report of this protocol-driven systematic review was approved by the Society for Vascular Surgery and adheres to the standards for reporting Meta-analysis Of Observational Studies in Epidemiology (MOOSE).11 Whenever possible, we used the nomenclatures and definitions as published in the “Recommended Standards for Reports Dealing with Arteriovenous Hemodialysis Accesses” by the Society for Vascular Surgery.12
Eligibility criteria
We sought to include randomized controlled trials (RCTs) and cohort studies that compared a group of patients that have an autogenous access with a concurrent comparison group that had a prosthetic access. The outcomes of interest were death, access infection, postoperative complications, the duration of hospitalization due to access complications, and patency. We included studies regardless of their language, size, or duration of patient follow-up.
Study identification
An expert reference librarian designed and conducted the electronic search strategy with input from study investigators with expertise in conducting systematic reviews. To identify eligible studies, we searched electronic databases (MEDLINE, EMBASE, Cochrane CENTRAL, Web of Science and SCOPUS) through March 2007. The search strategy, which was tailored to each database, included controlled vocabulary and text words describing vascular access in hemodialysis (including terms for renal disease, methods of vascular access, and access type). We also sought references from experts, bibliographies of included studies, and the ISI Science Citation Index for publications that cited included studies (details are available from the authors upon request).
References were uploaded in a Web-based software package developed for systematic review data management (SRS, TrialStat Corporation, Ottawa, Ontario Canada). Paired reviewers working independently screened all abstracts and titles for eligibility. References that were deemed potentially relevant were retrieved in full text and uploaded for full text evaluation against eligibility criteria. Disagreements were resolved by consensus (the two reviewers discussed the study and reached a consensus) and by arbitration (a third reviewer adjudicated the study) when disagreement continued.
Data collection
Teams of reviewers working independently and in duplicates and using standardized forms extracted descriptive, methodologic, and outcome data from all eligible studies. Outcomes were extracted from text, tables, and graphs (survival curves). Study quality was assessed using the Newcastle-Ottawa Scale for assessing the quality of observational studies.13 We sent e-mails to authors of all included studies to obtain missing data and to verify the presence of any collected but unreported data. When e-mail addresses were not published (particularly for older studies), we searched for authors' newer publications or attempted to contact their institutions to obtain current e-mail addresses.
Statistical analysis
Meta analysesWe pooled relative risks (RR) from each trial using the DerSimonian-Laird random effects model and estimated the 95% confidence intervals (CIs) for each outcome.14 Patency rates were converted to dichotomous outcomes for specific time periods (12 and 36 months).6 In all analyses in this review, a RR <1.0 indicates benefit from autogenous access vs prosthetic access. We assessed the heterogeneity among studies using the I2 statistic, which represents the proportion of variability across studies that is not due to chance or random error but rather is due to real differences in study design, population, or interventions.15 I2 values of 25%, 50%, and 75% indicate low, moderate, and high heterogeneity, respectively. Statistical analysis was conducted by using Comprehensive Meta-Analysis 2 software (Biostat Inc, Englewood, NJ; 2005).
Subgroup analysesA priori hypotheses to explain potential heterogeneity in the direction and magnitude of effect among included studies were patients' age (children vs adult, age ≥65 vs <65 years), gender, diabetes status, the presence of peripheral vascular disease, the location of the access (upper arm vs lower arm), and whether studies reported outcomes per patient or per access and whether patients were incidental or prevalent hemodialysis patients. Also, we conducted meta-regression to determine whether study quality or the length of study follow-up (predictor variables) affected patency outcomes (dependent variable).
Sensitivity analysesWe conducted sensitivity analyses to test the effect of including studies in which investigators determined study outcomes clinically or from administrative databases (eg, billing codes). Using billing/administrative data to determine outcomes reduces the bias caused by outcome assessors not being blinded but introduces misclassification bias (intentional or unintentional erroneous coding). We conducted sensitivity analysis with and without the assumption that denatured homologous vein grafts and saphenous vein grafts are considered autogenous accesses. We also explored the robustness of our results by analyzing the data with accounting for censoring in time-to-event outcomes according to the method of Pramar et al.16
Results
Study identification
Our search and selection procedures yielded 995 potentially eligible references, of which 99 proved eligible and 83 provided data for meta-analyses (Fig 1). Study characteristics are summarized in Table I.5, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98 The chance adjusted inter-reviewer agreement (κ statistic) for study eligibility averaged 0.78 (range, 0.61-1.00). These studies enrolled 69,816 participants (mean size, 850 patients; mean age, 55 years; mean follow-up, 2.8 years). Authors from 26 of the 83 included studies (31%) responded to our e-mail queries and provided missing data. Seven studies were translated to English.1, 24, 99, 40, 100, 101, 102
Table I. Baseline characteristics for included studies
| First author, year | Patients, No. | Mean Age, y | Incidental/prevalent | Autogenous | Prosthetic | F/U, d | Study design | ||
|---|---|---|---|---|---|---|---|---|---|
| Location | Vessels | Location | Vessels | ||||||
| Haimov,17 1980 | 126a | NR | Inc | Upper arm | Brachiocephalic | Forearm, upper arm, thigh | Radiocephalic, brachiocephalic, femoral | NR | Prosp |
| Mangiarotti,18 1983 | 205 | NR | NR | Forearm, upper arm, thigh | 36.96 brachial, 7.04 radial; 22.88 cephalic vein, 7.04 basilic, 14.08 other veins | Forearm, upper arm, thigh | 22 brachial, 1 arterial stump from prosthesis; 8 brachial, 8 basilic, 3 cephalic, 4 other veins | 1740 | Retro |
| ATordoir,19 1983 | 149 | 49 | Inc | Forearm | Radiocephalic | Forearm, upper arm, thigh | Radiocephalic, brachiocephalic, saphenofemoral | 1145 | Prosp |
| Louridas,20 1984 | 152 | 43 | NR | Forearm, upper arm | Radiocephalic, brachiocephalic | Forearm, upper arm, thigh | Brachial to axillary, axillary to femoral, axillary to basilic, axillary to cephalic | NR | Retro |
| Winsett,21 1985 | 508 | 45 | Prev | Forearm | Radiocephalic, brachiocephalic | Forearm | Radiocephalic, brachiocephalic, brachiocubital | 730 | Retro |
| Kherlakian,22 1986 | 200 | 52 | Inc | Forearm | Radiocephalic | Upper arm, thigh | Brachiocephalic, brachiobasilic, femoral | 1095 | Retro |
| Zibari,23 1988 | 230 | 52 | Mixed | Forearm, upper arm | Brachiocephalic, radiocephalic | Forearm, upper arm, thigh | Radiocephalic, brachioaxillary, femoral, femoral-popliteal | NR | Retro |
| Filiptsev,24 1989 | 84 | NR | NR | Multiple (shoulder, upper arm, thigh) | NR | Multiple (shoulder, upper arm, thigh) | NR | NR | Prosp |
| Nazzal,25 1990 | 125 | 37 | Inc | Forearm, upper arm | Radiocephalic, brachiocephalic | Upper arm | Brachioaxillary | 300 | Prosp |
| Sands,26 1992 | 111 | 64 | NR | NR | NR | NR | NR | 180 | Retro |
| Churchill,27 1992 | 347 | ≥18 | Inc | NR | NR | NR | NR | NR | Prosp |
| Tang,28 1992 | 63 | 50 | Prev | NR | NR | NR | NR | 300 | Prosp |
| Sanabia,29 1993 | 74 | 9 | Inc | Upper arm, forearm | Radiocephalic, ulnar basilic, antecubital | Forearm, upper arm, thigh, neck | Radiocephalic, brachiocephalic, brachiojugular, femoral | NR | Retro |
| Taylor,30 1993 | 1897 | NR | Inc | NR | NR | NR | NR | NR | Retro |
| Al-Wakeel,31 1994 | 105 | 42 | Inc | Forearm, upper arm | Radiocephalic, brachiocephalic | Forearm, upper arm | Radiocephalic, brachiocephalic | 1825 | Retro |
| Bender,32 1994 | 68 | 62 | Mixed | Elbow, wrist | Radiocephalic, brachiocephalic | Forearm, upper arm | NR | 1095 | Retro |
| Chalabi,33 1994 | 84 | 51 | Inc | NR | Saphenous vein | Upper arm | Humeroaxillary, humerobasilic, humerocephalic | 1825 | Retro |
| Coburn,34 1994 | 81 | 65 | Inc | Upper arm | Brachiobasilic | Upper arm | Brachiobasilic, Brachioaxillary, Brachiocephalic | NR | Retro |
| Riordan,35 1994 | 464 | 48 | Inc | Forearm | Radiocephalic | Forearm, upper arm, thigh | Radiocephalic, brachiocephalic, femoral | NR | Retro |
| Chazan,36 1995 | 117 | 57 | Prev | NR | NR | NR | NR | 425 | Prosp |
| Kim,37 1995 | 172 | 43 | NR | NR | NR | NR | NR | 510 | Retro |
| Sands,38 1995 | 107 | NR | Inc | NR | NR | NR | NR | 772 | Retro |
| Tedoriya,39 1995 | 113 | 47 | Inc | Forearm, upper arm | Radiocephalic, ulnar basilic, snuffbox, brachiocephalic | NR | NR | 6570 | Retro |
| Vaccaro,40 1995 | 276 | 56 | Prev | Forearm | Radiocephalic | Upper arm | PTFE | 730 | Retro |
| Enzler,41 1996 | 414 | 44 | Mixed | Forearm, upper arm | NR | Forearm, upper arm, thigh | NR | NR | Retro |
| Herzig,42 1997 | 391 | 58 | Inc | Multiple | NR | Multiple | NR | NR | Retro |
| Hodges,43 1997 | 350 | 59 | Inc | Forearm, upper arm | Radiocephalic, brachiocephalic | Forearm, upper arm, thigh | NR | NR | Retro |
| Miller,44 1997 | 76 | 64 | Inc | Forearm, upper arm | Cephalic, brachial, radial, basilic | Upper arm | Brachiocephalic loop or straight graft | 455 | Retro |
| Sparks,45 1997 | 427 | 54 | Inc | Forearm, upper arm | Radiocephalic, brachiocephalic, brachiocubital | Upper arm | Loop brachial-cephalic/basilic or a bridge radial-cephalic/basilic construction. | 1026 | Retro |
| Woods,46 1997 | 784 | 66 | Mixed | NR | NR | NR | NR | 365 | Retro |
| Bay,47 1998 | 2792 | 60 | Prev | Upper arm (6.4%), forearm (20.6%) | NR | Forearm straight (14.7%), forearm loop (24.8%), upper arm straight (26.1%), upper arm loop (3.8%), femoral graft (2.3%) | NR | 365 | Prosp |
| Miranda,48 1998 | 1308a | NR | Prev | Forearm or upper arm | Cephalic or basilic veins | Forearm, upper arm, thigh, chest | Cephalic, basilic, femoral, axillary | 180 | Retro |
| Berardinelli,49 1998 | 348 | 72 | Inc | Forearm, upper arm | Radiocephalic, brachiocephalic | Forearm, upper arm | Radiocephalic, brachiocephalic | 5475 | Retro |
| Bosman,50 1998 | 131 | 60 | Inc | Forearm, upper arm, thigh | Denatured homologous vein graft, straight radiocephalic, loop radiocephalic, brachiocephalic, femoral. | Forearm, thigh | PTFE: loop radiocephalic, straight radiocephalic, femoral | 326 | RCT |
| Cante,51 1998 | 51 | 74 | Inc | Forearm | NR | Forearm | NR | 730 | Retro |
| Jenkins,52 1980 | 56 | NR | Inc | Forearm, upper arm, thigh | Radiocephalic, brachiocephalic, femoral | Forearm, upper arm, thigh | Radiocephalic, brachiocephalic, femoral | NR | Prosp |
| Matsuura,53 1998 | 98 | 61 | Inc | Upper arm | Brachioaxillary, basilic vein transposition | Upper arm | Brachioaxillary | NR | Retro |
| Obialo,54 1998 | 36 | 42 | NR | Forearm | Radio cephalic | Upper arm | Brachiocephalic | 365 | Prosp |
| Silva,55 1998 | 172 | 63 | Inc | Forearm, upper arm | NR | Forearm, upper arm | Radiocephalic, brachioaxillary | 401 | Prosp |
| Wang,56 1998 | 131 | 60 | Prev | Multiple | NR | Multiple | NR | 180 | Prosp |
| Agarwal,57 1999 | 32 | 56 | Prev | NR | NR | NR | NR | 252 | Prosp |
| Turnbull,58 1999 | 166 | NR | Inc | Forearm, upper arm | Radiocephalic, brachiocephalic, brachiobasilic | Forearm, upper arm | Radiocephalic, brachiocephalic, straight, loop | NR | Retro |
| Ascher,59 2000 | 247 | 69 | Inc | Forearm, upper arm | Radiocephalic, brachiocephalic, brachiobasilic | NR | NR | 270 | Retro |
| Astor,5 2000 | 833 | 63 | Prev | NR | NR | NR | NR | 395 | Retro |
| Rodriguez,60 2000 | 544 | 56 | NR | Forearm, upper arm | Radiocephalic, brachiocephalic, humerobasilar | Upper arm, thigh | Humerocephalic, humerobasilic, femoro-femoral | 2532 | Retro |
| Staramos,61 2000 | 114 | 78 | Inc | Forearm, upper arm | Radiocephalic, brachiocephalic, basilic transposition | Forearm, upper arm, thigh | Brachiocephalic, brachioaxillary, femoral | 1095 | Prosp |
| Brunori,62 2000 | 203 | 68 | Inc | Forearm, upper arm | Radiocephalic, brachiocephalic | NR | NR | NR | Retro |
| Dhingra,63 2001 | 4469 | 59 | Prev | NR | NR | NR | NR | 730 | Prosp |
| Gibson,64 2001 | 152 | 56 | Mixed | NR | NR | NR | NR | 511 | Retro |
| Gibson,65 2001 | 1583 | 66 | Inc | NR | NR | NR | NR | 340 | Retro |
| Oliver,66 2001 | 195 | 57 | Inc | Upper arm | Brachiocephalic, brachiobasilic transposition | Upper arm | Brachioaxillary | 600 | Retro |
| Dixon,67 2002 | 204 | 56 | Inc | Forearm, upper arm | Radiocephalic, brachiocephalic | Forearm | Forearm loop radiocephalic | 1825 | Prosp |
| Lawrence,68 2002 | 71 | 57 | Prev | NR | NR | NR | NR | NR | Retro |
| Pastan,69 2002 | 7403 | 58 | Prev | NR | NR | NR | NR | 260 | Retro |
| Ridao-Cano,70 2002 | 872 | 56 | Inc | Forearm, upper arm | Radiocephalic, basiocephalic | Forearm, upper arm | Radiocephalic, brachiocephalic, straight, loop grafts | 1825 | Retro |
| Saxena,71 2002 | 218 | 48 | Prev | NR | NR | NR | NR | 1460 | Prosp |
| Sheth,72 2002 | 34 | 13 | Inc | Forearm, upper arm, thigh | Radiocephalic, brachiocephalic, femoral | Forearm, upper arm, thigh | Radiocephalic, brachiocephalic, femoral | 3650 | Retro |
| Valentine,73 2002 | 72 | 57 | Inc | Upper arm | Brachial-based arteriovenous fistula | Upper arm, forearm | Radiocephalic, brachiocephalic, straight or loop | 180 | Prosp |
| Johnson,74 2002 | 207 | > | NR | Wrist, elbow | NR | NR | NR | 360 | Prosp |
| Baaran,75 2003 | 2950 | 38 | Inc | Forearm, upper arm | Radiocephalic, brachiocephalic | Upper arm | NR | 1160 | Retro |
| Cernadas,76 2003 | 60 | 61 | Inc | Upper arm | Transposed brachiobasilic | Upper arm | PTFE brachioaxillary bridge fistula | 730 | Retro |
| Choi,77 2003 | 97 | 54 | NR | Forearm, upper arm | Radiocephalic, brachiocephalic, brachiobasilic, transposed, non-transposed | Forearm, upper arm | Brachioaxillary, mediocubital, cephalic or basilic vein | 545 | Retro |
| Culp,78 1995 | 267 | 62 | Inc | Forearm, upper arm | NR | Forearm, upper arm | NR | 365 | Prosp |
| Fisher,79 2003 | 197 | 61 | Inc | Forearm, upper arm | Radiocephalic, brachiocephalic | Forearm, upper arm, thigh | Forearm loop, upper arm loop, thigh loop | 780 | Retro |
| Shenoy,80 2003 | 1110 | 59 | Prev | NR | NR | NR | NR | 730 | Retro |
| Xue,81 2003 | 25226 | >=67 | Mixed | NR | NR | NR | NR | 365 | Retro |
| Yu,82 2003 | 82 | 61 | Prev | NR | NR | NR | NR | 365 | Prosp |
| Di Iorio,83 2004 | 2201 | 62 | Prev | NR | NR | NR | NR | 730 | Retro |
| Hazinedaroglu,84 2004 | 30 | 59 | Inc | Thigh | Femoral vein transposition | Thigh | Superficial femoral artery to saphenous or common femoral vein | 237 | Prosp |
| Kizilisik,85 2004 | 93 | 61 | Inc | Forearm, upper arm | Radiocephalic, brachiocephalic, brachiobasilic | Forearm, upper arm | Straight, loop | 600 | Retro |
| Perera,86 2004 | 209 | 57 | Inc | Upper arm | Radiocephalic mainly, brachiocephalic. Basilic vein used in 4 | Upper arm | Brachial mainly, radial. Outflow brachial/axillary, basilic vein | 1095 | Retro |
| Polkinghorne,87 2004 | 2632 | >18 | Inc | NR | NR | NR | NR | 1095 | Retro |
| Akoh,88 2005 | 151 | 62 | Inc | Forearm, upper arm | Brachiocephalic, radiocephalic | Forearm, upper arm, chest, thigh | Forearm straight, forearm loop, brachioaxillary, femoral, axillary | 567 | Retro |
| Astor,89 2005 | 206 | 59 | Inc | NR | NR | NR | NR | 810 | Retro |
| Fitzgerald,90 2005 | 146 | 56 | Inc | Upper arm | Brachiocephalic, brachiobasilic, brachiomedian | Forearm | Brachiobasilic, brachiocephalic, brachiomedian | 430 | Retro |
| Kawecka,91 2005 | 722 | 44 | Mixed | Upper and lower extremities | Radiocephalic, brachiocephalic and brachiobasilic | Upper and lower arm | NR | 570 | Retro |
| Manns,92 2005 | 239 | 63 | NR | Forearm, upper arm | Radiocephalic, brachiocephalic | Upper arm | Brachiocephalic | NR | Retro |
| Ramage,93 2005 | 114 | 12 | Inc | Upper arm | Radiocephalic, brachiocephalic | Forearm, upper arm, thigh | Radiocephalic, brachiocephalic, femoral | 7300 | Retro |
| Rooijens,94 2005 | 383 | 60 | Inc | Forearm | Radiocephalic | Forearm | Brachiocephalic | 365 | RCT |
| Ates,95 2006 | 920 | 42 | Inc | Forearm, upper arm | Radiocephalic, brachiocephalic | Upper arm | Brachioaxillary, brachiocephalic | 1825 | Retro |
| Roca-tey,96 2006 | 89 | 63 | Prev | Upper arm | Radiocephalic, brachiocephalic | Upper arm, thigh | Brachiocephalic, femoral | 354 | Prosp |
| Woo,97 2007 | 329 | 65 | Prev | Upper arm | NR | Upper arm | NR | 860 | Retro |
| Keuter,98 2008 | 105 | 63 | Prev | Upper arm | Brachial-basilic | Forearm | Brachial antecubital forearm loop | 365 | RCTb |
aThis is the number of accesses; number of patients is not reported. |
bCommunication with author indicates that patients and care givers were not blinded, data collectors were blinded, and allocation was concealed. |
Methodologic quality
Three studies were open randomized trials,50, 94, 98 and 80 were observational studies, of which 56 had a retrospective cohort design and 24 had a prospective cohort design. Allocation was concealed and data collectors were blinded in one of the randomized trials.98 The distribution of the Newcastle-Ottawa quality scale components that describe the quality of observational studies are summarized in Table II. Only 46% of the studies controlled for at least one possible confounder in cohort selection or analysis. The proportion lost to follow-up was <10% in only 19% of the studies. Only 20% of the studies reported a funding source. Inter-reviewer agreement (κ statistic) of the different components of quality averaged 0.70 (range, 0.53-1.00).
Table II. Distribution of components of the Newcastle-Ottawa quality scale of cohort studies
| Component | Studies, No. (%) |
|---|---|
| Cohort selection | |
| Study cohorts are representative of the typical patients encountered in practice | |
| 77 | |
| 3 | |
| Exposure ascertainment (type of access) | |
| 63 | |
| 17 | |
| Studies confirmed that the access was functional at the outset | |
| 20 | |
| 60 | |
| Cohort comparability | |
| Studies controlled for possible confounders in cohort selection or analysis | |
| 30 | |
| 7 | |
| 43 | |
| Outcome | |
| Outcome assessment | |
| 56 | |
| 24 | |
| The length of follow-up adequate to assess outcomes | |
| 47 | |
| 33 | |
| Proportion lost to follow-up | |
| 15 | |
| 65 |
Meta-analyses
The autogenous access was associated with a significant reduction in the risk of death (RR, 0.76; 95% CI, 0.67-0.86; I2 = 48%; 27 studies; Fig 2) and access infection (RR, 0.18; 95% CI, 0.11-0.31; I2 = 93%; 43 studies; Fig 3). The autogenous access was also associated with a nonsignificant reduction in the risk of postoperative complications of access placement other than infection, including hematoma, bleeding, pseudoaneurysm, and steal syndrome (RR, 0.73; 95% CI, 0.48-1.12; I2 = 65%, 31 studies; Fig 4). The length of hospitalization related to access complications was lower in patients who had autogenous accesses (pooled weighted mean difference –3.8 days; 95% CI –7.8 to 0.2; P = .06; 3 studies).

Fig 2.
Meta-analysis of the effect of access type on the risk of death. The vertical line indicates no treatment effect; the squares and horizontal lines, point estimates and associated 95% confidence intervals (CIs) for each study; diamonds, random-effects pooled relative risk (RR) of death.

Fig 3.
Meta-analysis of the effect of access type on the risk of access infection. The vertical line indicates no treatment effect; squares and horizontal lines, point estimates and associated 95% confidence intervals (CIs) for each study; diamonds, random-effects pooled relative risk (RR) of access infection.

Fig 4.
Meta-analysis of the effect of access type on the risk of access complications other than infection. The vertical line indicates no treatment effect; squares and horizontal lines, point estimates and associated 95% confidence intervals (CIs) for each study; diamonds, random-effects pooled relative risk (RR) of access complications.
Primary and secondary patency rates at 12 and 36 months were significantly higher in the autogenous than in the prosthetic access. RRs for access failure without interventions to maintain or re-establish patency were 0.72 (95% CI, 0.65-0.80) at 12 months and 0.67 (95% CI, 0.58-0.78 at 36 months. RRs for access failure including interventions to maintain or re-establish patency were 0.83 (95% CI, 0.70-0.99) at 12 months and 0.67 (95% CI, 0.61-0.74) at 36 months.
Subgroup analyses
One of the a priori established analyses to explain heterogeneity of results is autogenous access location (upper arm vs lower arm, both compared with prosthetic access at any location). We found a significant access location–access complications interaction (P = .02) demonstrating that the magnitude of benefit from autogenous access vs prosthetic access is significantly more when autogenous access was placed in the lower arm. There were no significant death–access location, access infection–access location or patency–access location interactions (P =.60, P = .18, and P = .33, respectively).
Only two studies compared the autogenous upper arm access with a prosthetic lower arm access (prosthetic looped forearm access).90, 98 Pooling the outcomes of the two studies (a total of 249 patients) demonstrates that the placement of autogenous access in the upper arm is associated with a significantly lower rate of infections (RR, 0.23; 95% CI, 0.07-0.83) and nonsignificant trends for better 12-month primary (RR, 0.88; 95% CI, 0.72-1.07) and secondary (RR, 0.81; 95% CI, 0.54-1.20) patency. Patency at 24 months was only reported by Fitzgerald et al90 and was similar between the two accesses. Both studies reported the upper arm placement of autogenous access to be associated with fewer complications and to require fewer interventions to maintain patency.
Interactions based on patient type (incidental vs prevalent hemodialysis) for outcomes of death, access infections, access complications, and patency were all nonsignificant (P = .4, P = .77, P = .43, and P = .33, respectively).
Several studies reported outcomes by access rather than by patient, a unit-of-analysis challenge given the likely correlation of outcomes for accesses in the same patient. However, the results in studies reporting patency, access complications, and access infection, per patient vs per access, were not different (P = .80, P = .43 and P = .33, respectively).
There were no significant patency-gender or patency-age (>65 or <65 years) interactions. A significant patency-age interaction (pediatric vs adults) was found in a single, small pediatric study that showed the autogenous access patency in children was inferior to that of the prosthetic access at 12 and 36 months (P = .02 and P = .07, respectively); however, autogenous patency regained superiority at 60 months of follow-up.72 Subgroup analyses are summarized in Table III.
Table III. Subgroup analyses
| Variable | Studies, No. | RR (95% CI) | P (interaction test) |
|---|---|---|---|
| Death | |||
| 6 | 0.68 | 0.55 | |
| 3 | 0.46 | ||
| 19 | 0.72 | 0.74 | |
| 5 | 0.76 | ||
| Access infection | |||
| 11 | 0.21 | 0.17 | |
| 5 | 0.10 | ||
| 29 | 0.21 | 0.33 | |
| 13 | 0.34 | ||
| 30 | 0.22 | 0.77 | |
| 5 | 0.26 | ||
| Access complications | |||
| 9 | 1.22 | 0.02 | |
| 5 | 0.20 | ||
| 21 | 0.69 | 0.43 | |
| 10 | 1.06 | ||
| 22 | 0.86 | 0.43 | |
| 4 | 0.56 | ||
| Primary patency at 12 months | |||
| 14 | 0.70 | 0.09 | |
| 11 | 0.94 | ||
| 2 | 0.50 | 0.64 | |
| 2 | 0.65 | ||
| 2 | 0.57 | 0.56 | |
| 2 | 0.89 | ||
| 28 | 0.68 | 0.51 | |
| 12 | 0.78 | ||
| 28 | 0.75 | 0.16 | |
| 6 | 0.63 | ||
| Primary patency at 36 months | |||
| 8 | 0.87 | 0.78 | |
| 4 | 0.80 | ||
| 13 | 0.65 | 0.08 | |
| 5 | 0.83 | ||
| 15 | 0.75 | 0.16 | |
| 6 | 0.59 | ||
| Secondary patency at 12 months | |||
| 9 | 0.70 | 0.07 | |
| 7 | 0.99 | ||
| 1 | 6.67 | 0.02 | |
| 22 | 0.82 | ||
| 18 | 0.82 | 0.45 | |
| 5 | 0.95 | ||
| 15 | 0.88 | 0.70 | |
| 4 | 0.97 | ||
| Secondary patency at 36 months | |||
| 8 | 0.73 | 0.33 | |
| 6 | 0.65 | ||
| 1 | 1.69 | 0.07 | |
| 18 | 0.67 | ||
| 16 | 0.67 | 0.80 | |
| 3 | 0.71 | ||
| 12 | 0.72 | 0.33 | |
| 4 | 0.61 |
Meta-regression revealed that neither study quality nor the length of study follow-up explained the between-study variability in patency reported across studies. In terms of diabetes status, the autogenous access was associated with longer patency36 and lower mortality63 than the prosthetic access in patients with and without diabetes. Hence, it appears that the presence of diabetes should not affect the choice of access.
Sensitivity analyses
Sensitivity analyses are summarized in Table IV. The exclusion of studies in which the autogenous access was denatured homologous vein graft or saphenous vein grafts and the exclusion of studies that used administrative and billing databases to determine outcomes caused no significant change in any of the results.
Table IV. Sensitivity analysis
| Variable | Studies, No. | RR (95% CI) |
|---|---|---|
| Death | ||
| 27 | 0.76 | |
| 25 | 0.71 | |
| 25 | 0.75 | |
| Primary patency at 12 months | ||
| 41 | 0.71 | |
| 39 | 0.70 | |
| 38 | 0.70 | |
| 30 | 0.72 | |
| 30 | 0.72 | |
| Primary patency at 36 months | ||
| 24 | 0.67(0.58-0.78) | |
| 22 | 0.68 | |
| 20 | 0.73 | |
| 20 | 0.72 | |
| Secondary patency at 12 months | ||
| 24 | 0.84 | |
| 22 | 0.84 | |
| 22 | 0.83 | |
| 21 | 0.84 | |
| 21 | 0.83 | |
| Secondary patency at 36 months | ||
| 20 | 0.67 | |
| 19 | 0.64 | |
| 19 | 0.63 |
Because the shortest and longest follow-up times for study participants, which are the key variables in the adjustment for censoring of time-to-event data reported in graphic form, were either not reported or were similar in both study arms, adjustments for censoring were either not feasible or led to proportionate decrements of the sizes of both study arms, slightly widening the CIs without affecting the estimates of RR for any of the outcomes examined or their statistical significance (data not shown).
Discussion
We conducted a systematic review and meta-analyses to compare the autogenous and prosthetic accesses for chronic hemodialysis in terms of patient-important outcomes. We found that very low-quality evidence103 with significant heterogeneity suggests that the autogenous access of hemodialysis is superior to the prosthetic access in terms of the risks of death, access infection, and primary and secondary patency. Overall, there were insufficient data to identify a subgroup to which the overall conclusions do not apply, although subgroup analyses were underpowered.
Limitations and strengths
Although systematic reviews and meta-analyses comparing autogenous vs prosthetics accesses exist, 6, 10 to our knowledge this is the first comprehensive review to assess patient-important outcomes other than patency. Efforts to reduce bias such as author contact, a review of the literature by two independent reviewers, and explicit quality assessment strengthen inferences from this review.
The main limitation of this review is the nonrandomized design of most of the included studies, which meant that the choice of access type was based on surgeons' preference, patients' comorbidities, and other unmeasured yet potentially important confounders. Although this inherent bias in observational studies can be remedied to some extent by controlling for factors that can affect study outcomes in either selecting cohorts or in analysis, we found that many studies did not control for these factors, rendering the cohort that received prosthetic access to include more patients with diabetes, patients with peripheral vascular disease, and older patients. This bias in selection has likely overestimated the benefit noted in patients who received the autogenous access. Moreover, the proportion of studies that contributed to each of the outcomes in this review was low; thus, reporting bias has likely affected the benefits noted with autogenous access placaement.104
Other limitations relate to extracting survival data from graphs and to the inconsistency of the taxonomy in the included studies, which underscores the need for standardized nomenclature.12 In addition, one study33 could not be retrieved and was extracted directly from a previously published systematic review.6
Conclusions
Although the available evidence is consistent with previous recommendations for using autogenous accesses for hemodialysis, the current review highlights that this inference is derived from very low-quality evidence. That is, large studies with better protection against bias—preferably randomized trials measuring patient important outcomes—are necessary to make recommendations with confidence because these may substantially change the estimates reported here. Patient and surgeon preferences, cost considerations, and clinical circumstances should inform the choice of access for specific patients. The accompanying practice guideline document includes the practical implication of this evidence from the standpoint of the expert members of the committee of the Society for Vascular Surgery.
Author contributions
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This review was funded by a contract from the Society for Vascular Surgery.
STATEMENT OF CONFLICT OF INTEREST: These authors report that they have no conflicts of interest with the sponsor of this supplement article or products discussed in this article.
PII: S0741-5214(08)01395-5
doi:10.1016/j.jvs.2008.08.044
© 2008 The Society for Vascular Surgery. Published by Elsevier Inc. All rights reserved.
Volume 48, Issue 5, Supplement , Pages S34-S47, November 2008

