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. 2016 Jul 5;57(4):240–248. doi: 10.4111/icu.2016.57.4.240

Table 1. Randomized controlled trials of prophylactic mesh placement.

Source Type of stoma Type of mesh Placement technique No. of patients Median follow-up Primary endpoint PH rate Mesh-related complications
Janes et al. [10] Permanent end colostomy Partially absorbable (Vypro) Sublay Mesh, 27; control, 27 14 months (95% CI, 12–17) Clinical PH At 12 months: None reported
 Mesh, 0/16 (0%); control; 8/18 (44.4%)
Serra-Aracil et al. [17] Permanent end colostomy Partially absorbable (Ultrapro) Sublay Mesh, 27; control, 27 29 mo (range, 13–49 mo) Clinical PH At 29 months (median) None reported
Radiographic PH Clinical PH
 Mesh, 4/27 (14.8%); control; 11/27 (40.7%)
Radiographic PH
 Mesh: 6/27 (22.2%); control; 12/27 (44.4%)
Hammond et al. [43] Loop stoma Xenogenic collagen Sublay Implant, 10; control, 10 6.5 mo Clinical PH At 12 months: None reported
 Implant: 0/10 (0%); control; 3/10 (33.3%)
Lambrecht et al. [44] Permanent end colostomy Polypropylene Sublay Mesh, 32; control, 26 40 mo (range, 3–87 mo) Clinical PH At 24 months: None reported
 Mesh, 2/32 (6.3%); control; 12/26 (46.2%)
Vierimaa et al. [46] Permanent end colostomy Partially absorbable (Dyna-Mesh IPOM) Intraperitoneal Onlay Mesh, 35; control, 35 12 mo Clinical PH At 12 months: None reported
Radiographic PH Clinical PH
 Mesh, 5/35 (14.3%); control; 12/32 (32.3%)
Radiographic PH
 Mesh, 18/35 (51.4%); control; 17/32 (53.1%)

CI, confidence interval; PH, parastomal hernia.