| Literature DB >> 34018122 |
Xavier Pereira1, Diego L Lima2, Patricia Friedmann3,4,5, Gustavo Romero-Velez6, Cosman C Mandujano6, Vicente Ramos-Santillan6, Ana Garcia-Cabrera6, Flavio Malcher2.
Abstract
Robotic-assisted abdominal wall repair (RAWR) has seen an exponential adoption over the last 5 years. Skepticism surrounding the safety, efficacy, and cost continues to limit a more widespread adoption of the platform. We describe our initial experience of 312 patients undergoing RAWR at a large academic center. A retrospective review of all patients undergoing any RAWR from July 1, 2016 to March 18, 2020 was completed. Patient specific, operation specific, and 30-day outcomes specific data were collected. Univariate analysis and multivariate logistic regression were used to assess factors associated with 30-day complications. There was a steady adoption of RAWR over the study period. A total of 312 patient were included, 138 (44%) were abdominal wall repairs and 174 (56%) were inguinal repairs. The mean age of the cohort was 54.2 years (SD 16), 69% were males, and the mean BMI was 29 kg/m2 (SD 4.8). There were two reported intraoperative events and nine operative conversions. 60 patients had at least one complication at 30-days. These include: 52 seromas, 4 hematomas, 2 surgical-site infections, 1 deep venous thrombus, and 1 recurrence at 30-days. BMI, type of hernia, and sex were not associated with complications at 30-days. The use of absorbable mesh, longer hospital stay, operative conversion, previous repair, and expert hernia surgeon were significant predictors of 30-day complications. Age, operative conversion, and previous repair were the only predictors of 30-day complications on multivariate regression. Our initial experience of 312 patients demonstrates the adoption and comparable short-term outcomes for a wide variety of robotic-assisted hernia repairs.Entities:
Keywords: Adoption; Hernia; Inguinal hernia; Minimally invasive; Robotic surgery; Safety; Ventral hernia
Mesh:
Year: 2021 PMID: 34018122 PMCID: PMC8136367 DOI: 10.1007/s11701-021-01251-2
Source DB: PubMed Journal: J Robot Surg ISSN: 1863-2483
Fig. 1Total hernia volume by modality at Montefiore Medical Center (MMC) between July of 2016 and March of 2020
Patient related information
| Total patients, | 312 |
|---|---|
| Male | 214 |
| Inguinal | 158 |
| Abdominal wall | 56 |
| Female | 98 |
| Inguinal | 16 |
| Abdominal wall | 82 |
| Age (years); mean (SD) | 54 (16) |
| ASA class, | |
| I | 41 (13) |
| II | 182 (58) |
| III | 89 (29) |
| Comorbidities, | |
| Diabetes mellitus | 62 (20) |
| COPD | 7 (2) |
| MI | 8 (3) |
| CHF | 4 (1) |
| Liver disease | 15 (5) |
| HIV/AIDS | 7 (2) |
| Cancer | 33 (11) |
| No. of comorbidities, | |
| 0 | 183 (59) |
| 1 | 66 (21) |
| ≥ 2 | 63 (20) |
| BMI (kg/m2); mean (SD) | 29 (4.8) |
| Recurrent hernia, | 50 (16) |
| Inguinal | 21 (12) |
| Ventral | 29 (21) |
| Type of previous repair, | |
| Unknown | 32 |
| Open | 5 |
| Open with mesh | 6 |
| Laparoscopic primary | 1 |
| Laparoscopic with mesh | 4 |
| Multiple previous repairs | 2 |
ASA American Society Anesthesiology Classification, BMI body mass index
Operative characteristics
| Total patients | 312 |
|---|---|
| Unilateral (4) | 126 |
| Bilateral | 48 |
| Primary ventral | 85 |
| Incisional | 52 |
| Parastomal | 1 |
| Inguinal unilateral | 107 (37) |
| Inguinal bilateral | 159 (63) |
| Abdominal wall | 163 (77) |
| Veress needle injury | 1 |
| Thermal injury | 1 |
| Hernia specialist | 110 (35) |
| Non-hernia specialist | 202 (65) |
| Laparoscopic | 4 |
| Open | 5 |
| TAPP | 174 (56) |
| IPOM | 57 (18) |
| Extraperitoneal | 81 (26) |
| Retro-muscular | 45 (14) |
| Preperitoneal | 34 (11) |
| Inlay | 1 (0.3) |
| Unilateral component separation | 4 |
| Bilateral component separation | 1 |
| Transversus abdominis release (TAR) | 9 |
Mesh type by location
| Extraperitoneal | |
| Bard™ Soft Mesh | 29 |
| Covidien Progrip™ | 23 |
| Prolene® | 12 |
| Covidien Symbotex™ | 10 |
| BD Ventralight™ ST | 3 |
| BD Phasix™ Mesh | 4 |
| BD Ventralex™ | 2 |
| Marlex (in situ) | 1 |
| GORE® SYNECOR | 1 |
| ULTRAPRO ADVANCED™ | 1 |
| IPOM | |
| Covidien Symbotex™ | 46 |
| BD Phasix™ Mesh | 3 |
| Prolene® | 2 |
| Parietene™ DS | 2 |
| OviTex® | 1 |
| BD Ventralight™ Echo | 1 |
| BD Ventralight™ Comp | 1 |
| Parietex™ Composite | 1 |
| Inguinal | |
| BD 3DMax™ Mesh | 99 |
| Covidien Progrip™ | 69 |
| GORE® SYNECOR | 3 |
| BD Phasix™ Mesh | 2 |
| Aborted/No mesh | 1 |
Univariate analysis
| OR conversion | 30-day complication | ||||
|---|---|---|---|---|---|
| No | Yes | No | Yes | ||
| 303 | 9 | 252 | 60 | ||
| Type of hernia | |||||
| Ventral | 96 | 4 | 80 | 20 | 0.757 |
| Inguinal | 98 | 2 | 79 | 21 | |
| Sex | |||||
| Female | 95 | 5 | 78 | 22 | 0.649 |
| Male | 98 | 2 | 80 | 20 | |
| No. of comorbidities | |||||
| 0 | 98 | 2 | 81 | 18 | 0.286 |
| 1 | 95 | 5 | 73 | 27 | |
| ≥ 2 | 95 | 5 | 81 | 19 | |
| BMI | |||||
| < 30 | 97 | 3 | 80 | 20 | 0.123 |
| 30–35 | 96 | 4 | 844 | 16 | |
| > 35 | 97 | 3 | 68 | 32 | |
| ASA class | |||||
| 1 | 98 | 2 | 90 | 10 | 0.152 |
| 2 | 96 | 4 | 80 | 20 | |
| 3 | 99 | 1 | 75 | 25 | |
| OR conversions | |||||
| No conversion | 81 | 19 | |||
| Convert to lap | – | – | 75 | 25 | |
| Convert to open | 20 | 80 | |||
| Surgeon type | |||||
| Hernia specialist | 98 | 2 | 72 | 28 | |
| Non-specialist | 96 | 4 | 84 | 16 | |
| Previous repair | |||||
| No | 98 | 2 | 83 | 17 | |
| Yes | 94 | 6 | 64 | 37 | |
| Mesh type | |||||
| Synthetic permanent | 82 | 18 | |||
| Synthetic absorbable | – | – | 25 | 75 | |
| Biologic | 0 | 100 | |||
| LOS | |||||
| 0 | 98 | 2 | 84 | 16 | |
| 1 | 100 | 0 | 74 | 26 | |
| 2–3 | 90 | 10 | 71 | 29 | |
| > 4 | 88 | 12 | 37 | 63 | |
Bold values represent the only variables that were statistically significant (i.e. the result was < 0.05)
Outcomes characteristics
| Total patients ( | 312 |
|---|---|
| 0 | 231 |
| 1 | 43 |
| 2–3 | 21 |
| ≥ 4 | 16 |
| Post-operative follow-up | 279 (89) |
| ED presentations | 6 (2) |
| Readmissions | 6 (2) |
| I | 52 |
| II | 3 |
| III | 3 |
| IV | 2 |
| V | 0 |
| Seroma | 52 (17) |
| Recurrence | 1 (0.2) |
| Hematoma | 4 (1) |
| SSI | 2 (1) |
| DVT | 1 (0.2) |
C–D Clavien–Dindo, SSI surgical-site infection, DVT deep venous thrombus, ED Emergency Department
Multivariate analysis
| Variables | Odds ratio | 95% IC | |
|---|---|---|---|
| Previous repair | 2.383 | 1.191–4.770 | |
| Age | 1.021 | 1.001–1.042 | |
| OR conversion | 3.085 | 1.184–8.038 | |
| Hernia type | 0.276 | – | – |
| ASA | 0.262 | – | – |
| No. of comorbidities | 0.268 | – | – |
| BMI | 0.288 | – | – |
| Type of surgeon | 0.223 | – | – |
Bold values represent the only variables that were statistically significant (i.e. the result was < 0.05)