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1.
Hernia ; 19(4): 549-55, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25092408

ABSTRACT

PURPOSE: Chronic postoperative inguinal pain (CPIP) is considered the most common and serious long-term problem after inguinal hernia repair. Young age has been described as a risk factor for developing chronic pain after several surgical procedures. Our aim was to assess if age has prognostic value on CPIP. METHODS: The database of a randomized trial; the LEVEL trial, 669 patients, TEP versus Lichtenstein, was used for analysis. Data on incidence and intensity of preoperative pain, postoperative pain and CPIP at 1 year were collected. The association of age with incidence and intensity of pain was assessed with regression analysis. Further, hernia type and surgical technique were studied in combination with age and CPIP as possible risk factors on CPIP over age alone. RESULTS: Younger patients (18-40 years) presented more often with CPIP than middle-aged patients (40-60 years) and elderly (>60 years); 43 vs. 29 vs. 19 %; overall 27 %. Younger and middle-aged patients had more frequently preoperative pain; 54 vs. 55 vs. 41 % and intensity of pain was higher during the first three postoperative days (VAS on day 1: 5.5 vs. 4.5 vs. 3.9 and on day 3: 3.8 vs. 2.9 vs. 2.6). Indirect-type hernias were seen more often in younger patients (77 vs. 51 vs. 48 %) and were not related to CPIP or with surgical technique. CONCLUSIONS: Almost one out of three patients experiences CPIP. The younger the patient, the higher the risk of CPIP. Hernia type and surgical technique did not influence CPIP.


Subject(s)
Hernia, Inguinal/surgery , Herniorrhaphy/adverse effects , Pain, Postoperative/etiology , Adult , Age Factors , Aged , Aged, 80 and over , Chronic Pain/etiology , Female , Herniorrhaphy/methods , Humans , Male , Middle Aged , Prognosis , Young Adult
2.
Hernia ; 11(5): 409-13, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17551808

ABSTRACT

OBJECTIVE: In patients with postoperative wound dehiscence in the presence of infection, extensive visceral oedema often necessitates mechanical containment of bowel. Prosthetic mesh is often used for this purpose. The aim of the present study was to assess the safety of the use of non-absorbable and absorbable meshes for this purpose. METHOD: All patients that had undergone mesh repair of abdominal wound dehiscence between January 1988 and January 1998 in the presence of intra-abdominal infection were included in a retrospective cohort study. All surviving patients had physical follow-up in February 2001. RESULT: Eighteen patients were included in the study. Meshes consisted of polyglactin (n = 6), polypropylene (n = 8), polyester (n = 1), or a combination of a polypropylene mesh with a polyglactin mesh on the visceral side (n = 3). All patients developed complications, consisting mainly of mesh infection (77%), intra-abdominal abscess (17%), enterocutaneous fistula (17%), or mesh migration through the bowel (11%). Mesh removal was necessary in eight patients (44%). Within four months postoperatively, six patients (33%) had died because of progressive abdominal sepsis. The incidence of progressive abdominal sepsis was significantly higher in the group with absorbable polyglactin mesh than in the group with nonabsorbable mesh (67 vs. 11%, p = 0.02) After a mean follow-up of 49 months, 63% of the surviving patients had developed incisional hernia. Absorbable meshes did not yield better outcomes than nonabsorbable meshes in terms of complications and mortality rate. CONCLUSION: Synthetic graft placement in the presence of intra-abdominal infection has a high risk of complications, regardless of whether absorbable (polyglactin) or non-absorbable mesh material (polypropylene or polyester) is used, and should be avoided if possible.


Subject(s)
Absorbable Implants , Polyglactin 910 , Polypropylenes , Surgical Mesh , Surgical Wound Dehiscence/therapy , Surgical Wound Infection/therapy , Abdomen/surgery , Adult , Aged , Aged, 80 and over , Cohort Studies , Female , Humans , Male , Middle Aged , Retrospective Studies , Surgical Wound Dehiscence/etiology , Surgical Wound Infection/etiology , Treatment Outcome
4.
Surg Endosc ; 18(4): 681-5, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15026899

ABSTRACT

INTRODUCTION: In laparoscopic incisional hernia repair with intraperitoneal mesh, concern exists about the development of adhesions between bowel and mesh, predisposing to intestinal obstruction and enterocutaneous fistulas. The aim of this study was to assess whether the addition of a collagen coating on the visceral side of a polypropylene mesh can prevent adhesion formation to the mesh. METHOD: In 58 rats, a defect in the muscular abdominal wall was created, and a mesh was fixed intraperitoneally to cover the defect. Rats were divided in two groups; polypropylene mesh (control group) and polypropylene mesh with collagen coating (Parieten mesh). Seven and 30 days postoperatively, adhesions and amount and strength of mesh incorporation were assessed. Wound healing was studied by microscopy. RESULTS: With Parieten mesh, the mesh surface covered by adhesions was reduced after 30 days (42% vs 69%, p = 0.01), but infection rate was increased after both 7 (p = 0.001) and 30 days (p = 0.03), compared to the polypropylene group with no mesh infections. If animals with mesh infection were excluded in the analysis, the mesh surface covered by adhesions was reduced after 7 days (21% vs 76%, p = 0.02), as well as after 30 days (21 vs 69%, p < 0.001). Percentage of mesh incorporation was comparable in both groups. Mean tensile strength of mesh incorporation after 30 days was higher with Parieten mesh. CONCLUSION: Although the coated Parieten mesh was more susceptible to mesh infection in the current model, a significant reduction of adhesion formation was still seen with the Parieten mesh after 30 days, with comparable mesh incorporation in the abdominal wall.


Subject(s)
Coated Materials, Biocompatible , Hernia, Ventral/surgery , Implants, Experimental , Polypropylenes , Surgical Mesh , Tissue Adhesions/prevention & control , Abdominal Wall/surgery , Animals , Male , Materials Testing , Random Allocation , Rats , Rats, Wistar , Tensile Strength , Wound Healing
5.
Br J Surg ; 89(11): 1350-6, 2002 Nov.
Article in English | MEDLINE | ID: mdl-12390373

ABSTRACT

BACKGROUND: Various randomized studies have evaluated techniques of abdominal fascia closure but controversy remains, leaving surgeons uncertain about the optimal method of preventing incisional hernia. METHOD: Medline and Embase databases were searched. All trials with a follow-up of at least 1 year that randomized patients with midline laparotomies to closure of the fascia by different suture techniques and/or suture materials were subjected to meta-analysis. Primary outcome was incisional hernia; secondary outcomes were wound dehiscence, wound infection, wound pain and suture sinus formation. RESULTS: Fifteen studies were identified with a total of 6566 patients. Closure by continuous rapidly absorbable suture was followed by significantly more incisional hernias than closure by continuous slowly absorbable suture (P < 0.009) or non-absorbable suture (P = 0.001). No difference in incisional hernia incidence was found between slowly absorbable and non-absorbable sutures (P = 0.75), but more wound pain (P < 0.005) and more suture sinuses (P = 0.02) occurred after the use of non-absorbable suture. Similar outcomes were observed with continuous and interrupted sutures, but continuous sutures took less time to insert. CONCLUSION: To reduce the incidence of incisional hernia without increasing wound pain or suture sinus frequency, slowly absorbable continuous sutures appear to be the optimal method of fascial closure.


Subject(s)
Hernia, Ventral/prevention & control , Laparoscopy/methods , Suture Techniques/standards , Humans , Postoperative Complications/prevention & control , Prospective Studies , Randomized Controlled Trials as Topic , Surgical Wound Dehiscence/prevention & control , Sutures , Wound Healing
6.
Surg Endosc ; 16(12): 1713-6, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12098028

ABSTRACT

BACKGROUND: Fixation of the mesh is crucial for the successful laparoscopic repair of incisional hernias. In the present experimental study, we used a pig model to compare the tensile strengths of mesh fixation with helical titanium coils (tackers) and transabdominal wall sutures. METHODS: Thirty-six full-thickness specimens (5 x 7 cm) of the anterior abdominal wall of nine pig cadavers were randomized for fixation of a polypropylene mesh (7 x 7 cm) by either tackers or transabdominal wall sutures. The number of fixation points varied from one to five per 7-cm tissue length, with distances between fixation points of 2.3, 1.8, 1.4, and 1.2 cm, respectively. The force required to disrupt the mesh fixation (tensile strength) was measured by a dynamometer. Statistical analysis was performed using the Wilcoxon test and the Spearman rank correlation test. RESULTS: The mean tensile strength of mesh fixation by transabdominal sutures was significantly greater than that by tackers for each number of fixation points: 67 N vs 28 N for a single fixation point (p <0.001), 115 N vs 42 N for two fixation points (p <0.001), 150 N vs 63 N for three fixation points (p <0.05), 151 N vs 73 N for four fixation points (p <0.05), and 150 N vs 82 N for five fixation points (p <0.05). Increasing the number of fixation points over three per 7 cm (distance between fixation points of 1.8 cm) did not improve tensile strength. CONCLUSION: The tensile strength of transabdominal sutures is up to 2.5 times greater than the tensile strength of tackers. Therefore, the use of transabdominal sutures for mesh fixation appears to be preferable for laparoscopic incisional hernia repair.


Subject(s)
Hernia, Ventral/surgery , Laparoscopy/methods , Surgical Mesh , Abdominal Wall/surgery , Animals , Disease Models, Animal , Female , Laparoscopy/standards , Male , Polypropylenes/metabolism , Polypropylenes/therapeutic use , Random Allocation , Secondary Prevention , Surgical Mesh/standards , Surgical Stapling/methods , Surgical Stapling/standards , Suture Techniques/standards , Sutures/standards , Swine , Tensile Strength
7.
Eur J Surg ; 168(12): 684-9, 2002.
Article in English | MEDLINE | ID: mdl-15362576

ABSTRACT

OBJECTIVE: To compare our results of open and laparoscopic mesh repair of incisional hernias. DESIGN: Retrospective cohort study. SETTING: Teaching hospitals, The Netherlands. SUBJECTS: All patients who had had a laparoscopic (n = 25) or an open (n = 76) mesh repair of incisional hernia between January 1996 and January 2000. INTERVENTIONS: Physical examination at the time of the study. MAIN OUTCOME MEASURES: Morbidity and recurrence. RESULTS: The groups were comparable. 11 patients (14%) developed postoperative infections after open repair and 1 (4%) after laparoscopic repair (p = 0.29). Median hospital stay was 5 days (range 1-19) in the open group and 4 (range 1-11) in the laparoscopic group (p = 0.28). The 2-year cumulative incidence of recurrence was 18% after open repair (median follow-up of 17 months (range 1-46) and 15% after laparoscopic repair (median follow-up of 15 months, range 1-44). Recurrences in the laparoscopic group were all among the first 7 cases in which the mesh was fixed with staples alone. CONCLUSION: There were fewer infections and hospital stay was shorter in the laparoscopic group, but not significantly so. Recurrence rates were comparable.


Subject(s)
Hernia, Ventral/surgery , Laparoscopy/methods , Laparotomy/methods , Surgical Mesh , Adult , Aged , Aged, 80 and over , Cohort Studies , Female , Follow-Up Studies , Hernia, Ventral/diagnosis , Humans , Length of Stay , Male , Middle Aged , Probability , Retrospective Studies , Risk Assessment , Statistics, Nonparametric , Treatment Outcome , Wound Healing/physiology
8.
Scand J Surg ; 91(4): 315-21, 2002.
Article in English | MEDLINE | ID: mdl-12558078

ABSTRACT

BACKGROUND AND AIMS: The choice of incision for laparotomy depends on the area that needs to be exposed, the elective or emergency nature of the operation and personal preference. Type of incision may however have its influence on the occurrence of postoperative wound complications. Techniques and features of various incisions are discussed, as well as the incidence of their postoperative complications. METHOD: A medline search was conducted identifying prospective randomised trials, as well as retrospective studies with sufficient follow-up, comparing midline, paramedian, transverse and oblique incisions. RESULTS: Significant differences in wound infection and wound dehiscence rates were not reported. Transverse, oblique and paramedian incisions caused significantly less incisional hernias than midline incisions. However, trials comparing transverse and midline incisions for larger laparotomies did not show significant differences. All four trials comparing lateral paramedian with midline incisions reported incisional hernia rates of 0% after the lateral paramedian incision. Differences with the midline incision were significant. CONCLUSION: Transverse or oblique incisions should be preferred for small unilateral operations. The paramedian incision should be used for major elective laparotomies. The use of the midline incision should be restricted to operations in which unlimited access to the abdominal cavity is useful or necessary.


Subject(s)
Laparotomy/adverse effects , Laparotomy/methods , Abdominal Wall/blood supply , Abdominal Wall/innervation , Hernia, Ventral/etiology , Humans , Pain, Postoperative , Surgical Wound Dehiscence/etiology , Wound Healing
9.
Br J Surg ; 87(9): 1229-33, 2000 Sep.
Article in English | MEDLINE | ID: mdl-10971433

ABSTRACT

BACKGROUND: Portal vein thrombosis is a rare but potentially fatal complication of splenectomy. The aim of this study was to assess the incidence, risk factors, treatment and outcome of portal vein thrombosis after splenectomy in a large series of patients. METHODS: All patients who had undergone a splenectomy in the University Hospital, Rotterdam, between 1984 and 1997 were reviewed retrospectively. Splenectomy that was followed by symptomatic portal vein thrombosis was selected for analysis. Risk factors for portal vein thrombosis were sought. RESULTS: Of 563 splenectomies, nine (2 per cent) were complicated by symptomatic portal vein thrombosis. All these patients had either fever or abdominal pain. Two of 16 patients with a myeloproliferative disorder developed portal vein thrombosis after splenectomy (P = 0.03), and four of 49 patients with haemolytic anaemia (P = 0.005). Treatment within 10 days after splenectomy was successful in all patients, while delayed treatment was ineffective. CONCLUSION: Portal vein thrombosis should be suspected in a patient with fever or abdominal pain after splenectomy. Patients with a myeloproliferative disorder or haemolytic anaemia are at higher risk; they might benefit from early detection and could have routine Doppler ultrasonography after splenectomy.


Subject(s)
Portal Vein , Splenectomy/adverse effects , Venous Thrombosis/diagnosis , Adolescent , Adult , Aged , Anticoagulants/therapeutic use , Child , Drug Combinations , Heparin/therapeutic use , Humans , Middle Aged , Retrospective Studies , Tissue Plasminogen Activator/therapeutic use , Venous Thrombosis/drug therapy , Venous Thrombosis/etiology , Warfarin/therapeutic use
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