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Issue: Vol.13 No.1 - January 2019
Management of non-absorbable mesh infection after hernia repair by negative pressure wound therapy
Authors:
Amreen Faruq
Amreen Faruq
Affiliations

Department of Surgery, BIRDEM General Hospital and Ibrahim Medical College, 122 Kazi Nazrul Islam Avenue, Shahbag, Dhaka-1000, Bangladesh

,
HM Sabbir Raihan
HM Sabbir Raihan
Affiliations

Department of Surgery, BIRDEM General Hospital and Ibrahim Medical College, 122 Kazi Nazrul Islam Avenue, Shahbag, Dhaka-1000, Bangladesh

,
Muhtarima Haque
Muhtarima Haque
Affiliations

Department of Surgery, BIRDEM General Hospital and Ibrahim Medical College, 122 Kazi Nazrul Islam Avenue, Shahbag, Dhaka-1000, Bangladesh

Abstract

Background and objectives: Mesh infection following hernia repair has previously often resulted in removal of mesh. The aim of this study was to evaluate if negative pressure wound therapy (NPWT) can be used to treat such complications and preserve the mesh.

Materials and method: A prospective study was carried in the Department of Surgery, BIRDEM General Hospital from January 2017 to January 2019. Patients with deep wound infection and exposed infected mesh after hernioplasty were included in the study. Patients’ demographics, existing comorbidities and outcome were recorded. All patients were treated with NPWT till the wound was covered with healthy granulation tissue and closed.

Results: NPWT was used to treat 7 patients with mesh infection following hernia repair. There was 2 male and 5 female cases and age ranged from 38-58 years. With NPWT the mesh in 6 patients (86%) out of 7 could be completely salvaged and wound closed with secondary suturing. However, in 1 patient although the mesh covered with granulation tissue by NPWT and wound was closed; but it had to be partly removed later on due to development of chronic discharging sinus 20 days after stitch removal.

Conclusion: The study demonstrated that NPWT was a useful technique for the treatment and preservation of infected mesh after hernia repair.

IMC J Med Sci 2019; 13(1): 008. EPub date: 20 June 2019. DOI: https://doi.org/10.3329/imcjms.v13i1.42041

Address for Correspondence: Dr. Amreen Faruq, Assistant Professor, Department of Surgery, BIRDEM General Hospital, 122 Kazi Nazrul Islam Avenue, Shahbag, Dhaka 1000. E-mail: [email protected]

 

Introduction

The use of prosthetic mesh in the repair of abdominal wall hernias that occur either due to open or laparoscopic surgery is the gold standard treatment. Mesh repair significantly reduces hernia recurrence by 30 % [1-3]. However, as with any prosthetic implant the mesh is susceptible to infection. The reported incidence of mesh infection following hernia repair varies from 1% to as high as 7-8% [4-8]. The rate of mesh infection following hernia repair in our hospital is not available. The exact incidence may be difficult to find probably due to its variable presentation with symptoms starting in early postoperative period to several years after surgery. Mesh infection is a misery for the patient as it is associated with longer hospital stay, added expenditure and emotional trauma. The recommended treatment for mesh infection involving non absorbable mesh is early surgical removal of the mesh and wound care [4-10]. However, this may leave behind a more complex open wound with an abdominal wall weakness, resulting in a recurrent hernia.

Negative pressure wound therapy (NPWT) is a newer technique used in the management of wound infection. This therapy enhances wound healing by (a) removing excess exudates, (b) providing a controlled moist environment, and (c) promoting neovascularization and granulation tissue formation. Moreover, it also stimulates shrinking of the wound size [11-13]. Taking into account of these properties, the present study was undertaken to evaluate the NPWT in the salvation/management of infected mesh of hernioplasty cases.

 

Materials and Methods

This prospective study was carried out in the department of Surgery, BIRDEM General Hospital from January 2017 to January 2019. Patients included in the study were informed of the treatment options and informed written consent was obtained.

Study population: All patients diagnosed with deep wound and mesh infection/exposure following hernia repair (incisional, inguinal, umbilical, paraumbilical) were included in the study. Minor superficial surgical site infection following mesh repair were excluded.

Mesh infection was defined as presence of local signs of wound infection namely purulent discharge /pus or abscess formation at the level of mesh with positive microbiological culture results. Superficial surgical site infection was defined as infection that occurred within 30 days of surgery involving skin and subcutaneous tissue of incision while deep surgical site infection was defined as infection involving deep soft tissue (fascia, muscle) [14].

Information regarding age, body mass index (BMI)), presence of comorbidities , site of hernia wound and size, type of mesh used for the repair of hernia and number of days when infection occurred after hernioplasty operation were recorded in a pre-designed data sheet.

Negative pressure wound therapy (NPWT): After obtaining consent, negative pressure wound therapy (NPWT) was employed for the management/ salvation of the infected mesh.

NPWT procedure involved controlled application of sub-atmospheric pressure to a local environment using a sealed wound dressing connected to a vacuum pump [15]. Initially the wound size was measured and surgical debridement of the wound was done under general or spinal anesthesia. Then, wound size was again measured after debridement and NPWT applied. A sterile black sponge was cut into specific size according to shape, size and depth of the prepared wound. A tube with multiple perforations at one end was placed within the sponge ensuring that the end with perforations remained inside the sponge and the rest taken out through the sponge. The sponge was soaked in 10% povidone iodine solution and wrapped with Sofratulle (medicated Vaseline gauge) to prevent adherence of the sponge to the wound. The sponge was then placed on the wound just above the mesh; ensuring that the mesh was in firm contact with the underlying wound surface. A transparent occlusive and adhesive dressing was applied over the sponge and the tube brought out through it making sure that the dressing was airtight (Fig 1a, b, c, d). The drainage tube was connected to commercially available portable suction machine or wall mounted suction devices.

 

Fig-1a. Wound infection after hernioplasty (mesh repair) in an incisional hernia (arrow); 1b: Wound showing exposed mesh after debridement; 1c: NPWT dressing- Black sponge wrapped in Sofratulle being placed in wound; 1d: Airtight occlusive dressing on abdominal wound.

 

The negative pressure was set to-100 to- 120 mm Hg during the entire NPWT treatment. Suction was automated at 10 minutes interval. Initially the NPWT dressing was opened every third day and a new dressing given, this was done for first 2 sessions then dressing changed every 5th day or once a week depending on the wound condition. The dressing was continued till the wound and mesh was covered with healthy granulation tissue (Fig 2a and 2b). The wound was irrigated with normal saline mixed with 10% povidone iodine (3:1) once daily through the tube. Systemic antibiotics were used according to the results of culture and sensitivity.

 

Fig-2a. Granulation tissue formation after two sessions of NPWT; 2b: Wound and exposed mesh covered with granulation tissue.

 

The NPWT was continued till the mesh was covered with granulation tissue. Once the wound was covered with healthy granulation it was cleaned with normal saline and wound closure planned. The wounds were closed either by suture or skin graft depending on the size of the wounds. Healing by secondary intention was allowed in cases where suture or skin graft was not possible. After wound closure, the patients were carefully followed up till wound healed and stitches were removed. Duration of NPWT and length of total hospital stay were also recorded. Sample of wound swab was taken from each case for culture and sensitivity test.

There was a follow up plan for 3 years for each patient from the time of wound closure to observe any delayed wound infection, fistula or hernia recurrence.

 

Results

A total of 7 patients were included in this study. Out of 7 cases, 4 were patients primarily operated at BIRDEM General Hospital and 3 were referred from different hospitals after developing wound infection following hernioplasty operation. Among the study patients, 71% (5/7) were female and 29% (2/7) were male. The mean age and BMI of the study patient were 47.85±6.84 years and 30.02 ± 4.97 kg/m2 respectively. About 57% of study patients presented with incisional hernia. Incisional hernia was present mostly in older patients (>50 years) and paraumbilical hernia was present in relatively younger patients (<45 years).

Polypropylene mesh was used in majority of the patients (5/7, 71%; Table-1). The mean postoperative day of diagnosis of wound infection was 7.71 ±2.56 days (range 4-11 days). Male patients developed infection earlier (< 6 post operative day) than female patients.

 

Table-1: Types of hernia and mesh used in study population

 

Table-2 describes the co-morbidities of the study patients. All the patients were diabetic. Hypertension, chronic kidney disease, bronchial asthma and hypothyroidism were present in 57.1%, 42.9%, 29% and 14% of the study patients respectively. Out 7 cases, 6 had multiple or more than one comorbidity.

 

Table-2: Details of co-morbidities present in all patients

 

Table-3 shows the pattern of bacteria isolated from the 7 cases prior to instituting NPWT. Pseudomonas sp was present in 42% patients either individually or in combination with other bacteria such as Esch. coli or Klebsiella sp. Out of 7 cases, 4 had wound infection with single bacteria while 3 had multiple organisms.

 

Table-3: Pattern of organisms isolated from wound samples of study cases (n=7)

 

Table-4 shows the size of the wound of the individual case before and after completion of NWPT. Wound size was measured after first debridement and after 3 sessions of NPWT in all patients and finally before closure. There was 22-24 % reduction in wound size after completion of NPWT in all 7 patients.

 

Table-4: Wound size before and after completion of NPWT

 

Out of the 7 patients with mesh infection, the mesh could be left in situ and infection controlled in 6 (86%) patients (Table-5). In 1(14%) patient after application of NPWT the mesh did cover with granulation tissue and secondary closure was done; but after 20 days of wound healing the patient developed a chronic discharging sinus. The wound was re-explored and the mesh partially removed and subsequently wound closure was done.

 

Table-5: Outcome of NPWT

 

The average duration of received NPWT therapy was 37±12.5 days. The average length of hospital stay was 48.5 ± 11.2 days (range 38 to 67 days; Table- 4). Length of hospital stay was the period of occurrence of infection/mesh exposure to the achievement of wound closure and release of patient from the hospital.

The first patient completed 2 years of follow up. No recurrence of hernia occurred in any patient after 6 to 24 months of follow up.

 

Discussion

Mesh infection after hernia repair is a dreadful complication. With regard to patient outcome, it is a surgical failure with a psychological trauma and financial burden to patient. Conventionally, the infected mesh is removed and the purpose of using prosthesis to strengthen the hernia defect is lost. When wound dehiscence exposes the abdominal mesh, biofilm forming bacteria colonize the implant. Aggregates of microorganisms embedded in biofilms become highly resistant to antibiotics [15]. Therefore, early removal of the infected mesh is the treatment of choice in order to remove the source. NPWT by virtue of its mechanical effect removes exudates; so if the exudates and the biofilm can be removed by the negative pressure effect then it will be possible to keep the mesh in situ. Wolvos in a retrospective study demonstrated reduction in bacterial load and exudates with a decrease in inflammatory markers with vacuum assisted closure instillation [16]. In addition, NPWT stimulates the formation of granulation tissue, promotes angiogenesis and cellular proliferation [11-13,17]; thus, expedites wound healing. With attribute to such qualities we decided to utilize NPWT in management of mesh infection following hernia repair and aimed at mesh preservation. By now, NPWT is an established modality of treatment of acute, chronic and non healing wounds. It has also proved its utility in patients with compromised healing [18]. Comorbidities such as diabetes, obesity, renal disease, steroid therapy, nutritional deficiency have been associated with increased chances of infection and slow wound healing [7,19-22]. The reasons identified for delayed wound healing are reduced perfusion of skin and subcutaneous tissue and immune suppression [23]. NPWT appeared a promising option for our patients as they had multiple associated comorbidities with mesh infection. Biologic mesh has been advocated as a useful option in high risk patients due to its ability to resist infection [24]. These are expensive and not readily available. In our study polypropylene mesh had been used in five patients and polyester mesh in two patients and we tried to preserve them. Although, Stremitzer et al in their study suggested conservative management for absorbable or biologic mesh grafts but recommended removal of infected non absorbable mesh [9]. We have tried to preserve non absorbable mesh and have been successful in six out of seven cases. Lehner et al in a prospective study reported 86.4% implant retention in thirty two patients with infected orthopaedic prostheses using VAC-instillation (NPWT) combined with systemic antibiotics [25]. Berrevot et al reported a similar study like ours where they used conventional VAC (NPWT) therapy and were able to salvage mesh in 60 patients of 63 and commented infected large pore meshes could be salvaged by topical negative pressure therapy [26]. However, we did not take pore size into consideration. It is important to mention that NPWT simplifies the management of such wound infection. It is comfortable to the patient though with some amount of restriction in movement but avoids heavy dressing or repeated change of dressing which is often required in such infections. Patients of infected mesh treated with conventional management and mesh removal have a long hospital stay. Length of hospital stay of our patients was apparently shorter, though we did not have any comparative control cases. In our present study, all patients remained in hospital till stitch removal. However, a retrospective study by Garcia-Ruano et al on 45 patients showed no statistical difference in hospital stay between the two groups [27]. In future cases, we plan to discharge our patients after first session of NPWT that is within 3-4 days of diagnosis of wound infection. We also planned to use available portable inexpensive VAC machines so that patients could be discharged early, monitored as outpatient then readmitted for wound closure. The patients will be taught how to maintain the portable device at home. This would significantly reduce both hospital stay and cost. Most important, NPWT can be used to avoid mesh removal thus reducing chance of hernia recurrence.

The study had some limitations. This study had small sample size and lacked control group. A larger control trial is necessary to prove the usefulness of NPWT as an effective method for salvation of the infected mesh used in hernioplasty.

Mesh infection after hernia repair usually necessitates a return trip to the operating theatre and removal of the infected mesh with a possibility of recurrence of hernia. NPWT may be cost effective compared to conventional method in terms of daily dressing expense, number of surgical procedures required and length of hospital stay till full recovery.

 

Authors’ contributions

AF designed the study, collected data and wrote the manuscript; HMSR and MH involved in patient follow up.

 

Conflict of Interest

The authors declare no conflict of interest.

 

Funding: None

 

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