Literature DB >> 26034725

Don't underestimate fournier's gangrene: report of 8 cases in 10 month survey.

Hosein Ali Danesh1, Mahdy Saboury2, Ameneh Sabzi3, Moosa Saboury4, Maryamsadat Jafary5, Shahriar Saboury6.   

Abstract

BACKGROUND: Fourniers gangrene caused by synergic aerobic and anaerobic organism is a life threatening disorder.
METHODS: The medical records of 8 among 839 patients admitted to imam ali general hospital Zahedan university of Medical Sciences with fourniers gangrene during the 10 months period between 2012 and 2013 were reviewed.
RESULTS: The most common etiology and presentation were abscess and perianal pain respectively. Mixed bacterial flora was common finding in patient. Single debridement was carried out in 2 patients and repeated procedure was needed in 6.
CONCLUSION: This disease is characterized with high mortality of up to 75% but in our study the rate was 37.5%. In other studies diabetes mellitus was found to be the common condition related to fourniers gangrene but in our study the common etiology was perianal abscess. Fourniers gangrene should be rule out in any patient with perianal pain and flulike, swelling skin.

Entities:  

Keywords:  Debridement; Fourniers gangrene; Mortality

Year:  2015        PMID: 26034725      PMCID: PMC4431430     

Source DB:  PubMed          Journal:  Med J Islam Repub Iran        ISSN: 1016-1430


Introduction

Fournier’s gangrene, caused by synergistic aerobic and anaerobic organisms, is a life-threatening disorder in which infectious agent of the perineum and scrotum spread along fascial planes, leading to soft-tissue necrosis. Majority of infections arise from anorectal, genitourinary and cutaneous sources. These patients usually present with erythema, pain and swelling. There is often crepitus, areas of gangrene or blister formation at the skin (1-3). Factors that benefit onset in all variants of this disease are: diabetes mellitus, alcoholism, drugs, immunological deficiencies, and malignant diseases, renal and hepatic insufficiency. Pathogenesis of this disease is still not completely known. Infection advances through genital fascia (Buck and Dartos), perineal fascia (Colles) as well as fascia of abdominal wall (Scarpa), in all directions, and can even reach up to armpit. Although it is evident that the combination of microorganisms play role in the development of this infection, but would cultures are usually negative (4). The common bacteria found are: E. Coli, Pseudomonas aeruginosa, Streptococcus putridis, Staphylococcus, Klebsiella, along with several anaerobic bacteria like Bacteroides,Clostridiumperfringens and Bacillus fragilis. The infection initiates under normal-looking skin. Although the symptoms usually are redness and edema of the skin of scrotum and perineum (and occasionally on penis), but it can also be discrete. It is more often in cases where deeply hidden abscesses (such asischiorectal) are observed. Suspected diagnosis is based on clinical presentation in up to 80% of cases. Due to potential severe complications, it is important to diagnose the disease as soon as possible. Mortality rate of Fournier gangrene can be reduced by intensive care and appropriate antibiotic therapy with the consideration of both aerobic gram-positive and negative bacteria as well as anaerobic microorganisms contaminant introduced during surgical treatment (5-6).

Methods

The medical records of 8 (among total 832) patients admitted to Imam Ali general hospital, Zahedan University of Medical Sciences, with a diagnosis of Fournier’s gangrene during the 10 months period between 2012 and 2013 were reviewed. The diagnosis of Fournier’s gangrene was established clinically on the basis of the patient’s history and physical examination and by radiological imaging in selected cases. The inclusion criteria included patients who underwent an invasivesurgical excision of scrotal and/or perineal necrosis along withother involved areas with a postoperative diagnosis of Fournier’sgangrene. Solitary perianal, scrotal and periurethral abscesseswere excluded, if no extension of cellulites and necrosisto surrounding tissues was existed. Before the operation, all patients underwent aggressive fluidresuscitation and treated with parenteral broad-spectrum ofantimicrobial agents, using a third-generation cephalosporin withan aminoglycoside and/or metronidazole, with dose adjustmentaccording to renal status and received haemodynamic support ifneeded. Prolonged mechanical ventilation, invasive monitoringand inotropic support were conducted in patients with cardiopulmonaryfailure due to sepsis. Coagulopathy was treated aggressively by blood component therapy. Following the optimum radical and aggressive debridement, all necrotic skin, subcutaneous tissue, fascia and obviously non-viable muscle were removed and sent for microbiological and histological examination. The areas of debridement were packed with dressings soaked inhydrogen peroxide and povidone iodine. After the initial surgery,the wound was closely monitored, and adequate nutrition was ensuredto support wound healing in addition to enteral or parenteral supplementation. Due to a high risk of ongoingprogression of the infection or the significant necrotic wound margins, patients underwent repeated debridement. The number of debridements defined as it was carriedout in operating room under general anaesthesia, not thoseapplied at bedside with local anaesthesia. Closure of wounds was commenced as soon as healthy, viabletissue allowed re-approximation. Whenever it was necessary, split-thickness skin graft or rotational cutaneous flaps were also used to repair large defects. If debridement resulted in exposure of the testes, thetestes were temporarily implanted into a medial thigh pouch untilhealing or until reconstruction completed. Colostomy was carried out for fecal diversion when the sourceof infection originated from the anorectum and the sphincter wasinfected. Furthermore, evidence of a rectal perforation and a largerectal wound or persistence of systemic sepsis were indications for performing colostomy, in spite of optimal radical debridement. Suprapubiccystostomy was required when there was gross urinary extravasationor periurethral inflammation. Orchidectomy was not necessaryunless testicular gangrene was present. If penile skin wasaffected, split-thickness skin graft was carried out with skin fromthe inguinal area. Mortality was defined as disease-related death during the hospitalstay and survival was measured in days.

Results

All patients were men, with the mean age of 44 years (range, 26 to 68 years). The mean delay between the onset of the symptoms and hospital admission was 13.8 days (range, 2 to 30 days). Five (62.5%), 1 (12.5%), and 2 (25 %) patients had colorectal, urologic, and cutaneous lesions,Of the 8 patients studied, 3 died and 5 survived and the overallmortality rate was 37.5%.2 patients (25%) had type 2 diabetes mellitus with a mean period of 4.7 years (range, 1 to 8 years) 1 (12.5%) was alcoholic. 1 (12.5%) was homosexual and 1 patient (12.5%) was IV drug abuser. None of the patients were immunocompromised. 3 patient (37.5%) had a history of the local trauma to perineum because of car accident. Hypocalcaemia wasdiagnosed in 3 cases (37.5%).Colostomy, suprapubic diversion,were performed in 4 (50%),1 (12.5%), patients respectively. The most common etiology of Fournier’s gangrene was perianalabscess (71.4%) and primary scrotal abscess (12.5%). Predisposing factors included diabetes mellitus (25%) and paraplegia (12.5%), The most common presentation was perianal/scrotal pain(78.6%) The mean duration of symptoms at presentation was11.8 days in survivor, and 17.3 days in non-survivors. The timefrom the onset of symptoms to presentation was not significantlydifferent in survivor and non-survivors (p> 0.05). Among infectious agents, ß-heamolythic streptococcus, Enterococcusfaecalis, Pseudomonas aeruginosa and Proteus were isolated, but mixed bacterial flora was also a common finding. The anaerobic bacterial commonly found included Bacillus fragilisand Clostridium perfringens.However, the bacterial organisms cultured from the wounds were not significantly different in outcomes. Single debridements were carried out in 2 (25%) patients and repeated debridements in 6 (75%). Table. 1 shows patient general informations.
Table 1

Patients general information

Patient12345678
Age (years)5527682653423050
SexMMMMMMMM
Duration ofdisease beforetreatment (days) 305463020214
Other factors DM,HTN DM,RF,HTNNONETrauma Paraplegiadue to Trauma Iv Drug AbuserHbvPositive,HomosexulTrauma
Microbiology Enterococcusfaecalis Proteus, PseudomonasProteus ChlostridiumEnterococcusPseudomonas _-hemolStreptoccocus _-hemolStreptoccocus _-hemolStreptoccocus EnterococcusPseudomonas
Antibiotics CefuroximGentamicinMetronidazolum CiprofloxacinMetronidazole GentamicinCefuroxim CefuroximGentamicinMetronidazolum AmpicilinGentamicin AmpicilinGentamicin AmpicilinGentamicin CefuroximGentamicinMetronidazolum
Colostoma+__++_+_
Cystostoma_+______
OutcomeDeathCureCureCureCureDeathDeathCure

Discussion

Various studies have characterized this disease with a high mortality, ranging from 7% up to 75% (7-10), but in our study, only 3 patients (37.5%) died from this condition. In other studies, diabetes mellitus was the most common condition associated with Fournier gangrene, up to 55.6% cases (11). But in our study the most common etiology of Fournier’s gangrene was perianalabscess (71.4%) Although extremely rare, it has been described in females and children (12-13). The clinical signs and symptoms of Fournier gangrene in our patients were similar to that explained in the literatures (14,15). After a nondistinctive prodromal period consisting of local discomfort and fever, typical presentations including crepitus,swelling, and erythema were also developed. In patients with severe clinical presentations, progression of the gangrenous process leading to malodorous drainage and sloughing in affected sites were present and resulted in the deterioration of the patients’conditions. Considering rapidity of the spread of the gangrenous area that can occur at the rate of 2 cm/h to 3 cm/h, prompt diagnosis and appropriateemergent management seems to be vital (16). Although in our and Laor et al studies the interval between the onset of the disease and the hospital admission does not play an important rolein the prognosis and clinical outcomes, the mortality rate may increase in patients with a significant delay before the reference to the medical center (17,18). Patient no.3: 68 years old male with history of scrotal swelling from 4 days ago,at emergency ward Patient no.3 at operation room after completed debridement and resection of necrotic tissue. In all patients died in our series the serum BUN level was higher than 30 mg/dL at presentation. Seyed Jalil Hosseini et al and Clayton and coworkers found that survival ofpatients with necrotizing fasciitis was associated significantly with a BUN level of less than 50 mg/dL at presentation (19,20). Prior investigators have stated that prompt diagnosis, wide-spectrum antibiotics, extensive debridement and surgery, as well as adequatenutrition could improve necrotizing fasciitis, patients' condition and reduce the mortality (21-23). Some published series have emphasized that hyperbaric oxygen therapy can be helpful for the management of Fournier gangrene wound site. Limitations in the availability and transfer of the patients to the hospital units offering this service restrict treatment of the patients with Fournier gangrene (24,25). Consequently, we did not utilize hyperbaric oxygen therapy for our patients. The possibility of recurrence of this condition even several years after treatment has been described in various studies (26).

Conclusion

based on other and our experience(8 cases in 10 months,among 832 patients), necrotizing fasciitis should be ruled out in any patient presented with pain, flulike symptoms, swelling, blisters, and necrotizing appearance in skin, especially if it is associated with: diabetes mellitus, IV drug abuse or recent trauma. Prompt diagnosis, suitable antibiotic administration,and extensive operation could significantly reduce mortality as well as morbidity.
  21 in total

Review 1.  Fournier's gangrene.

Authors:  Emilio Morpurgo; Susan Galandiuk
Journal:  Surg Clin North Am       Date:  2002-12       Impact factor: 2.741

2.  Hyperbaric oxygen therapy in the treatment of Fournier's disease in 11 male patients.

Authors:  R Pizzorno; F Bonini; A Donelli; R Stubinski; M Medica; G Carmignani
Journal:  J Urol       Date:  1997-09       Impact factor: 7.450

3.  Genital Fournier's gangrene: experience with 38 patients.

Authors:  M J Hejase; J E Simonin; R Bihrle; C L Coogan
Journal:  Urology       Date:  1996-05       Impact factor: 2.649

4.  Fournier's gangrene after unrelated cord blood stem cell transplantation.

Authors:  C Yoshida; K Kojima; K Shinagawa; D Hashimoto; S Asakura; S Takata; M Tanimoto
Journal:  Ann Hematol       Date:  2002-09-07       Impact factor: 3.673

Review 5.  Fournier's gangrene: a review of 1726 cases.

Authors:  N Eke
Journal:  Br J Surg       Date:  2000-06       Impact factor: 6.939

6.  Treatment and complications of Fournier's gangrene.

Authors:  M D Wolach; J P MacDermott; A R Stone; R W deVere White
Journal:  Br J Urol       Date:  1989-09

7.  Prognostic factors in Fournier gangrene.

Authors:  Hee Jong Jeong; Seung Chol Park; Ill Young Seo; Joung Sik Rim
Journal:  Int J Urol       Date:  2005-12       Impact factor: 3.369

8.  Management of Fournier's gangrene: an eleven year retrospective analysis of early recognition, diagnosis, and treatment.

Authors:  Kathryn S Norton; Lester W Johnson; Travis Perry; Katina H Perry; James K Sehon; Gazi B Zibari
Journal:  Am Surg       Date:  2002-08       Impact factor: 0.688

9.  Causes, presentation and survival of fifty-seven patients with necrotizing fasciitis of the male genitalia.

Authors:  M D Clayton; J E Fowler; R Sharifi; R K Pearl
Journal:  Surg Gynecol Obstet       Date:  1990-01

10.  Early recognition of potentially fatal necrotizing fasciitis. The use of frozen-section biopsy.

Authors:  I Stamenkovic; P D Lew
Journal:  N Engl J Med       Date:  1984-06-28       Impact factor: 91.245

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