Abstract
Clostridial myonecrosis is most often seen in settings of trauma, surgery, malignancy, and other underlying immunocompromised conditions. Since 1953 cases of gas gangrene have been reported in orthopaedic patients including open fractures, closed fractures, and orthopaedic surgeries. We present a case of 55-year-old obese woman who developed rapidly progressive gas gangrene in her right leg accompanied by tibial plateau fracture without skin lacerations. She was diagnosed with clostridial myonecrosis and above-the-knee amputation was carried out. This patient made full recovery within three weeks of the initial episode. We identified a total of 50 cases of gas gangrene in orthopaedic patients. Several factors, if available, were analyzed for each case: age, cause of injury, fracture location, pathogen, and outcome. Based on our case report and the literature review, emergency clinicians should be aware of this severe and potentially fatal infectious disease and should not delay treatment or prompt orthopedic surgery consultation.
1. Introduction
Emergency physicians and surgeons are confronted with patients of gas gangrene so uncommon in civilian practice that many are unfamiliar with its signs and symptoms and do not recognize its development quickly and accurately. The difficulties in diagnosis not only lie in unfamiliarity with the signs and symptoms of gas gangrene but also in the lack of differentiation between contamination and infection and to the confusion between gas gangrene and various clostridial infections and other bacterial and nonbacterial lesions simulating gas gangrene [1, 2]. Gas gangrene occurs in a variety of clinical settings that can be subdivided into three major types: posttraumatic origins, postoperative origins, and spontaneous occurrences. Clostridial myonecrosis, also known as true gas gangrene, is the most devastating kind of clostridial infection which requires aggressive, early surgical management. Its onset is insidious and subsequent progressive rapidly. Spontaneous types occurred in patients with compromised medical conditions including uncontrolled diabetes mellitus and various forms of malignancy, the more commonly reported being leukemia and breast cancer [3]. Clostridium septicum is the major cause of nontraumatic spontaneous gas gangrene in patients with immunosuppressant diseases [4].
2. Case Report
A 55-year-old female obese farmer (BMI 35) presented to the Emergency Department with a two-day history of the right leg progressing sensory deprivation and swelling. Eight days ago she had a car accident which caused her right tibial plateau fracture. Two days after her hospitalization, elective surgery for the fracture was performed at a local hospital. Afterwards, the patient felt increasing pain out of proportion to physical findings accompanied by progressive swelling, numbness, and weakness of the limb. She was unable to move her right lower extremity and had no sensation below the knee joint level. These signs were not taken seriously. Then she was transferred to our university hospital with the presumptive diagnosis of gas gangrene. She denied chills, anorexia, or other symptoms. She also reported no previous episodes or other recent illnesses. Previous medical history included mild type 2 diabetes mellitus which lasted over 20 years poorly controlled with metformin and hypertension treated with hydrochlorothiazide. She was not taking any other medications.
On physical examination this patient was febrile, alert, and comfortable; vital signs were temperature of 38.2 degrees centigrade, pulse of 110 beats/min, respiratory rate of 18 breaths/min, and blood pressure of 105/57 mmHg. Head, neck, cardiac, lung, and abdominal examinations were unremarkable. The physical examination revealed severe swollen and brownish skin of the limb with bullae exuding from the incision (Figure 1). Subcutaneous crepitus extended along the length of the limb and the skin discoloration spread from knee to ankle. Roentgenograms revealed gas in the interfacial planes of the leg. Extensive gas formation throughout all the muscle compartments of the right leg reaching to the level of knee joint was present. Laboratory evaluation showed that white blood cell count was 22.2 × 109/L, hemoglobin was 83 g/L, platelet count was 183 × 109/L, a serum glucose of 324 mg/dL, C-reactive protein was 48.0 mg/dL, and serum creatinine was 155 μmol/L. Examination of a needle aspirated from the incision showed gram-positive bacilli.
Figure 1.

The limb was severe swollen and skin was brownish with bullae exuding from the incision.
A diagnosis of gas gangrene was made and the patient was started on broad spectrum antibiotic coverage with intravenous penicillin, clindamycin, metronidazole, and fluid resuscitation. Urgent surgery was carried out immediately. Upon incision, the musculature was found to be extensive necrotic, foul smelling, and crepitant (Figure 2). An above-the-knee amputation remained the single best life-saving treatment and was performed, followed by extensive debridement of the remaining necrotic tissue. Then she was sent to the adult intensive care unit and all the wounds were kept open postoperatively. Two days later, the patient was taken to the operating room again for wound exploration. At this time, the muscle and tissue were found to be viable without evidence of spreading infection, and the wound was closed in a standard fashion. Hemocultures and intraoperative cultures both confirmed the presence of C. perfringens. With aggressive surgical and medical management, this patient made a full recovery and was subsequently discharged twenty days after his initial presentation.
Figure 2.

The muscle was found to be necrotic, foul smelling, and crepitant both superficially and deep.
3. Reviw of Published Gas Gangrene in Orthopaedic Patients
All published, English language and full-text available, Medline-reported orthopaedic patients with gas gangrene were included in this review. Several factors, if available, were analyzed for each case: age, cause of injury, fracture location, pathogen, and clinical outcome. As seen in Table 1, we identified a total of 50 cases of gas gangrene in orthopaedic patients. Of these, 24(48%) cases were caused by C. perfringens. Average age is 28.75 years old (range from 5 to 76).
Table 1.
Gas gangrene infections in traumatic orthopaedic patients.
| Source | Cause | Age | Fracture | Soft tissue | Pathogen | Outcome |
|---|---|---|---|---|---|---|
| Fee, 1977 [5] | Fall from a tree | 8 | Closed, forearm | A small laceration | Gram-positive Spore-forming rods | Lived with disarticulation |
| Fall from a tree | 10 | Open, right forearm | Two small lacerations | Clostridium perfringens | Lived with amputation | |
| Fall from a tree | 11 | Open, right forearm | A puncture wound | Clostridium perfringens | Lived with amputation | |
| Fall from a roof | 12 | Open, right forearm | Two openings | Clostridium perfringens | Lived with preserved forearm | |
| Fall on the street | 52 | Open, left radius | A puncture wound | Gram-positive rods | Lived with amputation | |
|
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| Buchanan and Gordon, 1980 [6] | Fall from 5 stories | 19 | Compound fracture of right tibia and fibula | Contaminated with dirt, gravel | Clostridium perfringens | Lived with amputation |
|
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| Fulford, 1969 [7] | Traffic accident | 19 | Open, right femur | Contaminated, No detail | Unknown | Lived with preserved limb |
|
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| Lucas et al., 1976 [8] | Kicked on right shin in a tackle | 24 | Tibia and fibula | 7 cm wound | Clostridium septicurn | Lived with preserved limb |
|
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| Woolley et al., 2004 [9] | Fall from high place | 39 | Open, left tibia, and fibula | Gustillo Grade III | Clostridium septicurn (no gas gangrene) | Lived with preserved limb |
|
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| Werry and Meek, 1986 [10] | Unknown | 32 | Distal radius | Abrasion of the volar wrist skin | Clostridium perfringens | Lived with amputation |
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| Goon et al., 2005 [11] | Local accident | 76 | No fracture | No traumatic history | Clostridium septicurn | Died |
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| Taylor et al., 2011 [12] | High-speed motor vehicle collision | 21 | Closed, right femur with traction pin | Multiple organ injuries | Clostridium perfringens | Died |
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| Mulier et al., 1993 [13] | Fall from a height of 8 feet | 45 | Closed, femoral fracture | Unknown | Clostridium septicurn | Survived with disarticulation |
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| Lorea et al., 2004 [14] | Muscle transfer for opponensplasty | 49 | No fracture | Normal muscle surgery | Clostridium perfringens, Sordellii | Survived with preserved forearm |
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| Sevitt, 1953 [15] | Playing football | 26 | Closed, left ankle | Unknown | Clostridium perfringens | Survived with amputation |
|
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| HILL, 1959 [16] | Fall from a gate | 6 | Left forearm fracture | A small wound on the forearm | Unknown | Survived with amputation |
|
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| Aufranc et al., 1969 [17] | Struck by a rotating truck wheel | 29 | Open, right tibia | Wringer-type injury of leg. | Presence of gram-positive rods | Survived with preserved limb |
|
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| Automobile accident | 13 | Compound, left tibia, and fibula | Unknown | Bacilli welchii | Died | |
| Fall from window to ground | 24 | Compound, left tibia | Unknown | Bacilli welchii | Survived with amputation | |
| Automobile accident | 37 | Compound, left tibia, and fibula | Unknown | Bacilli welchii | Died | |
| Hooked by a cow | 6 | Compound, right forearm | Unknown | Bacilli welchii | Survived with amputation | |
| Boland, 1929 [18] | Street accident | 52 | Compound, left tibia, and fibula | Unknown | Positive culture, detail Unknown | Survived with amputation |
| Truck Accident | 21 | Compound, left tibia, and fibula | Unknown | Positive culture, detail Unknown | Survived with preserved limb | |
| Motorcycle accident | 18 | Compound, right tibia, and fibula | Unknown | Bacilli welchii | Survived with amputation | |
| Struck by a truck | 5 | Compound, upper extremity, left femur, left tibia, and fibula | Unknown | Bacilli welchii | Died | |
| Street-car accident | 13 | Compound, both legs | Unknown | Bacilli welchii | Died | |
| Knee joint fracture from gun-shot | 30 | Knee joint fracture | Unknown | Positive culture, detail Unknown | Survived with amputation | |
| Auto accident | 36 | Compound, right tibia, and fibula | Unknown | Positive culture, detail Unknown | Survived with amputation | |
| Falling from freight train | 16 | Compound, both legs | Unknown | Positive culture, detail Unknown | Survived with amputation | |
| Motorcycle accident | 40 | Compound, left tibia, and fibula | Unknown | Positive culture, detail Unknown | Survived with preserved limb | |
| Automobile accident | 25 | Compound, both legs | Unknown | Positive culture, detail Unknown | Died | |
| Gun-shot | 20 | Compound, right ulnar, and radius | Unknown | Negative culture | Died | |
|
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| Brume and Ijagha, 1985 [19] | Unknown | 9 | Closed Colles' Fracture | Unknown | Unknown | Survived with amputation |
| Unknown | 27 | Closed, medical malleolus | Unknown | Unknown | Survived with amputation | |
| Unknown | 30 | Closed,tibia and fibula | Unknown | Unknown | Died | |
| Unknown | 14 | Closed Colles' Fracture | Unknown | Unknown | Survived with amputation | |
|
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| Moehring, 1988 [20] | Automobile accident | 13 | Right ankle region | Marked soft tissue swelling | Clostridium perfringens | Lived with preserved limb |
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| Oncel and Arsoy, 2010 [21] | Nail pierced the skin of hand | 16 | No fracture | A small wound on the hand | Gram-positive rods | Survived with amputation |
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| Hoffman et al., 1971 [22] | Working accident | 25 | Tibia fracture | Muscle and skin lacerated | Clostridium welchii | Survived |
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| DeHaven and Evarts, 1971 [23] | Fall from horseback | 10 | Open, both bones of forearms | Mild damage of soft tissue | Clostridium perfringens | Survived with amputation |
| Automobile accident | 44 | Open, Bilateral tibia, and fibulae | Damaged and contaminated severely | Pseudomonas, Klebsiella et al. | Survived with amputation | |
| Automobile accident | 21 | Open, pelvic | Multiple | Clostridium perfringens | Survived | |
| Fall from running | 10 | Open, both bones of forearms | Mild damage of soft tissue | Clostridium perfringens | Survived with amputation | |
| Automobile accident | 19 | Open, tibia, and fibula | Severe damage of soft tissue | Bacillus subtilis, Proteus | Survived with amputation | |
|
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| Johnson et al., 1994 [24] | Arthroscopic knee surgery | 36 | No fracture | No | Clostridium Septicum | Survived with amputation |
| Hip Arthroplasty | 57 | No fracture | No | Clostridium Septicum | Survived | |
|
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| Dykes, 1977 [25] | Hip nailing | 71 | Transcervical fracture of femur | No | Clostridium welchii | Died |
| Hip nailing and plate fixation | 68 | Subtrochanteric fracture of femur | No | Unknown | Died | |
| Hip nailing | 79 | Transcervical fracture of femur | No | Unknown | Died | |
| Miller et al., 1993 [26] | Iliac crest bone graft transplantation | 55 | Nonunion of closed fracture of clavicle | No | Clostridium perfringens | Survived |
(1) Compound fracture indicates open fracture, while simple fracture means closed fracture.
(2) Bacillus welchii is another expression of Clostridium perfringens.
(3) Clostridium perfringens (formerly known as C. welchii).
In our review of published orthopaedic gas gangrene literature, we found that conditions related with gas gangrene in orthopaedic patients can be grouped into three major categories: infection with clostridial myonecrosis, nonclostridial myonecrosis, unidentified; 38 patients survived, of which 25 survived with amputation, while 12 patients died. Gas gangrene followed by simple fracture occurred in 25 patients; 3 cases presented with gas gangrene after elective orthopaedic surgery and the rest cases were resulted from compound fracture. As for fracture location, most gas gangrene cases were involved with tibia and/or fibula fracture while forearm fractures ware ranked in the second place and following were femur, ankle, knee, and pelvic. Especially 5 patients developed gas gangrene with no fractures (three were selective orthopaedic surgeries, one was nail piercing, and the other one was soft tissue injury (see Table 2)).
Table 2.
Clinical outcome, pathogens, fractures locations, fractures, or surgeries types.
(a) Clinical outcome after infection with gas gangrene
| Outcome | Survived with amputation | Survived with no amputation | Died |
|---|---|---|---|
| Number | 25 | 13 | 12 |
(b) Pathogen of gas gangrene accompanied with traumatic orthopaedic patients
| Pathogen | Clostridium myonecrosis | Non-clostridial myonecrosis | Unidentified |
|---|---|---|---|
| Number | 28 | 3 | 19 |
Clostridium myonecrosis including Clostridium perfringen and septium while nonclostridial myonecrosis including culture negative; unidentified indicates no detail about the infection pathogen were reported.
(c) Fractures locations together with gas gangrene
| Location | Tibia and/or fibula | Forearm | Femur | Ankle | Clavicle | Knee | Pelvic | None |
|---|---|---|---|---|---|---|---|---|
| Number | 21 | 14 | 7 | 2 | 1 | 1 | 1 | S |
One case involved multiple locations of fractures: forearm, tibia and fibula, and femur; forearm including both or single bones of the forearm.
(d) Fractures or surgeries types associated with gas gangrene
| Fracture severity | Simple fracture | Compound fracture | Elective orthopaedic surgery |
|---|---|---|---|
| Number | 25 | 22 | 3 |
Compound (open) fracture: the bone breaks and pieces of the bone go through the internal soft tissue of the body and break through the skin from the inside.
4. Discussion
Gas gangrene is generally regarded as a disease associated with war or other mass casualty situations and is seldom a feature of normal peaceful time medical practice. The cause of gas gangrene could be grouped into following different types: clostridial myonecrosis, clostridial cellulitis, nonclostridial lesion simulation gas gangrene. Clostridial myonecrosis is the preferred term to denote the clinical syndrome of true gas gangrene [27]. More than 90% of these lesions occur in the extremities, thigh, shoulder, and so on. Clostridial cellulitis has been confused with clostridial myonecrosis by clinicians. Clostridial cellulitis has been noted to be a septic crepitant process involving epifascial, retroperitoneal, or other connective tissues, and its onset has been generally more gradual than clostridial myonecrosis. It is usually little pain, no edema, and little systemic toxicity. The wound is foul with brownish seropurulent exudates, and gas is found diffused through the tissues and bubbling up in the wound. The gas is much more evident than in clostridial myonecrosis, but it has never been found to be intramuscular. Also a large number of other bacterial and nonbacterial lesions which resemble clostridial myonecrosis may be seen in routine clinical practice. Many of these are diagnosed as gas gangrene and diagnostic skill knowledge is necessary for their differentiation [28]. For example, Streptococcal myonecrosis, which clinically resemble a subacute form of clostridial myonecrosis, is the second variety of anaerobic myonecrosis. Clinical considerations are listed in Table 3 when gas gangrene present.
Table 3.
Clinical consideration when gas gangrene is present.
| (I) Clostridial myonecrosis (true gas gangrene) | |
| (A) Localized: crepitant or noncrepitant | |
| (B) Diffuse: crepitant or noncrepitant together with toxemia | |
| (II) Clostridial cellulitis: anaerobic or crepitant | |
| (III) Nonclostridial | |
| (A) Bacterial: aerobic aerogenic infections; Staphylococcal fasciitis; anaerobic streptococcal infections |
|
| (B) Nonbacterial: mechanical trauma; infiltration from air-hose injury |
The most common causative organism of clostridial myonecrosis is C. perfringens while C. septicum is considered as the second most frequent agent. C. perfringens is commonly found in the human gastrointestinal tract, including the oral cavity. Myonecrosis resulting from C. perfringens alone after surgical procedures is rather uncommon. Clostridium myonecrosis following orthopaedic surgery is associated with a definite set of conditions: underlying malignancies, hematological and gastrointestinal solid tumors primarily, diabetes mellitus and atherosclerotic disease, and severe peripheral vascular disease [29].
Gas gangrene is an acute and life threatening infection characterized by fever, sudden onset of prominent pain, massive local edema, severe extensive myonecrosis, and the accumulation of gas at the site of infection. The typical manifestation of this disease usually starts with excruciating pain, out of proportion to physical findings, not relieved by pain killers. As the infection progresses, myonecrosis is accompanied by necrotizing fasciitis and cutaneous and muscle necrosis. The appearance of the skin around the site of infection usually becomes tense and changes from pale to bronze initially and then to purplish red, and multiple hemorrhagic bullae develop. Paramount to successful treatment for gas gangrene involves prompt recognition of the diagnosis and initiation multiple therapy including supportive measures, antimicrobial therapy, and timely surgical intervention. Despite this, in many cases of C. perfringens induced gas gangrene, radical amputation still remains the treatment of best choice [30]. If not controlled, it will always result in systemic toxemia, hypotension, shock, multiorgan failure, and death [31]. Hyperbaric oxygen therapy is recommended by some experts but is controversial because its effectiveness has not yet been established.
Still we cannot identify the definitive cause of the clostridial myonecrosis in our case, as both postoperative origins and spontaneously occurrences could be possible. Our case is unique in two aspects. First, as we all know, the responsible organism C. perfringens is mostly associated with development of traumatic gas gangrene but also can be associated with the nontraumatic spontaneous gas gangrene in patients with immunocompromised condition including malignancies and diabetes mellitus [2, 32]. Impaired evacuation and motility of the stomach (and the small intestine) has been described in diabetics with long lasting unsatisfactory diabetes compensation, microangiopathic complications, and diabetic autonomous neuropathy [33]. Postoperative infection of elective surgical wounds with Clostridium species has been linked to gastrointestinal tract lesions. As clostridia can multiply readily in low-oxygen conditions, infections are usually seen in the setting of decreased intestine lining blood supply which could account for a route of entry for hematogenous spread. Second, gas gangrene rarely occurs in the patients undergoing elective surgery. One of the basic principles of orthopedic surgery is that gas gangrene does not develop in closed fractures. Almost all cases of gas gangrene after orthopaedic surgery developed in open wounds which was not adequately debrided, in association with peripheral vascular disease and immunocompromised status. Even patients with closed fracture clostridium gas gangrene also had been found [11]. In our case, a possible mechanism is soil contamination of the skin near or at the infection site, as well as the severe injured soft tissue around the fracture together that contribute to the production histohypoxia environment. All these factors such as immunocompromised status, unviability of tissues, and local decrease of blood supply together nourished the gas gangrene. But the exact origin of the germ remains unknown.
5. Conclusion
Based on the case presented in the paper and our review of the literature on gas gangrene in orthopaedics patients, several following points should be emphasized.
Our emergency clinicians should be aware of this severe and potentially fatal infectious disease and should not delay treatment or prompt orthopedic surgery consultation. Gas gangrene, while rare in now peace days, can be a devastating complication of almost any small wound or surgical procedure even one as common as closed reduction of fractures. It is our experience that we should give sufficient extension of the wound to provide adequate visualization of surgical field so as to be certain that all the necrotic or foreign material has been removed.
Strict aseptic techniques should be observed for even the most minor procedure. Clostridial spores are ubiquitous and can reside in hospital environments, possibly on surgeons' hands, patients' skin, topical application, and so on.
The best way to prevent gas gangrene is meticulous wound debridement and delayed closure for all potentially contaminated wounds regardless of closed or open fractures.
Once gas gangrene is diagnosed, careful and adequate debridement should be instituted immediately to avoid further deterioration excision of necrotic tissue still the cornerstone of treatment, which should be involved with antibiotics and all other supportive treatments.
Systematic resuscitative efforts should be instituted immediately in whom the diagnosis of incipient gas gangrene is even considered. This cannot be overemphasized.
Recognized that gas gangrene may occur spontaneously and often in a immunocompromised patient, postoperative wounds may also develop gas gangrene due to the local soft tissue damage and decreasing blood supply.
Consent
Written informed consent was obtained from the patient for publication of this case report.
Conflict of Interests
The authors have no conflict of interests to declare.
References
- 1.Altemeier WA, Culbertson WR, Vetto M, Cole W. Problems in the diagnosis and treatment of gas gangrene. A.M.A. Archives of Surgery. 1957;74(6):839–845. doi: 10.1001/archsurg.1957.01280120017002. [DOI] [PubMed] [Google Scholar]
- 2.Altemeier WA. Diagnosis classification and general management of gas producing infections, particularly those produced by Clostridium Perfringens. proceedings of the 3rd International Conference on Hyperbaric Medicine; 1966; Washington, DC, USA. National Academy of Sciences; pp. 481–490. [Google Scholar]
- 3.Rich RS, Salluzzo RF. Spontaneous clostridial myonecrosis with abdominal involvement in a nonimmunocompromised patient. Annals of Emergency Medicine. 1993;22(9):1477–1480. doi: 10.1016/s0196-0644(05)82000-1. [DOI] [PubMed] [Google Scholar]
- 4.Shibuya H, Terashi H, Kurata S, et al. Gas gangrene following sacral pressure sores. Journal of Dermatology. 1994;21(7):518–523. doi: 10.1111/j.1346-8138.1994.tb01786.x. [DOI] [PubMed] [Google Scholar]
- 5.Fee NF, Dobranski A, Bisla RS. Gas gangrene complicating open forearm fractures. Report of 5 cases. Journal of Bone and Joint Surgery A. 1977;59(1):135–138. [PubMed] [Google Scholar]
- 6.Buchanan JR, Gordon SL. Gas gangrene in a wound treated without skin closure: a case report. Clinical Orthopaedics and Related Research. 1980;148:233–236. [PubMed] [Google Scholar]
- 7.Fulford PC. Gas gangrene following compound fracture of femur. Proceedings of the Royal Society of Medicine. 1969;62(7):p. 644. doi: 10.1177/003591576906200704. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Lucas HK, Speller DCE, Stephens M. Chronic Clostridium septicum infection of a tibal fracture: a case report. Injury. 1976;8(2):117–119. doi: 10.1016/0020-1383(76)90044-9. [DOI] [PubMed] [Google Scholar]
- 9.Woolley IJ, Love RL, Street AC. Clostridium septicum bacteremia without gas gangrene as a late consequence of a contaminated wound. Surgical Infections. 2004;5(3):315–317. doi: 10.1089/sur.2004.5.315. [DOI] [PubMed] [Google Scholar]
- 10.Werry DG, Meek RN. Clostridial gas gangrene complicating Colles’ fracture. Journal of Trauma. 1986;26(3):280–283. doi: 10.1097/00005373-198603000-00013. [DOI] [PubMed] [Google Scholar]
- 11.Goon PKY, O’Brien M, Titley OG. Spontaneous Clostridium septicum septic arthritis of the shoulder and gas gangrene: a case report. Journal of Bone and Joint Surgery A. 2005;87(4):874–877. doi: 10.2106/JBJS.D.02337. [DOI] [PubMed] [Google Scholar]
- 12.Taylor BC, Bramwell TJ, Formaini N. Gas gangrene as a result of femoral traction pin placement. Case Reports in Orthopedics. 2011;2011:3 pages. doi: 10.1155/2011/459812.459812 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Mulier T, Morgan M, Fabry G. Clostridium septicum gangrene complicating a closed femoral fracture. Acta Orthopaedica Belgica. 1993;59(4):416–419. [PubMed] [Google Scholar]
- 14.Lorea P, Baeten Y, Chahidi N, Franck D, Moermans J-P. A severe complication of muscle transfer: clostridial myonecrosis. Annales de Chirurgie Plastique et Esthetique. 2004;49(1):32–35. doi: 10.1016/j.anplas.2003.12.010. [DOI] [PubMed] [Google Scholar]
- 15.Sevitt S. Gas-gangrene infection in an operating-theatre. The Lancet. 1953;262(6796):1121–1123. doi: 10.1016/s0140-6736(53)91496-2. [DOI] [PubMed] [Google Scholar]
- 16.HILL MM. Gas-gangrene following fracture. The Lancet. 1959;1(7075):729–730. doi: 10.1016/s0140-6736(59)91909-9. [DOI] [PubMed] [Google Scholar]
- 17.Aufranc OE, Jones WN, Bierbaum BE. Gas gangrene complicating fracture of the tibia. Journal of the American Medical Association. 1969;209(13):2045–2047. [PubMed] [Google Scholar]
- 18.Boland FK. Gas gangrene in compound fractures. Annals of Surgery. 1929;90(4):603–613. doi: 10.1097/00000658-192910000-00016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Brume J, Ijagha EO. Traditional bone setters and gas gangrene. The Lancet. 1985;1(8432):p. 813. doi: 10.1016/s0140-6736(85)91465-5. [DOI] [PubMed] [Google Scholar]
- 20.Moehring HD. Postoperative clostridial infection. A case report. Clinical Orthopaedics and Related Research. 1988;(228):265–269. [PubMed] [Google Scholar]
- 21.Oncel S, Arsoy ES. Rapidly developing gas gangrene due to a simple puncture wound. Pediatric Emergency Care. 26(6):434–435. doi: 10.1097/PEC.0b013e3181e15e4f. [DOI] [PubMed] [Google Scholar]
- 22.Hoffman S, Katz JF, Jacobson JH. Salvage of a lower limb after gas gangrene. Bulletin of the New York Academy of Medicine. 1971;47(1):40–49. [PMC free article] [PubMed] [Google Scholar]
- 23.DeHaven KE, Evarts CM. The continuing problem of gas gangrene: a review and report of illustrative cases. Journal of Trauma. 1971;11(12):983–991. doi: 10.1097/00005373-197112000-00001. [DOI] [PubMed] [Google Scholar]
- 24.Johnson S, Driks MR, Tweten RK, et al. Clinical courses of seven survivors of Clostridium septicum infection and their immunologic responses to α toxin. Clinical Infectious Diseases. 1994;19(4):761–764. doi: 10.1093/clinids/19.4.761. [DOI] [PubMed] [Google Scholar]
- 25.Dykes RG. Gas gangrene after hip nailing. Australian and New Zealand Journal of Surgery. 1977;47(6):790–792. doi: 10.1111/j.1445-2197.1977.tb06625.x. [DOI] [PubMed] [Google Scholar]
- 26.Miller SD, Moed BR, Chess JL. Clostridium perfringens infection of an anterior iliac crest bone graft donor site: a case report. Clinical Orthopaedics and Related Research. 1993;(293):265–268. [PubMed] [Google Scholar]
- 27.Weinstein L, Barza MA. Gas gangrene. The New England Journal of Medicine. 1973;289(21):1129–1131. doi: 10.1056/NEJM197311222892107. [DOI] [PubMed] [Google Scholar]
- 28.Altemeier WA, Fullen WD. Prevention and treatment of gas gangrene. Journal of the American Medical Association. 1971;217(6):806–813. [PubMed] [Google Scholar]
- 29.Present DA, Meislin R, Shaffer B. Gas gangrene: a review. Orthopaedic Review. 1990;19(4):333–344. [PubMed] [Google Scholar]
- 30.Stevens DL, Bryant AE. The role of clostridial toxins in the pathogenesis of gas gangrene. Clinical Infectious Diseases. 2002;35(1):S93–S100. doi: 10.1086/341928. [DOI] [PubMed] [Google Scholar]
- 31.Stevens DL. The pathogenesis of clostridial myonecrosis. International Journal of Medical Microbiology. 2000;290(4-5):497–502. doi: 10.1016/S1438-4221(00)80074-0. [DOI] [PubMed] [Google Scholar]
- 32.Pereira De Godoy JM, Vasconcelos Ribeiro J, Caracanhas LA. Mortality and diabetes mellitus in amputations of the lower limbs for gas gangrene: a case report. International Journal of Lower Extremity Wounds. 2008;7(4):239–240. doi: 10.1177/1534734608324123. [DOI] [PubMed] [Google Scholar]
- 33.Nolan CJ, Damm P, Prentki M. Type 2 diabetes across generations: from pathophysiology to prevention and management. The Lancet. 2011;378(9786):169–181. doi: 10.1016/S0140-6736(11)60614-4. [DOI] [PubMed] [Google Scholar]
