Clostridial soft-tissue infections include cellulitis, myositis, and clostridial myonecrosis. They usually occur after trauma. Symptoms may include edema, pain, gas with crepitation, foul-smelling exudates, intense coloration of the site, and progression to shock and renal failure. Diagnosis is by inspection and smell, confirmed by culture. Treatment is with penicillin and surgical debridement. Hyperbaric O2 is sometimes beneficial.
Clostridium perfringens is the most common species involved. Infection develops hours or days after injury, usually in an extremity after severe crushing or penetrating trauma devitalizes tissue, creating anaerobic conditions. The presence of foreign material (even if sterile) markedly increases risk of clostridial infection. Infection may also occur in operative wounds, particularly in patients with underlying occlusive vascular disease. Rarely, spontaneous cases occur, usually involving C. septicum originating from occult colon perforation in patients with colon cancer, diverticulitis, or bowel ischemia. Infection typically results in gas collection in soft tissues.
In suitable conditions (low oxidation-reduction potential, low pH), as occur in devitalized tissue, infection progresses rapidly, from initial injury through shock, toxic delirium, and death within as little as 1 day.
Symptoms and Signs
Clostridial cellulitis occurs as a localized infection in a superficial wound, usually ≥ 3 days after injury. Infection may spread extensively along fascial planes, often with evident crepitation and abundant gas bubbling, but toxicity is much less severe than with extensive myonecrosis, and pain is minimal. Bullae are frequently evident, with foul-smelling, serous, brown exudate. Discoloration and gross edema of the extremity are rare. Clostridial skin infections associated with primary vascular occlusion of an extremity rarely progress to severe toxic myonecrosis or extend beyond the line of demarcation.
Clostridial myositis (suppurative infection of muscle without necrosis) is most common among parenteral drug users. It resembles staphylococcal pyomyositis and lacks the systemic symptoms of clostridial myonecrosis. Edema, pain, and frequently gas in the tissues occur. The infection spreads rapidly and may progress to myonecrosis.
In clostridial myonecrosis (gas gangrene), initial severe pain is common, sometimes even before other findings. The wound site may be pale initially, but it becomes red or bronze, often with blebs or bullae, and finally turns blackish green. The area is tensely edematous and tender to palpation. Crepitation is less obvious early than it is in clostridial cellulitis but is ultimately palpable in about 80%. Wounds and drainage have a particularly foul odor.
With progression, patients appear toxic, with tachycardia, pallor, and hypotension. Shock and renal failure occur, although patients often remain alert until the terminal stage. Unlike clostridial uterine infection, overt hemolysis is rare in gas gangrene of the extremities, even in terminally ill patients. Whenever massive hemolysis occurs, mortality of 70 to 100%, due to acute renal failure and septicemia, can be expected.
Early suspicion and intervention are essential; clostridial cellulitis responds well to treatment, but myonecrosis has a mortality rate of ≥ 40% with treatment and 100% without treatment.
Although localized cellulitis, myositis, and spreading myonecrosis may be clinically distinct, differentiation often requires surgical exploration. In myonecrosis, muscle tissue is visibly necrotic; the affected muscle is a lusterless pink, then deep red, and finally gray-green or mottled purple and does not contract with stimulation. X-rays may show local gas production, and CT and MRI delineate the extent of gas and necrosis.
Wound exudate should be cultured for anaerobic and aerobic organisms. Because of their short generation time, anaerobic cultures of Clostridia may be positive in as little as 6 h. However, other anaerobic and aerobic bacteria, including members of the Enterobacteriaceae family and Bacteroides, Streptococcus, and Staphylococcus spp, alone or mixed, can cause severe clostridia-like cellulitis, extensive fasciitis, or myonecrosis (see Bacterial Skin Infections: Necrotizing Subcutaneous Infection). Also, many wounds, particularly if open, are contaminated with both pathogenic and nonpathogenic clostridia that are not responsible for the infection.
The presence of clostridia is significant when
However, if PMNs are abundant and the smear shows many chains of cocci, an anaerobic streptococcal or staphylococcal infection should be suspected. Abundant gram-negative bacilli may indicate infection with one of the Enterobacteriaceae or a Bacteroides sp (see Anaerobic Bacteria: Mixed Anaerobic Infections). Detection of clostridial toxins in the wound or blood is useful only in the rare case of wound botulism (see Anaerobic Bacteria: Botulism).
When clinical signs of clostridial infection (eg, gas, myonecrosis) are present, rapid, aggressive intervention is mandatory. Thorough drainage and debridement are as important as antibiotics; both should be instituted rapidly. Penicillin G is the drug of choice; 1 to 2 million units IV q 2 to 3 h should be given immediately for severe cellulitis and myonecrosis. Addition of clindamycin 600 mg IV q 6 h is beneficial. If gram-negative organisms are seen or suspected, a broad-spectrum antibiotic (eg, ticarcillin plus clavulanate, ampicillin plus sulbactam, piperacillin plus tazobactam) should be added.
Hyperbaric O2 therapy may be helpful in extensive myonecrosis, particularly in the extremities, as a supplement to antibiotics and surgery. Hyperbaric O2 therapy may salvage tissue and lessen mortality and morbidity if it is started early, but it should not delay surgical debridement.
Last full review/revision August 2009 by Joseph R. Lentino, MD, PhD
Content last modified February 2012