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PEDIATRICS Vol. 108 No. 1 July 2001, p. e17
ELECTRONIC ARTICLE:
Recovery of Anaerobic Bacteria From Four Children With
Postthoracotomy Sternal Wound Infection
From the Department of Pediatrics, Georgetown University School
of Medicine, Washington, DC.
The cases of 4 children who developed
postthoracotomy sternal wound infection caused by anaerobic bacteria
are presented. The predominate anaerobes were
Peptostreptococcus species and pigmented
Prevotella species. Polymicrobial infection was present in all cases, and aerobic bacteria also were recovered in 2 instances. All patients responded to surgical debridement and antimicrobials effective against the isolated aerobic and anaerobic bacteria. These
findings highlight the potential importance of anaerobic bacteria in
postthoracotomy sternal wound infection.
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ABSTRACT
Top
Abstract
Methods
Results
Discussion
References
Postthoracotomy sternal wound infection (PTSWI) is a major
complication after cardiac surgery in adults1-3 and
children.4-8 The organisms that are recognized as causing
most of these infections in adults and children are mostly
Staphylococcus aureus, Staphylococcus epidermidis, and
members of the family Enterobacteriaceae, such as Escherichia coli, Klebsiella species, Enterobacter
species, and Proteus species.4,9,10 Although
anaerobic bacteria were described in PTSWI in adults,11 their recovery has not been documented previously in children. This
report describes 4 patients who developed PTSWI caused by anaerobic
bacteria.
The patients described were treated and studied by the author
for PTSWI in hospitals in the metropolitan Washington, DC, area between
1983 and 1998 and did not include all of the patients who had PTSWI
during this period. The hospitals included the Hospital for Sick
Children and Georgetown University Hospital in Washington, DC. The
total number of patients who had had a sternal thoracotomy procedure
performed on them at these institutions during these years was not
recorded. Included were only patients who had developed PTSWI caused by
anaerobic bacteria. Patients' medical and laboratory data were
reviewed.
Antimicrobial agents were given as surgical prophylaxis to all patients
and included a first-generation cephalosporin (patients 1-3; Table
1) and penicillin (patient 4).
TABLE 1
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METHODS
Top
Abstract
Methods
Results
Discussion
References
Clinical Features of Median Sternotomy Wound Infections in Children
Specimens were obtained by direct needle aspiration of the purulent contents into a syringe that was immediately sealed and transported to the laboratory within 30 minutes or by swab that was dipped into the pus and introduced into an anaerobic transport system (Port-A-Cul; BBL Microbiology Systems, Cockeysville, MD) or a Vacutainer (BD Vacutainer System, Rutherford, NJ) and transported to the laboratory within 2 hours.
Sheep's blood (5%), chocolate, and MacConkey agar plates were inoculated at 37°C aerobically (MacConkey) or under 5% CO2 (blood and chocolate) and examined at 24 and 48 hours. For isolation of anaerobes, the specimen material was plated onto prereduced vitamin K1-enriched Brucella blood agar, an anaerobic blood agar plate containing kanamycin and vancomycin, and an aerobic blood plate containing colistin and nalidixic acid and inoculated into an enriched thioglycolate broth,12 incubated in GasPak jars (BBL Microbiology Systems), and examined at 48 and 96 hours. Plates that showed growth were held until the organisms were processed and identified. All cultures that showed no growth were held for at least 5 days. Anaerobic and aerobic bacteria were identified as described previously.12,13
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RESULTS |
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Polymicrobial infection was present in all instances. The number of isolates varied from 2 to 3. The predominant anaerobes were Peptostreptococcus species (3) and pigmented Prevotella (2). Anaerobic bacteria only were recovered in 2 patients (patients 1 and 4; Table 1), and mixed aerobic and anaerobic bacteria were isolated in the 2 others (patients 2 and 3).
A median sternotomy incision was performed for repair of congenital defects in all cases. The infections were diagnosed between 18 to 31 days after surgery. All patients had factors that have been shown to predispose to infection.4,7 These included a perfusion time in excess of 1 hour, prolonged ventilation time (>200 hours), delayed sternal closure (>1 day), and inappropriate antimicrobial prophylaxis.
Signs and symptoms associated with PTSWI included fever (38°C-40°C; in all patients), erythema or cellulitis (in all patients), purulent (3 patients) or sanguinous (1 patient) wound discharge, foul-smelling discharge (3 patients), and instability of the sternum (2 patients). A leukocytosis of 16 600/mm3 to 23 800/mm3 with neutrophil predominance (64%-80%) was present when the diagnosis of PTSWI was made in all cases.
Therapy for the PTSWI included open (3 cases) or local (1 case) debridement and parenteral and oral antimicrobial therapy for 28 to 44 days. All patients recovered without complications.
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DISCUSSION |
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This report describes for the first time the isolation of anaerobic bacteria from PTSWI in children. These organisms were recovered as the sole isolates in 2 instances and mixed with aerobic bacteria in 2 instances. The isolation of these endogenous organisms from these infections may be attributable to their inoculation from the patient's normal flora. Peptostreptococcus and Prevotella species are part of the oropharyngeal flora14 and have been recovered previously from breast abscesses15 and head and neck abscesses.16 Similarly, Bacteroides fragilis group and E coli are part of the gastrointestinal flora14 and have been recovered previously from umbilical infections in newborns17 and from skin and soft-tissue infection in children.18
These findings are similar to our previous data collected from adults.11 Specimens from 65 adult patients with PTSWI were studied for aerobic and anaerobic bacteria. Aerobic or facultative bacteria only were recovered in 50 specimens (77%); anaerobic bacteria only in 6 (9%); and mixed aerobic, facultative, and anaerobic bacteria in 9 (14%). The predominant aerobes were S epidermidis (28 isolates), S aureus (21 isolates), and members of the family Enterobacteriaceae (14 isolates). The predominant anaerobes were Peptostreptococcus species (10 isolates), Bacteroides species (4), and Clostridium species (3).
Part of the reason that anaerobic bacteria were not reported previously in children may be attributable to inadequate methods for transportation and cultivation of specimens in previous studies.4,7 One of these studies reported observing Gram-negative rods in Gram-stain preparation of sternal drainage without obtaining any bacterial growth.4
Management of PTSWI includes surgical debridement and administration of
systemic antimicrobials. Many of the antimicrobials that are effective
against S aureus and Enterobacteriaceae are not effective
against all anaerobic bacteria. Anaerobic Gram-negative bacilli
isolated from clinical infections can be resistant to penicillins
through the production of
-lactamase.16 The presence of
penicillin-resistant anaerobic organisms may require the use of agents
that are effective against these bacteria. These antimicrobials include
clindamycin, metronidazole, imipenem, cefoxitin, chloramphenicol, or
the combination of a penicillin (eg, amoxicillin) and a
-lactamase
inhibitor (eg, clavulanate).19
Prospective studies are warranted to elucidate the role of anaerobic bacteria in PTSWI in children. It is recommended, however, that specimens from those sites be cultured for both aerobic and anaerobic bacteria so that when systemic antimicrobials are used, coverage for these organisms can be appropriate.
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ACKNOWLEDGMENT |
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The author thanks Sarah Blaisdell for secretarial help.
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FOOTNOTES |
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Received for publication Dec 8, 2000; accepted Feb 26, 2001.
Reprint requests to (I.B.) P.O.B. 70412, Chevy Chase, MD 20812. E-mail: dribrook{at}yahoo.com
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ABBREVIATIONS |
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PTSWI, postthoracotomy sternal wound infection.
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REFERENCES |
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-
Zacharias A,
Habib RH
Factors predisposing to median sternotomy
complications: deep vs. superficial infection.
Chest
1996;
110:1173-1178
[Abstract/Free Full Text] - Brunet F, Brusset A, Squara P, (The Parisian Mediastinitis Group). Risk factors for deep sternal wound infection after sternotomy: a prospective, multicenter study. J Thorac Cardiovasc Surg 1995; 11:1200-1207
- Dandalides PC, Rutala WA, Sarubbi FA Postoperative infections following cardiac surgery: association with an environmental reservoir in a cardiothoracic intensive care unit. Infect Control 1984; 5:378-384 [Medline]
- Edwards MS, Baker CJ Median sternotomy wound infections in children. Pediatr Infect Dis 1983; 2:105-109 [Medline]
- Pollock EM, Ford-Jones EL, Rebeyka I, Early nosocomial infections in pediatric cardiovascular surgery patients. Crit Care Med 1990; 18:378-384 [Medline]
-
Tabbutt S,
Duncan BW,
McLaughin D,
Delayed sternal closure after
cardiac operations in pediatric population.
J Thorac
Cardiovasc Surg
1997;
113:886-893
[Abstract/Free Full Text] - Farrington M, Webster M, Fenn A, Phillips I Study of cardiothoracic wound infection, St. Thomas Hospital. Br J Surg 1985; 72:759-762 [Medline]
- Kearns B, Sabella C, Mee RB, Moodie DS, Goldfarb J Sternal wound and mediastinal infections in infants with congenital heart disease. Cardiol Young. 1999; 9:280-284 [Medline]
- Hansen BG The occurrence of Staphylococcus epidermidis in a department of thoracic and cardiovascular surgery. A clinical and epidemiological investigation. Scand J Thorac Cardiovasc Surg 1982; 16:269-274 [Medline]
- Lilienfeld DE, Viahov D, Tenney JH, McLaughlin JS On antibiotic prophylaxis in cardiac surgery: a risk factor for wound infection. Ann Thorac Surg 1986; 42:670-674 [Abstract]
-
Brook I
Microbiology of postthoracotomy sternal wound infection.
J Clin Microbiol
1989;
27:806-807
[Abstract/Free Full Text] - Summanen P, Baron EJ, Citron DM, Strong CA, Wexler HM, Finefold SM. Wadsworth Anaerobic Bacteriology Manual. 5th ed. Belmonth, CA: Star Publishing; 1993
- Murray PR, Baron EJ, Pfaller MA, Trenover PC, Yolken RH. Manual of Clinical Microbiology. 5th ed. Washington, DC: American Society for Microbiology; 1993
- Brook I. Indigenous microbial of humans. In Howard RJ, Simmons RL, eds. Surgical Infectious Diseases. 3rd ed. Norwalk, CT: Appleton & Lange; 1995:37-46
- Brook I The aerobic and anaerobic microbiology of neonatal breast abscess. Pediatr Infect Dis J 1991; 10:785-786 [CrossRef][Medline]
- Brook I Microbiology of abscesses of the head and neck in children. Ann Otol Rhinol Laryngol 1987; 96:429-433 [Medline]
- Brook I Microbiology of necrotizing fasciitis associated with omphalitis in the newborn infant. J Perinatol 1998; 18:28-30 [Medline]
-
Brook I,
Finegold SM
Aerobic and anaerobic bacteriology of cutaneous
abscesses in children.
Pediatrics
1981;
67:891-895
[Abstract/Free Full Text] -
Sutter VL,
Finegold SM
Susceptibility of anaerobic bacteria to 23 antimicrobial agents.
Antimicrob Agents Chemother
1976;
10:736-752
[Abstract/Free Full Text]
Pediatrics (ISSN 0031 4005). Copyright ©2001 by the American Academy of Pediatrics
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