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American Journal of Respiratory and Critical Care Medicine Vol 179. pp. 257-258, (2009)
© 2009 American Thoracic Society


Correspondence

Death after Lung Transplantation in Cystic Fibrosis Patients Infected with Burkholderia cepacia

To the Editor:

We read with interest the article by Dr. Murray and colleagues (1), which examined the post–lung transplantation outcomes of patients with cystic fibrosis and Burkholderia cepacia complex infection. Excess mortality was largely seen in patients with B. cenocepacia infection, and infection with species other than B. cenocepacia was not associated with worse outcomes (1). These data support recent reports from other groups (2, 3).

We have had recent experience of early mortality in two patients with cystic fibrosis following lung transplant with chronic B. cepacia (genomovar I) infection. A 44-year-old female died 9 weeks post-transplant from overwhelming pulmonary infection. The early postoperative clinical course was excellent, including discharge from the hospital on Day 24 and no episodes of augmented immunosuppression. A male, 23 years of age, succumbed to progressive pulmonary infection 8 weeks post-transplant following the acquisition of an Influenza A and RSV coinfection on Day 53. The early postoperative clinical course was excellent, including discharge from hospital on Day 19. Treatment of the viral infection included ribavirin and pulse methylprednisolone therapy. Influenza vaccine had been administered pretransplant, but the antigenic component of the vaccine did not match the strain isolated from the patient.

Bronchoscopy washing and blood cultures revealed B. cepacia. These deaths occurred despite the use of routine protocols for patients with B. cepacia complex infection aimed at reducing risk of sepsis, including IL-2 receptor blocker monoclonal antibodies, cyclosporine targeting low therapeutic levels, intravenous antibiotics based on multiple combination bactericidal testing, and avoidance of surveillance transbronchial biopsies.

Kidd and colleagues (4) found that the proportion of Australian patients with cystic fibrosis and B. cepacia infection (previously known as genomovar I) is higher (11.2%) than most previous reports. Whereas early septic complications following lung transplantation have not been seen in our patients with B. cenocepacia, it has occurred in two patients with B. cepacia infection. The identification of a concurrent viral infection in one case could suggest a potential "priming" effect, which may have influenced the pathogenicity of B. cepacia infection. In each case, molecular typing demonstrated retention of the same B. cepacia strain after transplantation, but strains from each patient were unrelated. Despite antibiotic treatment based on available multiple combination bactericidal testing of B. cepacia (5), control of infection was not achievable. These cases exemplify the potential for "cepacia syndrome" post-transplant due to B. cepacia in patients with cystic fibrosis, adding to concerns about post-transplant outcomes in patients with B. cenocepacia and B. gladioli (13).

Peter M. Hopkins

The Prince Charles Hospital
Brisbane, Australia

Timothy J. Kidd

University of Queensland
and
Pathology Queensland
Brisbane, Australia

Chris Coulter

Pathology Queensland
Brisbane, Australia

Iain H. Feather

Gold Coast Hospital
Southport, Australia

Petra Derrington

Pathology Queensland
Southport, Australia

Scott C. Bell

University of Queensland
and
The Prince Charles Hospital
Brisbane, Australia

FOOTNOTES

Conflict of Interest Statement: P.M.H. does not have a financial relationship with a commercial entity that has an interest in the subject of this manuscript. T.J.K. does not have a financial relationship with a commercial entity that has an interest in the subject of this manuscript. C.C. served on a scientific advisory board for Wyeth Australia in 2005 and 2006, receiving AUD 1000; he received AUD 575 for chairing a meeting on behalf of Wyeth Australia in 2006; he was principal investigator for a laboratory research study which was supported by an unrestricted educational grant of $9,000 from Merck Sharp & Dohme (Australia). I.H.F. does not have a financial relationship with a commercial entity that has an interest in the subject of this manuscript. P.D. does not have a financial relationship with a commercial entity that has an interest in the subject of this manuscript. S.C.B. does not have a financial relationship with a commercial entity that has an interest in the subject of this manuscript.

REFERENCES

  1. Murray S, Charbeneau J, Marshall BC, LiPuma JJ. Impact of Burkholderia infection on lung transplantation in cystic fibrosis. Am J Respir Crit Care Med 2008;178:363–371.[Abstract/Free Full Text]
  2. Alexander BD, Petzold EW, Reller LB, Palmer SM, Davis RD, Woods CW, Lipuma JJ. Survival after lung transplantation of cystic fibrosis patients infected with Burkholderia cepacia complex. Am J Transplant 2008;8:1025–1030.[CrossRef][Medline]
  3. Boussaud V, Guillemain R, Grenet D, Coley N, Souilamas R, Bonnette P, Stern M. Clinical outcome following lung transplantation in patients with cystic fibrosis colonised with Burkholderia cepacia complex: results from two French centres. Thorax 2008;63:732–737.[Abstract/Free Full Text]
  4. Kidd TJ, Douglas JM, Bergh HA, Coulter C, Bell SC. Burkholderia cepacia complex epidemiology in persons with cystic fibrosis from Australia and New Zealand. Res Microbiol 2008;159:194–199.[Medline]
  5. Aaron SD, Vandemheen KL, Ferris W, Fergusson D, Tullis E, Haase D, Berthiaume Y, Brown N, Wilcox P, Yozghatlian V, et al. Combination antibiotic susceptibility testing to treat exacerbations of cystic fibrosis associated with multiresistant bacteria: a randomised, double-blind, controlled clinical trial. Lancet 2005;366:463–471.[CrossRef][Medline]




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