This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Friedl, J.
Right arrow Articles by Mühlbacher, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Friedl, J.
Right arrow Articles by Mühlbacher, F.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, March 1998, p. 818-819, Vol. 36, No. 3
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Haemophilus parainfluenzae Liver Abscess after Successful Liver Transplantation

J. Friedl,* A. Stift, G. A. Berlakovich, S. Taucher, M. Gnant, R. Steininger, and F. Mühlbacher

Department of Surgery, Division of Transplantation Surgery, University of Vienna, Vienna, Austria

Received 29 September 1997/Returned for modification 1 November 1997/Accepted 18 December 1997

    ABSTRACT
Top
Abstract
Text
References

Haemophilus parainfluenzae was isolated from a bile specimen and from an aspirate of a liver abscess in a 58-year-old liver-transplanted woman that was indicative of an invasion of the graft by an ascending route. Drug therapy, immunosuppression, rejection therapy, and Roux-en-Y choledochojejunostomy may have contributed to the septic course. Interdisciplinary cooperation was instrumental in diagnosis and successful management in this case.

    TEXT
Top
Abstract
Text
References

Infectious complications remain a major cause of morbidity and mortality after liver transplantation. The incidence of bacterial infections after liver transplantation differs considerably among transplantation centers, and reported infection rates range between 35 and 68% (1, 2, 8, 9, 12, 15). Patients under immunosuppressed conditions are at higher risk for infections and, in general, for infections which are caused by bacterial pathogens that are normally nonpathogenic. Herein we describe a patient who developed a nonbacteremic Haemophilus parainfluenzae liver abscess 1 year after successful orthotopic liver transplantation. H. parainfluenzae, a commensal organism of the upper respiratory tract, is an uncommon agent of human infection. It has been found to be associated with soft tissue infections, septic arthritis, genital tract infections, meningitis and brain abscesses (3), upper respiratory tract infections (10), endocarditis, bacteremia (7), and osteomyelitis (2). To date, only two cases of H. parainfluenzae liver abscess have been reported (3, 6).

Case report. A 58-year-old woman was admitted to our hospital 1 year after liver transplantation for extrahepatic cholangiocarcinoma. She was suffering from recurrent fever attacks and cholestasis. The diagnosis of purulent cholangitis, choledocholithiasis, and common bile duct stenosis was made. Despite stenting of the bile duct stricture, the patient acquired multiple infections (recurrent cholangitis and urinary tract infection) with different bacterial strains, including Klebsiella oxytoca, Pseudomonas spp., Staphylococcus aureus (methicillin resistant), a coagulase-negative staphyloccocus, and Streptococcus faecium. Vancomycin and rifampin or ciprofloxacin were used for treatment. Three weeks after the last infection, liver enzyme levels increased and a liver biopsy was performed, revealing graft rejection. A steroid pulse was given, and the immunosuppressive regimen was switched from cyclosporine (CsA) to tacrolimus and azathioprine. Three days later, the patient had fever again and a blood culture yielded methicillin-resistant S. aureus and Streptococcus faecalis. Vancomycin was readministered for 1 week until a Roux-en-Y choledochojejunostomy was performed. Vancomycin was also used as an intraoperative as well as a perioperative agent in combination with metronidazole. Intraoperative bile samples were obtained, and H. parainfluenzae and Enterococcus faecalis were isolated. Two weeks after the Roux-en-Y choledochojejunostomy, the patient had recurrent fever attacks with negative blood cultures. An abdominal computed tomography scan was performed, showing a hypodense area in the eighth liver segment. A fine-needle aspiration was done, and an initial Gram stain of the aspirate showed gram-negative coccobacilli. Since the further testing identified the isolate as H. parainfluenzae, daily intravenous treatment with fleroxacin led to a favorable outcome. Three years after liver transplantation, the patient is well with normal graft function.

Discussion. H. parainfluenzae is a commensal organism of the oropharynx and is present in over 20% of fecal samples analyzed (14). To date, only two cases of H. parainfluenzae biliary tract infections and only two H. parainfluenzae liver abscesses have been documented (Table 1). None of these infections was associated with bacteremia. This may indicate that H. parainfluenzae infection occurs via an ascending route. Two factors support this hypothesis. First, H. parainfluenzae grows well in the presence of V factor, which is abundant in the duodenum (11). Second, H. parainfluenzae bears iron-repressible outer membrane proteins closely related to those of enteric bacteria. These proteins may serve as adhesins, allowing colonization of the intestinal tract mucosa (13). Once H. parainfluenzae is established, it is provided with abundant V factor (NAD) excreted by the local flora.

                              
View this table:
[in this window]
[in a new window]
 
TABLE 1.   Documented cases of H. parainfluenzae hepatobiliary tract infection

Our report strongly supports this hypothesis because an H. parainfluenzae liver abscess was evident after H. parainfluenzae was isolated from the common bile duct and blood cultures showed no concomitant bacteremia. There are some possible reasons why this ascending infection occurred. One is that the patient suffered from recurrent cholangitis with concomitant cholestasis, which allowed bacterial overgrowth. This overgrowth was supported by graft rejection therapy, switching of the immunosuppression therapy, and Roux-en-Y choledochojejunostomy.

Metronidazole is widely distributed. It appears in most body tissues, including bile, bone, liver, brain, breast milk, saliva, and seminal fluid, and achieves concentrations similar to those in plasma. Metronidazole is metabolized by side chain oxidation and glucuronide formation, and the majority of a dose of metronidazole is excreted in the urine, mainly as metabolites. Some of the metabolites also have antibacterial activity (16). Thus, metronidazole, in contrast to vancomycin, which is not excreted in bile, may have induced a change in the local bacterial flora. To prevent a further infection in that critical situation, we treated the patient with fleroxacin, although the susceptibility profile of the isolated strain indicated no resistance to any of the tested agents, including amoxicillin-clavulanic acid, aminopenicillin derivatives, tetracyclines, and expanded- and broad-spectrum cephalosporins.

It seems that the combination of the factors mentioned above was responsible for the rapid ascending progression from a localized infection of the common bile duct to a general condition of sepsis due to a liver abscess.

    FOOTNOTES

* Corresponding author. Mailing address: Dept. of Surgery, Division of Transplantation Surgery, AKH Vienna, Währinger Gürtel 18-20, A-1090 Vienna, Austria. Phone: 43 1 40400 5621. Fax: 43 1 40400 5642. E-mail: Josef.Friedl{at}akh-wien.ac.at.

    REFERENCES
Top
Abstract
Text
References

1. Ascher, N. L., P. G. Stock, G. L. Bumgardner, W. D. Payne, and J. S. Najarian. 1988. Infection and rejection of primary hepatic transplant in 93 consecutive patients treated with triple immunosuppressive therapy. Surg. Gynecol. Obstet. 167:474-484[Medline].
2. Beauvais, C., F. Berenbaum, M. Spentchian, A. Prier, and G. Kaplan. 1992. Early diagnosis of vertebral osteomyelitis due to a rare pathogen: Haemophilus parainfluenzae. J. Rheumatol. 198:491-493.
3. Black, C. T., J. P. Kupferschmid, K. W. West, and J. J. Grosfeld. 1988. Haemophilus parainfluenzae infections in children with the report of a unique case. Rev. Infect. Dis. 10:342-346[Medline].
4. Bottone, E. J., and D. Y. Zhang. 1995. Haemophilus parainfluenzae biliary tract infection: rationale for an ascending route of infection from the gastrointestinal tract. J. Clin. Microbiol. 33:3042-3043[Abstract].
5. Cattier, B., J. Caillon, and R. Quentin. 1992. A case of biliary tract infection caused by Haemophilus parainfluenzae. Eur. J. Clin. Microbiol. Infect. Dis. 11:197-199[Medline].
6. Chattopadhyay, B., P. H. Silverstone, and R. S. Winwood. 1983. Liver abscess caused by Haemophilus parainfluenzae. Postgrad. Med. J. 59:788-789[Abstract/Free Full Text].
7. Chun, J. N., S. R. Jones, and A. McCutchan. 1978. Haemophilus parainfluenzae infective endocarditis. Medicine (Baltimore) 56:99-113.
8. Colonna, J. O., D. J. Winston, J. E. Brill, L. I. Goldstein, M. P. Hoff, J. R. Hiatt, W. Quinones-Baldrich, K. P. Ramming, and R. W. Busuttil. 1988. Infectious complication in liver transplantation. Arch. Surg. 123:360-364[Abstract/Free Full Text].
9. Jacobs, F., J. Van-de-Stadt, N. Bourgeois, M. J. Struelens, C. De Prez, M. Adler, J. P. Thys, and M. Gelin. 1989. Severe infections early after liver transplantation. Transplant. Proc. 21:2271-2273[Medline].
10. Kayser, F. H. 1992. Changes in the spectrum of organisms causing respiratory tract infections: a review. Postgrad. Med. J. Suppl. 68(Suppl. 3):S17-S23.
11. Kilian, M. 1985. Haemophilus, p. 387-393. In E. H. Lennette, A. Balows, W. J. Hausler, Jr., and H. J. Shadomy (ed.), Manual of clinical microbiology, 4th ed. American Society for Microbiology, Washington, D.C.
12. Kusne, S., J. S. Dummer, N. Singh, S. Iwatsuki, L. Makowka, C. Esquivel, A. G. Tsakis, T. E. Starzl, and M. Ho. 1988. Infections after liver transplantation. An analysis of 101 consecutive cases. Medicine (Baltimore) 67:132-143[Medline].
13. Liljemark, W. F., C. G. Bloomquist, and C. Lai. 1992. Clustering of an outer membrane adhesin of Haemophilus parainfluenzae. Infect. Immun. 60:687-689[Abstract/Free Full Text].
14. Megraud, F., C. Bebear, H. Dabernat, and C. Delmas. 1988. Haemophilus species in the human gastrointestinal tract. Eur. J. Clin. Microbiol. Infect. Dis. 7:437-438[Medline].
15. Paya, C. V., P. E. Hermans, J. A. Washington, T. F. Smith, J. P. Anhalt, R. H. Wiesner, and R. A. Krom. 1989. Incidence, distribution, and outcome of episodes of infection in 100 orthotopic liver transplantations. Mayo Clin. Proc. 64:555-564[Medline].
16. Reynolds, J. F. 1993. Metronidazole, p. 516-521. In W. Martindale (ed.), The extra pharmacopoeia. Pharmaceutical Press (UK), London, United Kingdom.


Journal of Clinical Microbiology, March 1998, p. 818-819, Vol. 36, No. 3
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.




This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Friedl, J.
Right arrow Articles by Mühlbacher, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Friedl, J.
Right arrow Articles by Mühlbacher, F.