BURKHOLDERIA CEPACIA EXIT-SITE INFECTION IN PERITONEAL DIALYSIS PATIENTS-CLINICAL CHARACTERISTICS AND TREATMENT OUTCOMES

被引:4
作者
Yap, Desmond Y. H. [1 ]
Chan, Jasper F. W. [2 ]
Yip, Terence [3 ]
Mok, Maggie M. Y. [1 ]
Kwan, Lorraine P. Y. [1 ]
Lo, Wai Kei [3 ]
Chan, Tak Mao [1 ]
机构
[1] Univ Hong Kong, Div Nephrol, Dept Med, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Queen Mary Hosp, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
[3] Tung Wah Hosp, Dept Med, Renal Unit, Hong Kong, Hong Kong, Peoples R China
来源
PERITONEAL DIALYSIS INTERNATIONAL | 2016年 / 36卷 / 04期
关键词
Burkholderia cepacia; exit-site infection; peritoneal dialysis; INTENSIVE-CARE-UNIT; CYSTIC-FIBROSIS; ANTIMICROBIAL SUSCEPTIBILITY; COMPLEX; PSEUDOMONAS; CATHETER; BACTEREMIA; CHLORHEXIDINE; HEMODIALYSIS;
D O I
10.3747/pdi.2015.00122
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Burkholderia cepacia is a hardy bacterium with intrinsic resistance to multiple antibiotics and high transmissibility. Opportunistic healthcare-associated B. cepacia infections among immunocompromised or critically ill patients have been reported, but there is limited data on the clinical characteristics and treatment outcomes of exit-site infection (ESI) in peritoneal dialysis (PD) patients. Patients and methods: Patients who suffered from B. cepacia ESI from 1 January 2004 to 31 December 2014 were reviewed. The clinical characteristics and treatment outcomes of the patients and the antibiotic susceptibility patterns of the bacterial isolates were analyzed. Results: Twenty-two patients were included for analysis. Eight patients (36.4%) had medical conditions which impaired host immunity, while 7 (31.8%) had pre-existing skin abnormalities. Three patients (13.6%) progressed to tunnel-tract infection and another 3 patients (13.6%) developed associated peritonitis. Fifteen patients (68.2%) responded to medical treatment while 7 (31.8%) required catheter removal. Eleven patients (50.0%) had recurrent B. cepacia ESI, which occurred at 7.8 months (95% confidence interval [CI] 0.1 - 19.4 months) after the first episode. Most B. cepacia strains were susceptible to ceftazidime (95.5%), piperacillin/tazobactam (95.5%), and piperacillin (90.9%). Besides aminoglycosides (80 - 100%), high rates of resistance were also observed for ticarcillin/clavulanate (90.9%). Conclusion: Burkholderia cepacia ESI is associated with low rates of tunnel-tract infection or peritonitis, but the risk of recurrence is high. Most cases can be managed with medical treatment alone, although one third of patients might require catheter removal.
引用
收藏
页码:390 / 394
页数:5
相关论文
共 25 条
  • [21] THE INFLUENCE OF PERITONEAL CATHETER EXIT-SITE INFECTIONS ON PERITONITIS, TUNNEL INFECTIONS, AND CATHETER LOSS IN PATIENTS ON CONTINUOUS AMBULATORY PERITONEAL-DIALYSIS
    PIRAINO, B
    BERNARDINI, J
    SORKIN, M
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 1986, 8 (06) : 436 - 440
  • [22] Outbreak of Burkholderia cepacia bacteremia caused by contaminated chlorhexidine in a hemodialysis unit
    Romero-Gomez, M. P.
    Quiles-Melero, M. I.
    Garcia, P. Pena
    Altes, A. Gutierrez
    de Miguel, M. A. Garcia
    Jimenez, C.
    Valdezate, Sylvia
    Nieto, J. A. Saez
    [J]. INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2008, 29 (04) : 377 - 378
  • [23] Antimicrobial susceptibility of uncommonly isolated non-enteric Gram-negative bacilli
    Sader, HS
    Jones, RN
    [J]. INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2005, 25 (02) : 95 - 109
  • [24] Burkholderia cepacia-An Uncommon Cause of Exit-Site Infection in a Peritoneal Dialysis Patient
    Yap, Desmond Y. H.
    Choy, Cindy B. Y.
    Mok, Maggie M. Y.
    Wong, Tin Kan
    Chan, Tak Mao
    [J]. PERITONEAL DIALYSIS INTERNATIONAL, 2014, 34 (04): : 471 - 472
  • [25] Antimicrobial susceptibility and synergy studies of Burkholderia cepacia complex isolated from patients with cystic fibrosis
    Zhou, Juyan
    Chen, Yunhua
    Tabibi, Setareh
    Alba, Luis
    Garber, Elizabeth
    Saiman, Lisa
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (03) : 1085 - 1088