Prognostic factors and antibiotics in Vibrio vulnificus septicemia

被引:80
作者
Liu, Jien-Wei
Lee, Ing-Kit
Tang, Hung-Jen
Ko, Wen-Chien
Lee, Hsin-Chun
Liu, Yung-Ching
Hsueh, Po-Ren
Chuang, Yin-Ching
机构
[1] Chimei Med Ctr, Dept Med Res, Yung Kang, Tainan, Taiwan
[2] Chimei Med Ctr, Dept Med, Yung Kang, Tainan, Taiwan
[3] Natl Cheng Kung Univ Hosp, Div Infect Dis, Tainan 70428, Taiwan
[4] Chang Gung Univ, Coll Med, Div Infect Dis, Chang Gung Mem Hosp,Kaohsiung Med Ctr, Kaohsiung, Taiwan
[5] Kaohsiung Vet Gen Hosp, Infect Dis Sect, Kaohsiung, Taiwan
[6] Natl Taiwan Univ Hosp, Dept Lab Med, Taipei, Taiwan
[7] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei, Taiwan
关键词
D O I
10.1001/archinte.166.19.2117
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Immunocompromised patients with Vibrio vulnificus septicemia are at high risk for fatality. When a hemorrhagic bullous necrotic cutaneous lesion (HBNCL) and decreased blood pressure develop, approximately 50% of V vulnificus septicemic patients die within 48 hours. This study aimed to evaluate the risk factor(s) for fatality among patients with V vulnificus septicemia, emphasizing the role of prescribed antimicrobial agents in general and the therapeutic efficacy of the combination of a third-generation cephalosporin and tetracycline or its analogue in particular. Methods: Patients with the diagnosis of V vulnificus infection admitted to 5 large medical centers in Taiwan between 1995 and 2003 were included in this retrospective study. Patients were divided into 2 groups: those with HBNCLs and those without HBNCLs. Patients were further divided into subgoups without fatalities (fatal subgroup) and those without fatalities (nonfatal subgroup). Results: A total of 93 patients participated in the study. In group 1, the fatal subgroup had higher Acute Physiology and Chronic Health Evaluation II (APACHE II) scores (P=.006) and a higher proportion of shock at arrival at the medical center (P=.015) than the nonfatal subgroup. In group 2, the effect of a first- or second-generation cephalosporin plus an aminoglycoside was negative (P=.01) and that of combined third-generation cephalosporin and tetracycline or its analogue was positive (P <.001); significant differences were found between the fatal and nonfatal subgroups in the APACHE II score (P <.001), number who were in shock at arrival at the medical center (P=.02), delayed surgical intervention (P=.03), and peripheral leukocytosis (P=.03). Shock at arrival at the medical center (odds ratio [OR], 19.25; 95% confidence interval [CI], 1.768-209.54; P=.02) was an independent risk factor for fatality in patients without HBNCLs. Use of a third-generation cephalosporin and tetracycline or its analogue significantly reduced fatality rates in patients with HBNCLs (OR, 0.037; 95% CI, 0.007-0.192; P <.001). Conclusion: Septic shock is a determinant of fatality in patients with V vulnificus septicemia without HBNCLs; our data suggest that the combination of a third-generation cephalosporin and tetracycline or its analogue may be a better choice in antimicrobial treatment of V vulnificus septicemic patients with HBNCLs.
引用
收藏
页码:2117 / 2123
页数:7
相关论文
共 42 条
[1]  
[Anonymous], MANUAL CLIN MICROBIO
[2]  
BECKMAN EN, 1981, AM J CLIN PATHOL, V76, P765
[3]   AMERICAN-COLLEGE OF CHEST PHYSICIANS SOCIETY OF CRITICAL CARE MEDICINE CONSENSUS CONFERENCE - DEFINITIONS FOR SEPSIS AND ORGAN FAILURE AND GUIDELINES FOR THE USE OF INNOVATIVE THERAPIES IN SEPSIS [J].
BONE, RC ;
BALK, RA ;
CERRA, FB ;
DELLINGER, RP ;
FEIN, AM ;
KNAUS, WA ;
SCHEIN, RMH ;
SIBBALD, WJ ;
ABRAMS, JH ;
BERNARD, GR ;
BIONDI, JW ;
CALVIN, JE ;
DEMLING, R ;
FAHEY, PJ ;
FISHER, CJ ;
FRANKLIN, C ;
GORELICK, KJ ;
KELLEY, MA ;
MAKI, DG ;
MARSHALL, JC ;
MERRILL, WW ;
PRIBBLE, JP ;
RACKOW, EC ;
RODELL, TC ;
SHEAGREN, JN ;
SILVER, M ;
SPRUNG, CL ;
STRAUBE, RC ;
TOBIN, MJ ;
TRENHOLME, GM ;
WAGNER, DP ;
WEBB, CD ;
WHERRY, JC ;
WIEDEMANN, HP ;
WORTEL, CH .
CRITICAL CARE MEDICINE, 1992, 20 (06) :864-874
[4]   SPECTRUM OF VIBRIO INFECTIONS IN A GULF-COAST COMMUNITY [J].
BONNER, JR ;
COKER, AS ;
BERRYMAN, CR ;
POLLOCK, HM .
ANNALS OF INTERNAL MEDICINE, 1983, 99 (04) :464-469
[5]  
BOWDRE JH, 1983, J PHARMACOL EXP THER, V225, P595
[6]  
*CDCP, 1993, MMWR-MORBID MORTAL W, V42, P405
[7]   VIBRIO-VULNIFICUS INFECTION [J].
CHUANG, YC ;
YOUNG, CD ;
CHEN, CW .
SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 1989, 21 (06) :721-726
[8]  
Chuang YC, 1997, J FORMOS MED ASSOC, V96, P677
[9]   Minocycline and cefotaxime in the treatment of experimental murine Vibrio vulnificus infection [J].
Chuang, YC ;
Ko, WC ;
Wang, ST ;
Liu, JW ;
Ku, CF ;
Wu, JJ ;
Huang, KY .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (06) :1319-1322
[10]   VIBRIO-VULNIFICUS INFECTION IN TAIWAN - REPORT OF 28 CASES AND REVIEW OF CLINICAL MANIFESTATIONS AND TREATMENT [J].
CHUANG, YC ;
YUAN, CY ;
LIU, CY ;
LAN, CK ;
HUANG, AHM .
CLINICAL INFECTIOUS DISEASES, 1992, 15 (02) :271-276