Our objective was to investigate the value of postmortem autopsy blood cultures performed with an iodine-subclavian technique relative to the classical method of atrial heat searing and antemortem blood cultures. The study consisted of a prospective autopsy series with each case serving as its own control relative to subsequent testing, and a retrospective survey of patients coming to autopsy who had both autopsy blood cultures and premortem blood cultures. A busy academic autopsy service (600 cases per year) at University of Texas Medical Branch Hospitals, Galveston, Texas, served as the setting for this work. The incidence of non-clinically relevant (false-positive) culture results were compared using different methods for collecting blood samples in a prospective series of 38 adult autopsy specimens. One hundred eleven adult autopsy specimens in which both postmortem and antemortem blood cultures were obtained were studied retrospectively. For both studies, positive culture results were scored as either clinically relevant or false positives based on analysis of the autopsy findings and the clinical summary. The rate of false-positive culture results obtained by an iodine-subclavian technique from blood drawn soon after death were statistically significantly lower (13%) than using the classical method of obtaining blood through the atrium after heat searing at the time of the autopsy (34%) in the same set of autopsy subjects. When autopsy results were compared with subjects' antemortem blood culture results, there was no significant difference in the rate of non-clinically relevant culture results in a paired retrospective series of antemortem blood cultures and postmortem blood cultures using the iodine-subclavian postmortem method (11.7% v 13.5%). The results indicate that autopsy blood cultures obtained using the iodine-subclavian technique have reliability equivalent to that of antemortem blood cultures. Copyright (C) 1998 by W.B. Saunders Company.
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Lutheran Gen Childrens Hosp, Dept Pediat, Div Neonatol, Park Ridge, IL USALutheran Gen Childrens Hosp, Dept Pediat, Div Neonatol, Park Ridge, IL USA
Fernandez, S
Mangurten, HH
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Lutheran Gen Childrens Hosp, Dept Pediat, Div Neonatol, Park Ridge, IL USALutheran Gen Childrens Hosp, Dept Pediat, Div Neonatol, Park Ridge, IL USA
Mangurten, HH
Stamos, J
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Lutheran Gen Childrens Hosp, Dept Pediat, Div Neonatol, Park Ridge, IL USALutheran Gen Childrens Hosp, Dept Pediat, Div Neonatol, Park Ridge, IL USA
Stamos, J
Angst, DB
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Lutheran Gen Childrens Hosp, Dept Pediat, Div Neonatol, Park Ridge, IL USALutheran Gen Childrens Hosp, Dept Pediat, Div Neonatol, Park Ridge, IL USA
Angst, DB
Schweig, LJ
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Lutheran Gen Childrens Hosp, Dept Pediat, Div Neonatol, Park Ridge, IL USALutheran Gen Childrens Hosp, Dept Pediat, Div Neonatol, Park Ridge, IL USA
机构:
Karolinska Inst, Dept Lab Med, Div Clin Microbiol, Stockholm, SwedenKarolinska Inst, Dept Lab Med, Div Clin Microbiol, Stockholm, Sweden
Ekwall-Larson, Anna
Yu, David
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Karolinska Inst, Dept Lab Med, Div Clin Microbiol, Stockholm, Sweden
Karolinska Univ Hosp, Funct Area Emergency Med, Stockholm, SwedenKarolinska Inst, Dept Lab Med, Div Clin Microbiol, Stockholm, Sweden
Yu, David
Dinnetz, Patrik
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Sodertorn Univ, Sch Nat Sci Technol & Environm Studies, Stockholm, SwedenKarolinska Inst, Dept Lab Med, Div Clin Microbiol, Stockholm, Sweden
Dinnetz, Patrik
Nordqvist, Hampus
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Stockholm South Hosp, Dept Infect Dis, Stockholm, SwedenKarolinska Inst, Dept Lab Med, Div Clin Microbiol, Stockholm, Sweden
Nordqvist, Hampus
Ozenci, Volkan
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Karolinska Inst, Dept Lab Med, Div Clin Microbiol, Stockholm, Sweden
Karolinska Univ Hosp, Dept Clin Microbiol, Stockholm, SwedenKarolinska Inst, Dept Lab Med, Div Clin Microbiol, Stockholm, Sweden