Comparison of Cox and Gray's survival models in severe sepsis

被引:28
作者
Kasal, J [1 ]
Jovanovic, Z
Clermont, G
Weissfeld, LA
Kaplan, V
Watson, S
Angus, DC
机构
[1] Univ Pittsburgh, CRISMA Lab, Dept Crit Care Med, Grad Sch Publ Hlth, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Dept Biostat, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Dept Hlth Policy & Management, Pittsburgh, PA 15261 USA
[4] Cumberland Med Ctr, Dept Crit Care Med Internal Med, Crossville, TN USA
[5] Univ Copenhagen, Inst Publ Hlth, Copenhagen, Denmark
[6] Univ Hosp, Dept Internal Med, Zurich, Switzerland
关键词
sepsis; sepsis syndrome; patient outcome assessment; survival analysis; proportional hazards models; Cox model; Gray's model;
D O I
10.1097/01.CCM.0000114819.37569.4B
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: Although survival is traditionally modeled using Cox proportional hazards modeling, this approach may be inappropriate in sepsis, in which the proportional hazards assumption does not hold. Newer, more flexible models, such as Gray's model, may be more appropriate. Objectives. To construct and compare Gray's model and two different Cox models in a large sepsis cohort. To determine whether hazards for death after sepsis were nonproportional. To explore how well the different survival modeling approaches describe these data. Design: Analysis of combined data from the treatment and placebo arms of a large, negative, sepsis trial. Setting., Intensive care units at 136 U.S. medical centers. Subjects. A total of 1090 adults aged 18 yrs or older with signs and symptoms of severe sepsis and documented or probable Gram-negative infection. Measurements. We considered 27 potential baseline risk factors and modeled survival over the 28 days after the onset of sepsis. We tested proportionality in single-variable Cox analysis using Schoenfeld residuals and log-log plots. We constructed a traditional multivariable Cox model, a multivariable Cox model with time-varying covariates, and a multivariable Gray's model. Results. In single-variable analyses, 20 of the 27 potential factors were significantly associated with mortality, and 10 of 20 had nonproportional hazards. In multivariate analysis, all three models retained a very similar set of significant covariates (two models retained the identical set of nine variables, and the third differed only in that it retained the same nine plus a tenth variable). Four of the nine common covariates had nonproportional hazards. Of the three models, Gray's model best captured these changing hazard ratios over time. Conclusion. We confirm that many of the important predictors of mortality in severe sepsis are nonproportional and find that Gray's model seems best suited for modeling survival in this condition.
引用
收藏
页码:700 / 707
页数:8
相关论文
共 20 条
[1]   E5 murine monoclonal antiendotoxin antibody in gram-negative sepsis - A randomized controlled trial [J].
Angus, DC ;
Birmingham, MC ;
Balk, RA ;
Scannon, PJ ;
Collins, D ;
Kruse, JA ;
Graham, DR ;
Dedhia, HV ;
Homann, S ;
MacIntyre, N .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 283 (13) :1723-1730
[2]   Surviving intensive care: a report from the 2002 Brussels Roundtable [J].
Angus, DC ;
Carlet, J .
INTENSIVE CARE MEDICINE, 2003, 29 (03) :368-377
[3]  
Angus DC, 2002, AM J RESP CRIT CARE, V165, P540
[4]   HOW BAD ARE BACTEREMIA AND SEPSIS - OUTCOMES IN A COHORT WITH SUSPECTED BACTEREMIA [J].
BATES, DW ;
PRUESS, KE ;
LEE, TH .
ARCHIVES OF INTERNAL MEDICINE, 1995, 155 (06) :593-598
[5]   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 .
CHEST, 1992, 101 (06) :1644-1655
[6]  
Bourdais-Mannone C, 1999, J Epidemiol Biostat, V4, P83
[7]   INCIDENCE, RISK-FACTORS, AND OUTCOME OF SEVERE SEPSIS AND SEPTIC SHOCK IN ADULTS - A MULTICENTER PROSPECTIVE-STUDY IN INTENSIVE-CARE UNITS [J].
BRUNBUISSON, C ;
DOYON, F ;
CARLET, J ;
DELLAMONICA, P ;
GOUIN, F ;
LEPOUTRE, A ;
MERCIER, JC ;
OFFENSTADT, G ;
REGNIER, B .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1995, 274 (12) :968-974
[8]   Bacteremia and severe sepsis in adults: A multicenter prospective survey in ICUs and wards of 24 hospitals [J].
BrunBuisson, C ;
Doyon, F ;
Carlet, J ;
Bedock, B ;
Annonay, CH ;
Valente, E ;
Lescale, O ;
Misset, B ;
Charbonneau, P ;
Vergnaud, M ;
Cohen, R ;
Coloignier, M ;
Frances, JL ;
Combes, A ;
Duval, O ;
Dellamonica, P ;
Descamps, JM ;
Domart, Y ;
Galiacy, JL ;
Gouin, F ;
Guivarch, G ;
Hennequin, C ;
Krajevitch, A ;
Delmas, P ;
Holzapfel, L ;
Lepeu, G ;
Loirat, P ;
Thaler, F ;
Knani, L ;
Mercier, JC ;
Mouton, Y ;
Libbrecht, E ;
Offenstadt, G ;
Pinaud, M ;
Pinsart, M ;
Girou, E ;
Portier, H ;
Grappin, M ;
Rebeix, MT ;
Regnier, B ;
Gachot, B ;
Ricome, JL ;
Sollet, JP ;
Mentec, H ;
Tempelhoff, G ;
Beuret, P ;
Lepoutre, A .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 154 (03) :617-624
[9]   New strategies for clinical trials in patients with sepsis and septic shock [J].
Cohen, J ;
Guyatt, G ;
Bernard, GR ;
Calandra, T ;
Cook, D ;
Elbourne, D ;
Marshall, J ;
Nunn, A ;
Opal, S .
CRITICAL CARE MEDICINE, 2001, 29 (04) :880-886
[10]  
COX DR, 1972, J R STAT SOC B, V34, P187