TY - JOUR
T1 - International normalized ratio increase before warfarin-associated hemorrhage
T2 - Brief and subtle
AU - Kucher, Nils
AU - Connolly, Shannon
AU - Beckman, Joshua A.
AU - Lay, Har Cheng
AU - Tsilimingras, Kanella V.
AU - Fanikos, John
AU - Goldhaber, Samuel Z.
PY - 2004/10/25
Y1 - 2004/10/25
N2 - Objective: To determine the relationship between serial international normalized ratios (INRs) in patients who have been undergoing long-term anticoagulation and the onset of warfarin-associated bleeding complications. Methods: The study cohort consisted of 2391 patients treated in the Anticoagulation Service at Brigham and Women's Hospital, Boston, Mass, from April 1999 through July 2003. For each patient with a bleeding event, we selected 2 controls who were matched for age, sex, indication for warfarin therapy, and duration of enrollment in our Anticoagulation Service. Results: Warfarin-related hemorrhage occurred in 32 patients (1.3%). The mean ± SD INRs at the time of the bleeding event or matched patient's event date (5.9 ± 5.9 vs 2.3 ± 0.7; P<.001) and the mean±SD last INRs before the bleeding event or matched patient's event date (3.0 ± 1.2 vs 2.1 ± 0.8; P<.001) were higher in the patients than in the controls. The last INRs before the bleeding event were obtained an average of 11.6 ± 17.8 (mean ± SD) days before the event in the patients and 18.3 ± 28.0 (mean ± SD) days before the matched date in the controls (P = .22). The mean second-to-last INRs were similar in both groups (2.8 ± 2.1 vs 2.3 ± 0.8; P = .11). When the INRs were plotted in relation to the time before the onset of bleeding, a marked increase in the patients' INRs was observed shortly before the bleeding began. Cenclualoiu: Serial INRs are poor predictors of hemorrhagic events. There appears to be only a brief warning period during which a slightly elevated INR predicts an imminent bleeding event.
AB - Objective: To determine the relationship between serial international normalized ratios (INRs) in patients who have been undergoing long-term anticoagulation and the onset of warfarin-associated bleeding complications. Methods: The study cohort consisted of 2391 patients treated in the Anticoagulation Service at Brigham and Women's Hospital, Boston, Mass, from April 1999 through July 2003. For each patient with a bleeding event, we selected 2 controls who were matched for age, sex, indication for warfarin therapy, and duration of enrollment in our Anticoagulation Service. Results: Warfarin-related hemorrhage occurred in 32 patients (1.3%). The mean ± SD INRs at the time of the bleeding event or matched patient's event date (5.9 ± 5.9 vs 2.3 ± 0.7; P<.001) and the mean±SD last INRs before the bleeding event or matched patient's event date (3.0 ± 1.2 vs 2.1 ± 0.8; P<.001) were higher in the patients than in the controls. The last INRs before the bleeding event were obtained an average of 11.6 ± 17.8 (mean ± SD) days before the event in the patients and 18.3 ± 28.0 (mean ± SD) days before the matched date in the controls (P = .22). The mean second-to-last INRs were similar in both groups (2.8 ± 2.1 vs 2.3 ± 0.8; P = .11). When the INRs were plotted in relation to the time before the onset of bleeding, a marked increase in the patients' INRs was observed shortly before the bleeding began. Cenclualoiu: Serial INRs are poor predictors of hemorrhagic events. There appears to be only a brief warning period during which a slightly elevated INR predicts an imminent bleeding event.
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U2 - 10.1001/archinte.164.19.2176
DO - 10.1001/archinte.164.19.2176
M3 - Article
C2 - 15505133
AN - SCOPUS:6944233685
SN - 2168-6106
VL - 164
SP - 2176
EP - 2179
JO - Archives of internal medicine (Chicago, Ill. : 1908)
JF - Archives of internal medicine (Chicago, Ill. : 1908)
IS - 19
ER -