TY - JOUR
T1 - Higher hemoglobin is associated with improved outcome after subarachnoid hemorrhage
AU - Naidech, Andrew M.
AU - Jovanovic, Borko
AU - Wartenberg, Katja E.
AU - Parra, Augusto
AU - Ostapkovich, Noeleen
AU - Connolly, E. Sander
AU - Mayer, Stephan A.
AU - Commichau, Christopher
PY - 2007/10
Y1 - 2007/10
N2 - OBJECTIVE: There are few data regarding anemia and transfusion after subarachnoid hemorrhage (SAH). We addressed the hypothesis that higher hemoglobin (HGB) levels are associated with less death and disability after SAH. DESIGN: Prospective registry with automated data retrieval. PATIENTS: Six hundred eleven patients enrolled in the Columbia University SAH Outcomes Project between August 1996 and June 2002. SETTING: Neurologic intensive care unit. INTERVENTIONS: Patients were treated according to standard management protocols. MEASUREMENTS AND MAIN RESULTS: We electronically retrieved all HGB readings during the acute hospital stay for 611 consecutively admitted SAH patients. Outcomes were measured with the modified Rankin Scale at 14 days or discharge, and at 3 months. Patients who were independent (modified Rankin Scale, 0-3) at discharge or 14 days had higher mean (11.7 ± 1.5 vs. 10.9 ± 1.2, p < .001) and nadir (9.9 ± 2.1 vs. 8.6 ± 1.8, p < .001) HGB, and had higher HGB values every day in the hospital. There were similar results when patients were stratified by mortality. Higher HGB was associated with reduced risk of poor outcome (modified Rankin Scale, 4-6) at 14 days/discharge and 3 months after correcting for Hunt and Hess grade, age, history of diabetes, and cerebral infarction. Length of stay and HGB interacted such that lower HGB has a more pronounced effect with length of stay > 14 days. CONCLUSIONS: Higher HGB values are associated with improved outcomes after SAH at 14 days/discharge and 3 months. In contrast to general critical care patients, SAH patients may benefit from higher HGB. Determination of the optimal goal HGB after SAH will require separate prospective research.
AB - OBJECTIVE: There are few data regarding anemia and transfusion after subarachnoid hemorrhage (SAH). We addressed the hypothesis that higher hemoglobin (HGB) levels are associated with less death and disability after SAH. DESIGN: Prospective registry with automated data retrieval. PATIENTS: Six hundred eleven patients enrolled in the Columbia University SAH Outcomes Project between August 1996 and June 2002. SETTING: Neurologic intensive care unit. INTERVENTIONS: Patients were treated according to standard management protocols. MEASUREMENTS AND MAIN RESULTS: We electronically retrieved all HGB readings during the acute hospital stay for 611 consecutively admitted SAH patients. Outcomes were measured with the modified Rankin Scale at 14 days or discharge, and at 3 months. Patients who were independent (modified Rankin Scale, 0-3) at discharge or 14 days had higher mean (11.7 ± 1.5 vs. 10.9 ± 1.2, p < .001) and nadir (9.9 ± 2.1 vs. 8.6 ± 1.8, p < .001) HGB, and had higher HGB values every day in the hospital. There were similar results when patients were stratified by mortality. Higher HGB was associated with reduced risk of poor outcome (modified Rankin Scale, 4-6) at 14 days/discharge and 3 months after correcting for Hunt and Hess grade, age, history of diabetes, and cerebral infarction. Length of stay and HGB interacted such that lower HGB has a more pronounced effect with length of stay > 14 days. CONCLUSIONS: Higher HGB values are associated with improved outcomes after SAH at 14 days/discharge and 3 months. In contrast to general critical care patients, SAH patients may benefit from higher HGB. Determination of the optimal goal HGB after SAH will require separate prospective research.
KW - Anemia
KW - Cerebrovascular disorders
KW - Disability
KW - Outcomes
KW - Subarachnoid hemorrhage
KW - Transfusion
UR - http://www.scopus.com/inward/record.url?scp=34748859202&partnerID=8YFLogxK
U2 - 10.1097/01.CCM.0000284516.17580.2C
DO - 10.1097/01.CCM.0000284516.17580.2C
M3 - Article
C2 - 17717494
AN - SCOPUS:34748859202
SN - 0090-3493
VL - 35
SP - 2383
EP - 2389
JO - Critical Care Medicine
JF - Critical Care Medicine
IS - 10
ER -