TY - JOUR
T1 - Establishing guidelines for pharmacotherapy trials in bulimia nervosa and anorexia nervosa
AU - Mitchell, James E.
AU - Tareen, Basir
AU - Sheehan, William
AU - Agras, Stewart
AU - Brewerton, Timothy D.
AU - Crow, Scott
AU - Devlin, Michael
AU - Eckert, Elke
AU - Halmi, Katherine
AU - Herzog, David
AU - Marcus, Marsha
AU - Powers, Pauline
AU - Stunkard, Albert
AU - Walsh, B. Timothy
PY - 2000
Y1 - 2000
N2 - Objective: This paper addresses the lack of a standard protocol for pharmacotherapy trials for patients with bulimia nervosa (BN) and anorexia nervosa (AN). Method: Twenty-two surveys were sent to established researchers in the field of eating disorders to elicit their opinions regarding medication trials, including baseline laboratory tests, the optimal length/frequency of medication management sessions, and the information that should or should not be included in these sessions. Results: Sixteen of 22 researchers completed and returned the survey. Their answers are the basis of the data presented. Discussion: We propose a battery of screening laboratory tests for both conditions. We suggest 30-45-min initial medication management sessions in both AN and BN trials with 15-min follow-ups to be held weekly for AN subjects, and weekly for 2 weeks, then biweekly for 2 weeks, then monthly, for BN subjects. We also recommend that published trials should include explicit details of medication management. (C) 2000 by John Wiley and Sons, Inc.
AB - Objective: This paper addresses the lack of a standard protocol for pharmacotherapy trials for patients with bulimia nervosa (BN) and anorexia nervosa (AN). Method: Twenty-two surveys were sent to established researchers in the field of eating disorders to elicit their opinions regarding medication trials, including baseline laboratory tests, the optimal length/frequency of medication management sessions, and the information that should or should not be included in these sessions. Results: Sixteen of 22 researchers completed and returned the survey. Their answers are the basis of the data presented. Discussion: We propose a battery of screening laboratory tests for both conditions. We suggest 30-45-min initial medication management sessions in both AN and BN trials with 15-min follow-ups to be held weekly for AN subjects, and weekly for 2 weeks, then biweekly for 2 weeks, then monthly, for BN subjects. We also recommend that published trials should include explicit details of medication management. (C) 2000 by John Wiley and Sons, Inc.
KW - Laboratory tests
KW - Medication management
KW - Pharmacotherapy trials
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U2 - 10.1002/(SICI)1098-108X(200007)28:1<1::AID-EAT1>3.0.CO;2-H
DO - 10.1002/(SICI)1098-108X(200007)28:1<1::AID-EAT1>3.0.CO;2-H
M3 - Article
C2 - 10800008
AN - SCOPUS:0034028181
SN - 0276-3478
VL - 28
SP - 1
EP - 7
JO - International Journal of Eating Disorders
JF - International Journal of Eating Disorders
IS - 1
ER -