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Adjunct Aripiprazole Reduces Prolactin and Prolactin-Related Adverse Effects in Premenopausal Women With Psychosis: Results From the DAAMSEL Clinical Trial.
Kelly, Deanna L; Powell, Megan M; Wehring, Heidi J; Sayer, MacKenzie A; Kearns, Ann Marie; Hackman, Ann L; Buchanan, Robert W; Nichols, Rebecca B; Adams, Heather A; Richardson, Charles M; Vyas, Gopal; McMahon, Robert P; Earl, Amber K; Sullivan, Kelli M; Liu, Fang; Luttrell, Sarah E; Dickerson, Faith B; Feldman, Stephanie M; Narang, Supriya; Koola, Maju M; Buckley, Peter F; RachBeisel, Jill A; McEvoy, Joseph P.
Afiliação
  • Powell MM; Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD.
  • Wehring HJ; Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD.
  • Sayer MA; Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD.
  • Kearns AM; Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD.
  • Hackman AL; Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD.
  • Buchanan RW; Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD.
  • Nichols RB; Department of Psychiatry, Georgia Regents University, Augusta, GA.
  • Adams HA; Spring Grove Hospital Center and Maryland Psychiatric Research Center, Department of Psychiatry, University of Maryland School of Medicine.
  • Richardson CM; Spring Grove Hospital Center and Maryland Psychiatric Research Center, Department of Psychiatry, University of Maryland School of Medicine.
  • Vyas G; Spring Grove Hospital Center and Maryland Psychiatric Research Center, Department of Psychiatry, University of Maryland School of Medicine.
  • McMahon RP; Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD.
  • Earl AK; MS Thread, Inc, Baltimore, MD.
  • Sullivan KM; Cystic Fibrosis/Pulmonary Research and Treatment Center, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Liu F; Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD.
  • Luttrell SE; Department of Pharmacy, University of Maryland Eastern Shore School of Pharmacy, Princess Anne, MD.
  • Dickerson FB; Department of Psychology and.
  • Feldman SM; Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD.
  • Narang S; Mosaic Community Services, Sheppard Pratt Health System, Baltimore, MD.
  • Koola MM; Department of Psychiatry and Behavioral Sciences, George Washington University School of Medicine and Health Sciences, Washington, DC.
  • Buckley PF; Department of Psychiatry, Virginia Commonwealth University School of Medicine, Richmond, VA.
  • RachBeisel JA; Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD.
  • McEvoy JP; Department of Psychiatry, Georgia Regents University, Augusta, GA.
J Clin Psychopharmacol ; 38(4): 317-326, 2018 Aug.
Article em En | MEDLINE | ID: mdl-29912799
ABSTRACT
PURPOSE/

BACKGROUND:

Prolactin-related adverse effects contribute to nonadherence and adverse health consequences, particularly in women with severe mental illness. Treating these adverse effects may improve treatment acceptability, adherence, and long-term outcomes. METHODS/PROCEDURES Premenopausal women with a Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision diagnosis of schizophrenia, schizoaffective disorder, or bipolar disorder were recruited for a randomized, double-blind, placebo-controlled 16-week trial of adjunct aripiprazole (5-15 mg/d). Participants had elevated prolactin (>24 ng/mL) and were experiencing galactorrhea, amenorrhea, oligomenorrhea, or sexual dysfunction on a prolactin-elevating antipsychotic. Participants were evaluated biweekly for prolactin elevation and galactorrhea and completed a menstrual diary review. Psychiatric symptoms and adverse effects were closely monitored. FINDINGS/

RESULTS:

Forty-six women were randomized (n = 25 aripiprazole, n = 21 placebo). Thirty-seven completed at least 8 weeks of the study (n = 20 [80%] aripiprazole and n = 17 [81%] placebo). Aripiprazole (mean dose, 11.7 ± 2.4 mg/d) was effective for lowering prolactin relative to placebo (P = 0.04). In addition, 45% (9/20) of the aripiprazole group had a normalized prolactin (<24 mg/mL) compared with 12% (2/17) of the placebo group (P = 0.028). Galactorrhea resolved in 77% (10/13) of the aripiprazole-treated participants compared with 33% (4/12) in the placebo group (P = 0.028). Normalization of sexual function (<16 on the Arizona Sexual Experience Scale) occurred in 50% on aripiprazole (7/14) versus 9% (1/11) on placebo (P = 0.030). No differences between groups in symptoms or adverse effects were noted. Overall, women rated a mean score of 4.6 ± 0.6 on a 5-point Likert scale for sexual function improvement, suggesting their particular satisfaction with improvement in this domain. IMPLICATIONS/

CONCLUSIONS:

Building upon prior studies, this rigorous evaluation confirms the utility of adjunctive aripiprazole as a strategy for improving prolactin and managing prolactin-related adverse effects in premenopausal women with psychosis.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Prolactina / Transtornos Psicóticos / Antipsicóticos / Pré-Menopausa / Quimioterapia Combinada / Aripiprazol Tipo de estudo: Clinical_trials / Guideline Limite: Adult / Female / Humans Idioma: En Revista: J Clin Psychopharmacol Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Prolactina / Transtornos Psicóticos / Antipsicóticos / Pré-Menopausa / Quimioterapia Combinada / Aripiprazol Tipo de estudo: Clinical_trials / Guideline Limite: Adult / Female / Humans Idioma: En Revista: J Clin Psychopharmacol Ano de publicação: 2018 Tipo de documento: Article