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TRATAMIENTO DE LOS SÍNTOMAS MANÍACOS Y DEPRESIVOS EN EL TRASTORNO BIPOLAR I
Journal of Affective Disorders 366:136-145
Difundido en siicsalud: 7 nov 2024
IMPORTANCIA PREDICTIVA DE LA RESPUESTA TEMPRANA A CARIPRAZINA
Journal of Affective Disorders 362:197-200
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DOS AÑOS DESPUES DE LA APARICION DE LOS ANTIPSICOTICOS DE SEGUNDA GENERACION, "LA CANCION SIGUE SIENDO LA MISMA"

(especial para SIIC © Derechos reservados)
Si se considera indispensable tratar con antipsicóticos de segunda generación a los pacientes con trastorno bipolar, se debe preferir la olanzapina, a pesar de sus limitaciones en cuanto a seguridad, porque esta droga presenta el mayor número de estudios bien diseñados con resultados tranquilizadores en cuanto a su eficacia.
gentile9.jpg Autor:
Salvatore Gentile
Columnista Experto de SIIC

Institución:
Mental Health Center Nº 4


Artículos publicados por Salvatore Gentile
Recepción del artículo
19 de Diciembre, 2008
Aprobación
27 de Enero, 2009
Primera edición
16 de Junio, 2009
Segunda edición, ampliada y corregida
7 de Junio, 2021

Resumen
A pesar del entusiasmo creciente por el uso de los antipsicóticos de segunda generación (ASG) en pacientes bipolares, una revisión sistemática publicada en 2007 generó varias dudas sobre la efectividad de estos medicamentos, tanto para el tratamiento de episodios agudos como para la prevención de los cambios del estado de ánimo. Existe, por lo tanto, la necesidad de verificar si durante los dos últimos años se han realizado nuevos estudios que validen la inclusión de los ASG entre las opciones farmacológicas de primera línea para el tratamiento del trastorno bipolar. Sin embargo, desafortunadamente, los estudios más recientes resultaron inadecuados cualtitava y cuantitativamente para aminorar las dudas sobre la seguridad y eficacia de los ASG en esos pacientes. Por esta razón, en la actualidad, los ASG deberían considerarse agentes de cuarta línea en todas las diferentes fases que caracterizan el curso fluctuante de este trastorno. De hecho, el uso de estos fármacos debería sólo considerarse en el caso de que los estabilizadores del estado de ánimo, los anticonvulsivos, los antidepresivos o los antipsicóticos de primera generación (APG) fallaran. Si a pesar de ello los clínicos insisten que es indispensable el tratamiento de estos pacientes con ASG, se debería preferir a la olanzapina, a pesar de sus limitaciones en cuanto a seguridad, porque esta droga presenta el mayor número de estudios bien diseñados con resultados tranquilizadores en cuanto a su eficacia.

Palabras clave
neurolépticos, antipsicóticos atípicos/segunda generación, risperidona, quetiapina, olanzapina, ziprasidona, aripiprazol, trastorno afectivo/bipolar, manía, depresión, efectividad, seguridad, eficacia, tasa de interrupción


Artículo completo

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Abstract
Despite the growing enthusiasm for the effective use of second-generation antipsychotics (SGAs) in bipolar patients, a systematic review article published in 2007 raised several concerns about the effectiveness of such medications both for treating acute mood episodes and/or for preventing mood changes. Hence, the necessity exists to verify if, during the last two years, there have been new studies which could fully validate the inclusion of SGAs among the first-line pharmacological options for treating bipolar disorder. Unfortunately, however, the most recent studies were quantitatively and qualitatively inadequate to attenuate doubts about the safe and effective use of SGAs in such patients. For this reason, until now SGAs should be considered as fourth-line agents in all various phases characterizing the fluctuating course of the disorder. Indeed, the use of such medications should be taken into consideration only in the case of failure of therapy with classic mood stabilizing, anticonvulsivant, antidepressant agents, and/or first-generation antipsychotics (FGAs). Nonetheless, if clinicians deem it indispensable to treat these patients with SGA-therapy, olanzapine should still be preferred despite its safety limitations, because the drug continues to show the highest number of well-designed studies with reassuring efficacy findings.

Key words
neuroleptics, atypical/second-generation antipsychotics, risperidone, quetiapine, olanzapine, quetiapine, ziprasidone, aripiprazole, affective/bipolar disorder, mania, depression, effectiveness, safety, efficacy, discontinuation rate


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Especialidades
Principal: Salud Mental
Relacionadas: Bioética, Farmacología, Medicina Farmacéutica



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Enviar correspondencia a:
Salvatore Gentile, Mental Health Center Nº 4 Asl Salerno 1 Department of Mental Health, 84013, Piazza Galdi - Cava de'Tirreni, Salerno, Italia
Patrocinio y reconocimiento:
El Dr. Gentile ha recibido honorarios como conferencista/consultor de Boehringer Ingelheim y Eli Lilly Italia SpA. Durante los últimos cinco años, el también recibió fondos para viajes de Bristol-Myers Squibb, Eli Lilly, Lundbeck y Novartis. No ha recibido apoyo financiero para este estudio.
Bibliografía del artículo

1. Zyprexa (olanzapine) tablets and Zyprexa Zydis (olanzapine) orally disintegrating tablets [prescribing information]. Indianapolis, Ind: Eli Lilly and Company, 2004.
2. Abilify (aripiprazole) tablets and oral solution [prescribing information]. Princeton, NJ, and Rockville, Md: Bristol-Myers Squibb Company and Otsuka Amarica Pharmaceutical, Inc, 2005.
3. Department of Health & Human Services. Public Health Service. Food and Drug Administration. Supplemental new drug (Seroquel®) application. Rockville, October 20, 2006.
4. Bret MC, Bret P, Pariente A, Fourier-Réglat A. The use of atypical antipsychotics in French psychiatric hospitals. Pharm World Sci 29(5):551-6, 2007.
5. Woo YS, Bahk WM, Min KJ, et al. Medication prescription pattern for outpatients with bipolar disorder: focusing on atypical antipsychotics. Korean J Psychopharmacol 17(6):538-49, 2006.
6. Cooper WO, Arbogast PG, Hickson GB, Fuchs C, Ray WA. Trends in prescribing of antipsychotic medications for US children. Amb Pediatr 6:79-83, 2006.
7. Gentile S. Atypical antipsychotic for the treatment of bipolar disorder. More shadows than lights. CNS Drugs 21(5):367-87, 2007.
8. Bekelman JE, Li Y, Gross CP. Scope and impact of financial conflicts of interest in biomedical research: a systematic review. JAMA 289(4):454-65, 2003.
9. Boyd EA, Cho MK, Bero LA. Financial conflict-of-interest policies in clinical research: issues for clinical investigators. Acad Med 78(8):769-74, 2003.
10. Gentile S. Long term atypical antipsychotics treatment and risk of weight gain. A literature analysis. Drug Saf 29(4):303-19, 2006.
11. Rendell JM, Gijsman HJ, Keck P, Goodwin GM, Geddes JR. Risperidone alone or in combination for acute mania. Cochrane Database Syst Rev (1):CD004043, 2006.
12. Gentile S. Extrapyramidal adverse events associated with atypical antipsychotic treatment of bipolar disorder. J Clin Psychopharmacol 27(1):35-45, 2007.
13. Patel NC, Crismon ML, Pondrom M. Rehospitalization rates of patients with bipolar disorder discharged on a mood stabilizer versus a mood stabilizer plus an atypical or typical antipsychotic. J Behav Health Serv Res 32(4):438-45, 2005.
14. Keck PE Jr, Calabrese JR, McQuade RD, Carson WH, Carlson BX, Rollin LM, for the Aripiprazole Study Group. A randomized, double-blind, placebo-controlled 26-week trial of aripiprazole in recently manic patients with bipolar I disorder. J Clin Psychiatry 67:626-37, 2006.
15. Keck PE Jr, Calabrese JR, McIntyre RS, McQuade RD, Carson WH, Eudicone JM, et al., for the Aripiprazole Study Group. Aripiprazole monotherapy for maintenance therapy in bipolar I disorder: a 100-week, double-blind study versus placebo. J Clin Psychiatry 68:1480-91, 2007.
16. Keck PE, McElroy SL. Aripiprazole: a partial dopamine D2 receptor agonist antipsychotic. Expert Opin Invest Drugs 12:655-62, 2003.
17. Muzina DJ, Momah C, Eudicone JM, et al. Aripiprazole monotherapy in patients with rapid-cycling bipolar I disorder: an analysis from a long-term, double-blind, placebo-controlled study. Int J Clin Pract 62(5):679-87, 2008.
18. Suppes T, Eudicone J, McQuade R, Pikalov III A, Carlson B. Efficacy and safety of aripiprazole in subpopulations of patients with acute or mixed episodes. J Affect Disord 107:145-54, 2008.
19. Sachs G, Sanchez R, Marcus R, Stock E, McQuade R, Carson W, et al., for the Aripiprazole Study Group. Aripiprazole in the treatment of acute manic or mixed episodes in patients with bipolar I disorder: a 3-week, placebo-controlled study. J Psychopharm 20:536-46, 2006.
20. Keck Jr. PE, Marcus R, Tourkodimitris S, Ali M, Liebeskind A, Saha S, Ingenito G, and Aripiprazole Study Group. A placebo-controlled, double-blind study of the efficacy and safety of aripiprazole in patients with acute bipolar mania. Am J Psychiatry 160:1651-8, 2003.
21. Zimbroff DL, Marcus RN, Manos G, Stock E, McQuade RD, Auby P, et al. Management of acute agitation in patients with bipolar disorder. Efficacy and safety of intramuscolar aripiprazole. J Clin Psychopharm 27(2):171-6, 2007.
22. Young AH, Oren DA, Lowy A, McQuade RD, Marcus RN, Carson WH, et al. Aripiprazole monotherapy in acute mania: 12-week randomized placebo- and haloperidol-controlled study. Br J Psychiatry 194:40-8, 2009.
23. Thase ME, Jonas A, Khan A, Bowden CL, Wu X, McQuade RD, et al. Aripiprazole monotherapy in non-psychotic bipolar I depression. Results of 2 randomized, placebo-controlled studies. J Clin Psychopharmacol 28(1):13-20, 2008.
24. Niufan G, Tohen M, Qiuqing A, Fude Y, Pope E, McElroy H, et al. Olanzapine versus lithium in the acute treatment of bipolar mania: a double-blind, randomized, controlled trial. J Affect Disord 105:101-8, 2008.
25. Tohen M, Vieta E, Goodwin GM, Sun B, Amsterdam JD, Banov M, et al. Olanzapine versus divalproex versus placebo in the treatment of mild to moderate mania: a randomized, 12-week, double-blind study. J Clin Psychiatry, published online ahead of print: October 7 e1-e14 (pii:ej07m03788), 2008.
26. Moreno RA, Hanna MM, Tavares SM, Wang YP. A double-blind comparison of the effect of the antipsychotics haloperidol and oanzapine on sleep in mania. Braz J Med Biol Res 40:357-66, 2007.
27. Tamayo JM, Mazzotti G, Tohen M, Gattaz WF, Zapata R, Castillo JJ, et al. Outcomes for Latin American versus White patients suffering from acute mania in a randomized, double-blind trial comparing olanzapine and haloperidol. J Clin Psychopharmacol 27(2):126-34, 2007.
28. Tohen M, Bowden CL, Smulevich AB, Bergstrom R, Quinlan T, Osuntokun O, et al. Combination of olanzapine and carbamazepine compared with carbamazepine alone in treating manic episodes. Br J Psychiatry 192:1-9, 2008.
29. Maina G, Albert U, Salvi V, Mancini M, Bogetto F. Valproate or olanzapine add-on to lithium: an 8-week, randomized, open-label study on Italian patients with a manic relapse. J Affect Disord 99:247-51, 2007.
30. Maina G, Albert U, Rosso G, Bogetto F. Olanzapine or lamotrigine addition to lithium in remitted bipolar disorder patients with anxiety disorder comorbidity: a randomized, single-blind, pilot study. J Clin Psychiatry 69:609-16, 2008.
31. Ling H, Ma C, Wang G, Zhu X, Peng M, Gu N. Response and remission rates in Chinese patients with bipolar mania treated for 4 weeks with either quetiapine or lithium: a randomized and double-blind study. Curr Med Res Opin 24(1):1-10, 2008.
32. Severus WE, Kleindienst N, Seemüller F, Frangou S, Möller S, Greil W. What is the optimal serum lithium level in the long-term treatment of bipolar disorder? A review. Bipolar Disord 10(2):231-7, 2008.
33. Langosch JM, Drieling T, Biedermann NC, et al. Efficacy of quetiapine monotherapy in rapid-cycling bipolar disorder in comparison with sodium valproate. J Clin Psychopharm 28(5):555-60, 2008.
34. Endicott J, Rajagopalan K, Minkwitz M, Macfadden W, for the BOLDER study group. A randomized, double-blind, placebo-controlled study of quetiapine in the treatment of bipolar I and II depression: improvement in quality of life. Int J Psychopharmacol 22(1):29-37, 2007.
35. Calabrese JR, Keck PE, Macfadden W, Minkwitz M, Ketter TA, Weisler RH, et al. A randomized, double-blind, placebo-controlled trial of quetiapine in the treatment of bipolar I or II depression. Am J Psychiatry 162:1351-60, 2005.
36. Gentile S. A systematic review of quality of life and weight gain related issues in patients treated for severe and persistent mental disorders: focus on aripiprazole. Neuropsychiatr Dis Treat, in press.
37. Suppes T, Hirschfeld RM, Vieta E, Raines S, Paulsson B. Quetiapine for the treatment of bipolar II depression: analysis of data from two randomized, double-blind, placebo-controlled studies. World J Biol Psychiatry 9(3):198-211, 2008.
38. Harvey PD, Hassman H, Mao L, Gharabawi GM, Mahmoud RA, Engelhart LM. Cognitive functioning and acute sedative effects of risperidone and quetiapine in patients with stable bipolar I disorder: a randomised, double-blind, crossover study. J Clin Psychiatry 68:1186-94, 2007.
39. Sheehan DV, McElroy SL, Harnett-Sheehan K, et al. Randomized, placebo-controlled trial of risperidone for acute treatment of bipolar anxiety. J Aff Disord, in press.
40. Yatham LN, Fallu A, Binder CE. A 6-month randomized open-label comparison of continuation of oral antipsychotic therapy or switch to long acting injectable risperidone in patients with bipolar disorder. Acta Psychiatr Scand 116(Suppl. 434):30-56, 2007.
41. Mech AV. High-dose ziprasidone monotherapy in bipolar I disorder patients with depressed or mixed episodes. J Clin Psychopharm 28(2):240-1, 2008.
42. Vieta E, Sanchez-Moreno J. Acute and long-term treatment of mania Dialogues Clin Neurosci 10(2):165-79, 2008.
43. Keating GM, Robinson DM. Spotlight on quetiapine in bipolar depression. CNS Drugs 21(8):695-7, 2007.
44. Tohen M, Vieta E, Calabrese J, Ketter TA, Sachs G, Bowden C, et al. Efficacy of olanzapine and olanzapine-fluoxetine combination in the treatment of bipolar I depression. Arch Gen Psychiatry 60:1079-1088, 2003.
45. Amsterdam JD, Shults J. Comparison of fluoxetine, olanzapine, and combined fluoxetine plus olanzapine initial therapy of bipolar I and type II major depression - lack of manic induction. J Affect Dis 87:121-130, 2005.
46. Gentile S. Antipsychotic-associated weight gain. Ann Pharmacother 38(5):903-4, 2004.
47. Soares-Weiser K, Bravo Vergel Y, Beynon S, et al. A systematic review and economic model of the clinical effectiveness and cost-effectiveness of interventions for preventing relapse in people with bipolar disorder. Health Technol Assess 11(39):iii-iv, ix-206, 2007.
48. Led Zeppelin. The House of the Holy: The Song Remains the Same. Available from URL: http://discography.ledzeppelin.com/disc_hoth.html. Accessed: 15 December 2008.

 
 
 
 
 
 
 
 
 
 
 
 
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