Chen Hua, Kennedy William K, Dorfman Jeffrey H, Fincham Jack E, Reeves Jaxk, Martin Bradley C
Department of Clinical Sciences and Administration, University of Houston, Houston, TX, USA.
Curr Med Res Opin. 2007 Jun;23(6):1351-65. doi: 10.1185/030079907X187883. Epub 2007 May 1.
Prescribing adjunctive mood stabilizers to manage schizophrenia is prevalent, despite the lack of substantial evidence to support the long-term use of this treatment regimen.
The objective of this study was to assess the impact of using adjunctive mood stabilizers on antipsychotic utilization, total health expenditures, inpatient hospitalizations, long-term care stays, and emergency room (ER) visits for patients with schizophrenia.
Georgia Medicaid claims from 1999 through 2001 were analyzed to identify recipients diagnosed with schizophrenia (International Classification of Diseases, Ninth Revision, Clinical Modification [ICD-9-CM]: 295. XX). The treatment groups consisted of subjects who received combination therapy of mood stabilizers and antipsychotics (including both atypical and typical medications), while the comparison group consisted of subjects who were on antipsychotic medications without exposure to the mood stabilizers under investigation. Four treatment groups (valproate, lithium, carbamazepine, and combination mood stabilizer therapy) were formed based on the mood stabilizers patient received. Differences in annual health care use and expenditures were estimated between propensity score matched treatment and comparison groups controlling for comorbidity, prior utilization, demographic, and health provider specialty.
During the 1-year observation period, subjects in treatment groups filled an average of 200-days supply of adjunctive mood stabilizers. These adjunctive mood stabilizer recipients had significantly longer antipsychotic treatment durations than the subjects who did not have exposure to mood stabilizers (valproate + antipsychotic vs. antipsychotic only, net difference: 56.47 days, p < 0.0001; lithium + antipsychotic vs. antipsychotic only, net difference: 90.25 days, p < 0.0001; carbamazepine + antipsychotic vs. antipsychotic only, net difference: 41.27 days, p = 0.0439; multiple mood stabilizers + antipsychotic vs. antipsychotic only, net difference: 83.14 days, p < 0.0001). The intensive pharmacotherapy associated with treatment groups resulted in $900-$1300 higher pharmacy costs than the comparison groups (valproate + antipsychotic vs. antipsychotic only, net difference: $1218.43, p < 0.0001; lithium + antipsychotic vs. antipsychotic only, net difference: $985.79, p = 0.0015; carbamazepine + antipsychotic vs. antipsychotic only, net difference: $911.63, p = 0.0497; multiple mood stabilizers + antipsychotic vs. antipsychotic only, net difference: $1281.91, p < 0.0047). However, there were no statistically significant differences for total health expenditures, hospitalizations, emergency room visits, and nursing home admissions between propensity-matched treatment and control groups.
There were no differences in health care costs or utilization of ER, long-term care, and inpatient services between schizophrenia patients who did and did not receive adjunctive mood stabilizer; however, longer antipsychotic treatment durations were observed in patients receiving adjunctive mood stabilizers. Interpretation of these results is limited by the unknown selection bias between the treatment and the comparison groups and the relatively small number of patients in some treatment groups. The development of a better-controlled study to further evaluate this treatment regimen is warranted.
尽管缺乏充分证据支持长期使用这种治疗方案,但开具辅助情绪稳定剂来治疗精神分裂症的情况却很普遍。
本研究的目的是评估使用辅助情绪稳定剂对精神分裂症患者抗精神病药物使用、总医疗费用、住院治疗、长期护理住院时间以及急诊就诊的影响。
分析了1999年至2001年佐治亚州医疗补助索赔数据,以识别被诊断为精神分裂症的患者(国际疾病分类第九版临床修订本[ICD - 9 - CM]:295.XX)。治疗组由接受情绪稳定剂和抗精神病药物联合治疗的受试者组成(包括非典型和典型药物),而对照组由仅接受抗精神病药物治疗且未使用所研究情绪稳定剂的受试者组成。根据患者接受的情绪稳定剂形成了四个治疗组(丙戊酸盐、锂盐、卡马西平和联合情绪稳定剂治疗)。在控制合并症、既往使用情况、人口统计学和医疗服务提供者专业的倾向得分匹配治疗组和对照组之间,估计年度医疗保健使用和费用的差异。
在1年的观察期内,治疗组的受试者平均开具了200天用量的辅助情绪稳定剂。这些接受辅助情绪稳定剂治疗的受试者的抗精神病治疗持续时间明显长于未使用情绪稳定剂的受试者(丙戊酸盐 + 抗精神病药物组与仅使用抗精神病药物组相比,净差异:56.47天,p < 0.0001;锂盐 + 抗精神病药物组与仅使用抗精神病药物组相比,净差异:90.25天,p < 0.0001;卡马西平 + 抗精神病药物组与仅使用抗精神病药物组相比,净差异:41.27天,p = 0.0439;多种情绪稳定剂 + 抗精神病药物组与仅使用抗精神病药物组相比,净差异:83.14天,p < 0.0001)。与治疗组相关的强化药物治疗导致药房费用比对照组高出900 - 1300美元(丙戊酸盐 + 抗精神病药物组与仅使用抗精神病药物组相比,净差异:1218.43美元,p < 0.0001;锂盐 + 抗精神病药物组与仅使用抗精神病药物组相比,净差异:985.79美元,p = 0.0015;卡马西平 + 抗精神病药物组与仅使用抗精神病药物组相比,净差异:911.63美元,p = 0.0497;多种情绪稳定剂 + 抗精神病药物组与仅使用抗精神病药物组相比,净差异:1281.91美元,p < 0.0047)。然而,在倾向得分匹配的治疗组和对照组之间,总医疗费用、住院治疗、急诊就诊和疗养院入院方面没有统计学上的显著差异。
接受和未接受辅助情绪稳定剂治疗的精神分裂症患者在医疗费用或急诊、长期护理和住院服务的使用方面没有差异;然而,接受辅助情绪稳定剂治疗的患者观察到更长的抗精神病治疗持续时间。这些结果的解释受到治疗组和对照组之间未知选择偏倚以及一些治疗组中患者数量相对较少的限制。有必要开展一项控制更好的研究来进一步评估这种治疗方案。