评估根据不同治疗方案提供的综合康复计划对减少脑外伤后脑内血肿神经外科手术后 10 年患者的慢性额叶综合征的效果

IF 1 Q4 PSYCHOLOGY
Rafał Morga, Jolanta Góral-Półrola, M. Pąchalska
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引用次数: 0

摘要

这项研究旨在评估根据不同治疗方案提供的综合康复计划(CPReh)在减少脑内血肿神经外科手术后10年患者慢性额叶综合征方面的效果。克拉科夫市的雅盖隆大学医学院神经外科和神经创伤学系在2004年至2010年间对568名成年车祸患者进行了脑内血肿创伤后神经外科手术,其中90名患者患有OFC损伤和慢性额叶综合征。患者被分为 A、B 和 C 三组,每组 30 人,年龄、性别和损伤严重程度均匹配。综合康复计划(CPReh)(参见 Pąchalska 2008)适用于因脑内血肿住院和手术治疗十年后的所有组别,并按照三个治疗方案进行:方案 1 在 A 组实施,结合认知训练(CT)和 "生命学院 "计划,每周实施两次。方案 2 在 B 组实施,包括 CT 和 "生命学院 "课程,也是每周两次,但标准持续时间为一年左右(平均 12 个月,1.03 个月)。- 方案 3 在 C 组实施,包括 CT 和 "社区基础治疗 "计划,同样每周实施两次,标准持续时间约为一年(平均 12 个月 1.27):研究 I(基线,术后 10 年随访)--在康复治疗开始之前;研究 II(随访)--在康复治疗结束后,按照所有方案进行。FBInv 测试的所有或大部分阳性或阴性症状,包括神经、认知、情绪和行为症状。与采用方案 2 或方案 3 实施的标准 CPReh 方案相比,采用方案 1 实施的改良 CPReh 方案(其中结合了认知训练(CT)和 "生命学院 "方案,每周两次,但只要患者有能力并愿意继续,该方案就会继续实施)能更有效地减少这些症状,而采用方案 2 或方案 3 实施的标准 CPReh 方案只能作为标准实施一年。研究还发现,与社区基础治疗相比,"生活学院 "计划也被证明是 CPReh 更为有效的组成部分。A 组所取得的改善是,对于 B 组和 C 组的患者而言,与标准的 CPReh 方案 2 和方案 3 相比,修改后的 CPReh 方案 1 在减轻慢性额叶综合征方面更为有效,该方案为患者提供了继续康复的机会,只要患者有能力并愿意继续。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EVALUATION OF THE EFFECTIVENESS OF A COMPREHENSIVE PROGRAM OF REHABILITATION OFFERED ACCORDING TO DIFFERENT THERAPEUTIC PROTOCOLS IN REDUCING CHRONIC FRONTAL SYNDROME IN PATIENTS 10-YEARS FOLLOWING NEUROSURGERY FOR POST-TRAUMATIC INTRACEREBRAL HEMATOMA
The aim of the study was to evaluate the effectiveness of a Comprehensive Program of Rehabilitation (CPReh) offered according to different therapeutic protocols in reducing chronic frontal syndrome in patients 10 years following neurosurgery for post-traumatic intracerebral hematoma.Out of 568 adult car accident patients who underwent neurosurgery for post-traumatic intracerebral hematoma between 2004 and 2010 at the Department of Neurosurgery and Neurotraumatology of the Jagiellonian University's Collegium Medicum in Krakow, 90 patients with OFC injury and Chronic Frontal Syndrome were selected for the study. Patients were divided into three groups A, B and C of 30 each, matched for age, gender and injury severity. The Comprehensive Rehabilitation Program (CPReh) (cf. Pąchalska 2008) was applied in all groups ten years after hospitalization and surgery for intracerebral hematoma and was conducted according to three therapeutic Protocols:- Protocol 1 administered in group A, combained cognitive training (CT) and the "Life Academy" program administered twice a week. The activities were continued as long as the patient was able and willing to continue (average 24 months 1.18).- Protocol 2 administered in group B, included CT and the "Academy of Life" program also administered twice a week but lasting for the standard period of about a year (average 12 months 1.03).- Protocol 3 administered in group C, included CT and the "Community Base Treatment" program similarly administered twice a week and also lasting about a year as standard (average 12 months 1.27).Evaluation of the effects of rehabilitation using the Frontal Behavioral Inventory (FBInv) was conducted 2 times: Study I (baseline, 10 years follow up after operation)-before the start of rehabilitation, Study II (follow up) after the end of rehabilitation according to all protocols.all or most of the positive or negative symptoms tested by FBInv, including neurological, cognitive, emotional and behavioral ones. A modified CPReh program administered with Protocol 1. in which combined cognitive training (CT) and the "Academy of Life" program is provided twice a week, but which continues as long as the patient was able and willing to continue, is more effective in reducing these symptoms, like the standard CPReh program administered with Protocol 2 or 3 administered only up to a year as a standard. It was also found that the "Academy of Life " program has also been shown to be a more effective component of CPReh than the Community Base Treatment.The improvement achieved by group A, in which a modified CPReh administered with Protocol 1. that provided the patient the opportunity to continue rehabilitation as long as the patient was able and willing to continue was more effective in the reduction of Chronic Frontal Syndrome than the standard CPReh administered with Protocols 2. and 3. for the patients in groups B and C.
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CiteScore
1.50
自引率
42.90%
发文量
8
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