南印度格林-巴利综合征患者治疗结果和临床特征的预测因素。

IF 1.4 Q4 PHARMACOLOGY & PHARMACY Reviews on recent clinical trials Pub Date : 2023-01-01 DOI:10.2174/0115748871254419231019053136
Nitin Joseph, Soumya Shrigiri
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引用次数: 0

摘要

背景:格林-巴利综合征(GBS)是世界范围内急性神经肌肉无力和瘫痪的主要原因之一。对其在发展中国家的临床流行病学概况和影响其治疗结果的因素的研究很少。目的:本研究旨在研究两所三级护理医院收治的GBS患者的危险因素、临床表现、管理和治疗结果的预测因素。材料和方法:在2017年6月至2022年5月的近五年时间里,检查了121名根据布莱顿标准确诊的GBS住院患者的医疗记录。使用Hughes功能分级量表对GBS的严重程度进行评估。结果:平均发病年龄为36.8±18.9岁。大多数患者[82(67.8%)]为男性。34名(28.1%)患者在GBS发作后1个月内出现既往疾病。大多数患者出现呼吸道疾病[13例(38.2%)]。4例(3.3%)患者有GBS复发史。既往疾病发作和GBS发作之间的中位时间间隔为5天(IQR 3,10)。GBS患者最常见的症状是四肢肌肉无力[117(96.7%)]。其中53(45.3%)患者的无力发展模式是从下肢到上肢。最常见的体征是64例(52.9%)患者的肌张力减退。在12名(9.9%)患者中观察到由于GBS引起的并发症。最常见的并发症是11例(91.7%)患者的呼吸窘迫,其次是8例(66.7%)的自主神经功能障碍。48例(39.7%)患者出现脑脊液白蛋白细胞学分离。神经传导研究中的大多数患者患有急性炎症性脱髓鞘性多发性神经病[61(50.4%)]。大多数GBS患者[68(56.2%)]使用静脉注射免疫球蛋白(IVIG)进行治疗。95名(78.5%)患者在出院时通过治疗得到改善。在多变量分析中,既往疾病的缺失(p=0.029)、GBS的Brighton诊断确定性水平1和2(p=0.024)以及继续接受IVIG治疗(p=0.05)与患者病情的改善有关。结论:利用临床和实验室证据对GBS进行适当的诊断,并在有既往病史的GBS患者中提供适当的治疗和更多的监督,将有助于改善他们出院时的预后。
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Predictors of Treatment Outcome and Clinical Profile among Guillain- Barre Syndrome Patients in South India.

Background: Guillain-Barre syndrome (GBS) is one of the principal causes of acute neuromuscular weakness and paralysis worldwide. Its clinic-epidemiological profile and factors influencing its treatment outcomes in developing countries are very minimally studied.

Objective: The study aimed to find out the risk factors, clinical presentation, management, and predictors of treatment outcomes among GBS patients admitted in two tertiary care hospitals.

Materials and methods: Medical records of 121 inpatients with GBS confirmed based on the Brighton criteria over the recent five-year period from June 2017 to May 2022 were examined. Assessment of the severity of GBS was done using the Hughes functional grading scale.

Results: The mean age at onset was 36.8 ± 18.9 years. The majority of the patients [82 (67.8%)] were males. Antecedent illnesses within 1 month of onset of GBS were present among 34 (28.1%) patients. The majority of them developed respiratory tract illnesses [13 (38.2%)]. Recurrent history of GBS was observed among 4 (3.3%) patients. The median time gap between the onset of antecedent illnesses and the onset of GBS was 5 days (IQR 3, 10). The most common symptom among GBS patients was the weakness of the muscles of the extremities [117 (96.7%)]. The pattern of progression of weakness among 53 (45.3%) of these patients was from the lower to upper limbs. The most common sign noted was hypotonia [64(52.9%)]. Complications due to GBS were observed among 12 (9.9%) patients. The most common complication among them was respiratory distress in 11 (91.7%) patients, followed by autonomic dysfunctions in 8 (66.7%). Albuminocytological dissociation in cerebrospinal fluid was noted among 48 (39.7%) patients. The majority of patients in nerve conduction studies had acute inflammatory demyelinating polyneuropathy [61(50.4%)]. The majority of the GBS patients [68 (56.2%)] were treated using intravenous immunoglobulin (IVIG). 95 (78.5%) patients improved with treatment at the time of discharge. In multivariable analysis, the absence of antecedent illnesses (p =0.029), Brighton's diagnostic certainty levels 1 and 2 of GBS (p =0.024), and being on IVIG treatment (p =0.05) were associated with improvement in disease condition among the patients.

Conclusion: Appropriate diagnosis of GBS using both clinical and laboratory evidence and providing appropriate treatment along with more supervision among GBS patients with a history of antecedent illnesses will help improve their prognosis at the time of discharge.

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来源期刊
Reviews on recent clinical trials
Reviews on recent clinical trials PHARMACOLOGY & PHARMACY-
CiteScore
3.10
自引率
5.30%
发文量
44
期刊介绍: Reviews on Recent Clinical Trials publishes frontier reviews on recent clinical trials of major importance. The journal"s aim is to publish the highest quality review articles in the field. Topics covered include: important Phase I – IV clinical trial studies, clinical investigations at all stages of development and therapeutics. The journal is essential reading for all researchers and clinicians involved in drug therapy and clinical trials.
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