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Published on: August 30, 2020
Risk Factors for Atorvastatin as a Monotherapy for Chronic Subdural Hematoma: A Retrospective Multifactor Analysis
Xinjie Zhang1,2, Dong Wang1,2, Ye Tian1,2
1Department of Neurosurgery, Tianjin Medical University General Hospital, Tianjin, China.
Insights
Atorvastatin effectively treats moderate chronic subdural hematoma (CSDH) in most patients. High-density hematoma, basal cistern compression, and hematoma volume predict treatment efficacy, guiding non-surgical management decisions.
Area of Science:
- Neurosurgery
- Neurology
- Pharmacology
Background:
- Chronic subdural hematoma (CSDH) is a prevalent intracranial hemorrhage in elderly individuals.
- Identifying predictors of treatment efficacy is crucial for managing CSDH.
Purpose of the Study:
- To investigate predictive factors for atorvastatin monotherapy efficacy in moderate CSDH.
- To evaluate atorvastatin's role as a non-surgical treatment for CSDH.
Main Methods:
- Retrospective review of 89 patients with moderate CSDH treated with atorvastatin monotherapy.
- Univariate, multivariate, and ROC curve analyses were used to identify predictive factors.
- Assessment of clinical and radiological data including MGS-GCS, ADL-BI, ASA-PS, and CT findings.
Main Results:
- Atorvastatin demonstrated an overall efficacy rate of 87.6% at 6 months.
- High-density hematoma, basal cistern compression, and hematoma volume were independent risk factors for poor efficacy.
- Activities of Daily Life-Barthel Index (ADL-BI) showed higher sensitivity than MGS-GCS and ASA-PS for outcome prediction.
Conclusions:
- Atorvastatin is an effective monotherapy for moderate CSDH.
- High-density hematoma, basal cistern compression, and hematoma volume predict non-surgical treatment outcomes.
- ADL-BI is a sensitive tool for assessing patient outcomes in CSDH.
Abstract:
Chronic subdural hematoma (CSDH) is a common form of intracranial hemorrhage in the aging population. We aimed to investigate the predictive factors for atorvastatin efficacy as a monotherapy for moderate CSDH. We retrospectively reviewed the medical records of patients who were diagnosed with moderate CSDH and received atorvastatin monotherapy between February 5, 2014, and November 7, 2015, in multiple neurosurgical departments. Univariate, multivariate and receiver operating characteristic curve analyses were performed to identify the potential significant factors indicative of the good therapeutic efficacy or poor therapeutic efficacy of atorvastatin for mild CSDH, such as age, sex, history of injury, Markwalder grading scale-Glasgow Coma Scale (MGS-GCS), Activities of Daily Life-the Barthel Index scale (ADL-BI), American Society of Anesthesiologists Physical Status classification system (ASA-PS), blood cell counts, serum levels and computed tomography findings. A total of 89 patients (75 men and 14 women) aged 24-88 years (mean age 61.95 ± 15.30 years) were followed-up for 24 weeks. Computed tomography findings at admission showed mixed-density hematoma in 22 patients, isodense hematoma in 13 patients, high-density hematoma in 26 patients, and low-density hematoma in 28 patients. In total, 3, 80, and 6 patients had MGS-GCS grades of 0, 1, and 2, respectively. The efficacy rate at 6 months was 87.6% (78/89). Eleven patients were switched to surgery due to a worsened neurological condition, of whom 8, 1, 1, and 1 had high-density, low-density, isodense and mixed-density hematomas, respectively. These patients were switched to surgery over a range of 2-27 days, with a median interval of 12 days after the medication treatment. Univariate and multivariate analyses, confirmed by ROC curves, revealed that high-density hematoma, basal cistern compression, and hematoma volume to be independent risk factors for the efficacy of atorvastatin monotherapy in patients with moderate CSDH. Atorvastatin is an effective monotherapy for the treatment of mild CSDH. High-density hematoma, basal cistern compression, and hematoma volume are independent predictors of the efficacy of atorvastatin as a non-surgical treatment. The results suggested that ADL-BI was more sensitive than the MGS-GCS and ASA-PS for determining patient outcomes in our moderate CSDH cohort.
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