https://www.ajol.info/index.php/eajns/issue/feed East African Journal of Neurological Sciences 2024-07-02T06:47:11+00:00 Dr Philip Maseghe Mwachaka, eajnseditor@gmail.com Open Journal Systems <p>The East African Journal of Neurological Sciences (ISSN: 2957-4323 (online) &amp; 2957-4315 (print)) is the official journal of the East African Association of Neurological Surgeons (EAANS).<br /><br /><strong>Aims and Scope</strong><br />The East African Journal of Neurological Sciences (EAJNS) is dedicated to advancing the field of neurological sciences through the dissemination of high-quality research and innovative findings. As the official journal of the East African Association of Neurological Surgeons (EAANS), EAJNS aims to provide a platform for researchers, clinicians, and practitioners to share knowledge and contribute to the development of neurosurgery and related disciplines in Africa and beyond. The journal covers a wide range of topics in the neurological sciences, including clinical and experimental neurosurgery, clinical neurophysiology, neuroanatomy, neurology, neuro-ophthalmology, neuroradiology, neuropathology, neuro-otology, neuro-oncology, and molecular biology. <br /><br />You can see this journal's own website <a href="https://theeajns.org/index.php/eajns/index" target="_blank" rel="noopener">here</a>.</p> https://www.ajol.info/index.php/eajns/article/view/273135 Management of Chronic Subdural Hematomas with Bedside Placement of Twist Drill Subdural Evacuation Port System: A Single Center Retrospective Review 2024-07-02T06:06:46+00:00 Ryan T. Kellogg rkellogg9@gmail.com Stephen R. Lowe rkellogg9@gmail.com Jeff Wessell rkellogg9@gmail.com Zachary Hubbard rkellogg9@gmail.com Orgest Lajthia rkellogg9@gmail.com Laura Wolgamott rkellogg9@gmail.com Guilherme Porto rkellogg9@gmail.com Thomas Larrew rkellogg9@gmail.com Jaime Martinez Santos rkellogg9@gmail.com Ahmed Alshareef rkellogg9@gmail.com Fraser Henderson Jr rkellogg9@gmail.com Mohammed Alshareef rkellogg9@gmail.com <p><strong>Objective</strong>: Chronic subdural hematoma (cSDH) is prevalent globally and its management is evolving to minimize morbidity while&nbsp; optimizing theater utilization. We present our institution’s experience with subdural evacuation port system (SEPS) as a first-line&nbsp; treatment approach to cSDHs.</p> <p><strong>Methods</strong>: A retrospective review was performed of patients undergoing bedside SEPS placement in a&nbsp; single institution. Pre- and post-procedural radiographic and clinical data were collected and analyzed to identify predictive variables of&nbsp; procedural success for the SEPS approach. For procedure failures, subsequent procedures were analyzed for rates of success.</p> <p><strong>Results</strong>:&nbsp; 268 patients were identified for a total of 326 initial procedures. Pre-procedural variables associated with improved odds of a good&nbsp; outcome were: unilateral cSDH, prior use of anticoagulation, GCS &gt; 13 at presentation, larger cSDH, and greater degree of midline shift (MLS). 65% success rate was observed for initial SEPS placement and an overall success of 78% after repeat SEPS. Bilateral SDH with&nbsp; bilateral SEPS placement had 56% success, a significantly lower success rate than unilateral placement (p=0.0147). Patients with&nbsp; subsequent failures underwent craniotomy. Patients who had a successful SEPS procedure had an average LOS of 13 ± 39 days compared&nbsp; to 25 ± 65 in incidents of failure (p=0.047). Average follow-up after discharge was 2.8 ± 3.8 months.</p> <p><strong>Conclusions</strong>: Bedside SEPS&nbsp; placement is a low-risk option for first-line treatment of cSDH and may spare patients from the risks of general anesthesia while&nbsp; reducing burden on surgical theaters in resource-limited settings. Performing a repeat SEPS procedure is a reasonable surgical option if&nbsp; the first procedure fails to completely evacuate the cSDH.&nbsp;</p> 2024-07-02T00:00:00+00:00 Copyright (c) 2024 East African Journal of Neurological Sciences https://www.ajol.info/index.php/eajns/article/view/273136 Blood Pressure Variability and Shifting in Clinical Outcome Amongst Stroke Patients in Southwestern Uganda 2024-07-02T06:14:48+00:00 Nicholas Kulaba Kulnic21@gmail.com Kayanja Adrian Kulnic21@gmail.com Denis Serubiri Kulnic21@gmail.com Sofia Najjingo Kulnic21@gmail.com Shirley M. Moore Kulnic21@gmail.com Mark Kaddu Mukasa Kulnic21@gmail.com Cumara B O'Carroll Kulnic21@gmail.com Muyingo Anthony Kulnic21@gmail.com <p><strong>Background</strong>: Higher blood pressure variability is associated with shifting towards worse outcome among stroke patients.</p> <p><strong>Methods</strong>: We&nbsp; conducted a prospective cohort study of CT head confirmed ischemic and hemorrhagic stroke admitted within 7 days of onset of motor weakness. Blood Pressure Variability (BPV) indice; Standard Deviation (SD) of systolic and diastolic Blood pressure (BP) between 0 and 7&nbsp; days after admission was calculated with subsequent modified Rankin Scale (mRS) score on day 14 and day 30 post-stroke. Ordinal logistic regression was fitted to determine the adjusted odds ratios (aOR) for shifting towards worse clinical outcome at 30 days among&nbsp; patients with stroke that had survived beyond 14 days with 95% CI and p value&lt;0.05 used as statistical significance.</p> <p><strong>Results</strong>: Out of 120&nbsp; patients, 32 patients passed on by day 14, 88 patients survived beyond day 14. Fourteen patients had a 1 point shift in MRS towards worse&nbsp; outcome at 30 days of stroke onset. Blood pressure variability SD systolic BP tertiles (2&amp;3) had aOR: 1.6, p= 0.306 (95%C.I: 0.6-4.1)&nbsp; and 5.8, p = 0.002 (95%C.I: 1.9-17.5) respectively. NIHSS≥16 had aOR=3.8 (95%CI: 1.5-9.6) P=0.004 and time to presentation ≥ 3 days had&nbsp; aOR=2.8 (95% C.I:1.2-6.3) p=0.013.</p> <p><strong>Conclusion</strong>: Higher BPV (tertile 3), late presentation ≥ 3 days and high NIHSS conferred statistically&nbsp; significant odds of shifting towards a bad functional outcome.&nbsp;</p> 2024-07-02T00:00:00+00:00 Copyright (c) 2024 East African Journal of Neurological Sciences https://www.ajol.info/index.php/eajns/article/view/273137 Statins: An Alternative To Surgical Treatment Of Chronic Subdural Haematoma In The Poly Pathological Elderly? 2024-07-02T06:23:42+00:00 Faye Mohameth fayeneurocchir92@gmail.com Celebre Mualaba fayeneurocchir92@gmail.com Roger Ilunga Mulumba fayeneurocchir92@gmail.com Barry Lounceny Fatoumata fayeneurocchir92@gmail.com Cisse Yakhya fayeneurocchir92@gmail.com Magatte Gaye Sakho fayeneurocchir92@gmail.com Momar Code Ba fayeneurocchir92@gmail.com <p>Chronic subdural haematoma is a frequent pathology of the elderlý especially in comorbid terrain. The treatment is almost always&nbsp; surgical. Sometimes this surgery is not possible and a medical treatment based on corticosteroids is most often required. We report the&nbsp; cases of two patients followed for chronic subdural haematoma with several comorbidities and ineligible for surgery. A statin-based&nbsp; treatment was initiated. The aim is to consolidate the hypothesis of medical management of chronic subdural haematoma. The first case&nbsp; was about an 87-year-old patient followed in cardiology for cardiac arrhythmia with a Pacemaker insertion in 2021 on Aspirin 100mg and&nbsp; oral anti-diabetic and insulin therapy for 15 years. Clinically, he presented with intense headaches without neurological deficit. The brain&nbsp; scan performed revealed a chronic left hemispheric subdural hematoma with mass effect. Treatment with atorvastatin at a dose of 20mg/ day for three months was initiated. The evolution was marked by the disappearance of headaches after two weeks. After three months of&nbsp; treatment, the haematoma disappeared completely. The second patient was an 83-year-old man also followed in cardiology for heart&nbsp; failure and in gastroenterology for a gastric tumour undergoing chemotherapy who had been suffering for three weeks from intense&nbsp; headaches with left hemiparesis. Brain CT scan: right hemispheric subdural hematoma with mass effect. Treatment with atorvastatin&nbsp; 20mg was started for three months with radiological controls at one month and three months with a favourable evolution.&nbsp;</p> 2024-07-02T00:00:00+00:00 Copyright (c) 2024 East African Journal of Neurological Sciences https://www.ajol.info/index.php/eajns/article/view/273138 Conus Medularis Neuroschistosomiasis In A 12-Year-Old Boy 2024-07-02T06:34:26+00:00 Felix Nyatigo Nyang'wech felixnyatigo@gmail.com Brian Makini Atuti felixnyatigo@gmail.com Orlando Manuel felixnyatigo@gmail.com Rios Mastrapa felixnyatigo@gmail.com <p><strong>Introduction</strong>: Neuroschistosomiasis, an infrequent consequence of schistosomal infection, typically presents with deteriorating motor&nbsp; and sensory function coupled with sphincter dysfunction. Diagnosis involves a clinical history, physical examination, cerebrospinal fluid studies, and imaging.</p> <p><strong>Case report</strong>: We detail the case of a 12-year-old boy hailing from Machakos County, who manifested lower limb&nbsp; weakness and urine retention for two weeks. Examination unveiled diminished lower limb tone and areflexia, with a power grade of 0 in distal muscles below the knee and normal muscle bulk. Magnetic resonance imaging revealed a cauda equina region tumor. Subsequent&nbsp; histopathology after tumor-debulking surgery unveiled schistosomal-associated necrotizing granulomatous inflammation. Following&nbsp; tumor resection at T1-L1 and receipt of histopathology results, the patient underwent optimum pain management and praziquantel&nbsp; therapy. Clinical improvement ensued, albeit with distal paralysis.</p> <p><strong>Conclusion</strong>: Our case highlights the necessity of heightened suspicion&nbsp; for cauda equina tumors in young patients from schistosoma-endemic regions, advocating early diagnosis and management involving&nbsp; praziquantel treatment.&nbsp;</p> 2024-07-02T00:00:00+00:00 Copyright (c) 2024 East African Journal of Neurological Sciences https://www.ajol.info/index.php/eajns/article/view/273140 Mood Disorders Associated With Pituitary Adenoma 2024-07-02T06:42:37+00:00 Michael A. Magoha faisalnageyle@gmail.com Faisal Nageyle faisalnageyle@gmail.com <p>Pituitary adenomas have been found to exhibit associations with various mood disorders, including depression, mania, and anxiety&nbsp; disorders. Additionally, these adenomas have been observed to manifest other psychiatric symptoms, such as psychosis, eating&nbsp; disorders, apathy, and suicidal ideation. A comprehensive literature review was conducted, employing diverse search engines including&nbsp; PubMed, Cochrane, and Google Scholar. The search terms utilised encompassed "pituitary adenomas," "mood disorders,"&nbsp; "Hypothalamo-pituitary axis," "hypopituitarism," "acromegaly," "depression," "mania," and "psychosis." The publications that were&nbsp; chosen consisted of case reports and relevant research articles. There is a high prevalence of comorbidity between pituitary adenomas&nbsp; and depressive and anxiety disorders. The manifestation of these symptoms can be attributed to the endocrine dysfunction associated with pituitary adenomas, as well as the physical impact and infiltration of the tumours into the brain. Furthermore, it has been noted that&nbsp; apathy syndrome and chronic fatigue syndrome may be mistakenly diagnosed as depression among individuals within this specific&nbsp; patient demographic. Mood disorders can impact the process of diagnosing and treating pituitary adenomas. Diseases of this nature can&nbsp; potentially impact patients' daily functioning and their ability to engage in social activities. These individuals require suitable medical&nbsp; intervention to enhance their prognosis.&nbsp;</p> 2024-07-02T00:00:00+00:00 Copyright (c) 2024 East African Journal of Neurological Sciences