Kumara Tini
Department of Neurology, Faculty of Medicine, Universitas Udayana, Denpasar, Indonesia

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Admission Mean Platelet Volume and Poor Functional Outcome After Reperfusion Therapy for Acute Ischaemic Stroke: A Systematic Review and Meta-Analysis Ivan Agusta Dwi Kristiawan; Kumara Tini; Ida Ayu Sri Wijayanti; Anak Agung Ayu Putri Laksmidewi; Ketut Widyastuti; Ni Putu Ayu Putri Mahadewi
Sriwijaya Journal of Neurology Vol. 4 No. 1 (2026): Sriwijaya Journal of Neurology
Publisher : Phlox Institute: Indonesian Medical Research Organization

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.59345/sjn.v4i1.309

Abstract

Background: Mean platelet volume (MPV), an inexpensive index of platelet activation from the routine admission full blood count, has been linked to poor outcome in unselected ischaemic stroke, but its prognostic value in reperfusion-treated patients is uncertain and conflicting. Objective: To quantify the association between admission MPV and poor functional outcome after reperfusion therapy, and to test whether it depends on treatment modality and MPV operationalisation. Methods: PubMed was searched for cohort or case–control studies reporting admission MPV against poor functional outcome (modified Rankin Scale 3–6) in adults with acute ischaemic stroke treated with intravenous thrombolysis and/or mechanical thrombectomy. Odds ratios (OR) were pooled using DerSimonian–Laird random-effects models, with a-priori subgroups by modality and MPV metric and leave-one-out, adjusted-only and Hartung–Knapp sensitivity analyses. This review was not registered in a public registry. Results: Ten studies were included and seven (1,597 patients) pooled. Higher MPV was associated with poor outcome (OR 1.62, 95% CI 1.22–2.16; I²=68.5%). The effect was strong with dichotomised MPV after thrombectomy (OR 2.56, 95% CI 1.60–4.08) but modest with continuous or quartile MPV in broad reperfusion (OR 1.27, 95% CI 1.08–1.49); the between-subgroup difference was significant (p=0.005) yet not robust to removing the most weighted study per arm. Conclusion: Higher admission MPV was associated with poor functional outcome after reperfusion therapy, but its magnitude depended on modality and measurement; certainty was low (GRADE). MPV is a promising, essentially free supplementary marker best used within multivariable models, requiring confirmation in standardised prospective studies.
Vitamin D Deficiency and the Risk and Severity of Chemotherapy-Induced Peripheral Neuropathy in Adults with Cancer: A Systematic Review and Meta-Analysis Chrissanty; Ida Ayu Sri Wijayanti; Kumara Tini
Sriwijaya Journal of Neurology Vol. 4 No. 1 (2026): Sriwijaya Journal of Neurology
Publisher : Phlox Institute: Indonesian Medical Research Organization

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.59345/sjn.v4i1.332

Abstract

Background: Chemotherapy-induced peripheral neuropathy is the commonest neurological complication of cancer treatment and has no established preventive therapy. Vitamin D deficiency is a plausible, cheaply correctable risk factor, but the only previous pooled estimate rested on two studies. Objective: To estimate the association between vitamin D deficiency or insufficiency and the risk and severity of chemotherapy-induced peripheral neuropathy, and to determine how much of the between-study variation is attributable to how neuropathy was ascertained. Methods: PubMed/MEDLINE and Europe PMC were screened, with four further sources and citation tracking. Cohort, cross-sectional and trial-embedded studies reporting serum 25-hydroxyvitamin D against neuropathy in adults were eligible. ROBINS-E was used. Random-effects models pooled odds ratios and, separately, Hedges g for 25-hydroxyvitamin D concentration. Ascertainment method was a pre-specified moderator. Results: Fourteen studies (3,654 participants) were included, seven poolable (2,118). The unstratified pooled odds ratio was 3.45 (95% confidence interval 1.97 to 6.03), I² 74.6%. Ascertainment explained 93.5% of between-study variance: patient-reported instruments gave 5.27 (3.41 to 8.13, I² 0%) and clinician-graded NCI-CTCAE gave 1.72 (1.29 to 2.29, I² 8.0%); ratio of odds ratios 3.01 (1.69 to 5.35). 25-Hydroxyvitamin D was lower in affected patients (g 0.58, 0.28 to 0.88). Bias-adjusted estimates ranged from 1.44 to 2.40. Certainty was very low, rising to low for the clinician-graded estimate. Conclusion: Vitamin D deficiency was associated with chemotherapy-induced peripheral neuropathy, but the magnitude depended almost entirely on how neuropathy was measured. The defensible estimate is a 1.7- to 2.4-fold increase in odds, not threefold.