| Literature DB >> 29065915 |
Leonard Baatiema1,2, Carina K Y Chan3, Adem Sav4, Shawn Somerset4.
Abstract
BACKGROUND: The past decades have witnessed a rapid evolution of research on evidence-based acute stroke care interventions worldwide. Nonetheless, the evidence-to-practice gap in acute stroke care remains variable with slow and inconsistent uptake in low-middle income countries (LMICs). This review aims to identify and compare evidence-based acute stroke management interventions with alternative care on overall patient mortality and morbidity outcomes, functional independence, and length of hospital stay across Africa.Entities:
Keywords: Africa; Evidence-based practice; Implementation; Organised care; Stroke; Stroke service
Mesh:
Year: 2017 PMID: 29065915 PMCID: PMC5655819 DOI: 10.1186/s13643-017-0594-4
Source DB: PubMed Journal: Syst Rev ISSN: 2046-4053
Fig. 1Flow chart on selection of eligible studies
Characteristics of studies on interventions for acute stroke care
| Lead author year and country | Study aim | Study design | Intervention | Level of evidence | Duration | Population sample | Outcome measures | Key results |
|---|---|---|---|---|---|---|---|---|
| Villiers et al. 2009 | Examine the impact of multidisciplinary stroke care on in-hospital mortality, resource utilisation and access to in-patient rehabilitation facilities for stroke patients admitted to the stroke unit | Retrospective study | Stroke unit | Level 3 | December 2001–February 2002 | 195 patients | Length of hospital stay in-patient death transfer to a tertiary hospital number of patients who accessed CT brain | In-hospital mortality was 31 (33%) in general ward compared to 16 (16%) in the stroke unit ( |
| Wasserman and Bryer 2012 | To evaluate early outcomes and safety of stroke thrombolysis in a South African setting | Prospective study | Thrombolytic therapy | Level 3 | January 2000–February 2011 | 42 patients | Early neurological recovery functional independence at discharge rate of symptomatic intracranial haemorrhage (SICH) | Mean time to t-PA infusion was 160 min (SD 50; range 60–270). 72.5% patients were thrombolysed within 180 min |
| Klemperer et al. 2014 | To evaluate the performance of SITS-SICH and SEDAN scores in predicting the risk of SICH after thrombolysis | Retrospective Study | Thrombolytic therapy | Level 3 | 2000–2012 | 41 patients | Bleeding complications | 2 (4.9%) patients experienced SICH, (95% CI: 0–11.5%), SITS-SICH (5.1%) and SEDAN (6.5%) cohorts |
| Naima Chtaou et al. 2016 | To report the case series of all patients who were treated with rt-PA in a stroke unit of HASSAN II University hospital between 2010 and 2013 | Case series | Thrombolytic therapy | Level 4 | 2010–2013 | 52 patients | 17 patients (32.7%) were treated within a 3-h window of stroke onset and 35 (67.3%) within 3–4.5 h |
Risk and quality assessment of eligible studies
| Appraisal questions for cohort studies | Bryer and Wasserman 2012 | Villiers et al. 2009 | Klemperer et al. 2014 | |
| 1 | Were the groups similar and recruited from the same population? | Yes | Yes | Yes |
| 2 | Were the exposures measured similarly to assign people to both exposed and unexposed groups? | Yes | Yes | Yes |
| 3 | Was the exposure measured in a valid and reliable way? | Yes | Yes | Yes |
| 4 | Were confounding factors identified? | Yes | Yes | Yes |
| 5 | Were strategies to deal with confounding factors stated? | No | No | Yes |
| 6 | Were the groups/participants free of the outcome at the start of the study (or at the moment of exposure)? | Yes | Yes | Yes |
| 7 | Were the outcomes measured in a valid and reliable way? | Yes | Yes | Yes |
| 8 | Was the follow up time reported and sufficient to belong enough for outcomes to occur? | Yes | No | Yes |
| 9 | Was follow-up complete, and if not, were the reasons to loss to follow-up described and explored? | NA | NA | NA |
| 10 | Were strategies to address incomplete follow-up utilised? | NA | NA | NA |
| 11 | Was appropriate statistical analysis used? | Yes | Yes | Yes |
| Critical appraisal questions for case series study | Naima Chtaou et al. 2016 | |||
| 1 | Were there clear criteria for inclusion in the case series? | Yes | – | – |
| 2 | Was the condition measured in a standard, reliable way for all participants included in the case series? | Yes | – | – |
| 3 | Were valid methods used for identification of the condition for all participants included in the case series? | Yes | – | – |
| 4 | Did the case series have consecutive inclusion of participants? | Yes | – | – |
| 5 | Did the case series have complete inclusion of participants? | Yes | – | – |
| 6 | Was there clear reporting of the demographics of the participants in the study? | Yes | – | – |
| 7 | Was there clear reporting of clinical information of the participants? | Yes | – | – |
| 8 | Were the outcomes or follow up results of cases clearly reported? | Yes | – | – |
| 9 | Was there clear reporting of the presenting site(s)/clinic(s) demographic information? | No | – | – |
| 10 | Was statistical analysis appropriate? | Yes | – | – |
| 11 | Were there clear criteria for inclusion in the case series? | Yes | – | – |