| Literature DB >> 28959488 |
Ali Zohair Nomani1, Sumaira Nabi1, Mazhar Badshah1, Shahzad Ahmed1.
Abstract
Ischaemic stroke is a major cause of neurological morbidity and mortality. The objective of this review article is to summarise facts pertaining to acute ischaemic stroke and its various aspects in a developing country like Pakistan, where resources are limited and the healthcare system is underdeveloped. No large-scale epidemiological studies are available to determine the true incidence of stroke in Pakistan. We reviewed the available literature on stroke from Pakistan and through this article we primarily aim to present the current acute ischaemic stroke management in Pakistan in juxtaposition to that of the developed world. We also intend to highlight areas for future development and improvement in management. The routine practice in Pakistan is that of using stat dose of aspirin in emergency (ER) at large with only a handful of centres offering thrombolytic therapy with recombinant tissue plasminogen activator for acute ischaemic stroke. This too is faced with the problem of long window periods before the patient reaches a proper stroke care centre. The facilities of interventional therapies like arterial thrombolysis and endovascular surgery are non-existent and rehabilitation facilities limited. The opportunities for training physicians in acute stroke are also scarce. Stroke in children is underdiagnosed and that in women not availing facilities at stroke care centres. While basic research has gained pace regarding local demographic data, advanced research and genetic studies are extremely limited. The field of stroke neurology needs to grow at a substantial pace in Pakistan to be at par with the developed world.Entities:
Keywords: Cerebrovascular accident; Pakistan stroke management.; acute ischemic stroke; recombinant tissue Plasminogen Activator; window period
Mesh:
Substances:
Year: 2017 PMID: 28959488 PMCID: PMC5435212 DOI: 10.1136/svn-2016-000041
Source DB: PubMed Journal: Stroke Vasc Neurol ISSN: 2059-8696
Figure 1Risk factors for ischaemic stroke. An algorithm showing the risk factors for ischaemic stroke. SAH, subsarachnoid hemorrhage.
Figure 2Bedside clinical signs to be noted in stroke; (A) a patient who has not suffered a stroke can generally hold the arms in an extended position with eyes closed. (B) A patient with stroke will often display ‘arm drift’ (pronator drift)—one arm will remain extended when held outwards with eyes closed, but the other arm will drift or drop downwards and pronate (palm turned downwards).
Figure 3Graphical representation of patients within and outside window period for IV thrombolysis in a study conducted by Ali and colleagues in 2015–2016 (adapted from ref. 28). Out of the cohort of 100 patients, 29% had presented within the window period for IV thrombolysis. IV, intravenous.
Figure 4Process of tissue damage and time intervals for possible salvage in acute ischaemic stroke.
Acute ischaemic stroke: an ER protocol (routinely followed protocols across Pakistan)
| Acute ischaemic stroke: an ER protocol | ||||
|---|---|---|---|---|
| 1. | ||||
| 2. | Plain CT head STAT | |||
| 3. | CBC and platelet count | |||
| 4. | prothrombin time (PT), INR | |||
| 5. | Electrolytes, creatinine, glucose, Trop, liver function tests (LFTs) | |||
| 6. | 0.9% normal saline (NS) at 100 to 120 mL/hour for 24 hours. No dextrose saline (if congestive cardiac failure (CCF), use 0.9% NS at ≤60 to 70 mL/hour) | |||
| 7. | If systolic BP>185 mm Hg or diastolic BP>110 mm Hg for ≥2 readings taken 5–10 min apart, use hypertension management protocol | |||
| 8. | If random blood glucose >150 mg/dL, use S/C insulin protocol | |||
| 9. | Metoclopramide 10 mg IV every 8 hours (for nausea/vomiting) | |||
| 10. | Acetaminophen 1000 mg IV every 8 hours (for headache or fever >37.5°C) | |||
| 11. | Aspirin 300 mg loading dose PO in ER if haemorrhagic stroke ruled out | |||
BP, blood pressure; CBC, complete blood count; INR, international normalised ratio; IV, intravenous; PO, orally; S/C, subcutaneous; Trop, troponin.
Hypertension management protocol (routinely followed protocols across Pakistan)
| Hypertension management protocol | ||||
|---|---|---|---|---|
| 12. | ||||
| 13. | If systolic BP>185 mm Hg or diastolic BP>110 mm Hg for ≥2 readings taken 5–10 min apart, use hypertension management protocol | |||
| 14. | If systolic BP>185 mm Hg or diastolic BP>110 mm Hg, treat with labetalol bolus or infusion | |||
| 15. | Give: IV labetalol 10–20 mg over 1–2 min | |||
| 16. | If still elevated after 10–15 min:The dose may be repeated every 10–15 min up to a total of no more than 300 mg/24 hours or give labetalol initial loading dose followed by infusion at 2–8 mg/min | |||
| 17. | Hold treatment if BP<185/110 mm Hg | |||
BP, blood pressure; IV, intravenous.
Clinical pathway for acute ischaemic stroke (routinely followed protocols across Pakistan)
| Clinical pathway for acute ischaemic stroke | ||||
|---|---|---|---|---|
| 18. | ||||
| 19. | Admit to stroke unit or ICU for 48–72 hours (at a few centres only), then shift to general ward if stable | |||
| 20. | National Institute of Health Stroke Scale (NIHSS)/GCS (individual centre adapted protocols may differ) once/twice daily | |||
| 21. | CT scan of head repeated STAT if decreased level of consciousness or new deficit | |||
| 22. | Monitor vital signs (BP, HR, cardiac rhythm, scores, metabolic acidemia, pulse oximeter (SaPO2) (give oxygen as indicated), Temp and respiratory rate (RR)) | |||
| 23. | Monitor vital signs: every 30×3; every 1 hour×every 6 hours, then every 3 hours×every 10 hours (individual centre adapted protocols may differ) | |||
| 24. | Start mobilisation (in bed or chair) if stable (after functional assessment) | |||
| 25. | Bed rest for 24 hours | |||
| 26. | Keep nothing per oral (NPO) until swallowing screen done (if dysphagia present, keep NPO and repeat screen in 24 hours) | |||
BP, blood pressure; GCS, Glasgow Coma Scale; ICU, intensive care unit; NPO, nothing per oral; SaPO2, scores, metabolic acidemia, pulse oximeter; Temp, temperature.
Clinical stroke extended management pathway (routinely followed protocols across Pakistan)
| Clinical stroke extended management pathway | ||||
|---|---|---|---|---|
| 27. | ||||
| 28. | Extracranial imaging: carotid Doppler, CTA, MRA) in 2–7 days | |||
| 29. | ECG in 2–7 days (trans thoracic echocardiography (TTE)/trans esophageal echocardiography (TEE) as indicated) | |||
| 30. | DVT prophylaxis | |||
| 31. | Stroke educational material for patient and family | |||
| 32. | Removal of Foley's catheter and start bladder management (if stable and feasible) | |||
| 33. | Discharged on:
Antithrombotic therapy OR Anticoagulation therapy for atrial fibrillation/flutter Antihypertensives (as indicated) Statins/cholesterol lower agent (as indicated) Antidiabetic agent (if indicated) | |||
| 34. | Fasting lipid profile, HbA1c | |||
| 35. | Holter monitor (if indicated | |||
| 36. | Specialised workup for young stroke (like anti nuclear antibody (ANA), extractable Nuclear Antigen (eNA), etc) | |||
| 37. | Referral to:
Rehabilitation specialist Speech therapist Dietician Medical team (if otherwise indicated or required) | |||
| 38. | Follow-up | |||
CTA, CT angiography; HbA1c, glycated haemoglobin; MRA, MR angiography.