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Nurse Practitioner
Susan E. Wilson, DNP, ANP-BC, and Susan Ashcraft, DNP, ACNS-BC
ABSTRACT
Approximately 800,000 people living in the United States are diagnosed with a stroke
each year. Nurse practitioners are positioned to impact and improve stroke survivor’s
outcomes in the primary and acute care setting. This article provides an overview of
stroke management pre- and postdischarge in the primary care setting and addresses
acute stroke treatment during hospitalization.
A
pproximately 800,000 people in the United objective is to identify symptoms consistent with a
States experience a stroke each year. Stroke neurologic focal deficit and determine the
ranks as the fifth leading cause of death and timing of symptom onset. Once a stroke is
the leading cause of disability, with over $40 billion suspected, emergency medical services (EMS) dispatch
annual cost.1 The nurse practitioner (NP) may is crucial.
significantly impact patient outcomes during the
prehospital, acute, and posthospital phase of care. History
This article addresses preischemic stroke, acute, and A quick comprehensive history includes identifi-
postischemic stroke care by the NP with a focus on cation of symptoms, time of symptom onset,
the American Heart Association 8 D’s of stroke chain medical history, and medication use. The identifi-
of survival. The 8 D’s include detection, dispatch, cation of symptoms aids the clinician in deter-
delivery, door, data, decision, drug/device, and mining focal neurologic deficits, assisting in ruling
disposition.2 out stroke mimics. The timing of symptom onset is
crucial because treatment initiation must occur
COMMUNITY PRESTROKE MANAGEMENT within 24 hours of symptom presentation.
Case Study Comorbidities that increase the risk of stroke
A 63-year-old man with coronary artery disease, include atrial fibrillation, coronary artery disease,
hypertension, hyperlipidemia, and tobacco use, diabetes, high cholesterol, and hypertension. It is
currently taking aspirin, enalapril, and atorvastatin, important to determine medication history
presents with a sudden onset (at 8:45 AM) of slurred because the use of anticoagulants impacts
speech, aphasia, and right-sided weakness. treatment decision.
48 The Journal for Nurse Practitioners - JNP Volume 15, Issue 1, January 2019
Rapid transport to the closest hospital is crucial to Table 3. American Heart Associationerecommended
receiving prompt treatment, recovery, and prognosis. Stroke Evaluation Benchmarks7
There are currently 4 levels of stroke care: acute Evaluation Vital Components Time Target
stroke-ready, primary stroke, thrombectomy Door to doctor/nurse 10 minutes
capable, and comprehensive stroke. All levels are practitioner/physician assistant
capable of providing initial acute stroke evaluation; Evaluation by neurology expert 15 minutes
the ability to provide complex care increases with
Arrival to CT scan completion 20-25 minutes
each level. The stroke systems of care literature
emphasizes both professional and community Arrival to CT scan interpretation 30-45 minutes
awareness of facilities with systems and teams in Arrival to treatment with 45-60 minutes
place to expedite care.5 intravenous thrombolysis
The immediate objective of ischemic stroke treat- Arrival to admission to stroke unit 3 hours
ment is to improve perfusion and prevent further or intensive care unit
50 The Journal for Nurse Practitioners - JNP Volume 15, Issue 1, January 2019
Postprocedure National Institutes of Health include aspirin, clopidogrel, and dipyridamole/
Stroke Scale ¼ 3 (right-sided drift with some aspirin, decreasing the risk of stroke by approxi-
effort against gravity) mately 22%.13
The patient was discharged on aspirin, atorvastatin Aspirin is accessible, inexpensive, and reduces
80 mg, nicotine patch, enalapril, and outpa- stroke risk between 13% and 23%. A dose of 81 mg
tient therapy. provides a similar benefit as 325 mg with less bleeding
risk associated with lower doses.14
COMMUNITY POSTSTROKE MANAGEMENT: Clopidogrel as a single agent is comparable with
DISPOSITION aspirin in stroke prevention. A Cochrane review re-
Postacute discharge needs focus on poststroke ported a nonsignificant benefit of clopidogrel over
complications and secondary stroke prevention. aspirin in secondary stroke prevention.15 Compared
Unfortunately, compared with the organized with aspirin, clopidogrel has a lower risk of serious
guideline-driven acute hospital care, the same level of hemorrhage but causes diarrhea and rash more
organized guideline-driven postdischarge community frequently.16
care does not exist. Patients may have limited contact The Prevention Regimen for Effectively Avoid-
with health care providers, making patients and ing Second Strokes (PRoFESS) trial found similar
their families responsible for health maintenance, stroke rates between dipyridamole/aspirin (9%) and
monitoring, and management activities.10 clopidogrel (8.8%) with similar hemorrhage rates.
Stroke survivors are encouraged to schedule an Yet, a high discontinuation rate because of headaches
appointment with their primary care provider within occurred in the dipyridamole/aspirin group
2 weeks and a neurology specialist within 1 month. compared with clopidogrel (5.9 vs 0.9%).15 If
During the follow-up visit, the NP has an opportu- dipyridamole/aspirin is prescribed, start at half dose (1
nity to review medications prescribed at discharge tablet daily) for the first 2 weeks before increasing to
and provide education on the importance of their use the full dose (1 tablet twice daily).
in secondary prevention of stroke. Knowledge of Dual antiplatelet therapy may be beneficial for
medications and understanding of their necessity have early stroke prevention. The Clopidogrel in High-
been found to promote medication adherence in Risk Patients with Acute Nondisabling Cerebrovas-
stroke patients.11 Hence, the NP is in a position to cular Events (CHANCE) trial evaluated clopidogrel/
effectively oversee and meet the comprehensive aspirin combination and aspirin alone begun within
needs of the stroke survivor. Individualized care plans 24 hours of symptom onset and treating patients with
should focus on modifiable risk factors, prevention of dual antiplatelet (DAP) for 21 days. Stroke occurred
poststroke complications, and continued 8.2% in the clopidogrel/aspirin group and 11.7% in
rehabilitation to assist in community reintegration. the aspirin group. The Clopidogrel and Aspirin in
At 1 year, recurrent stroke risk is reported at 1%, Acute Ischemic Stroke and High-Risk TIA (POINT)
at 5 years 16%, and at 10 years 25%.12 trial, which treated subjects with DAP for 90 days,
Comprehensive treatment involves risk assessment supports CHANCE’s findings, reporting lower
and strategies targeting individual risk factors. To ischemic events occurring in the clopidogrel/aspirin
decrease stroke risk, effective modification of risk group (5.0%) compared with aspirin alone (6.5%).
factors involves patient education and compliance to However, POINT reported an increased hemorrhage
meet guideline targets for modifiable risk factors risk in the longer DAP treatment period (0.9%)
(Table 5, available online). The hospital discharge compared with CHANCE’s reported hemorrhage
summary should address the cause of stroke, risk of zero. For stroke prevention, it is reasonable to
complications, and modifiable risk factors. treat patients with combination therapy for 21 days.5
52 The Journal for Nurse Practitioners - JNP Volume 15, Issue 1, January 2019
SUPPLEMENTARY DATA 11. Crayton E. Psychological determinants of medication adherence in stroke
survivors: a systematic review of observational studies. Ann Behav Med.
Supplementary tables associated with this article can 2017;51:833-845. https://doi.org/10.1007/s12160-017-9906-0.
12. Pennlert J. Long-term risk and predictors of recurrent stroke beyond the acute
be found in the online version at https://doi.org/10 phase. Stroke. 2014;45(6):1839-1841. https://doi.org/10.1161/STROKEAHA.
114.005060.
.1016/j.nurpra.2018.07.019. 13. Kernan W, Ovbiagele B, Black HR, et al. Guidelines for the prevention of
stroke in patients with stroke and transient ischemic attack: a guideline for
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the department of neurology at the University of North Carolina-
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FAST Facial droop Sensitivity 79%-85%, Easy to use Does not detect 38% of
Arm weakness specificity 68% for posterior strokes
Slurred speech or anterior cerebral strokes
difficulty speaking
Time is important, call 911
LAPSS Age ¼ over 45 Sensitivity 91% with Rapid identification of Takes longer to
Seizure ¼ no history trained EMS personnel stroke; excludes mimics complete
New-onset neurologic
symptoms
Walks at baseline
Glucose range: 60-400 mg/dL
Facial droop
Arm weakness
NIHSS Using the NIHSS4 Reliable when performed Reliable rapid Requires training and
by different professionals assessment certification
CPSS ¼ Cincinnati Prehospital Stroke Scale; EMS ¼ emergency medical services; FAST ¼ Face, Arm, Speech, Time; LAPSS ¼ Los Angeles Prehospital Stroke Screen;
NIHSS ¼ National Institutes of Health Stroke Scale.
53.e1 The Journal for Nurse Practitioners - JNP Volume 15, Issue 1, January 2019
Table 5. Modifiable Risk Factors and Interventions13
Modifiable Risk Risk Reduction Goal/Percent
Factor Stroke Risk Reduction Intervention
Hypertension < 130/80-140/90 Mediterranean diet, regular physical activity,
Risk reduction: limited alcohol intake, and use of
25%-32% antihypertension medications
Hyperlipidemia < 70-100 mg/dL Mediterranean diet, regular physical activity;
Risk reduction: high-intensity statin therapy (eg, atorvastatin
11.2% 80 mg) in patients 75 and in patients > 75,
moderate-intensity statin therapy (eg,
atorvastatin 40 mg) regardless of LDL
Diabetes < 6.5%-8% HbA1C Diet modification and blood glucose control with
Risk reduction: medication
Type 1: 57%
Type 2: no data
Atrial Risk reduction: Warfarin INR goal: 2.0-3.0
fibrillation Warfarin: 68% May use aspirin 325 mg if anticoagulant
Aspirin: 20% contraindicated
DOAC: similar to warfarin
Smoking Risk reduction: 50% at Smoking cessation counseling, nicotine
cessation 1 year, no risk by year 5 replacement, oral smoking cessation medication
DOAC ¼ directing-acting oral anticoagulant; INR ¼ international normalized ratio; LDL ¼ low-density lipoprotein.