The European Cooperative Acute Stroke Study (ECASS) III trial indicated that intravenous rtPA can be given safely to, and can improve outcomes for, carefully selected patients treated 3 to 4.5 hours after stroke; however, as the NINDS investigators concluded, the earlier that IV thrombolytic therapy is initiated, the better the patient outcome. Therefore, the target for IV alteplase initiation remains within 3 hours of time last known well. The administration of IV alteplase beyond 3 hours of stroke symptom onset has not been FDA approved.
Although the benefit of IV alteplase has been well established, only a minority of patients with acute ischemic stroke actually receive this medication across the United States. Recent recommendations from the American Heart Association/American Stroke Association and FDA remove or make less specific many previous contraindications and warnings for therapy.
Type Of Measure: Process Improvement Noted As: Increase in the rateIncluded Populations: Not applicable Excluded Populations: None Data Elements:Denominator Statement: Acute ischemic stroke patients whose time of arrival is within 2 hours (less than or equal to 120 minutes) of time last known well.
Included Populations: Discharges with an ICD-10-CM Principal Diagnosis Code for ischemic stroke as defined in Appendix A, Table 8.1 Excluded Populations:Risk Adjustment: No. Data Collection Approach: Retrospective data sources for required data elements include administrative data and medical records. Some hospitals may prefer to gather data concurrently by identifying patients in the population of interest. This approach provides opportunities for improvement at the point of care/service. However, complete documentation includes the principal or other ICD-10 diagnosis and procedure codes, which require retrospective data entry. Data Accuracy: Variation may exist in the assignment of ICD-10 codes; therefore, coding practices may require evaluation to ensure consistency. Measure Analysis Suggestions: None Sampling: Yes. Please refer to the measure set specific sampling requirements and for additional information see the Population and Sampling Specifications section. Data Reported As: Aggregate rate generated from count data reported as a proportion. Selected References:Data Elements:
- Patients less than 18 years of age
- Patients who have a Length of Stay greater than 120 days
- Patients enrolled in clinical trials
- Patients admitted for Elective Carotid Intervention
- Time Last Known Well to arrival in the emergency department greater than 2 hours
- Patients with a documented Reason For Extending the Initiation of IV Alteplase
- Patients with a documented Reason For Not Initiating IV Alteplase
- Admission Date
- Arrival Date
- Arrival Time
- Birthdate
- Clinical Trial
- Date Last Known Well
- Discharge Date
- ED Patient
- Elective Carotid Intervention
- ICD-10-CM Principal Diagnosis Code
- Last Known Well
- Reason for Extending the Initiation of IV Alteplase
- Reason for Not Initiating IV Alteplase
- Time Last Known Well
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