Dosing Tissue Plasminogen Activator on a Mobile Stroke Unit: Comparison Between Estimated and Hospital-Measured Weights. Issue 4 (August 2021)

• Record Type: Journal Article
• Authors: Jacob, Asha P.; Wang, Mengxi; Okpala, Munachi; Yamal, Jose-Miguel; Grotta, James C.; Parker, Stephanie A.
• Is Part Of: Journal of neuroscience nursing. Volume 53:Issue 4(2021)
• Publication Date: 2021-08
• Subjects: emergency medical services -- ischemic stroke -- mobile stroke -- tissue plasminogen activator -- transport nursing -- weight; Neurological nursing -- Periodicals; 616.80231
• DOI: 10.1097/JNN.0000000000000598
• Languages: English
• ISSNs: 0888-0395

Abstract

Abstract : ABSTRACT: BACKGROUND: Prehospital tissue plasminogen activator dosing in a mobile stroke unit (MSU) is estimated by the paramedic and nurse. We aimed to determine the accuracy of the estimated weight method compared with the actual weight of patients treated with tissue plasminogen activator on the MSU. METHODS: We prospectively collected the estimated weight used on the MSU for treatment and the first-documented hospital-measured weight (bed scale) within 24 hours of hospital arrival. Median absolute and percent difference in weights were calculated; less than 10% of difference in weights was considered acceptable. To compare the estimated and measured weights, we conducted a Wilcoxon signed rank test and Fisher exact test to explore the association between weight difference of greater than 10% and patient outcomes. RESULTS: Among 337 patients, median estimated and hospital-measured weights were 79.0 kg (interquartile range [IQR], 66.0–94.5) and 78.5 kg (IQR, 65.0–91.7), respectively. The median of the absolute value of the difference in estimated versus measured weight was 2.7 kg (IQR, 0.6–7.6; P < .0001). The median percent difference in weight was 3.6% (IQR, 0.8%–9.4%). The median difference between the tissue plasminogen activator dosage administered on the MSU and the recommended dose based on the actual weight was 1.3 mg (IQR, 0.06–4.8) in absolute value. In 56 patients (16.6% of the entire sample) with overestimation of weight by greater than 10%, there were no symptomatic intracerebral hemorrhages. There was no association between weight difference and discharge modified Rankin score ( P = .59). CONCLUSION: Weight estimation on an MSU can lead to similar tissue plasminogen activator dosing for 83.4% of subjects compared with if dosing were determined based on actual weight. Weight overestimation or underestimation had no detected impact on tissue plasminogen activator outcomes.