With the outbreak of coronavirus disease 2019 (COVID-19), usual stroke care logistics have been disrupted worldwide.Reference Markus and Brainin1 Guidelines currently recommend screening suspected stroke patients for COVID-19 and employing appropriate precautions to prevent contamination of healthcare workers and other patients,Reference Lyden2,Reference Smith, Mountain and Hill3 while some groups have proposed protected acute stroke evaluation algorithms.Reference Nguyen, Abdalkader and Jovin4 Our institution’s modified code stroke protocol includes use of personal protective equipment during all acute stroke evaluations and systematic COVID-19 screening for all code stroke patients with a nasopharyngeal swab and polymerase chain reaction (PCR). We aimed to study the impact of the COVID-19 pandemic on stroke treatment metrics.
We conducted an observational cohort study at a high-volume comprehensive stroke center for which exposure was defined as the emerging COVID-19 pandemic. Montreal, Quebec, is currently the epicenter of the COVID-19 pandemic in Canada (21,912 confirmed cases as of May 31, 2020). Using data from the Montreal Neurovascular and Stroke Data Repository (MONSTER), a routine electronic medical record tool allowing systematic guideline-based quality assurance, we compared a prospective cohort of consecutive adult patients evaluated for acute stroke between March 30 (date of formal implementation of our modified code stroke protocol) and May 31, 2020, with a retrospective reference cohort of consecutive adult patients evaluated for stroke during the corresponding time period of 2019. We collected baseline characteristics, prestroke modified Rankin scale (mRS) and NIH stroke scale (NIHSS) scores, discharge diagnosis (stratified into ischemic stroke, hemorrhagic stroke, stroke mimic), reperfusion treatment (thrombolysis, thrombectomy), time between symptom onset and hospital presentation, stroke management metrics (door-to-imaging, door-to-needle, door-to-puncture, and door-to-recanalization delays), and the COVID-19 screening results. Statistical testing was performed using t-tests (continuous parametric data), Wilcoxon rank-sum tests (continuous nonparametric data), and χ 2 tests (dichotomous data). For ischemic stroke patients, multivariate logistic regressions were used with the following prespecified variables: stroke evaluation during the pandemic period, patient age, sex, prestroke mRS, NIHSS, transfer from another institution, and delay from symptom onset. The outcomes of interest were treatment with thrombolysis and thrombectomy, hospital presentation within 4.5 h from symptom onset, and referral from another institution for thrombectomy. The project was approved by our institutional Research Ethics Board (#20.013).
Overall, 156 patients were included in the pandemic cohort and 138 in the reference cohort. Baseline characteristics and stroke subtypes were similar between cohorts (Table 1; see Supplementary Table for data on confirmed ischemic stroke patients). Delays to hospital presentation were longer during the pandemic for all evaluated patients (median [interquartile range]: 147 [64–363] vs. 102 [57–205] min, p = 0.02) and for ischemic stroke patients (197 [64–501] vs. 116 [60–212] min, p = 0.03). During the pandemic, a significantly smaller proportion of ischemic stroke patients was treated with thrombolysis or thrombectomy (36% vs. 54% for both interventions, p = 0.01) and fewer patients were transferred from another institution for thrombectomy (22% vs. 35%, p = 0.02). Furthermore, patients directly evaluated at our institution had longer door-to-needle (34 [25–41] vs. 22 [21–30] min, p < 0.01) and door-to-recanalization delays (100 [90–124] vs. 89 [64–97] min, p = 0.04).
SD = standard deviation; IQR = interquartile range; ED = emergency department.
The proportion of COVID-19 positive cases was 3% (4/146); two patients presented with stroke mimics (septic encephalopathy) and two had confirmed ischemic strokes. Ten patients, all diagnosed as stroke mimics, had declined screening.
When controlling for confounders, the pandemic period was not statistically associated with thrombolysis treatment (adjusted odds ratio [aOR]: 0.49, 95% confidence interval [CI]: 0.23–1.03) or thrombectomy (aOR: 0.70, 95% CI: 0.26–1.86; Table 2). However, the pandemic period was inversely associated with hospital presentation within 4.5 h from symptom onset (aOR: 0.46, 95% CI: 0.21–0.96) and with referral from another institution for thrombectomy (aOR: 0.40, 95% CI: 0.19–0.82; Table 3).
aOR = adjusted odds ratio; 95% CI = 95% confidence interval.
aOR = adjusted odds ratio; 95% CI = 95% confidence interval.
This study provides additional evidence that the COVID-19 pandemic has an impact on the presentation and management of acute stroke patients. While in some areas stroke centers have reported a lower number of acute stroke evaluations overall,Reference Kansagra, Goyal, Hamilton and Albers5–Reference Rudilosso, Laredo and Vera8 we observed a similar acute stroke caseload during the first 2 months of the pandemic. This may reflect increased referrals to our center resulting from temporary closures of nearby stroke centers due to institutional outbreaks during the study period. Importantly, delays between symptom onset and hospital presentation were significantly longer, and fewer patients underwent reperfusion therapy. Our analysis suggests that the pandemic may be affecting reperfusion therapy eligibility through increased delays to hospital presentation and decreased referrals from other institutions.
In addition, we observed longer delays to reperfusion (door-to-needle and door-to-recanalization) and only 3% of patients testing positive for COVID-19 (Figure 1). Albeit necessary, in-hospital infection control measures, including the use of appropriate protective equipment and secure patient transportation, may be delaying acute stroke management. Other than these safety procedures, we avoided modifications to our established, guideline-based code stroke protocol. For instance, patient transfer from first evaluation to CT scan remained streamlined with prenotification and dedicated transport staff, which may explain why we did not observe an increase in door-to-imaging delays. While some authors have advocated greater use of elective intubation for endovascular therapy during the pandemic,Reference Sharma, Rasmussen and Han9 our approach remained unchanged in order to avoid further delays. Existence of an established code stroke protocol with prior favorable metrics, as well as collaborative implementation of required protocol modifications, may explain why despite greater delays our in-house metrics still remained within the accepted range of recommended clinical standards during the pandemic.
Our study is limited by its single-center design and by the relatively short observation period. Although demographics and clinical characteristics were similar between cohorts, the possibility of systematic or random bias cannot be excluded. Whether the longer delays observed in this study will be sustained over time and translate into worse functional outcomes for patients remains to be determined and will be evaluated in longer term studies.
In conclusion, the first two months of the COVID-19 pandemic were not associated with a decrease in acute stroke evaluations in our comprehensive stroke center. Despite only 3% of code stroke patients being diagnosed with concomitant COVID-19, we observed longer delays between stroke onset, initial evaluation, and reperfusion therapy. In addition, a lower proportion of acute stroke patients in the pandemic cohort benefited from such therapies. These findings support concerns that the current pandemic may have a negative impact on the acute management of non-COVID-19-related conditions such as acute stroke. Further research will be needed to investigate the long-term effects of the pandemic on population-based acute stroke incidence, hospital stroke volumes, treatment metrics, and long-term outcomes.
Disclosures
The authors report no disclosures relevant to the study.
Statement of Authorship
JNB, CD, and AYP: Conceptualized and designed the study, collected and analyzed the data, and drafted the manuscript. GJ: Collected and analyzed the data, and reviewed the manuscript for intellectual content. WA, WB, ND, YD, JE, LCG, DI, CO, JR, DR, CS, and AW: Reviewed the manuscript for intellectual content.
Supplementary Material
To view supplementary material for this article, please visit https://doi.org/10.1017/cjn.2020.160.