Literature DB >> 33722432

Telehealth follow up in emergency department patients discharged with COVID-like illness and exertional hypoxia.

Peter A D Steel1, Jonathan Siegal2, Yiye Zhang3, Kenrick Cato4, Peter Greenwald3, Laura D Melville5, Kriti Gogia3, Zachary Smith3, Rahul Sharma3, Marie Romney4.   

Abstract

Entities:  

Year:  2021        PMID: 33722432      PMCID: PMC7919584          DOI: 10.1016/j.ajem.2021.02.052

Source DB:  PubMed          Journal:  Am J Emerg Med        ISSN: 0735-6757            Impact factor:   2.469


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Introduction

New York City was the initial US epicenter of the 2020 Covid-19 global pandemic. Early models predicted a crisis of hospital capacity. Our healthcare system's nine emergency departments (EDs) developed a disaster care pathway (Fig. 1 ) designed to preserve inpatient capacity for the most severely ill Covid patients. The pathway included the discharge of a subgroup of patients with Covid Like Illness (CLI) who otherwise would have been admitted to the hospital [1,2]. We monitored these patients with a combination of post-ED telemedicine (virtual) follow up (VF) and remote patient monitoring (RPM) with home pulse oximetry. During the Covid-19 pandemic, telemedicine and RPM models have been described to monitor pulse oximetry (SpO2) in patients discharged from both inpatient and ED care, including escalation protocols as intervention for clinical deterioration [[3], [4], [5], [6]]. Our objective is to describe the crisis pathway we employed and assess the available outcomes.
Fig. 1

Evaluation pathway for ED patients with possible COVID Infection.

Evaluation pathway for ED patients with possible COVID Infection.

Clinical protocol

Our enterprise's Evaluation Pathway for ED Patients with Possible Covid Infection (Fig. 1) triaged ED patients into mild, moderate and severe CLI, based on early severity classification tools [7]. Patients determined to have severe CLI were admitted to the hospital. Patients who maintained saturation above 94% were discharged with standardized Covid precautions. Patients with oxygen saturation between 90% and 94% who met additional criteria for discharge were enrolled in the follow up program. Patients were enrolled via electronic health record (EHR). All enrolled patients were discharged with a portable consumer pulse oximeter (Drive Medical MQ3200; Medline HCSM70C). Patients with exertional SpO2 between 90 and 91% were also given a home oxygen concentrator set at 2 l oxygen (O2) per minute via nasal cannula (SimplyGo by Philips; Esclipse by CAIRE; OxLife Independence by O2 Concepts; Inogen One G3 by Inogen). Devices were provided to patients without additional charge. Enrolled patients were monitored post-discharge via virtual follow up (VF). VF visits were initiated within 24 h of ED discharge, performed as video visits when possible, with telephone as alternate. VF visits were attempted at least once a day for a total of 7 days, performed by advanced practice providers and physicians. Visits included an assessment of the patient's symptoms, as well measurement of pulse oximetry at rest and with exertion. At the end of each VF visit a recommendation was made for i) continuing care at home supported by VF visits, if improving or stable; ii) discontinuation of further VF visits (and supplementary oxygen), if interval resolution of symptoms for 2 days; iii) return to ED, if worsening symptoms or hypoxia (SpO2 less than 90%). VF providers could contact an ED attending physician in real time as an escalation pathway for clinical decision making. Patient outcome data were collected retrospectively from 4 regional hospitals and 2 quaternary care medical centers in New York between March 29th 2020 and April 17th, 2020. Collected variables are shown in Table 1, Table 2, Table 3, Table 4, Table 5 . Additional follow-up information after the 7-day period was obtained by calling patients at 90–120 days post index visit. Patients who returned to non-study-site EDs were included in 30-day mortality rates only. For continuous variables, Student t-test was used for variables with normal distribution and equal variances, and Wilcoxon rank sum test was used for variables with unnormal distribution. For categorical variables, Chi-square test was used for variables whose all of the cells of a contingency table are not below 5, and Fisher's exact test was used for other variables.
Table 1

Index ED visits.

CharacteristicPatient (N = 677)Pulse oximeter only (N = 483)Pulse oximeter and O2 concentrator (N = 194)
Age – median (IQR) (N = 677)54 (42–62)52 (41–61)57 (45–67)
Female sex — no. (%) (N = 677)273 (40.3)205 (42.4)69 (35.6)
Days since symptom onset – median (IQR) (N = 654)7 (4–10)7 (4–10)7 (4–10)
Vitals – median (IQR)
 Triage SpO2 (N = 677)94 (93–96)95 (93–97)94 (92–96)
 Triage RR (N = 672)20 (18–22)20 (18–22)20 (18–22)
 Heart Rate (N = 677)99 (87–110)99 (87–109)99 (88–111)
Blood pressure (N = 674)
 Systolic128 (116–140)128 (117–141)128 (116–139)
 Diastolic80 (73–85)80 (73–86)79 (73–85)
Temperature (N = 677)37 (37–38)37 (37–38)37 (37–38)
Discharge SpO2 (%) (N = 560)95 (94–97)96 (94–97)95 (93–96)
Discharge RR (breaths/min) (N = 406)18 (18–20)18 (18–20)18 (18–20)
Exertional SpO2 (%) (N = 604)93 (92–94)94 (93–95)91 (90–92)
Chest X-ray performed — no. (%)443 (65.4)289 (59.8)154 (79.4)
 Any consolidation334 (49.3)205 (42.4)129 (66.5)
 Unilateral Findings279 (41.2)169 (35.0)110 (56.7)
 Bilateral Findings54 (8.0)35 (7.2)19 (9.8)
Discharged w/Antibiotics — no. (%) (N = 673)127 (18.8)93 (19.3)34 (17.5)
Coexisting condition — no. (%) (N = 677)
 Hypertension247 (36.5)165 (34.2)82 (42.3)
 Diabetes140 (20.7)83 (17.2)57 (29.4)
 Chronic Vascular Disease27 (4.0)13 (2.7)14 (7.2)
 Chronic Kidney Disease21 (3.1)10 (2.1)11 (5.7)
 COPD8 (1.2)7 (1.4)1 (0.5)
 Interstitial Lung Disease2 (0.3)0 (0.0)2 (1.0)
 Asthma74 (10.9)62 (12.8)12 (6.2)
 Immunosuppression8 (1.2)6 (1.2)2 (1.0)
 Active Malignancy11 (1.6)10 (2.1)1 (0.5)
 At least 3 coexisting conditions101 (14.9)65 (13.5)36 (18.6)
Lost to follow up during study period — no. (%)36 (5.3)26 (5.4)10 (5.2)
 Lost to follow up*— no. (%)21 (3.1)14 (2.9)7 (3.6)
Returned to any ED — no. (%)158 (23.3)116 (24.0)42 (21.6)
30-day mortality — no. (%)13 (1.9)10 (2.1)3 (1.5)
Table 2

Virtual follow-up visits.

CharacteristicTotalED returnNo ED return
Unique patients participated — no. (% of total cohort)586 (86.5)120 (17.7)466 (68.8)
Index visit to first follow–up visit - days median (IQR)1 (1–2)1 (1–1)1 (1–2)
Total number of visits completed18253201505
Number of visits per patient – median (IQR)3 (2–4)2 (1–4)3 (2–4)
Mode of visits — no. (%)

Denominator 441.

Table 3

Index ED visit characteristics of patients with return visits.

CharacteristicPatient (N = 138)Admitted on return visit (N = 86)Discharged on return visit⁎⁎ (N = 52)P value
Age – median (IQR) (N = 138)56 (44–62)58 (45–66)51 (40–60)0.016
Female sex — no. (%) (N = 138)53 (38.4)28 (32.6)25 (48.1)0.102
Days since symptom onset – median (IQR) (N = 135)7 (4–10)7 (4–10)7 (4–10)0.944
Vitals – median (IQR)
 Triage SpO2 (N = 138)95 (93–96)94 (93–96)95 (94–97)0.082
 Triage RR (N = 137)20 (18–22)20 (18–21)20 (18–22)0.426
 Heart Rate (N = 138)97 (82–108)99 (80–110)94 (84–105)0.689
Blood pressure (N = 138)
 Systolic125 (115–140)125 (112–138)126 (118–142)0.281
 Diastolic79 (72–87)78 (71–85)82 (73–89)0.047
 Temperature (N = 138)37 (37–38)38 (37–38)37 (37–38)0.006
 Discharge SpO2 (%) (N = 119)95 (94–97)95 (94–97)97 (95–98)0.010
 Discharge RR (breaths/min) (N = 89)18 (18–20)18 (18–20)18 (18–20)0.983
 Exertional SpO2 (%) (N = 121)93 (92–94)93 (91–94)94 (93–95)0.001
Chest X-ray performed — no. (%)99 (71.7)60 (69.8)39 (75.0)0.641
 Any consolidation77 (55.8)51 (59.3)26 (50.0)0.058
 Unilateral Findings17 (12.3)9 (10.5)8 (15.4)0.329
 Bilateral Findings59 (42.8)41 (47.7)18 (34.6)0.329
Discharged w/Antibiotics — no. (%) (N = 136)30 (21.7)20 (23.3)10 (19.2)0.680
Coexisting condition — no. (%) (N = 138)
 Hypertension54 (39.1)39 (45.3)15 (28.8)0.081
 Diabetes31 (22.5)20 (23.3)11 (21.2)0.939
 Chronic vascular disease8 (5.8)6 (7.0)2 (3.8)0.710
 Chronic kidney disease4 (2.9)2 (2.3)2 (3.8)0.632
 COPD2 (1.4)1 (1.2)1 (1.9)1.000
 Interstitial lung disease1 (0.7)1 (1.2)0 (0)1.000
 Asthma17 (12.3)8 (9.3)9 (17.3)0.263
 Immunosuppression1 (0.7)1 (1.2)0 (0)1.000
 Active Malignancy4 (2.9)3 (3.5)1 (1.9)1.000
 At least 3 coexisting conditions25 (18.1)19 (22.1)6 (11.5)0.183
30-day mortality — no. (%)12 (8.7)10 (11.6)2 (3.8)0.211

p-value < 0.05.

Including 1 patient deceased in ED.

Table 4

Characteristics of patients with return visits.

CharacteristicPatient (N = 138)Admitted (N = 86)Discharged (N = 52)⁎⁎P value
Age – median (IQR) (N = 138)56 (44–62)58 (45–66)51 (40–60)0.016
Female sex — no. (%) (N = 138)53 (38.4)28 (32.6)25 (48.1)0.102
Days since symptom onset – median (IQR) (N = 134)9 (6–14)9 (7–12)9 (6–17)0.518
Vitals – median (IQR)
 Triage SpO2 (N = 136)94 (91–97)93 (89–95)96 (94–98)<0.001
 Triage RR (N = 135)20 (18–24)22 (19–25)20 (18–20)<0.001
 Heart Rate (N = 118)99 (87–110)101 (90–112)96 (83–106)0.067
Blood pressure (N = 117)
 Systolic125 (112–136)123 (111–135)130 (114–137)0.365
 Diastolic78 (72–85)78 (73–85)79 (72–85)0.791
 Temperature (N = 117)37.2 (36.8–37.9)37.3 (37.0–38.2)37.0 (36.8–37.3)0.003
Mortality — no. (%)
 Death within 24 h of ED arrival1 (0.7)0 (0.0)1 (1.9)0.377
 Death anytime during hospitalization11 (8.0)11 (12.8)N/AN/A

p-value < 0.05.

Including 1 patient deceased in ED.

Table 5

Characteristics of patients admitted in return visits.

CharacteristicPatient (N = 86)
Admitted to floor79 (57.2)
Admitted to stepdown5 (3.6)
Admitted to ICU2 (1.4)
Admitted to ICU within 24 h of hospitalization7 (5.1)
Admitted to ICU anytime during hospitalization16 (11.6)
Intubated within 24 h of hospitalization2 (1.4)
Intubated anytime during hospitalization11 (8.0)
Index ED visits. Virtual follow-up visits. Denominator 441. Index ED visit characteristics of patients with return visits. p-value < 0.05. Including 1 patient deceased in ED. Characteristics of patients with return visits. p-value < 0.05. Including 1 patient deceased in ED. Characteristics of patients admitted in return visits.

Results

A total of 677 patients were enrolled in the program. A total of 138 patients returned to a study site ED within 7 days, 86 patients were subsequently admitted, 16 required ICU level care. The overall 30-day mortality rate was 13. Table 1 describes the demographic and baseline characteristics from the index ED visit for all patients in the cohort. Table 2 describes data pertaining to VF visits, received by 86.5% of all patients. A median number of 3 visits occurred per patient, and 58.7% of the visits were audio-only. Of the 80 patients who were instructed to return to the ED during a follow-up visit, 18 did not return but none of these patients died or were lost to follow up. Of patients who reported an exertional SpO2 < 90% at home, 33 (57.9%) returned to an ED, and 22 (38.6%) were subsequently admitted. Table 3 describes the patients who returned to a study site ED. Those admitted on the repeat visit were older (58 vs 51, p-value = 0.016*) compared to those discharged home on the return visit. Additional information of patients who returned to the study site EDs within 7 days of index visit are outlined in Table 4. Table 5 describes the outcomes of patients admitted on their return visit. 79 (57.2%) were admitted to the floor, 5 (3.6%) were admitted to the step-down unit, and 2 (1.4%) were admitted to the intensive care unit (ICU) directly from the ED. Of all ED returns, there were 11 patients who died during admission, including one patient who died within 24 h of ED return (1.7%). There were 36 (5.3%) patients lost to follow-up during the 7-day study period, and 20 (2.9%) of patients documented to have returned to non-study site EDs. A total of 21 (3.1%) patients remained lost to follow-up at 120 days.

Discussion

This study describes the large-scale implementation of a novel post-ED care pathway utilizing telehealth virtual visits and remote patient monitoring for CLI patients discharged from 6 heterogeneous urban EDs. Outside of the Covid-19 crisis, this cohort would likely have been admitted to hospital. Subsequent to this study, the National Institute of Health classified Covid-19 patients with an SpO2 < 94% as severe, requiring supplementary oxygen, admission, and therapeutic management, including corticosteroid and antiviral therapy [8, [9], [10], [11], [12], [13], [14], [15], [16]]. While the enrollment criteria of this study (SpO2 90–94%) are now outdated, the care model may be useful in determining how best to use telemedicine resources and remote self-monitoring of SpO2 to increase safety for patients with Covid-19. The 30-day mortality of our cohort was 1.9%, significantly lower than the 10–21% inpatient mortality described in New York during approximately the same time, although there are limits to comparing these patient populations [17,18]. Common inpatient interventions not performed on the VF-RPM cohort, such as general nursing care and rapid escalation of care, limit further comparisons to inpatient management during the study time. Given 5.3% of the cohort was lost to follow up, similar models should focus on both patient education and discerning enrollment criteria. Future studies should examine the relatively low rates of video use (41%) for follow-up visits. The growing discussion regarding disparities associated with telemedicine care may play a role, although we were not able to collect race and ethnicity data [19,20]. While we became aware of some patients admitted to other hospitals during the course of initial follow-up protocol calls, as well as the follow up calls performed at 90–120 days post index visit to determine 30-day mortality, we did not utilize other data systems to gather information on patients lost to follow up. During the Covid-19 crisis, there has been great expansion of telemedicine care, incentivized by the US government and patients growing acceptance [21,22]. Healthcare systems who leverage telehealth technologies may offer more dynamic care during disaster scenarios. With many communities still experiencing surges in Covid-19 cases, post-ED care models incorporating telemedicine may be a useful strategy to provide flexible and safe care.

Funding

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.”

Declaration of Competing Interest

None.
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