1. Introduction
The occurrence of acute exacerbation of chronic pulmonary disease (AECOPD) is a common cause for individuals seeking medical attention at the emergency department (ED) [
1]. The urgency in providing rapid treatment arises from the high mortality associated with this condition [
2,
3]. Non-invasive ventilation support (NIV) has been established as a gold standard treatment for AECOPD over the last couple of years [
3]. However, the advent of the COVID-19 pandemic in early 2020 ushered in practical challenges that impacted the implementation of this established treatment.
A great proportion of COVID-19 patients initially present with respiratory symptoms. Subjects suffering from chronic lung disease are at higher risk for severe disease progression and have an increased risk of mortality [
4,
5,
6]. Despite the acknowledged efficacy of aerosol-forming treatments such as NIV or bronchodilator inhalation for AECOPD, a cautious approach was taken to discourage their use until the exclusion of a concurrent COVID-19 infection [
6]. This is especially true for intensive or intermediate care units integrated into an emergency department (ED) with little to no means of isolating a potentially infectious patient. During the first wave of the COVID-19 pandemic, when antigen tests were not yet widely available and reliable, it took two to four hours until the results of PCR tests were available and the SARS-CoV2 status of a patient was known.
A combination of these factors could lead to a delay in respiratory therapy for patients with AECOPD.
These multifaceted challenges arising from the COVID-19 pandemic, including the potential delay in initiating respiratory therapy for AECOPD patients, were compounded by a global decrease in overall patient numbers at EDs. This was partly due to measures taken by the hospital. For example, for patients seeking care on their own (without consulting emergency medical services first), access was often restricted to individuals under long-term treatment at the hospital (e.g., patients being treated for cancer) or those referred by a specialist.
This was, in some aspects, similar to previous catastrophes such as Hurricane Sandy in 2012 and outbreaks of MERS 2015 or SARS 2003, when a significant decline in patient numbers was observed at EDs [
7,
8,
9,
10]. This effect was particularly noticeable in patients with chronic or non-urgent health problems. Those who seek help in a hospital despite a catastrophe often suffer from serious illness and require extensive testing and therapy [
11,
12].
The cumulative impact of these factors during the COVID-19 pandemic translated into a significant decrease in overall patient volumes seeking emergency care.
One of the key functions of an ED is the quick evaluation of patients and deciding whether they require intensive care, can be treated on a regular hospital ward, or if outpatient management is possible. In many cases, this decision can be made based on clinical presentation, medical history, and only a very limited set of necessary additional (laboratory or imaging) tests, saving precious resources. This quick-decision approach was severely impaired by the COVID-19 pandemic. Inpatient admission was dependent on PCR test results, which could take up to four hours. Treatment in the emergency department itself, especially non-invasive ventilation support, might also have been delayed. Available space was limited due to the need for isolation, and fear of an increased infection risk might have influenced the decision to start such potentially aerosol-forming treatments.
Goals of this Investigation
Considering the limited understanding surrounding the implications of a pandemic involving an airborne virus on the care of patients grappling with respiratory insufficiency, our primary objective was to conduct a comprehensive analysis delineating the repercussions of the COVID-19 pandemic on patient flow and treatment for individuals experiencing acute exacerbation of chronic obstructive pulmonary disease.
Specifically, we analyzed data to ascertain whether there was a surge in patients necessitating comprehensive respiratory therapy such as oxygen insufflation, employment of HFNC, utilization of NIV, or invasive ventilation as a last resort. Moreover, our investigation extended beyond the immediate treatment realm, aiming to unravel the ripple effects of the pandemic on the operational aspects of the emergency department. One key aspect scrutinized was whether the pandemic triggered an extension in the boarding time experienced by patients at the ED, potentially indicative of an increased strain on the healthcare system. We probed further into whether there was a notable fluctuation in the rates of hospital admissions or intensive care unit (ICU) admissions, reflecting the systemic impact of the pandemic on the broader spectrum of healthcare services. In our quest for a comprehensive understanding, we also embarked on an exploration of longer-term consequences, delving into the potential influence of the pandemic on one-year mortality rates among patients presenting with AECOPD.
2. Materials and Methods
2.1. Study Design and Setting
We conducted a retrospective chart review investigating the temporal dynamics of the COVID-19 pandemic’s impact on healthcare delivery. The study period encompassed the initial wave of the pandemic, spanning from 15 March 2020 to 14 March 2021, and was compared with the corresponding time frame exactly one year prior, extending from 15 March 2019 to 14 March 2020. To ensure a thorough understanding of the long-term implications, all patients were followed up for a duration of one year.
In adherence to robust research methodologies, our study findings are presented in accordance with the REporting of studies Conducted using Observational Routinely collected health Data (RECORD) Statement, an extension that augments the STrengthening the Reporting of OBservational studies in Epidemiology (STROBE) statement [
13]. The study was approved by our local institutional review board.
The study setting was a 2300-bed tertiary care university hospital, which is the largest of seven public hospitals in a city with 1.9 million inhabitants. The Department of Emergency Medicine is a pivotal component of this healthcare center and shoulders the responsibility for the treatment of all medical emergencies in adult patients. The department is divided into three parts, including an intensive care unit consisting of seven positions, a seven-bed intermediate care unit, and an outpatient clinic, each tailored to meet the diverse medical needs of the patient population.
Patient triage, a critical facet in the emergency care continuum, is expertly handled by qualified nurses who employ the internationally recognized Emergency Severity Index (ESI). This stratification system categorizes patients into five groups, ranging from 1 (life-threatening) to 5 (no medical resources needed) [
14]. Collaborative care is a cornerstone of the department’s operational philosophy and sees physicians working in tandem with consultant physicians from various specialties such as ENT, surgery, orthopedics, and others, ensuring a thorough approach to patient well-being.
In the context of the Austrian healthcare landscape, characterized by a universal healthcare system, our study benefits from insights derived within a framework that ensures healthcare coverage for all, including hospitalization, outpatient care, and ambulance services. Noteworthy is the absence of regulations dictating the level of care, allowing patients the autonomy to choose their preferred level of care without the need to navigate through a general practitioner or any other intermediary healthcare provider.
2.2. Study Population and Inclusion and Exclusion Criteria
The study population consisted of all patients treated for acute exacerbations of COPD at the department during the study period, as determined by the treating physician. We decided to analyze full calendar years to allow for the known seasonal fluctuation in patient numbers and case mix. Patients who left without being seen were excluded from this study.
2.3. Measurements
All data were collected through the hospital’s electronic health record and retrospectively retrieved for this study.
Collected data included:
Patient age and gender
Date and time of arrival at the ED and leaving the ED (discharge or admission)
Further management (discharge, admission to normal ward or ICU)
Use of long-term oxygen therapy (LTOT) at home
Vital signs on admission (heart rate, blood pressure, blood gas analysis)
Laboratory findings (inflammatory signs, renal function parameters)
Respiratory therapy according to the WHO ordinal scale for COVID-19 clinical research:
- 0
no clinical or virological evidence of infection
- 1
ambulatory, no activity limitation
- 2
ambulatory, activity limitation
- 3
hospitalized, no oxygen therapy
- 4
hospitalized, oxygen mask or nasal prongs
- 5
hospitalized, noninvasive mechanical ventilation (NIMV) or high-flow nasal cannula (HFNC)
- 6
hospitalized, intubation and invasive mechanical ventilation (IMV)
- 7
hospitalized, IMV + additional support such as pressors or extracardiac membranous oxygenation (ECMO)
- 8
death
Chest X-ray findings (emphysema, pulmonary infiltrates)
Re-admission within one year
Death within one year
The research team had full access to the health record database and all members were carefully trained in coding before beginning the chart review process. This pre-emptive training was a crucial step in enhancing the accuracy and consistency of data coding throughout the research project. To maintain a high standard of data quality and accuracy, the coded information underwent monitoring by the primary investigator, who conducted random checks at various stages of the process. Any observed discrepancies in the coding were promptly flagged, triggering a comprehensive review and clarification process by the research team. We used an electronic form for data abstraction. Prior to full-scale implementation, a small-scale and informal test pilot was conducted to ensure the seamless functionality and effectiveness of the electronic abstraction system. This pilot phase served as a proactive measure to identify and address any potential glitches or challenges in the system, thereby optimizing the data abstraction workflow for the main phase of the study. One year subsequent to the initial presentation at the emergency department, the research team engaged in a follow-up stage by accessing the patient’s national electronic health record once again. This revisit aimed to ascertain whether, and if so, when the patient had experienced any subsequent hospital re-admissions or had succumbed to their health challenges. This longitudinal approach to data collection not only provided valuable insights into the immediate outcomes following the emergency department visit but also enabled the exploration of longer-term health trajectories and potential correlations between initial interventions and sustained health outcomes.
2.4. Outcomes and Analysis
The primary outcome was the type of respiratory therapy (HFNC/non-invasive ventilation support/intubation) received by patients treated for AECOPD. Secondary outcomes included waiting time from arrival at the emergency department to admission, total number of patients treated, admitted to the ward, and admitted to the ICU for AECOPD, and proportion of patients receiving invasive and non-invasive ventilation at the emergency department.
We compared the “before” and “pandemic” groups using standard methods (the chi-square test for comparison of categorical variables and the t-test and Mann–Whitney U test for comparison of normally distributed and non-normally distributed continuous variables, respectively). We calculated absolute differences in outcomes using linear (for continuous outcomes) and binary (for categorical outcomes) regression, calculating robust 95% confidence intervals as described by Hamilton et al. We used Stata 17MP for all calculations.
4. Discussion
In our comprehensive study analyzing emergency department (ED) visits for AECOPD both before and during the initial wave of the COVID-19 pandemic, a pronounced and statistically significant reduction in ED visits emerged—a trend consistent with a plethora of analogous findings in the existing literature [
16,
17,
18,
19]. Interestingly, in our study, this was true, although we included only patients with AECOPD, whereas Gutovitz et al. in their analysis of ED utilization in America during the pandemic identified infectious disease and respiratory illnesses as exceptions from the general decrease in ED visits [
17]. Our findings also deviate from earlier research [
18], as we did not observe any discernible differences regarding gender in the context of ED visits for AECOPD.
While our investigation revealed no alterations in the relative frequency of simple oxygen insufflation, high-flow nasal cannulas, or invasive ventilation, a substantial and statistically significant increase was observed in the overall utilization of respiratory therapy, escalating from 71% to 80%. Moreover, there was a conspicuous increase in the proportion of patients receiving non-invasive ventilation support, rising from 12% to 18%. This surge in therapeutic interventions was notably mirrored by an increase in the percentage of patients treated at the ED’s own Intensive Care Unit (ICU), surging from 39% to 64%.
These observed shifts in treatment patterns likely represent a confluence of factors, including an influx of more severe cases, as indicated by the distinctly heightened one-year mortality rates—a trend aligning with findings in other studies [
18,
19]. Additionally, alterations in management strategies may be at play, potentially influenced by a heightened “fear of aerosols”. This fear could explain the exclusive increase in therapy involving non-invasive ventilation support, utilizing tight face masks, without a corresponding rise in HFNC. The concern for potential transmission between patients due to insufficient isolation capacity in the general ED area might have prompted physicians to opt for broader transfers to the ED’s ICU. The stability in the transfer rates to other ICUs after initial ED treatment could be considered supportive evidence for this hypothesis.
Healthcare provision during the pandemic undoubtedly bore the imprint of numerous influences. Medical considerations, such as the perceived severity of cases and evolving knowledge about COVID-19, likely played a pivotal role in guiding treatment decisions. Concurrently, non-medical factors, including the prevailing “fear of aerosols” and concerns about transmission risks within the healthcare setting, may have exerted a notable influence. These factors collectively highlight the complex decision-making processes that healthcare providers navigated, balancing the obligation to provide effective care with the necessity to mitigate potential transmission risks.
In summary, our study underscores the complex relationship of many medical and non-medical factors that have left a permanent mark on patient numbers and management practices during the pandemic.
Figure 5 provides a visual representation, illustrating potential interactions between the various phenomena encountered in the complicated healthcare landscape during this unprecedented period.
Limitations
This was a before–after study with all the limitations inherent to this design. In particular, no causal inference should be drawn from the findings. The nature of this study design restricts our interpretation to a description of observed changes. For instance, while our study sheds light on notable shifts in therapy choices, such as the potential influence of a “fear of aerosols”, we must underscore the inability to conclusively prove the reasons behind providers opting for one therapeutic approach over another.
Furthermore, the scope of our investigation was specifically tailored to patients treated for AECOPD within the emergency department (ED), thereby confining the generalizability of our findings to this specific clinical setting. The outcomes and dynamics observed in our study might not necessarily be extrapolated to other medical contexts or patient populations. Additionally, the study was conducted as a single-center study, although within the confines of a large tertiary care center. While this singular focus allows for a detailed exploration within a specific institutional framework, physicians have to be cautious when extending these findings to a broader healthcare landscape.
We nevertheless believe that our findings carry meaningful implications, particularly in shedding light on the challenges faced by an especially vulnerable group of patients—those undergoing treatment for AECOPD—during the unprecedented era of the COVID-19 pandemic. This population’s unique vulnerabilities and healthcare needs warrant focused attention, and our study may contribute valuable insights into the nuanced changes observed in their care within the ED setting. It is essential to contextualize our study within the broader context of existing research because the impact of the pandemic on the general ED population has been extensively studied. By focusing on this specific subset of patients, our study addresses a crucial gap in the literature, providing a better understanding of the challenges and adaptations encountered in the care of individuals grappling with AECOPD amidst the evolving landscape of the COVID-19 pandemic.