Literature DB >> 33910601

Effect of the coronavirus disease pandemic on bronchoscopic diagnosis of lung cancer in a provincial city in Japan.

Taichiro Goto1.   

Abstract

Entities:  

Keywords:  Bronchoscopy; COVID-19; Diagnosis; Lung cancer; Pandemic

Mesh:

Year:  2021        PMID: 33910601      PMCID: PMC8080994          DOI: 10.1186/s13019-021-01501-2

Source DB:  PubMed          Journal:  J Cardiothorac Surg        ISSN: 1749-8090            Impact factor:   1.637


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Since its detection in Japan in January 2020, the coronavirus disease (COVID-19) has rapidly spread. Strict mitigating measures helped end the first wave of the outbreak. However, there is increasing concern of a second wave of infection. As effective vaccines and drugs for COVID-19 are still underway, long-term management plans are necessary to prevent the spread of infection. Moreover, “new clinical practice models” are necessary to accommodate both COVID-19 and non-COVID-19 patients. Recently, the incidence of lung cancer has steadily increased in Japan and the world [1]. Bronchoscopy is an important diagnostic method for lung cancer; however, performing bronchoscopy is challenging considering the threat of nosocomial infections during the COVID-19 pandemic [2, 3]. Similar to other coronavirus diseases, COVID-19 is mostly transmitted via droplets and contact [4]. Additionally, studies suggest aerosol transmission during specific medical procedures [5]. In particular, if a person is exposed to elevated aerosol concentrations in closed spaces such as bronchoscopy rooms, aerosol transmission of COVID-19 may occur causing nosocomial infection [6]. In this study, we compared characteristics of lung cancer patients who underwent surgery at our hospital from March to August 2020 with those of such patients from previous years (March to August 2017 to 2019) to examine the effects of the pandemic on bronchoscopic diagnosis of lung cancer. At our hospital, a core facility in the provincial city of Yamanashi, we perform surgeries for 160–170 lung cancer cases yearly. During the pandemic, the number of lung cancer patients who underwent surgery (n = 89) from March to August 2020 was comparable with that of previous years (Table 1) and did not decrease even though computed tomography (CT) screening was not routinely performed and the number of medical examinations substantially reduced. A possible reason could be that several local smaller-sized hospitals refrained from providing certain health care services such as lung cancer surgery during the pandemic.
Table 1

Changes in diagnosis of lung cancer at our hospital from March to August 2017 to 2020

2017201820192020p value
Number of surgical cases of lung cancera
 Stage 0-IV82807989
 Stage I-II56605862
Age (mean ± SD)b69.4 ± 5.169.9 ± 7.169.1 ± 6.569.6 ± 8.9NS
SexNS
 Male37394042
 Female19211820
Bronchoscopy< 0.05
 Performed4948474
 Not performed7121158
Method for preoperative definitive diagnosis< 0.05
 Sputum cytology0100
 Bronchoscopic examination2726282
 CT-guided needle biopsy1010
 None28332960
Rapid pathological examination during surgery among those without a preoperative definitive diagnosis< 0.05
 Done45421
 Not done24282539
Surgical procedureNS
 Lobectomy49555257
 Segmentectomy6454
 Partial resection1211
HistologyNS
 Adenocarcinoma43464546
 Squamous cell carcinoma12121214
 Others1212
Pathological stage< 0.05
 IA35444326
 IB98712
 IIA76516
 IIB5238
Number of days waiting to have surgery24.1 ± 6.326.3 ± 5.624.5 ± 6.113.9 ± 4.5*< 0.05
Total hospitalization period (hospitalization for tests plus hospitalization for surgery)10.1 ± 4.211.1 ± 4.310.6 ± 3.98.0 ± 1.7*< 0.05
Diagnostic unpredictability4.24.64.14.0< 0.05

CT computed tomography, NS not significant, SD standard deviation

aHistological typing was performed according to the World Health Organization classification (3rd edition), and clinical staging was performed according to the International Union Against Cancer Tumor-Node-Metastasis classification (8th edition)

bContinuous variables were presented as mean ± SD, and one-way analysis of variance and the Tukey–Kramer multiple comparison test were used to detect significant differences between groups

†Chi-square tests were used to compare categorical data between groups

*P < 0.05, compared to previous years. P -values < 0.05 in the two-tailed analyses were considered to denote statistical significance

Changes in diagnosis of lung cancer at our hospital from March to August 2017 to 2020 CT computed tomography, NS not significant, SD standard deviation aHistological typing was performed according to the World Health Organization classification (3rd edition), and clinical staging was performed according to the International Union Against Cancer Tumor-Node-Metastasis classification (8th edition) bContinuous variables were presented as mean ± SD, and one-way analysis of variance and the Tukey–Kramer multiple comparison test were used to detect significant differences between groups †Chi-square tests were used to compare categorical data between groups *P < 0.05, compared to previous years. P -values < 0.05 in the two-tailed analyses were considered to denote statistical significance On comparing the characteristics of stage I-II lung cancer patients between 2017 and 2019 and 2020, no significant differences in age or sex were found; however, the number of bronchoscopy procedures and endoscopic diagnoses of lung cancer were significantly lower in 2020 (Table 1). We do not now perform CT-guided biopsy at our hospital despite its high diagnostic accuracy because of the potential risk of air embolism and dissemination [7]. Therefore, the number of patients who underwent surgery without a preoperative definitive diagnosis substantially increased during the pandemic in 2020. Additionally, among these patients, the number of those undergoing rapid pathological examinations during surgery significantly increased. Comparing the data with those from 2017 to 2019 revealed no significant changes in surgical procedures or histology. However, the number of patients with advanced stage disease (IIA or IIB) increased in 2020. This could be because fewer individuals undergo CT screening and more lung cancers are being detected based on subjective symptoms. As previously reported, there is a sudden change in the distribution of stages of diagnosed lung cancers owing to the pandemic [8]. In addition, the waiting period (days) for surgery and total hospitalization period (hospitalization for tests and surgery) significantly reduced in 2020 because bronchoscopy was omitted in almost all patients. Most importantly, the diagnostic unpredictability, measured by the number of patients who underwent surgery for suspected lung cancer but were found to have benign disease, did not increase. This situation is ongoing, and the challenges in performing bronchoscopy persist. To address it, cancer board conferences aimed at enhancing diagnostic imaging capabilities are being conducted more frequently than in past years. Furthermore, as we perform preoperative CT twice to evaluate sequential changes in tumor and virtual bronchoscopy, as a substitute, to determine the location of the bronchial bifurcation and tumor, we theorize that bronchoscopy is not indispensable in diagnosing stage I-II lung cancer and can be omitted considering the need for infection control. However, it should be noted that this study only investigated patients with clinical stage I or II lung cancer. For patients suspected to have mediastinal lymph node metastasis (N2 disease), it is important to perform bronchoscopy, including endobronchial ultrasound. In such cases, bronchoscopy should be performed with sufficient precautions, and if that is unavailable, mediastinoscopy may be performed as a substitute. Besides the risk of nosocomial infection with COVID-19, bronchoscopic examination has its own merits and demerits. On the one hand, it can help guide appropriate treatment strategies when a diagnosis (cancer or other) is obtained, and it may help avoid unnecessary surgery. Airway observation by bronchoscopy enables the endoscopic detection of early lung cancer and confirmation of the tracheal bifurcation. Furthermore, biopsy of the bronchial epithelium enables evaluation of the extent of tumor invasion. On the other hand, bronchoscopy is relatively invasive and may prolong the time to surgery [9]. Moreover, the diagnostic rate of lung cancer is unsatisfactory; it is approximately 50–60% for resectable types and is particularly low for small-sized peripheral types [10]. In our hospital, bronchoscopy is performed according to the following guidelines: (i) the diagnosis of lung cancer is mainly based on imaging analyses, and unnecessary bronchoscopies are avoided; (ii) all patients undergo polymerase chain reaction-based testing for COVID-19 infection before undergoing bronchoscopy; (iii) staff wear medical caps, N95 masks, goggles, long sleeve gowns, and gloves while conducting bronchoscopic examinations; (iv) oropharyngeal anesthesia via xylocaine spray (8%) is used instead of applying local anesthesia using Jackson’s spray (face-to-face application); (v) systemic administration of sedative drugs (benzodiazepine and opioid etc.) is performed to prevent cough during the procedure, (vi) one-hour intervals are taken for cleaning between examinations, during which ventilation and sterilization of the room are performed, and (vii) the maximum number of examinations per day is restricted to three as opposed to eight (prior to the pandemic). Because prolonged mitigating measures against new coronavirus infection are expected and bronchoscopy may not be readily available, we believe that as clinicians it is important to critically examine the need of bronchoscopic diagnosis of lung cancer to establish a flexible, feasible, and novel clinical system in compliance with the “new lifestyle.”
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