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Annals of Clinical and Medical
Case Reports
Case Report ISSN 2639-8109 Volume 9
Germana Lages Gandra, Fábio José Araújo do Carmo, Gustavo Pinto de Moraes Kiffer, and Ricardo Mesquita Camelo*
Hospital Unimed Betim, Unimed-BH, Av. Juiz Marco Túlio Isaac, 3400 - Betim Industrial, Betim - MG, 32671-150, Brazil
COVID-19-Associated Pneumothorax: Case Reports
*
Corresponding author:
Ricardo Mesquita Camelo,
Hospital Unimed Betim, Unimed-BH, Av. Juiz
Marco Túlio Isaac, 3400 - Betim Industrial,
Betim - MG, 32671-150, Brazil,
E-mail: rmcamelo@hotmail.com
Received: 21 Sep 2022
Accepted: 01 Sep 2022
Published: 07 Sep 2022
J Short Name: ACMCR
Copyright:
©2022 Ricardo Mesquita Camelo. This is an open ac-
cess article distributed under the terms of the Creative
Commons Attribution License, which permits unrestrict-
ed use, distribution, and build upon your work non-com-
mercially
Citation:
Gandra et al, COVID-19-AssociatedPneumothorax: Case
Reports. Ann Clin Med Case Rep. 2022; V9(17): 1-5
http://www.acmcasereport.com/ 1
Abstract
Spontaneous pneumothorax associated with COVID-19 is rare.
We reported four cases and reviewed the literature. Among the
reports, 29% and 42% were a-/oligosymptomatic or symptomatic
but improving, respectively. Clinicians must be aware of this com-
plication because it can happen when the patient with COVID-19
was a-/oligosymptomatic or had improving symptoms.
1. Introduction
Pneumothorax is the presence of air in the pleural space due to
communications between the pleural and the alveolar/external
spaces or the presence of gas-producing organisms in the pleural
space. Spontaneous pneumothorax (SP) is diagnosed when no in-
jury has been inflicted to the thorax. There are two types of SP: pri-
mary SP, without apparent underlying lung disease, and secondary
SP, when there is a clinically apparent disease. SP is a rare event
among people with severe acute respiratory syndrome coronavirus
2 (SARS-CoV-2) pneumonia or COVID-19.1
We described four
cases of COVID-19-associated SP in patients treated at our hos-
pital.
2. Case Reports
The study was approved by the Committee on Ethics on Research
of the Hospital Eduardo de Menezes. Between March/1/2020-
June/30/2021, we prospectively searched all patients hospitalized
because of SP during or after COVID-19. The enrolled patients
signed the Consent Form. COVID-19 was diagnosed by reverse
transcriptase polymerase chain reaction for SARS-CoV-2 from
nasopharyngeal swab. We defined SP as pneumothorax detected
by any image modality without previous positive-pressure ventila-
tion, neck/chest manipulation, or trauma. We collected data using
a standardized form.
2.1. Case 1
An 84-year-old man with motor sequelae of stroke, hyperlipidem-
ia, mood disorder, benign prostatic disease, and previous smoker
presented to the Emergency Department (ED) with one-day fever,
cough, and dyspnea. He was afebrile, tachypneic with mild breath-
ing effort, normal lung sounds, and desaturating. He was dis-
charged home three days before, after a two-week hospitalization
due to COVID-19 and complaining fever, dry cough, and diarrhea.
During this hospitalization, his chest computed tomography (CT)
evidenced ground-glass opacities in 50% of the lung parenchyma
(Figure 1A). He received oxygen by nasal cannula, dexametha-
sone, amoxycillin+clavulanate, azithromycin, and enoxaparin.
Upon his return, he had elevated reactive C-protein (RCP). Other
laboratory tests were unremarkable. The new chest CT evidenced
sparse ground-glass opacities, and a small left-sided pneumotho-
rax with bilateral small pleural effusion (Figure 1B). He received
oxygen by nasal cannula, and dexamethasone was reintroduced.
He received piperacillin+tazobactam and thromboprophylaxis.
Pneumothorax was treated conservatively. He was discharged
home after one week.
Keywords:
COVID-19; Spontaneous pneumothorax; Respiratory
failure
ORCID IDs:
Germana Lages Gandra: https://orcid.org/0000-0003-4712-4185
Ricardo Mesquita Camelo: https://orcid.org/0000-0001-9025-0289
http://www.acmcasereport.com/ 2
Volume 10 Issue 1 -2022 Case Report
2.2. Case 2
A 77-year-old man with dementia and stroke sequelae presented to
the ED with COVID-19 after one day of agitation, without cough.
He stopped smoking for approximately 30 years. He was afebrile,
with normal lung sounds, tachypneic and desaturating, tachycar-
dic, and mildly hypertensive. He had leucocytosis, with elevated
RCP, lactic acid, and lactic-dehydrogenase. Other laboratory tests
were unremarkable. Ground-glass opacities covered less than 25%
of the lung parenchyma, with a large right-sided pneumothorax and
collapse of the right lung (Figure 2A). A chest drain was inserted
with a water-seal. He received oxygen by face mask, amoxycillin+-
clavulanate, azithromycin, dexamethasone, and enoxaparin. Clin-
ical conditions improved and the follow-up chest CT confirmed
lung expansion, with right-sided pleural effusion and bilateral con-
solidations (Figure 2B). The drain was removed three days after
insertion. One week after hospitalization, his respiratory condition
worsened. He was febrile with leucocytosis and increased RCP. A
new chest CT evidenced sparse ground-glass opacities, but a larg-
er pleural effusion associated with pleural thickness (Figure 2C).
Pleural decortication was performed, and piperacillin+tazobactam
and teicoplanin were prescribed. Vancomycin was prescribed, due
to Staphylococcus haemoliticus vancomycin-sensitive on a cathe-
ter tip culture. Fluconazole was associated, due to skin candidiasis
on seborrheic dermatitis. Since fever was recurrent and he started
diarrhea, a new course of piperacillin+tazobactam with metronida-
Figure 1: Chest computed tomography (CT) of the Case #1. A. Chest CT (topogram, axial view, and coronal view) of the first hospitalization. Some
ground-glass opacities were highlighted by large white arrows. B. Chest CT (topogram, axial view, and coronal view) of the second hospitalization,
when left-sided pneumothorax was diagnosed (thin white arrows). Some ground-glass and confluent opacities were also highlighted by large white
arrows.
zole was initiated, with Saccharomyces boulardii and racecadotril.
Clostridium difficile glutamate dehydrogenase was negative. Kleb-
siella pneumoniae ssp. pneumoniae and Pseudomonas aeruginosa
amikacin-sensitive were identified on the culture of his calcaneus
tissue injury, and he received amikacin. He was discharged home
after 86 days of hospitalization.
2.3. Case 3
A 67-year-old woman presented to the ED complaining fever, con-
fusion, dizziness, dry cough, and tachypnea, in the last seven days.
She had lung emphysema due to previous smoking with oxygen
supplementation at least three-quarters of the daytime. She was
treating systemic arterial hypertension, dyslipidemia, hypovita-
minosis D, and hypothyroidism. She also had a hearing sequela
due to previous stroke. She had mild COVID-19 two months be-
fore. She was afebrile, dyspneic with moderate effort, desaturating
at room air, and hypertensive. Laboratory tests were unremarkable.
SARS-CoV-2 was not detected. Chest CT evidenced a centrolobu-
lar emphysema and a large left pneumothorax with a mild right-de-
viated mediastinum (Figure 3). Low-flow oxygen was provided,
and she received azithromycin and piperacillin+tazobactam, cor-
ticosteroids, bronchodilators, codeine, and thromboprophylaxis. A
chest drain was inserted, connected to a water-seal. Bullectomy
and pleurodesis were performed 5 days after tube insertion, be-
cause of a high-flow air drainage. Chest tube was removed 5 days
later. She was discharged home after 14 days of hospitalization.
http://www.acmcasereport.com/ 3
Volume 10 Issue 1 -2022 Case Report
Figure 2. Chest computed tomography (CT) of the Case #2. A. Chest CT (topogram, axial view, and coronal view) at hospitalization, when right-sided
pneumothorax was diagnosed (thin white arrows). Some ground-glass opacities were highlighted by large white arrows. B. Chest CT (topogram and
axial view) showing lung expansion after chest tube insertion and air drainage. Some ground-glass opacities were also highlighted by large white
arrows. C. Chest CT (topogram and axial view) evidencing sparse ground-glass opacities (large white arrow), and a larger pleural effusion associated
with pleural thickness (thin black arrow).
Figure 3. Chest computed tomography (CT) of the Case #3. Chest CT (topogram, axial view, and coronal view) at hospitalization, when right-sided
pneumothorax was diagnosed (thin white arrows). Some ground-glass opacities were highlighted by large white arrows.
http://www.acmcasereport.com/ 4
Volume 10 Issue 1 -2022 Case Report
2.4. Case 4
A previously healthy 22-year-old man with COVID-19 was ad-
mitted after one week of sore throat and dry cough. At admission,
he was dyspneic with moderate effort, desaturating, tachycardic,
and normotensive. He denied smoking. He had elevated RCP. The
other blood tests were unremarkable. Chest CT showed ground-
glass opacities covering more than 50% of the lung parenchyma
and few consolidation foci (Figure 4A). A mild-to-moderate bi-
lateral pneumothorax associated with pneumomediastinum and
pneumopericardium was also noted. Oxygen was offered by face
mask. He received dexamethasone, thromboprophylaxis, and
amoxycillin+clavulanate and azithromycin. His respiratory effort
worsened, and he was intubated and mechanically ventilated in
prone position. Two chest tubes were inserted in both his right and
left hemithoraces, all connected to water-seals. Chest tubes were
withdrawn after four days. He self-extubated three days later. He
was discharged home, with a normal chest CT and breathing at
room air (Figure 4B).
Figure 4. Chest computed tomography (CT) of the Case #4. A. Chest CT (topogram and both inspired and expired axial views) at hospitalization, when
bilateral pneumothoraces were diagnosed (thin white arrows). Pneumomediastinum (large-narrow white arrows) and pneumopericardium (black ar-
rows) were also detected. Some ground-glass opacities were highlighted by large-long white arrows. B. Chest CT (topogram, axial, and coronal views)
before discharge. Small volume of gas was noted in the upper thorax. The other pneumatoses resolved completely.
http://www.acmcasereport.com/ 5
Volume 10 Issue 1 -2022 Case Report
3. Discussion
Since the beginning of the pandemic, many cases of COVID-19
-associated SP were reported. SARS-CoV-2 causes a diffuse
alveolar damage with perivascular immune cell infiltration,
severe endothelial injury, and widespread thrombosis, which may
lead to air leak and dilatation of some alveoli and hemorrhagic/
edematous collapse of others.2
The final rupture of the alveolar
wall is a consequence of a shear stress (e.g., coughing), developing
a communication with the pleural space. Ultimately, COVID-19
may also be considered a cause of SP. However, it should be
highlighted it is an unusual complication of COVID-19 (relative
frequency of 0.57‰), although more common in affected than in
non-affected individuals.1,2
A recent case-control study described
40 COVID-19-associated SP (i.e., without previous positive-
pressure ventilation, chest manipulation or trauma) among 71,904
patients attending in 50 Spanish EDs.3
Patients with COVID-19
who developed SP more frequently were men and their median
age similar to our search.3
They also more frequently had dyspnea/
tachypnea and chest pain, desaturation, and increased leukocyte
count, than those without COVID-19.3
Another registry held in
16 centers in the United Kingdom which reported 20 patients
with COVID-19-associated SP.4
Nine patients had the diagnosis
of pneumothorax at presentation to the ED, from which five
were readmissions.4
All cases we described had the diagnosis of
pneumothorax at admission, after improving or complaining mild
symptoms.
4. Conclusion
COVID-19-associated SP is a potentially severe, although rare,
complication. Physicians should be aware of this important pneu-
matosis because it can happen in people without previous diag-
References
1. Miro O, Llorens P, Jiménez S. Frequency of five unusual presenta-
tions in patients with COVID-19: Results of the UMC-19-S1. Epi-
demiol Infect. 2020; 148: e189-92.
2. Menter T, Haslbauer JD, Nienhold R. Postmortem examination of
COVID-19 patients reveals diffuse alveolar damage with severe
capillary congestion and variegated findings in lungs and other
organs suggesting vascular dysfunction. Histopathology. 2020;
77(2):198-209.
3. Miro O, Llorens P, Jiménez S. Frequency, Risk Factors, Clinical
Characteristics, and Outcomes of Spontaneous Pneumothorax in
Patients With Coronavirus Disease 2019: A Case-Control, Emergen-
cy Medicine-Based Multicenter Study. Chest. 2021; 159(3): 1241-
1255.
4. Martinelli AW, Ingle T, Newman J. COVID-19 and pneumotho-
rax: A multicentre retrospective case series. Eur Respir J. 2020;
56(5):2002697.

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COVID-19-associated pneumothorax

  • 1. Annals of Clinical and Medical Case Reports Case Report ISSN 2639-8109 Volume 9 Germana Lages Gandra, Fábio José Araújo do Carmo, Gustavo Pinto de Moraes Kiffer, and Ricardo Mesquita Camelo* Hospital Unimed Betim, Unimed-BH, Av. Juiz Marco Túlio Isaac, 3400 - Betim Industrial, Betim - MG, 32671-150, Brazil COVID-19-Associated Pneumothorax: Case Reports * Corresponding author: Ricardo Mesquita Camelo, Hospital Unimed Betim, Unimed-BH, Av. Juiz Marco Túlio Isaac, 3400 - Betim Industrial, Betim - MG, 32671-150, Brazil, E-mail: rmcamelo@hotmail.com Received: 21 Sep 2022 Accepted: 01 Sep 2022 Published: 07 Sep 2022 J Short Name: ACMCR Copyright: ©2022 Ricardo Mesquita Camelo. This is an open ac- cess article distributed under the terms of the Creative Commons Attribution License, which permits unrestrict- ed use, distribution, and build upon your work non-com- mercially Citation: Gandra et al, COVID-19-AssociatedPneumothorax: Case Reports. Ann Clin Med Case Rep. 2022; V9(17): 1-5 http://www.acmcasereport.com/ 1 Abstract Spontaneous pneumothorax associated with COVID-19 is rare. We reported four cases and reviewed the literature. Among the reports, 29% and 42% were a-/oligosymptomatic or symptomatic but improving, respectively. Clinicians must be aware of this com- plication because it can happen when the patient with COVID-19 was a-/oligosymptomatic or had improving symptoms. 1. Introduction Pneumothorax is the presence of air in the pleural space due to communications between the pleural and the alveolar/external spaces or the presence of gas-producing organisms in the pleural space. Spontaneous pneumothorax (SP) is diagnosed when no in- jury has been inflicted to the thorax. There are two types of SP: pri- mary SP, without apparent underlying lung disease, and secondary SP, when there is a clinically apparent disease. SP is a rare event among people with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pneumonia or COVID-19.1 We described four cases of COVID-19-associated SP in patients treated at our hos- pital. 2. Case Reports The study was approved by the Committee on Ethics on Research of the Hospital Eduardo de Menezes. Between March/1/2020- June/30/2021, we prospectively searched all patients hospitalized because of SP during or after COVID-19. The enrolled patients signed the Consent Form. COVID-19 was diagnosed by reverse transcriptase polymerase chain reaction for SARS-CoV-2 from nasopharyngeal swab. We defined SP as pneumothorax detected by any image modality without previous positive-pressure ventila- tion, neck/chest manipulation, or trauma. We collected data using a standardized form. 2.1. Case 1 An 84-year-old man with motor sequelae of stroke, hyperlipidem- ia, mood disorder, benign prostatic disease, and previous smoker presented to the Emergency Department (ED) with one-day fever, cough, and dyspnea. He was afebrile, tachypneic with mild breath- ing effort, normal lung sounds, and desaturating. He was dis- charged home three days before, after a two-week hospitalization due to COVID-19 and complaining fever, dry cough, and diarrhea. During this hospitalization, his chest computed tomography (CT) evidenced ground-glass opacities in 50% of the lung parenchyma (Figure 1A). He received oxygen by nasal cannula, dexametha- sone, amoxycillin+clavulanate, azithromycin, and enoxaparin. Upon his return, he had elevated reactive C-protein (RCP). Other laboratory tests were unremarkable. The new chest CT evidenced sparse ground-glass opacities, and a small left-sided pneumotho- rax with bilateral small pleural effusion (Figure 1B). He received oxygen by nasal cannula, and dexamethasone was reintroduced. He received piperacillin+tazobactam and thromboprophylaxis. Pneumothorax was treated conservatively. He was discharged home after one week. Keywords: COVID-19; Spontaneous pneumothorax; Respiratory failure ORCID IDs: Germana Lages Gandra: https://orcid.org/0000-0003-4712-4185 Ricardo Mesquita Camelo: https://orcid.org/0000-0001-9025-0289
  • 2. http://www.acmcasereport.com/ 2 Volume 10 Issue 1 -2022 Case Report 2.2. Case 2 A 77-year-old man with dementia and stroke sequelae presented to the ED with COVID-19 after one day of agitation, without cough. He stopped smoking for approximately 30 years. He was afebrile, with normal lung sounds, tachypneic and desaturating, tachycar- dic, and mildly hypertensive. He had leucocytosis, with elevated RCP, lactic acid, and lactic-dehydrogenase. Other laboratory tests were unremarkable. Ground-glass opacities covered less than 25% of the lung parenchyma, with a large right-sided pneumothorax and collapse of the right lung (Figure 2A). A chest drain was inserted with a water-seal. He received oxygen by face mask, amoxycillin+- clavulanate, azithromycin, dexamethasone, and enoxaparin. Clin- ical conditions improved and the follow-up chest CT confirmed lung expansion, with right-sided pleural effusion and bilateral con- solidations (Figure 2B). The drain was removed three days after insertion. One week after hospitalization, his respiratory condition worsened. He was febrile with leucocytosis and increased RCP. A new chest CT evidenced sparse ground-glass opacities, but a larg- er pleural effusion associated with pleural thickness (Figure 2C). Pleural decortication was performed, and piperacillin+tazobactam and teicoplanin were prescribed. Vancomycin was prescribed, due to Staphylococcus haemoliticus vancomycin-sensitive on a cathe- ter tip culture. Fluconazole was associated, due to skin candidiasis on seborrheic dermatitis. Since fever was recurrent and he started diarrhea, a new course of piperacillin+tazobactam with metronida- Figure 1: Chest computed tomography (CT) of the Case #1. A. Chest CT (topogram, axial view, and coronal view) of the first hospitalization. Some ground-glass opacities were highlighted by large white arrows. B. Chest CT (topogram, axial view, and coronal view) of the second hospitalization, when left-sided pneumothorax was diagnosed (thin white arrows). Some ground-glass and confluent opacities were also highlighted by large white arrows. zole was initiated, with Saccharomyces boulardii and racecadotril. Clostridium difficile glutamate dehydrogenase was negative. Kleb- siella pneumoniae ssp. pneumoniae and Pseudomonas aeruginosa amikacin-sensitive were identified on the culture of his calcaneus tissue injury, and he received amikacin. He was discharged home after 86 days of hospitalization. 2.3. Case 3 A 67-year-old woman presented to the ED complaining fever, con- fusion, dizziness, dry cough, and tachypnea, in the last seven days. She had lung emphysema due to previous smoking with oxygen supplementation at least three-quarters of the daytime. She was treating systemic arterial hypertension, dyslipidemia, hypovita- minosis D, and hypothyroidism. She also had a hearing sequela due to previous stroke. She had mild COVID-19 two months be- fore. She was afebrile, dyspneic with moderate effort, desaturating at room air, and hypertensive. Laboratory tests were unremarkable. SARS-CoV-2 was not detected. Chest CT evidenced a centrolobu- lar emphysema and a large left pneumothorax with a mild right-de- viated mediastinum (Figure 3). Low-flow oxygen was provided, and she received azithromycin and piperacillin+tazobactam, cor- ticosteroids, bronchodilators, codeine, and thromboprophylaxis. A chest drain was inserted, connected to a water-seal. Bullectomy and pleurodesis were performed 5 days after tube insertion, be- cause of a high-flow air drainage. Chest tube was removed 5 days later. She was discharged home after 14 days of hospitalization.
  • 3. http://www.acmcasereport.com/ 3 Volume 10 Issue 1 -2022 Case Report Figure 2. Chest computed tomography (CT) of the Case #2. A. Chest CT (topogram, axial view, and coronal view) at hospitalization, when right-sided pneumothorax was diagnosed (thin white arrows). Some ground-glass opacities were highlighted by large white arrows. B. Chest CT (topogram and axial view) showing lung expansion after chest tube insertion and air drainage. Some ground-glass opacities were also highlighted by large white arrows. C. Chest CT (topogram and axial view) evidencing sparse ground-glass opacities (large white arrow), and a larger pleural effusion associated with pleural thickness (thin black arrow). Figure 3. Chest computed tomography (CT) of the Case #3. Chest CT (topogram, axial view, and coronal view) at hospitalization, when right-sided pneumothorax was diagnosed (thin white arrows). Some ground-glass opacities were highlighted by large white arrows.
  • 4. http://www.acmcasereport.com/ 4 Volume 10 Issue 1 -2022 Case Report 2.4. Case 4 A previously healthy 22-year-old man with COVID-19 was ad- mitted after one week of sore throat and dry cough. At admission, he was dyspneic with moderate effort, desaturating, tachycardic, and normotensive. He denied smoking. He had elevated RCP. The other blood tests were unremarkable. Chest CT showed ground- glass opacities covering more than 50% of the lung parenchyma and few consolidation foci (Figure 4A). A mild-to-moderate bi- lateral pneumothorax associated with pneumomediastinum and pneumopericardium was also noted. Oxygen was offered by face mask. He received dexamethasone, thromboprophylaxis, and amoxycillin+clavulanate and azithromycin. His respiratory effort worsened, and he was intubated and mechanically ventilated in prone position. Two chest tubes were inserted in both his right and left hemithoraces, all connected to water-seals. Chest tubes were withdrawn after four days. He self-extubated three days later. He was discharged home, with a normal chest CT and breathing at room air (Figure 4B). Figure 4. Chest computed tomography (CT) of the Case #4. A. Chest CT (topogram and both inspired and expired axial views) at hospitalization, when bilateral pneumothoraces were diagnosed (thin white arrows). Pneumomediastinum (large-narrow white arrows) and pneumopericardium (black ar- rows) were also detected. Some ground-glass opacities were highlighted by large-long white arrows. B. Chest CT (topogram, axial, and coronal views) before discharge. Small volume of gas was noted in the upper thorax. The other pneumatoses resolved completely.
  • 5. http://www.acmcasereport.com/ 5 Volume 10 Issue 1 -2022 Case Report 3. Discussion Since the beginning of the pandemic, many cases of COVID-19 -associated SP were reported. SARS-CoV-2 causes a diffuse alveolar damage with perivascular immune cell infiltration, severe endothelial injury, and widespread thrombosis, which may lead to air leak and dilatation of some alveoli and hemorrhagic/ edematous collapse of others.2 The final rupture of the alveolar wall is a consequence of a shear stress (e.g., coughing), developing a communication with the pleural space. Ultimately, COVID-19 may also be considered a cause of SP. However, it should be highlighted it is an unusual complication of COVID-19 (relative frequency of 0.57‰), although more common in affected than in non-affected individuals.1,2 A recent case-control study described 40 COVID-19-associated SP (i.e., without previous positive- pressure ventilation, chest manipulation or trauma) among 71,904 patients attending in 50 Spanish EDs.3 Patients with COVID-19 who developed SP more frequently were men and their median age similar to our search.3 They also more frequently had dyspnea/ tachypnea and chest pain, desaturation, and increased leukocyte count, than those without COVID-19.3 Another registry held in 16 centers in the United Kingdom which reported 20 patients with COVID-19-associated SP.4 Nine patients had the diagnosis of pneumothorax at presentation to the ED, from which five were readmissions.4 All cases we described had the diagnosis of pneumothorax at admission, after improving or complaining mild symptoms. 4. Conclusion COVID-19-associated SP is a potentially severe, although rare, complication. Physicians should be aware of this important pneu- matosis because it can happen in people without previous diag- References 1. Miro O, Llorens P, Jiménez S. Frequency of five unusual presenta- tions in patients with COVID-19: Results of the UMC-19-S1. Epi- demiol Infect. 2020; 148: e189-92. 2. Menter T, Haslbauer JD, Nienhold R. Postmortem examination of COVID-19 patients reveals diffuse alveolar damage with severe capillary congestion and variegated findings in lungs and other organs suggesting vascular dysfunction. Histopathology. 2020; 77(2):198-209. 3. Miro O, Llorens P, Jiménez S. Frequency, Risk Factors, Clinical Characteristics, and Outcomes of Spontaneous Pneumothorax in Patients With Coronavirus Disease 2019: A Case-Control, Emergen- cy Medicine-Based Multicenter Study. Chest. 2021; 159(3): 1241- 1255. 4. Martinelli AW, Ingle T, Newman J. COVID-19 and pneumotho- rax: A multicentre retrospective case series. Eur Respir J. 2020; 56(5):2002697.