Delayed Tension Pneumothorax Complicating Staphylococcal Pneumonia S.P
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Spontaneous Pneumothorax in COVID-19 Patients Treated with High-Flow Nasal Cannula Outside the ICU: a Case Series
International Journal of Environmental Research and Public Health Case Report Spontaneous Pneumothorax in COVID-19 Patients Treated with High-Flow Nasal Cannula outside the ICU: A Case Series Magdalena Nalewajska 1, Wiktoria Feret 1 , Łukasz Wojczy ´nski 1, Wojciech Witkiewicz 2 , Magda Wi´sniewska 1 and Katarzyna Kotfis 3,* 1 Department of Nephrology, Transplantology and Internal Medicine, Pomeranian Medical University, 70–111 Szczecin, Poland; [email protected] (M.N.); [email protected] (W.F.); [email protected] (Ł.W.); [email protected] (M.W.) 2 Department of Cardiology, Pomeranian Medical University, 70–111 Szczecin, Poland; [email protected] 3 Department of Anesthesiology, Intensive Therapy and Acute Intoxications, Pomeranian Medical University in Szczecin, 70–111 Szczecin, Poland * Correspondence: katarzyna.kotfi[email protected] Abstract: The coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has become a global pandemic and a burden to global health at the turn of 2019 and 2020. No targeted treatment for COVID-19 infection has been identified so far, thus supportive treatment, invasive and non-invasive oxygen support, and corticosteroids remain a common therapy. High-flow nasal cannula (HFNC), a non-invasive oxygen support method, has become a prominent treatment option for respiratory failure during the SARS-CoV-2 pandemic. Citation: Nalewajska, M.; Feret, W.; HFNC reduces the anatomic dead space and increases positive end-expiratory pressure (PEEP), Wojczy´nski,Ł.; Witkiewicz, W.; allowing higher concentrations and higher flow of oxygen. Some studies suggest positive effects of Wi´sniewska,M.; Kotfis, K. HFNC on mortality and avoidance of intubation. -
Legionnaires' Disease
epi TRENDS A Monthly Bulletin on Epidemiology and Public Health Practice in Washington Legionnaires’ disease Vol. 22 No. 11 Legionellosis is a bacterial respiratory infection which can result in severe pneumonia and death. Most cases are sporadic but legionellosis is an important public health issue because outbreaks can occur in hotels, communities, healthcare facilities, and other settings. Legionellosis Legionellosis was first recognized in 1976 when an outbreak affected 11.17 more than 200 people and caused more than 30 deaths, mainly among attendees of a Legionnaires’ convention being held at a Philadelphia hotel. Legionellosis is caused by numerous different Legionella species and serogroups but most epiTRENDS P.O. Box 47812 recognized infections are due to Olympia, WA 98504-7812 L. pneumophila serogroup 1. The extent to which this is due to John Wiesman, DrPH, MPH testing bias is unclear since only Secretary of Health L. pneumophila serogroup 1 is Kathy Lofy, MD identified via commonly used State Health Officer urine antigen tests; other species Scott Lindquist, MD, MPH Legionella pneumophila multiplying and serogroups must be identified in a human lung cell State Epidemiologist, through PCR or culture, tests Communicable Disease www.cdc.gov which are less commonly ordered. Jerrod Davis, P.E. Assistant Secretary The disease involves two clinically distinct syndromes: Pontiac fever, Disease Control and Health Statistics a self-limited flu-like illness without pneumonia; and Legionnaires’ disease, a potentially fatal pneumonia with initial symptoms of fever, Sherryl Terletter Managing Editor cough, myalgias, malaise, and sometimes diarrhea progressing to symptoms of pneumonia which can be severe. Health conditions that Marcia J. -
Pneumonia: Prevention and Care at Home
FACT SHEET FOR PATIENTS AND FAMILIES Pneumonia: Prevention and Care at Home What is it? On an x-ray, pneumonia usually shows up as Pneumonia is an infection of the lungs. The infection white areas in the affected part of your lung(s). causes the small air sacs in your lungs (called alveoli) to swell and fill up with fluid or pus. This makes it harder for you to breathe, and usually causes coughing and other symptoms that sap your energy and appetite. How common and serious is it? Pneumonia is fairly common in the United States, affecting about 4 million people a year. Although for many people infection can be mild, about 1 out of every 5 people with pneumonia needs to be in the heart hospital. Pneumonia is most serious in these people: • Young children (ages 2 years and younger) • Older adults (ages 65 and older) • People with chronic illnesses such as diabetes What are the symptoms? and heart disease Pneumonia symptoms range in severity, and often • People with lung diseases such as asthma, mimic the symptoms of a bad cold or the flu: cystic fibrosis, or emphysema • Fatigue (feeling tired and weak) • People with weakened immune systems • Cough, without or without mucus • Smokers and heavy drinkers • Fever over 100ºF or 37.8ºC If you’ve been diagnosed with pneumonia, you should • Chills, sweats, or body aches take it seriously and follow your doctor’s advice. If your • Shortness of breath doctor decides you need to be in the hospital, you will receive more information on what to expect with • Chest pain or pain with breathing hospital care. -
Obliterative Bronchiolitis, Cryptogenic Organising Pneumonitis and Bronchiolitis Obliterans Organizing Pneumonia: Three Names for Two Different Conditions
Eur Reaplr J EDITORIAL 1991, 4, 774-775 Obliterative bronchiolitis, cryptogenic organising pneumonitis and bronchiolitis obliterans organizing pneumonia: three names for two different conditions R.M. du Bois, O.M. Geddes Over the last five years, increasing confusion has has been applied to conditions in which airflow obstruc developed over the use of the terms "bronchiolitis tion is prominent and in which response to treatment is obliterans" and "bronchiolitis obliterans organizing poor. pneumonia". The confusion stems largely from the common use of the term "bronchiolitis obliterans" or "obliterative bronchiolitis" in the diagnostic labels applied "Cryptogenic organizing pneumonitis" or "bronchi· to two entities which are quite distinct clinically but which otitis obliterans organizing pneumonia" (BOOP) bear certain resemblances histologically. Cryptogenic organizing pneumonitis was first described by DAVISON et al. [7] in 1983. The clinical syndrome ObUterative bronchiolitis consisted of breathlessness, malaise, fever, high erythrocyte sedimentation rate (ESR), pneumonic In 1977, GEODES et al. [1] reported the case histories shadowing on chest radiograph with a restrictive of six patients whose clinical condition was characterized pulmonary function defect and low gas transfer coeffi by airways obliteration in association with rheumatoid cient. On histological examination of lung biopsy mate· arthritis. The striking clinical features were of rapidly rial, the typical and distinguishing feature was the progressive breathlessness and the fmding on examination presence of connective tissue within the alveoli, alveolar of a high-pitched mid-inspiratory squeak heard over the ducts and, occasionally, in respiratory bronchioles. This lung fields. Chest radiographs showed hyperinflated lungs connective tissue consisted of "loosely woven fibres of but were otherwise normal. -
Allergic Bronchopulmonary Aspergillosis: a Perplexing Clinical Entity Ashok Shah,1* Chandramani Panjabi2
Review Allergy Asthma Immunol Res. 2016 July;8(4):282-297. http://dx.doi.org/10.4168/aair.2016.8.4.282 pISSN 2092-7355 • eISSN 2092-7363 Allergic Bronchopulmonary Aspergillosis: A Perplexing Clinical Entity Ashok Shah,1* Chandramani Panjabi2 1Department of Pulmonary Medicine, Vallabhbhai Patel Chest Institute, University of Delhi, Delhi, India 2Department of Respiratory Medicine, Mata Chanan Devi Hospital, New Delhi, India This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. In susceptible individuals, inhalation of Aspergillus spores can affect the respiratory tract in many ways. These spores get trapped in the viscid spu- tum of asthmatic subjects which triggers a cascade of inflammatory reactions that can result in Aspergillus-induced asthma, allergic bronchopulmo- nary aspergillosis (ABPA), and allergic Aspergillus sinusitis (AAS). An immunologically mediated disease, ABPA, occurs predominantly in patients with asthma and cystic fibrosis (CF). A set of criteria, which is still evolving, is required for diagnosis. Imaging plays a compelling role in the diagno- sis and monitoring of the disease. Demonstration of central bronchiectasis with normal tapering bronchi is still considered pathognomonic in pa- tients without CF. Elevated serum IgE levels and Aspergillus-specific IgE and/or IgG are also vital for the diagnosis. Mucoid impaction occurring in the paranasal sinuses results in AAS, which also requires a set of diagnostic criteria. Demonstration of fungal elements in sinus material is the hall- mark of AAS. -
Pneumothorax in Patients with Idiopathic Pulmonary Fibrosis
Yamazaki et al. BMC Pulm Med (2021) 21:5 https://doi.org/10.1186/s12890-020-01370-w RESEARCH ARTICLE Open Access Pneumothorax in patients with idiopathic pulmonary fbrosis: a real-world experience Ryo Yamazaki, Osamu Nishiyama* , Kyuya Gose, Sho Saeki, Hiroyuki Sano, Takashi Iwanaga and Yuji Tohda Abstract Background: Some patients with idiopathic pulmonary fbrosis (IPF) develop pneumothorax. However, the charac- teristics of pneumothorax in patients with IPF have not been elucidated. The purpose of this study was to clarify the clinical course, actual management, and treatment outcomes of pneumothorax in patients with IPF. Methods: Consecutive patients with IPF who were admitted for pneumothorax between January 2008 and Decem- ber 2018 were included. The success rates of treatment for pneumothorax, hospital mortality, and recurrence rate after discharge were examined. Results: During the study period, 36 patients with IPF were admitted with pneumothorax a total of 58 times. During the frst admission, 15 patients (41.7%) did not receive chest tube drainage, but 21 (58.3%) did. Of the 21 patients, 8 (38.1%) received additional therapy after chest drainage. The respective treatment success rates were 86.6% and 66.7% in patients who underwent observation only vs chest tube drainage. The respective hospital mortality rates were 13.3% and 38.0%. The total pneumothorax recurrence rate after hospital discharge was 34.6% (n 9). = Conclusions: Pneumothorax in patients with IPF was difcult to treat successfully, had a relatively poor prognosis, and showed a high recurrence rate. Keywords: Idiopathic pulmonary fbrosis, Hospitalization, Pneumothorax, Recurrence, Treatment Background pneumothorax was signifcantly associated with poor Idiopathic pulmonary fbrosis (IPF) is a specifc form survival in patients with IPF [11]. -
Legionellosis: Legionnaires' Disease/ Pontiac Fever
Legionellosis: Legionnaires’ Disease/ Pontiac Fever What is legionellosis? Legionellosis is an infection caused by the bacterium Legionella pneumophila, which acquired its name in 1976 when an outbreak of pneumonia caused by this newly recognized organism occurred among persons attending a convention of the American Legion in Philadelphia. The disease has two distinct forms: • Legionnaires' disease, the more severe form of infection which includes pneumonia, and • Pontiac fever, a milder illness. How common is legionellosis in the United States? An estimated 8,000 to 18,000 people get Legionnaires' disease in the United States each year. Some people can be infected with the Legionella bacterium and have mild symptoms or no illness at all. Outbreaks of Legionnaires' disease receive significant media attention. However, this disease usually occurs as a single isolated case not associated with any recognized outbreak. When outbreaks do occur, they are usually recognized in the summer and early fall, but cases may occur year-round. About 5% to 30% of people who have Legionnaires' disease die. What are the usual symptoms of legionellosis? Patients with Legionnaires' disease usually have fever, chills, and a cough. Some patients also have muscle aches, headache, tiredness, loss of appetite, and, occasionally, diarrhea. Chest X-rays often show pneumonia. It is difficult to distinguish Legionnaires' disease from other types of pneumonia by symptoms alone; other tests are required for diagnosis. Persons with Pontiac fever experience fever and muscle aches and do not have pneumonia. They generally recover in 2 to 5 days without treatment. The time between the patient's exposure to the bacterium and the onset of illness for Legionnaires' disease is 2 to 10 days; for Pontiac fever, it is shorter, generally a few hours to 2 days. -
Top 20 Pneumonia Facts—2019
American Thoracic Society Top 20 Pneumonia Facts—2019 1. Pneumonia is an infection of the lung. The lungs fill 12. Antibiotics can be effective for many of the bacteria with fluid and make breathing difficult. Pneumonia that cause pneumonia. For viral causes of pneumonia, disproportionately affects the young, the elderly, and antibiotics are ineffective and should not be used. There are the immunocompromised. It preys on weakness and few or no treatments for most viral causes of pneumonia. vulnerability. 13. Antibiotic resistance is growing amongst the bacteria 2. Pneumonia is the world’s leading cause of death among that cause pneumonia. This often arises from the overuse children under 5 years of age, accounting for 16% of all and misuse of antibiotics in and out of the hospital. New deaths of children under 5 years old killing approximately and more effective antibiotics are urgently needed. 2,400 children a day in 2015. There are 120 million episodes 14. Being on a ventilator raises especially high risk for of pneumonia per year in children under 5, over 10% of serious pneumonia. Ventilator-associated pneumonia is which (14 million) progress to severe episodes. There was an more likely to be caused by antibiotic-resistant microbes estimated 880,000 deaths from pneumonia in children under and can require the highest antibiotic use in the critically ill the age of five in 2016. Most were less than 2 years of age. population. 3. In the US, pneumonia is less often fatal for children, but 15. Our changing interactions with the microbial world mean it is still a big problem. -
Legionella Pneumonia (Legionnaires' Disease)
ROY COOPER • Governor MANDY COHEN, MD, MPH • Secretary BETH LOVETTE, MPH, BSN, RN• Acting Director Division of Public Health Legionella Pneumonia (Legionnaires’ Disease) Background on Legionella Pneumonia (Legionnaires’ Disease): Legionella is a bacterium commonly found in the environment, particularly in warm water. Legionella bacteria can cause two different illnesses: A kind of pneumonia (lung disease) called Legionnaire’s disease, and a milder infection without pneumonia, known as Pontiac fever. People can come in contact with Legionella when they breathe in a mist or vapor (small droplets of water in the air) containing the bacteria. Most people who come in contact with the bacteria do not become ill. Key points: • Legionnaires’ disease is a form of pneumonia caused by the Legionella bacteria. • Symptoms include high fever, chills, cough, body aches, headache and fatigue. Individuals with Legionnaires’ disease may need to be hospitalized. The disease typically begins 2–10 days after exposure to the bacteria. It can be treated effectively with antibiotics. • Legionella bacteria are found naturally in the environment, usually in warm water, such as in hot tubs, cooling towers, hot water tanks, large plumbing systems and decorative fountains. They do not seem to grow in car or window air-conditioners. • People can get infected when they breathe in a mist or vapor (small droplets of water in the air) that has been contaminated with Legionella bacteria. • Legionella does not spread from person-to-person. • Most people who are exposed -
Secondary Spontaneous Pneumothorax in a Patient of Allergic Bronchopulmonary Aspergillosis: an Unusual Presentation
International Journal of Research in Medical Sciences Sandal S et al. Int J Res Med Sci. 2021 Apr;9(4):1205-1208 www.msjonline.org pISSN 2320-6071 | eISSN 2320-6012 DOI: https://dx.doi.org/10.18203/2320-6012.ijrms20211377 Case Report Secondary spontaneous pneumothorax in a patient of allergic bronchopulmonary aspergillosis: an unusual presentation Shivali Sandal1, Surender Kumar2* 1Department of Critical Care Medicine, Inderaprastha Apollo, New Delhi, India 2Department of Cardiology, UN Mehta Institute of Cardiology and Research Centre, Ahmedabad, Gujarat, India Received: 23 January 2021 Accepted: 01 March 2021 *Correspondence: Dr. Surender Kumar, E-mail: [email protected] Copyright: © the author(s), publisher and licensee Medip Academy. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. ABSTRACT Allergic bronchopulmonary aspergillosis (ABPA) is a complex immunologic pulmonary disorder caused by hypersensitivity to fungus, Aspergillus fumigates. It clinically manifests with non-specific respiratory and systemic symptoms. ABPA is typically seen in patients with long-standing asthma or cystic fibrosis. Pleural involvement in ABPA is uncommon and secondary spontaneous pneumothorax is very rare. Herein, we report a case of 33 years old male patient presented with dyspnoea, low grade fever and productive cough. High Resolution Computed tomography (HRCT) scan of thorax was suggestive of ABPA with secondary pneumothorax. Keywords: Allergic bronchopulmonary aspergillosis, Aspergillus fumigates, High resolution computed tomography, Secondary spontaneous pneumothorax INTRODUCTION episodes of increasing dyspnea, cough with sputum production, pleuritic pain and fever. -
IDSA/ATS Consensus Guidelines on The
SUPPLEMENT ARTICLE Infectious Diseases Society of America/American Thoracic Society Consensus Guidelines on the Management of Community-Acquired Pneumonia in Adults Lionel A. Mandell,1,a Richard G. Wunderink,2,a Antonio Anzueto,3,4 John G. Bartlett,7 G. Douglas Campbell,8 Nathan C. Dean,9,10 Scott F. Dowell,11 Thomas M. File, Jr.12,13 Daniel M. Musher,5,6 Michael S. Niederman,14,15 Antonio Torres,16 and Cynthia G. Whitney11 1McMaster University Medical School, Hamilton, Ontario, Canada; 2Northwestern University Feinberg School of Medicine, Chicago, Illinois; 3University of Texas Health Science Center and 4South Texas Veterans Health Care System, San Antonio, and 5Michael E. DeBakey Veterans Affairs Medical Center and 6Baylor College of Medicine, Houston, Texas; 7Johns Hopkins University School of Medicine, Baltimore, Maryland; 8Division of Pulmonary, Critical Care, and Sleep Medicine, University of Mississippi School of Medicine, Jackson; 9Division of Pulmonary and Critical Care Medicine, LDS Hospital, and 10University of Utah, Salt Lake City, Utah; 11Centers for Disease Control and Prevention, Atlanta, Georgia; 12Northeastern Ohio Universities College of Medicine, Rootstown, and 13Summa Health System, Akron, Ohio; 14State University of New York at Stony Brook, Stony Brook, and 15Department of Medicine, Winthrop University Hospital, Mineola, New York; and 16Cap de Servei de Pneumologia i Alle`rgia Respirato`ria, Institut Clı´nic del To`rax, Hospital Clı´nic de Barcelona, Facultat de Medicina, Universitat de Barcelona, Institut d’Investigacions Biome`diques August Pi i Sunyer, CIBER CB06/06/0028, Barcelona, Spain. EXECUTIVE SUMMARY priate starting point for consultation by specialists. Substantial overlap exists among the patients whom Improving the care of adult patients with community- these guidelines address and those discussed in the re- acquired pneumonia (CAP) has been the focus of many cently published guidelines for health care–associated different organizations, and several have developed pneumonia (HCAP). -
Cryptogenic Organizing Pneumonia
462 Cryptogenic Organizing Pneumonia Vincent Cottin, M.D., Ph.D. 1 Jean-François Cordier, M.D. 1 1 Hospices Civils de Lyon, Louis Pradel Hospital, National Reference Address for correspondence and reprint requests Vincent Cottin, Centre for Rare Pulmonary Diseases, Competence Centre for M.D., Ph.D., Hôpital Louis Pradel, 28 avenue Doyen Lépine, F-69677 Pulmonary Hypertension, Department of Respiratory Medicine, Lyon Cedex, France (e-mail: [email protected]). University Claude Bernard Lyon I, University of Lyon, Lyon, France Semin Respir Crit Care Med 2012;33:462–475. Abstract Organizing pneumonia (OP) is a pathological pattern defined by the characteristic presence of buds of granulation tissue within the lumen of distal pulmonary airspaces consisting of fibroblasts and myofibroblasts intermixed with loose connective matrix. This pattern is the hallmark of a clinical pathological entity, namely cryptogenic organizing pneumonia (COP) when no cause or etiologic context is found. The process of intraalveolar organization results from a sequence of alveolar injury, alveolar deposition of fibrin, and colonization of fibrin with proliferating fibroblasts. A tremen- dous challenge for research is represented by the analysis of features that differentiate the reversible process of OP from that of fibroblastic foci driving irreversible fibrosis in usual interstitial pneumonia because they may determine the different outcomes of COP and idiopathic pulmonary fibrosis (IPF), respectively. Three main imaging patterns of COP have been described: (1) multiple patchy alveolar opacities (typical pattern), (2) solitary focal nodule or mass (focal pattern), and (3) diffuse infiltrative opacities, although several other uncommon patterns have been reported, especially the reversed halo sign (atoll sign).