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Incidence of Air Leaks in Critically Ill Patients with Acute Hypoxemic Respiratory Failure Due to COVID-19

Goossen, Robin L; Verboom, Mariëlle; Blacha, Mariëlle; Smesseim, Illaa; Beenen, Ludo F M; Meenen, David M P van; Paulus, Frederique; Schultz, Marcus J; ,
Subcutaneous emphysema, pneumothorax and pneumomediastinum are well-known complications of invasive ventilation in patients with acute hypoxemic respiratory failure. We determined the incidences of air leaks that were visible on available chest images in a cohort of critically ill patients with acute hypoxemic respiratory failure due to coronavirus disease of 2019 (COVID-19) in a single-center cohort in the Netherlands. A total of 712 chest images from 154 patients were re-evaluated by a multidisciplinary team of independent assessors; there was a median of three (2-5) chest radiographs and a median of one (1-2) chest CT scans per patient. The incidences of subcutaneous emphysema, pneumothoraxes and pneumomediastinum present in 13 patients (8.4%) were 4.5%, 4.5%, and 3.9%. The median first day of the presence of an air leak was 18 (2-21) days after arrival in the ICU and 18 (9-22)days after the start of invasive ventilation. We conclude that the incidence of air leaks was high in this cohort of COVID-19 patients, but it was fairly comparable with what was previously reported in patients with acute hypoxemic respiratory failure in the pre-COVID-19 era.
PMCID:10046975
PMID: 36980464
ISSN: 2075-4418
CID: 5993452

Broadening the scope for three-dimensional printed airway stents

van Beelen, Sophia; Smesseim, Illaa; Guibert, Nicolas; Wijma, Inge; Burgers, Sjaak
PMCID:9986767
PMID: 36891070
ISSN: 2312-0541
CID: 5993442

Focal 18 F-FDG uptake predicts progression of pre-invasive squamous bronchial lesions to invasive cancers

Smesseim, Illaa; van Boerdonk, Robert A; Dickhoff, Chris; Heineman, David J; Dahele, Max R; Radonic, Teodora; Bahce, Idris; Rauh, Simone P; Comans, Emile F I; Daniels, Hans J M A
INTRODUCTION:F-FDG) positron emission tomography (PET) scans in predicting progression in patients with pre-invasive squamous endobronchial lesions. METHODS:F-FDG PET scan at the VU University Medical Center Amsterdam, between January 2000 and December 2016, were included. Autofluorescence bronchoscopy (AFB) was used for tissue sampling and was repeated every 3 months. The minimum and median follow-up was 3 and 46.5 months. Study endpoints were the occurrence of biopsy proven invasive carcinoma, time-to-progression and overall survival (OS). RESULTS:F-FDG PET positive and negative groups, respectively. CONCLUSIONS:F-FDG PET scan were at high-risk for developing lung carcinoma, highlighting that this patient group requires early radical treatment.
PMCID:10040284
PMID: 36802171
ISSN: 1759-7714
CID: 5993432

High flow nasal cannula for acute respiratory failure due to COVID-19 in patients with a 'do-not-intubate' order: A survival analysis

Smesseim, Illaa; Mooij-Kalverda, Kirsten; Hessels, Lisa; Korevaar, Daniel A; Atasever, Burak; de Graaff, Hjalmar; Goorhuis, Abraham; Nossent, Esther; Bos, Lieuwe; Bonta, Peter; ,; van den Aardweg, Joost; Boersma, Wim; van der Lee, Ivo; Reesink, Herre J
INTRODUCTION/BACKGROUND:High flow nasal cannula (HFNC) reduces the need for intubation in patients with hypoxaemic acute respiratory failure (ARF), but its added value in patients with severe coronavirus disease 2019 (COVID-19) and a do-not-intubate (DNI) order is unknown. We aimed to assess (variables associated with) survival in these patients. MATERIALS AND METHODS/METHODS:We described a multicentre retrospective observational cohort study in five hospitals in the Netherlands and assessed the survival in COVID-19 patients with severe acute respiratory failure and a DNI order who were treated with high flow nasal cannula. We also studied variables associated with survival. RESULTS AND DISCUSSION/CONCLUSIONS:One-third of patients survived after 30 days. Survival was 43.9% in the subgroup of patients with a good WHO performance status and only 16.1% in patients with a poor WHO performance status. Patients who were admitted to the hospital for a longer period prior to HFNC initiation were less likely to survive. HFNC resulted in an increase in ROX values, reflective of improved oxygenation and/or decreased respiratory rate. CONCLUSION/CONCLUSIONS:Our data suggest that a trial of HFNC could be considered to increase chances of survival in patients with ARF due to COVID-19 pneumonitis and a DNI order, especially in those with a good WHO performance status.
PMCID:9880618
PMID: 36584670
ISSN: 1752-699x
CID: 5993422

Bronchoscopic Intrapulmonary Recombinant Factor VIIa for Diffuse Alveolar Hemorrhage-induced Acute Respiratory Failure in MPO-ANCA Vasculitis: A Case Report

Smesseim, Illaa; Schaepman-Ruys, Titia; Duitman, Jan Willem; Vegting, Yosta; Raasveld, Jorinde; Hilhorst, Marc; Vlaar, Alexander; van Es, Josien; Bonta, Peter
INTRODUCTION/UNASSIGNED:Diffuse alveolar haemorrhage (DAH) is a potentially life-threatening disease, characterized by diffuse accumulation of red blood cells within the alveoli. It can be caused by a variety of disorders. In case DAH results in severe respiratory failure, veno-venous extracorporeal membrane oxygenation (VV-ECMO) can be required. Since VV-ECMO coincides with the need for anticoagulation therapy, this results in a major clinical challenge in DAH patients with hemoptysis. CASE PRESENTATION/UNASSIGNED:We report a patient case with severe DAH-induced acute respiratory failure and hemoptysis in need for VV-ECMO complicated by life-threatening membrane oxygenator thrombosis. The DAH-induced hemoptysis was successfully treated with local bronchoscopic recombinant factor VIIa (rFVIIa), allowing systemic anticoagulation to prevent further membrane oxygenator thrombosis. Neither systemic clinical side effects nor differences in the serum coagulation markers occurred after applying recombinant factor VIIa (rFVIIa) treatment endobronchially. CONCLUSION/UNASSIGNED:This is, to our knowledge, the first case that reports the use of rFVIIa in a patient with DAH due to vasculitis and in need for VV-ECMO complicated by membrane oxygenator thrombosis.
PMCID:9097647
PMID: 35950153
ISSN: 2393-1809
CID: 5993412

The Legend of the Buffalo Chest

Blacha, Marielle M J; Smesseim, Illaa; van der Lee, Ivo; van den Aardweg, Joost G; Schultz, Marcus J; Kik, Marja L J; van Sonsbeek, Linda; de Bakker, Bernadette S; Light, Richard W
BACKGROUND:The "buffalo chest" is a condition in which a simultaneous bilateral pneumothorax occurs due to a communication of both pleural cavities caused by an iatrogenic or idiopathic fenestration of the mediastinum. This rare condition is known by many clinicians because of a particular anecdote which stated that Native Americans could kill a North American bison with a single arrow in the chest by creating a simultaneous bilateral pneumothorax, due to the animal's peculiar anatomy in which there is one contiguous pleural space due to an incomplete mediastinum. RESEARCH QUESTION:What evidence is there for the existence of buffalo chest? STUDY DESIGN AND METHODS:The term "buffalo chest" and its anecdote were first mentioned in a ''personal communication'' by a veterinarian in the Annals of Surgery in 1984. A mixed method research was performed on buffalo chest and its etiology. A total of 47 cases of buffalo chest were identified in humans. RESULTS:This study found that all authors were referring to the article from 1984 or to each other. Evidence was found for interpleural communications in other mammal species, but no literature on the anatomy of the mediastinum of the bison was found. The main reason for this research was fact-checking the origin of the anecdote and search for evidence for the existence of buffalo chest. Autopsies were performed on eight bison, and four indeed were found to have had interpleural communications. INTERPRETATION:We hypothesize that humans can also have interpleural fenestrations, which can be diagnosed when a pneumothorax occurs.
PMCID:8692104
PMID: 34216606
ISSN: 1931-3543
CID: 5993402

Close Surveillance with Long-Term Follow-up of Subjects with Preinvasive Endobronchial Lesions

van Boerdonk, Robert A A; Smesseim, Illaa; Heideman, Daniëlle A M; Coupé, Veerle M H; Tio, Darryl; Grünberg, Katrien; Thunnissen, Erik; Snijders, Peter J F; Postmus, Pieter E; Smit, Egbert F; Daniels, Johannes M A; Sutedja, Thomas G
RATIONALE/BACKGROUND:Autofluorescence bronchoscopy (AFB) and computed tomography (CT) enable lung cancer (LC) detection at the early (pre-)invasive stage. However, LC risk in patients with preinvasive endobronchial lesions is unclear. OBJECTIVES/OBJECTIVE:To assess LC incidence and identify potential risk determinants in patients with preinvasive lesions. METHODS:In our tertiary care referral center, 164 subjects with preinvasive lesions were monitored up to 12.5 years by repeated AFB and CT. Occurrence of LC was monitored. Clinical management depended on histological grade, with cancer patients receiving standard care. Potential risk determinants (smoking status, baseline histology, cancer history, and chronic obstructive pulmonary disease [COPD] status) were evaluated in relation to cancer occurrence, event-free survival (EFS), and overall survival (OS). MEASUREMENTS AND MAIN RESULTS/RESULTS:During surveillance (median of 30 mo, range 4-152) of 164 subjects with preinvasive lesions (80 high grade and 84 low grade at inclusion), 61 LCs were detected in 55 subjects (median time to event 16.5 mo). Twenty-three LCs (38%) were detected by CT, and 38 (62%) were detected by AFB. More cancers (36 of 61; 59%) developed from separate, rather than initial lesional sites. Subjects with high-grade lesions were more likely to be diagnosed with LC at the same or another site in the lungs than those with low-grade lesions (P = 0.03). Independent risk determinants for OS were previous curatively treated cancer and COPD (P ≤ 0.05). CONCLUSIONS:Presence of preinvasive lesions, especially high-grade lesions, may serve as LC risk markers. LCs occur both at preinvasive lesion sites and elsewhere in the bronchial epithelium or lung parenchyma. Prospective validation of biomarkers and randomized intervention studies are needed to determine optimal management strategies.
PMID: 26275031
ISSN: 1535-4970
CID: 5993392