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Minimally Invasive Tissue Sampling Findings in 12 Patients With Coronavirus Disease 2019
Author(s) -
Natalia Rakislova,
Maria Teresa RodrigoCalvo,
Lorena Marimón,
Inmaculada RiberaCortada,
Mamudo R. Ismail,
Carla Carrilho,
Fabiola Fernandes,
Melania Ferrando,
Esther Sanfeliu,
Paola Castillo,
José Guerrero,
José Ramírez,
Karmele Sáez de Gordoa,
Ricardo López del Campo,
Rosanna Bishop,
Estrella Ortiz,
Abel Muñoz-Beatove,
Jordi Vilà,
Juan Carlos Hurtado,
Mireia Navarro,
María Maixenchs,
Vima Delgado,
Ibán Aldecoa,
Antonio Martı́nez,
Pedro Castro,
Clara Menéndez,
Quique Bassat,
Miguel J. Martínez,
Jaume Ordï
Publication year - 2021
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1093/cid/ciab812
Subject(s) - medicine , autopsy , gold standard (test) , covid-19 , coronavirus , personal protective equipment , biopsy , cause of death , pathology , infectious disease (medical specialty) , disease
Background Minimally invasive tissue sampling (MITS), a postmortem procedure that uses core needle biopsy samples and does not require opening the body, may be a valid alternative to complete autopsy (CA) in highly infectious diseases such as coronavirus disease-19 (COVID-19). This study aimed to (1) compare the performance of MITS and CA in a series of COVID-19 deaths and (2) evaluate the safety of the procedure. Methods From October 2020 to February 2021, MITS was conducted in 12 adults who tested positive before death for COVID-19, in a standard, well-ventilated autopsy room, where personnel used reinforced personal protective equipment. In 9 cases, a CA was performed after MITS. A thorough histological evaluation was conducted, and the presence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was evaluated by real-time reverse-transcription polymerase chain reaction (RT-PCR) and immunohistochemistry. Results The diagnoses provided by MITS and CA matched almost perfectly. In 9 patients, COVID-19 was in the chain of events leading to death, being responsible for diffuse alveolar damage and mononuclear T-cell inflammatory response in the lungs. No specific COVID-19 features were identified. Three deaths were not related to COVID-19. All personnel involved in MITS repeatedly tested negative for COVID-19. SARS-CoV-2 was identified by RT-PCR and immunohistochemistry in the MITS samples, particularly in the lungs. Conclusions MITS is useful for evaluating COVID-19–related deaths in settings where a CA is not feasible. The results of this simplified and safer technique are comparable to those of CA.

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