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Contribution of the clinical information to the accuracy of the minimally invasive and the complete diagnostic autopsy.
Fernandes, Fabiola; Castillo, Paola; Bassat, Quique; Quintó, Llorenç; Hurtado, Juan Carlos; Martínez, Miguel J; Lovane, Lucilia; Jordao, Dercio; Bene, Rosa; Nhampossa, Tacilta; Ritchie, Paula Santos; Bandeira, Sónia; Sambo, Calvino; Chicamba, Valeria; Mocumbi, Sibone; Jaze, Zara; Mabota, Flora; Ismail, Mamudo R; Lorenzoni, Cesaltina; Sanz, Ariadna; Rakislova, Natalia; Marimon, Lorena; Cossa, Anelsio; Mandomando, Inacio; Vila, Jordi; Maixenchs, Maria; Munguambe, Khátia; Macete, Eusebio; Alonso, Pedro; Menéndez, Clara; Ordi, Jaume; Carrilho, Carla.
Afiliação
  • Fernandes F; Department of Pathology, Maputo Central Hospital, 1100 Maputo, Mozambique; Faculty of Medicine, Eduardo Mondlane University, 1100 Maputo, Mozambique.
  • Castillo P; ISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Department of Pathology, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain.
  • Bassat Q; ISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Centro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique; ICREA, Catalan Institution for Research and Advanced Studies, Pg. Lluís Companys 23, 08010 Barcelona, Spain; Pediatric Infectious Diseases Unit, Pediatric
  • Quintó L; ISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain.
  • Hurtado JC; ISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Department of Microbiology, Hospital Clinic of Barcelona, Universitat de Barcelona, 08036 Barcelona, Spain.
  • Martínez MJ; ISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Department of Microbiology, Hospital Clinic of Barcelona, Universitat de Barcelona, 08036 Barcelona, Spain.
  • Lovane L; Department of Pathology, Maputo Central Hospital, 1100 Maputo, Mozambique.
  • Jordao D; Department of Pathology, Maputo Central Hospital, 1100 Maputo, Mozambique.
  • Bene R; Department of Medicine, Maputo Central Hospital, 1100 Maputo, Mozambique.
  • Nhampossa T; Centro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique.
  • Ritchie PS; Department of Pediatrics, Maputo Central Hospital, 1100 Maputo, Mozambique.
  • Bandeira S; Department of Pediatrics, Maputo Central Hospital, 1100 Maputo, Mozambique.
  • Sambo C; Department of Pediatrics, Maputo Central Hospital, 1100 Maputo, Mozambique.
  • Chicamba V; Department of Pediatrics, Maputo Central Hospital, 1100 Maputo, Mozambique.
  • Mocumbi S; Department of Gynecology and Obstetrics, Maputo Central Hospital, 1100 Maputo, Mozambique.
  • Jaze Z; Department of Gynecology and Obstetrics, Maputo Central Hospital, 1100 Maputo, Mozambique.
  • Mabota F; Department of Gynecology and Obstetrics, Maputo Central Hospital, 1100 Maputo, Mozambique.
  • Ismail MR; Department of Pathology, Maputo Central Hospital, 1100 Maputo, Mozambique; Faculty of Medicine, Eduardo Mondlane University, 1100 Maputo, Mozambique.
  • Lorenzoni C; Department of Pathology, Maputo Central Hospital, 1100 Maputo, Mozambique; Faculty of Medicine, Eduardo Mondlane University, 1100 Maputo, Mozambique.
  • Sanz A; ISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain.
  • Rakislova N; ISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Department of Pathology, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain.
  • Marimon L; ISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain.
  • Cossa A; Centro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique.
  • Mandomando I; Centro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique.
  • Vila J; ISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Department of Microbiology, Hospital Clinic of Barcelona, Universitat de Barcelona, 08036 Barcelona, Spain.
  • Maixenchs M; ISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Centro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique.
  • Munguambe K; Centro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique.
  • Macete E; Centro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique.
  • Alonso P; ISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Centro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique.
  • Menéndez C; ISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Centro de Investigação em Saúde de Manhiça, 1100 Maputo, Mozambique; Consorcio de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), 28029 Madrid, Spain.
  • Ordi J; ISGlobal, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain; Department of Pathology, Hospital Clinic, Universitat de Barcelona, 08036 Barcelona, Spain. Electronic address: jordi@clinic.ub.es.
  • Carrilho C; Department of Pathology, Maputo Central Hospital, 1100 Maputo, Mozambique; Faculty of Medicine, Eduardo Mondlane University, 1100 Maputo, Mozambique.
Hum Pathol ; 85: 184-193, 2019 03.
Article em En | MEDLINE | ID: mdl-30496801
ABSTRACT
Although autopsy diagnosis includes routinely, a thorough evaluation of all available pathological results and also of any available clinical data, the contribution of this clinical information to the diagnostic yield of the autopsy has not been analyzed. We aimed to determine to which degree the use of clinical data improves the diagnostic accuracy of the complete diagnostic autopsy (CDA) and the minimally invasive autopsy (MIA), a simplified pathological postmortem procedure designed for low-income sites. A total of 264 coupled MIA and CDA procedures (112 adults, 57 maternal deaths, 54 children, and 41 neonates) were performed at the Maputo Hospital, Mozambique. We compared the diagnoses obtained by the MIA blind to clinical data (MIAb), the MIA adding the clinical information (MIAc), and the CDA blind to clinical information (CDAb), with the results of the gold standard, the CDA with clinical data, by comparing the International Classification of Diseases, Tenth Revision codes and the main diagnostic classes obtained with each evaluation strategy (MIAb, MIAc, CDAb, CDAc). The clinical data increased diagnostic coincidence to the MIAb with the gold standard in 30 (11%) of 264 cases and modified the CDAb diagnosis in 20 (8%) of 264 cases. The increase in concordance between MIAb and MIAc with the gold standard was significant in neonatal deaths (κ increasing from 0.404 to 0.618, P = .0271), adult deaths (κ increasing from 0.732 to 0.813, P = .0221), and maternal deaths (κ increasing from 0.485 to 0.836, 0.;P < .0001). In conclusion, the use of clinical information increases the precision of MIA and CDA and may strengthen the performance of the MIA in resource-limited settings.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Autopsia / Morte Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Autopsia / Morte Tipo de estudo: Diagnostic_studies Limite: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article