Informed consent and use of biological samples from clinical care for research: A case in northern Peru Hospital

Authors

  • Emma Vanesa Arriaga-Deza Dirección de Investigación, Hospital Regional Lambayeque, Chiclayo, Perú. Universidad San Martín de Porres, Facultad de Medicina Humana. Chiclayo, Perú
  • Antero Enrique Yacarini-Martínez Universidad Católica Santo Toribio de Mogrovejo, Chiclayo, Perú
  • Franco Ernesto León-Jiménez Vicerrectorado de Investigación, Universidad Privada Norbert Wiener, Lima, Perú https://orcid.org/0000-0002-9418-3236

DOI:

https://doi.org/10.35434/rcmhnaaa.2023.163.1982

Keywords:

Informed consent, Bioethics, Laboratory personnel, Clinical laboratory services

Abstract

Objective: To describe the frequency and characteristics of the use of Informed Consent (IC) for the use of biological samples from clinical care for research purposes in a Peruvian hospital. Setting: Northern Peru Hospital. Material and methods: Cross-sectional descriptive study developed during 2018, in 50 laboratory workers, through an interview using a questionnaire validated by 5 bioethic experts. Results: 30/50 were women; mean years of service: 6.5; 42% biologists, 30% medical technologists, and 25% technicians; according to academic degree: 46% Bachelor, 26% Master and 24% technicians; 24/50 reported training in ethics, being: 15/26 (talks), 8/26 (short courses) and 3/26 (graduates); 76% know of the need for IC to use samples; 78% and 64% of those surveyed explain the procedure to hospitalized patients and relatives of unconscious patients, respectively; 74% of those surveyed explain the sampling; 24% report that sometimes/almost always, “keep part of the sample” without the patient's IC; 52% do not explain to the patient/relative the confidentiality of the information; 44% state that they always/sometimes carry out “additional analyzes to those requested” with the sample. Conclusion: there are deficiencies in the ethical training of the respondents, and despite knowing the importance of the IC for the use of biological samples intended for clinical care, its use for research was evidenced.

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Author Biographies

Emma Vanesa Arriaga-Deza, Dirección de Investigación, Hospital Regional Lambayeque, Chiclayo, Perú. Universidad San Martín de Porres, Facultad de Medicina Humana. Chiclayo, Perú

1. Bióloga

2. Maestra en Bioética y Biojurídica

3. Maestra en Ciencias con Mención en Microbiología

Antero Enrique Yacarini-Martínez, Universidad Católica Santo Toribio de Mogrovejo, Chiclayo, Perú

1. Biólogo

2. Máster en Bioética

3. Maestro en Ciencias con mención en Microbiología

Franco Ernesto León-Jiménez, Vicerrectorado de Investigación, Universidad Privada Norbert Wiener, Lima, Perú

1. Médico internista

2. Maestro en Epidemiología Clínica

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Published

2023-12-03

How to Cite

1.
Arriaga-Deza EV, Yacarini-Martínez AE, León-Jiménez FE. Informed consent and use of biological samples from clinical care for research: A case in northern Peru Hospital. Rev. Cuerpo Med. HNAAA [Internet]. 2023 Dec. 3 [cited 2024 Nov. 21];16(3). Available from: https://cmhnaaa.org.pe/ojs/index.php/rcmhnaaa/article/view/1982

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