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1.
Lijec Vjesn ; 136(3-4): 104-9, 2014.
Artículo en Croata | MEDLINE | ID: mdl-24988746

RESUMEN

Respecting the informed consent and its implementation is one of the fundamental components of high-quality health care. This article discusses the informed consent with an overview of Croatian and international legal documents and scientific studies dealing with this issue. Based on the review of the literature it can be concluded that this is an important issue that contains several key components that should be observed and investigated. It is necessary to evaluate the purposefulness and quality of the implementation of the informed consent, to systematically examine respect of the patients' right to information regarding the medical procedure during treatment, to explore decision-making model in the physician-patient encounter in Croatian hospitals, to determine the content and amount of information shared between physicians and patients, to determine the content and readability of consent forms and written patient information on the medical procedure. In order to assure higher quality of the implementation of the informed consent it is necessary to define by law a list of medical procedures that require written consent and to uniform consent forms for the same medical procedures country-wide.


Asunto(s)
Consentimiento Informado/ética , Consentimiento Informado/legislación & jurisprudencia , Derechos del Paciente/ética , Autonomía Personal , Relaciones Médico-Paciente/ética , Barreras de Comunicación , Croacia , Humanos , Médicos/ética , Garantía de la Calidad de Atención de Salud/ética , Percepción Social
3.
Lijec Vjesn ; 133(3-4): 133-9, 2011.
Artículo en Croata | MEDLINE | ID: mdl-21612111

RESUMEN

Informed consent represents the standard for adequate protection of all participants in biomedical research. This standard is affirmed in international legal documents concerning biomedical research, as well as in Croatian legislation. However, some questions regarding informed consent remain open. One of such questions that research ethics committees around the world and in the Republic of Croatia often deal with, is the question of whether to obtain informed consent for the research on archived material or previously collected research data taken from the patients during diagnostic or therapeutic procedures. This contribution provides an overview of both Croatian and international legal documents and guidelines that deal with this issue, together with an overview of the literature concerning this issue. Since in the Republic of Croatia there are no regulations regarding this type of research, the authors of this contribution are presenting conduct guidelines for researchers and ethics committees in such cases. The implementation of the proposed guidelines would facilitate scientific research and international cooperation for Croatian scientific institutions.


Asunto(s)
Investigación Biomédica/ética , Consentimiento Informado/ética , Registros Médicos , Bancos de Tejidos/ética , Croacia , Humanos
4.
Croat Med J ; 43(4): 417-24, 2002 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-12187519

RESUMEN

AIM: To examine the citizens' attitudes toward health insurance and its reform in Croatia, and their views on private payments for health care services. METHOD: In 1999 and 2000, we surveyed 500 randomly selected adults from all regions of Croatia, aged 40 years and over. The questionnaire included questions on social health insurance, private payments for health care, and background information. The net response was 393 (79%). The analysis of the data collected included univariate and multivariate analyses to test the differences in the attitudes among sociodemographic and socioeconomic groups. RESULTS: Most interviewed Croatian citizens (83.2%) expressed the opinion that everybody should have access to health care services, irrespective of the health insurance contributions. However, 32.1% agreed that the utilization of services should depend on the payment of contribution; 39.1% believed that the money they contributed to health insurance corresponded to health care services they received; 60.1% agreed that insurance rate should increase proportionally to income. When asked about reforms, more than half (53.4%) thought that the current health insurance covered less benefits than 10 years earlier, whereas more than a third believed that changes offered more choice (36.9%) but less equity (37.7%), and 46% disagreed with the introduction of the basic package of health care benefits and supplementary insurance. About the same percentage of respondents thought that they had already been paying too much for health care out of their own pockets. CONCLUSION: Citizens in Croatia do not hold a positive opinion on health insurance reform. They fear the changes would bring about limitations in their social rights and increase their financial burden.


Asunto(s)
Actitud Frente a la Salud , Reforma de la Atención de Salud , Seguro de Salud/legislación & jurisprudencia , Programas Nacionales de Salud/legislación & jurisprudencia , Opinión Pública , Adulto , Croacia , Femenino , Financiación Gubernamental , Humanos , Seguro de Salud/economía , Entrevistas como Asunto , Masculino , Programas Nacionales de Salud/economía , Sector Privado , Encuestas y Cuestionarios
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