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  1. "As escolhas são do paciente?", por Ana Maria Malik e Martha Oliveira (artigo que integra a publicação “Temas avançados em qualidade de vida – Volume 5”, organizado por Alberto José Niituma Ogata) (.pdf)

  2. Jamoulle M, Gomes LF. Prevenção Quaternária e limites em medicina. Rev Bras Med Fam Comunidade. 2014;9(31):186-91. (link)

  3. MORITZ, Rachel Duarte. Como melhorar a comunicação e prevenir conflitos nas situações de terminalidade na Unidade de Terapia Intensiva. Revista Brasileira de Terapia Intensiva, v. 19, n. 4, p. 485-489, 2010.

  4. SINDING, Christina et al. “I like to be an informed person but…” negotiating responsibility for treatment decisions in cancer care. Social Science & Medicine, v. 71, n. 6, p. 1094-1101, 2010.

  5. SOUSA, Karla Carolina; CARPIGIANI, Berenice. Ditos, não ditos e entreditos: a comunicação em cuidados paliativos. Psicologia: teoria e prática, v. 12, n. 1, p. 97-108, 2010.

  6. HOLMSTRÖM, Inger; RÖING, Marta. The relation between patient-centeredness and patient empowerment: a discussion on concepts. Patient education and counseling, v. 79, n. 2, p. 167-172, 2010.

  7. GERBER, Ben S.; EISER, Arnold R. The patient-physician relationship in the Internet age: future prospects and the research agenda. Journal of medical Internet research, v. 3, n. 2, p. e15, 2001.

  8. MOULTON, Benjamin; KING, Jaime S. Aligning ethics with medical decision-making: the quest for informed patient choice. The Journal of Law, Medicine & Ethics, v. 38, n. 1, p. 85-97, 2010.

  9. HOLWERDA, Nynke et al. Do patients trust their physician? The role of attachment style in the patient-physician relationship within one year after a cancer diagnosis. Acta oncologica, v. 52, n. 1, p. 110-117, 2013.

  10. LONGTIN, Yves et al. Patient participation: current knowledge and applicability to patient safety. In: Mayo Clinic Proceedings. Elsevier, 2010. p. 53-62.

  11. ELWYN, Glyn et al. Shared decision making: a model for clinical practice. Journal of general internal medicine, v. 27, n. 10, p. 1361-1367, 2012.

  12. Lakasing E. Michael Balint: an outstanding medical life. British J Gen Pract. 2005; 55 (518):724-5.

  13. Johnson AH. The Balint movement in America. Family Med. 2001;33(3):174-7.

  14. Engel GL. The need for a new medical model: a challenge for biomedicine. Science. 1977;196(4286):129-136. (link)

  15. Cheraghi-Sohi S. Contractual change and UK general practitioners: still a case of street-level bureaucrats? [dissertation]. Manchester, UK: Faculty of Medicine and Human Sciences, Manchester University School; 2011.

  16. EMANUEL, Ezekiel J.; EMANUEL, Linda L. Four models of the Physician-Patient Relationships. Readings in Health Care Ethics, 2000.

  17. XIAO, Nan et al. Factors influencing online health information search: An empirical analysis of a national cancer-related survey. Decision Support Systems, v. 57, p. 417-427, 2014.

  18. SHALLER, D. Patient-centred care: What does it take? The Commonwealth Fund. 2013.

  19. DROSSMAN, Douglas A. 2012 David Sun Lecture: Helping Your Patient by Helping Yourself--How to Improve the Patient-Physician Relationship by Optimizing Communication Skills. The American journal of gastroenterology, v. 108, n. 4, p. 521, 2013.

  20. SANTOS, Margarida Custódio dos et al. Comunicação em saúde e a segurança do doente: problemas e desafios. Revista Portuguesa de Saúde Pública, p. 47-57, 2010.

  21. MENDONÇA, Mariana Barreira. Análise do processo de comunicação entre médico, paciente acompanhante em onco-hematologia pediátrica. 2010.

  22. SILVA, CMGCH et al. Relação médico-paciente em oncologia: medos, angústias e habilidades comunicacionais de médicos na cidade de Fortaleza (CE). Ciência e Saúde Coletiva, v. 16, n. Supl 1, p. 1457-1465, 2011.

  23. CHEWNING, Betty et al. Patient preferences for shared decisions: a systematic review. Patient education and counseling, v. 86, n. 1, p. 9-18, 2012.

  24. VOLKMAN, Julie E. et al. The National Cancer Institute’s Health Information National Trends Survey [HINTS]: a national cross-sectional analysis of talking to your doctor and other healthcare providers for health information. BMC family practice, v. 15, n. 1, p. 111, 2014.

  25. DOWRICK, Christopher; FRANCES, Allen. Medicalising unhappiness: new classification of depression risks more patients being put on drug treatment from which they will not benefit. BMJ, v. 347, n. 7, p. f7140, 2013.

  26. LEE, Yin-Yang; LIN, Julia L. Do patient autonomy preferences matter? Linking patient-centered care to patient–physician relationships and health outcomes. Social science & medicine, v. 71, n. 10, p. 1811-1818, 2010.

  27. TARIMAN, Joseph D. et al. Patient, physician and contextual factors are influential in the treatment decision making of older adults newly diagnosed with symptomatic myeloma. Cancer treatment communications, v. 2, n. 2, p. 34-47, 2014.

  28. FENTON, Joshua J. et al. A cluster randomized trial of a patient-centered communication intervention in advanced cancer: The Values and Options In Cancer Care (VOICE) study. 2016.

  29. CLAYMAN, Marla L. et al. The impact of patient participation in health decisions within medical encounters: a systematic review. Medical Decision Making, v. 36, n. 4, p. 427-452, 2016.

  30. MCCULLOUGH, Dennis; WOOTTON, Jacqueline C. My mother, your mother: Embracing “slow medicine,” the compassionate approach to caring for your aging loved ones. 2008.

  31. BONALDI, Antonio; VERNERO, Sandra. Slow Medicine: un nuovo paradigma in medicina. Recenti progressi in medicina, v. 106, n. 2, p. 85-91, 2015.

  32. LEVINSON, Wendy et al. ‘Choosing Wisely’: a growing international campaign. BMJ quality & safety, p. bmjqs-2014-003821, 2014.


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