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Twelve Tips

Twelve tips for teaching a comprehensive disease-focused course with a global perspective: A sickle cell disease example

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References

  • Adeyemo TA, Ojewunmi OO, Diaku-Akinwumi IN, Ayinde OC, Akanmu AS. 2015. Health related quality of life and perception of stigmatisation in adolescents living with sickle cell disease in Nigeria: a cross sectional study. Pediatr Blood Cancer. 62:1245–1251.
  • Aygun B, Odame I. 2012. A global perspective on sickle cell disease. Pediatr Blood Cancer. 59:386–390.
  • Borrell-Carrió F, Suchman AL, Epstein RM. 2004. The biopsychosocial model 25 years later: principles, practice, and scientific inquiry. Ann Family Med. 2:576–582.
  • Bortolusso Ali S. 2015. Sickle cell disease: the clinical care guidelines of the Sickle Cell Unit TMRI UWI Jamaica. Kingston (Jamaica): Sickle Unit, TMRI, University of the West Indies.
  • Brauer DG, Ferguson KJ. 2015. The integrated curriculum in medical education: AMEE Guide No. 96. Med Teach. 37:312–322.
  • Chib A, van Velthoven MH, Car J. 2015. mHealth adoption in low-resource environments: a review of the use of mobile healthcare in developing countries. J Health Commun. 20:4–34.
  • Epstein RM, Fiscella K, Lesser CS, Stange KC. 2010. Why the nation needs a policy push on patient-centered health care. Health Aff (Millwood). 29:1489–1495.
  • Freiermuth CE, Haywood C, Silva S, Cline DM, Kayle M, Sullivan D, Thornton V, Tanabe P. 2014. Attitudes toward patients with sickle cell disease in a multicenter sample of emergency department providers. Adv Emerg Nurs J. 36:335–347.
  • Glassberg JA, Tanabe P, Chow A, Harper K, Haywood C Jr, DeBaun MR, Richardson LD. 2013. Emergency provider analgesic practices and attitudes toward patients with sickle cell disease. Ann Emerg Med. 62:293–302.
  • Grosse SD, Odame I, Atrash HK, Amendah DD, Piel FB, Williams TN. 2011. Sickle cell disease in Africa: a neglected cause of early childhood mortality. Am J Prev Med. 41:S398–S405.
  • Harirforoosh S, Stewart DW. 2016. A descriptive investigation of the impact of student research projects arising from elective research courses. BMC Res Notes. 9:48.
  • Haywood C, Bediako S Jr, Lanzkron S, Diener-West M, Strouse J, Haythornthwaite J, Onojobi G, Beach MC. 2014. An unequal burden: poor patient-provider communication and sickle cell disease. Patient Educ Couns. 96:159–164.
  • Haywood C Jr, Tanabe P, Naik R, Beach MC, Lanzkron S. 2013. The impact of race and disease on sickle cell patient wait times in the emergency department. Am J Emerg Med. 31:651–656.
  • IOM. 2015. The six domains of health care quality. March 2016. http://www.ahrq.gov/professionals/quality-patient-safety/talkingquality/create/sixdomains.html
  • Jenerette CM, Brewer CA, Ataga KI. 2014. Care seeking for pain in young adults with sickle cell disease. Pain Manag Nurs. 15: 324–330.
  • Jenerette CM, Pierre-Louis BJ, Matthie N, Girardeau Y. 2015. Nurses’ attitudes toward patients with sickle cell disease: a worksite comparison. Pain Manag Nurs. 16:173–181.
  • Jenkins JF, Prows C, Dimond E, Monsen R, Williams J. 2001. Recommendations for educating nurses in genetics. J Prof Nurs. 17:283–290.
  • Lanzkron S, Carroll CP, Haywood C Jr. 2013. Mortality rates and age at death from sickle cell disease: U.S., 1979–2005. Public Health Rep. 128:110–116.
  • McCleskey PE, Gilson RT, DeVillez RL. 2009. Medical student core curriculum in dermatology survey. J Am Acad Dermatol. 61:30–35.
  • Mulumba LL, Wilson L. 2015. Sickle cell disease among children in Africa: an integrative literature review and global recommendations. Int J Africa Nurs Sci. 3:56–64.
  • Okpala I, Thomas V, Westerdale N, Jegede T, Raj K, Daley S, Costello-Binger H, Mullen J, Rochester-Peart C, Helps S, et al. 2002. The comprehensiveness care of sickle cell disease. Eur J Haematol. 68:157–162.
  • Oswald A, Czupryn J, Wiseman J, Snell L. 2014. Patient-centred education: what do students think? Med Educ. 48:170–180.
  • PCORI. 2012. Patient-centered outcomes research. https://www.pcori.org/research-results/patient-centered-outcomes-research.
  • Piel FB, Hay SI, Gupta S, Weatherall DJ, Williams TN, Osrin D. 2013. Global burden of sickle cell anaemia in children under five, 2010–2050: modelling based on demographics, excess mortality, and interventions. PLoS Med. 10:e1001484.
  • SCD Coalition. 2017. Global issues sickle cell disease coalition. http://www.scdcoalition.org/priorities/global.html.
  • Traxler J, Kukulska-Hulme A. 2005. Mobile learning in developing countries.
  • WHO. 2011. Sickle-cell disease and other haemoglobin disorders. Media Centre. http://www.who.int/mediacentre/factsheets/fs308/en/
  • Wierenga KJJ, Hambleton IR, Lewis NA, Unit SC. 2001. Survival estimates for patients with homozygous sickle-cell disease in Jamaica: a clinic-based population study. Lancet. 357:680–683.
  • Yawn BP, Buchanan GR, Afenyi-Annan AN, Ballas SK, Hassell KL, James AH, Jordan L, Lanzkron SM, Lottenberg R, Savage WJ, et al. 2014. Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel members. JAMA. 312: 1033–1048.

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