Literature DB >> 14560435

Sickle cell disease: health promotion and maintenance and the role of primary care nurse practitioners.

Ruth A Tanyi1.   

Abstract

PURPOSE: To discuss the role of nurse practitioners (NPs) with regard to early identification of affected individuals, effective monitoring and screening, effective pain management and prophylaxis, and health education for patients with sickle cell disease (SCD). DATA SOURCES: Electronic database searches were performed using Medline, Cinahl, and PsycINFO. Data were obtained from medical textbooks, research, and review articles.
CONCLUSIONS: SCD is a chronic inherited disease belonging to a group of conditions called hemoglobinopathies. Individuals with SCD often require close medical care from specialists. Nonetheless, NPs are in ideal positions to facilitate the health promotion and health maintenance necessary to decrease the high rate of morbidity and mortality associated with this disease. IMPLICATIONS FOR PRACTICE: NPs must understand the importance of early identification of affected individuals, effective monitoring and screening, effective monitoring and screening, effective pain treatment, and prophylaxis. The unpredictable trajectory of SCD can lead to frustration, fear, helplessness, hopelessness, and emotional distress. Ineffective pain management is a major problem for people with SCD. NPs can overcome this problem by initiating effective and prompt pain management in a nonjudgmental manner.

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Year:  2003        PMID: 14560435     DOI: 10.1111/j.1745-7599.2003.tb00413.x

Source DB:  PubMed          Journal:  J Am Acad Nurse Pract        ISSN: 1041-2972


  6 in total

Review 1.  Adherence monitoring with chronic opioid therapy for persistent pain: a biopsychosocial-spiritual approach to mitigate risk.

Authors:  Deborah Matteliano; Barbara J St Marie; June Oliver; Candace Coggins
Journal:  Pain Manag Nurs       Date:  2012-10-23       Impact factor: 1.929

2.  The Effects of Sickle Cell Disease on the Quality of Life: A Focus on the Untold Experiences of Parents in Tanzania.

Authors:  Manase Kilonzi; Dorkasi L Mwakawanga; Fatuma Felix Felician; Hamu J Mlyuka; Lulu Chirande; David T Myemba; Godfrey Sambayi; Ritah F Mutagonda; Wigilya P Mikomangwa; Joyce Ndunguru; Agnes Jonathan; Paschal Ruggajo; Irene Kida Minja; Emmanuel Balandya; Julie Makani; Nathanael Sirili
Journal:  Int J Environ Res Public Health       Date:  2022-06-04       Impact factor: 4.614

3.  Knowledge of family health program practitioners in Brazil about sickle cell disease: a descriptive, cross-sectional study.

Authors:  Ludmila M X Gomes; Magda M Vieira; Tatiana C Reis; Thiago L A Barbosa; Antônio P Caldeira
Journal:  BMC Fam Pract       Date:  2011-08-19       Impact factor: 2.497

4.  Knowledge and attitude of secondary school students in Jos, Nigeria on sickle cell disease.

Authors:  Olarewaju Sunday Olakunle; Enwerem Kenneth; Adebimpe Wasiu Olakekan; Olugbenga-Bello Adenike
Journal:  Pan Afr Med J       Date:  2013-08-08

5.  Healthcare Workers' Knowledge and Resource Availability for Care of Sickle Cell Disease in Dar es Salaam, Tanzania.

Authors:  Agnes Jonathan; Hilda Tutuba; William Lloyd; Joyce Ndunguru; Julie Makani; Paschal Ruggajo; Irene K Minja; Emmanuel Balandya
Journal:  Front Genet       Date:  2022-02-11       Impact factor: 4.599

6.  Quality of assistance provided to children with sickle cell disease by primary healthcare services.

Authors:  Ludmila Mourão Xavier Gomes; Tatiana Carvalho Reis; Magda Mendes Vieira; Thiago Luis de Andrade-Barbosa; Antônio Prates Caldeira
Journal:  Rev Bras Hematol Hemoter       Date:  2011
  6 in total

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