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Nursing Care Plan for Patients with Hajdu–Cheney Syndrome

Hajdu–Cheney syndrome is a rare genetic disease. Its main features include phenotypic variability, age-dependent progression and the presence of acroosteolysis of the distal phalanges and generalized osteoporosis, which have significant disabling potential. Currently, there is no effective curative...

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Autores principales: Cortés-Martín, Jonathan, Díaz-Rodríguez, Lourdes, Piqueras-Sola, Beatriz, Sánchez-García, Juan Carlos, Menor-Rodríguez, María José, Rodríguez-Blanque, Raquel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9223558/
https://www.ncbi.nlm.nih.gov/pubmed/35742738
http://dx.doi.org/10.3390/ijerph19127489
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author Cortés-Martín, Jonathan
Díaz-Rodríguez, Lourdes
Piqueras-Sola, Beatriz
Sánchez-García, Juan Carlos
Menor-Rodríguez, María José
Rodríguez-Blanque, Raquel
author_facet Cortés-Martín, Jonathan
Díaz-Rodríguez, Lourdes
Piqueras-Sola, Beatriz
Sánchez-García, Juan Carlos
Menor-Rodríguez, María José
Rodríguez-Blanque, Raquel
author_sort Cortés-Martín, Jonathan
collection PubMed
description Hajdu–Cheney syndrome is a rare genetic disease. Its main features include phenotypic variability, age-dependent progression and the presence of acroosteolysis of the distal phalanges and generalized osteoporosis, which have significant disabling potential. Currently, there is no effective curative treatment, so nursing care is essential to ensure the maintenance of the quality of life of these patients. The main objective of this study was to establish a specific standardized nursing care plan using the NANDA–NIC–NOC taxonomy. The application of a care plan as such would improve the quality of life of patients affected by this rare disease, will contribute to increasing healthcare professionals’ knowledge on this matter and will support future studies on this disease.
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spelling pubmed-92235582022-06-24 Nursing Care Plan for Patients with Hajdu–Cheney Syndrome Cortés-Martín, Jonathan Díaz-Rodríguez, Lourdes Piqueras-Sola, Beatriz Sánchez-García, Juan Carlos Menor-Rodríguez, María José Rodríguez-Blanque, Raquel Int J Environ Res Public Health Article Hajdu–Cheney syndrome is a rare genetic disease. Its main features include phenotypic variability, age-dependent progression and the presence of acroosteolysis of the distal phalanges and generalized osteoporosis, which have significant disabling potential. Currently, there is no effective curative treatment, so nursing care is essential to ensure the maintenance of the quality of life of these patients. The main objective of this study was to establish a specific standardized nursing care plan using the NANDA–NIC–NOC taxonomy. The application of a care plan as such would improve the quality of life of patients affected by this rare disease, will contribute to increasing healthcare professionals’ knowledge on this matter and will support future studies on this disease. MDPI 2022-06-18 /pmc/articles/PMC9223558/ /pubmed/35742738 http://dx.doi.org/10.3390/ijerph19127489 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cortés-Martín, Jonathan
Díaz-Rodríguez, Lourdes
Piqueras-Sola, Beatriz
Sánchez-García, Juan Carlos
Menor-Rodríguez, María José
Rodríguez-Blanque, Raquel
Nursing Care Plan for Patients with Hajdu–Cheney Syndrome
title Nursing Care Plan for Patients with Hajdu–Cheney Syndrome
title_full Nursing Care Plan for Patients with Hajdu–Cheney Syndrome
title_fullStr Nursing Care Plan for Patients with Hajdu–Cheney Syndrome
title_full_unstemmed Nursing Care Plan for Patients with Hajdu–Cheney Syndrome
title_short Nursing Care Plan for Patients with Hajdu–Cheney Syndrome
title_sort nursing care plan for patients with hajdu–cheney syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9223558/
https://www.ncbi.nlm.nih.gov/pubmed/35742738
http://dx.doi.org/10.3390/ijerph19127489
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