Literature DB >> 18639753

Parental stress and quality of life in children with neuromuscular disease.

Jean K Mah1, Jennifer E Thannhauser, Hanna Kolski, Deborah Dewey.   

Abstract

This study examined health-related quality of life and parental stress among pediatric neuromuscular patients with or without home mechanical ventilation. Parents completed the Parenting Stress Index or Stress Index for Parents of Adolescents, depending on their child's age. The Pediatric Quality of Life Inventory measured quality of life in children with neuromuscular disease. One hundred and nine families participated; 19 (17%) families had a child with neuromuscular disease requiring home mechanical ventilation. Overall, children on home mechanical ventilation had significantly lower mean total Pediatric Quality of Life Inventory scores than nonventilated children (47.9 versus 61.5, respectively; P = 0.013). No significant difference in mean total stress scores was found between parents of pediatric neuromuscular patients with or without home mechanical ventilation. Despite their child's lower health-related quality of life, parents of pediatric neuromuscular patients requiring home mechanical ventilation did not report significantly higher parental stress than parents of nonventilated children or parents in the normative sample. We postulated that for parents living with the constant demands of caring for their child with neuromuscular disease requiring home mechanical ventilation, these caretaking demands, over time, had become part of "normal" life and were not identified as creating additional stress.

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Year:  2008        PMID: 18639753     DOI: 10.1016/j.pediatrneurol.2008.04.011

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  12 in total

1.  Risk factors for hospitalizations due to bacterial respiratory tract infections after tracheotomy.

Authors:  Christopher J Russell; Cary Thurm; Matt Hall; Tamara D Simon; Michael N Neely; Jay G Berry
Journal:  Pediatr Pulmonol       Date:  2018-01-04

2.  Factors affecting the health-related quality of life of caregivers of patients with muscular dystrophy.

Authors:  Yi-Jing Lue; Shun-Sheng Chen; Yen-Mou Lu
Journal:  J Neurol       Date:  2018-04-26       Impact factor: 4.849

3.  The PedsQL in pediatric patients with Spinal Muscular Atrophy: feasibility, reliability, and validity of the Pediatric Quality of Life Inventory Generic Core Scales and Neuromuscular Module.

Authors:  Susan T Iannaccone; Linda S Hynan; Anne Morton; Renee Buchanan; Christine A Limbers; James W Varni
Journal:  Neuromuscul Disord       Date:  2009-10-28       Impact factor: 4.296

4.  Relationship between clinical outcome measures and parent proxy reports of health-related quality of life in ambulatory children with Duchenne muscular dystrophy.

Authors:  Craig M McDonald; Dawn A McDonald; Anita Bagley; Susan Sienko Thomas; Cathleen E Buckon; Eric Henricson; Alina Nicorici; Michael D Sussman
Journal:  J Child Neurol       Date:  2010-06-17       Impact factor: 1.987

Review 5.  Home Mechanical Ventilation in Children.

Authors:  Aroonwan Preutthipan
Journal:  Indian J Pediatr       Date:  2015-07-31       Impact factor: 1.967

Review 6.  Consensus statement on standard of care for congenital muscular dystrophies.

Authors:  Ching H Wang; Carsten G Bonnemann; Anne Rutkowski; Thomas Sejersen; Jonathan Bellini; Vanessa Battista; Julaine M Florence; Ulrike Schara; Pamela M Schuler; Karim Wahbi; Annie Aloysius; Robert O Bash; Christophe Béroud; Enrico Bertini; Kate Bushby; Ronald D Cohn; Anne M Connolly; Nicolas Deconinck; Isabelle Desguerre; Michelle Eagle; Brigitte Estournet-Mathiaud; Ana Ferreiro; Albert Fujak; Nathalie Goemans; Susan T Iannaccone; Patricia Jouinot; Marion Main; Paola Melacini; Wolfgang Mueller-Felber; Francesco Muntoni; Leslie L Nelson; Jes Rahbek; Susana Quijano-Roy; Caroline Sewry; Kari Storhaug; Anita Simonds; Brian Tseng; Jiri Vajsar; Andrea Vianello; Reinhard Zeller
Journal:  J Child Neurol       Date:  2010-11-15       Impact factor: 1.987

7.  Quantifying the burden of caregiving in Duchenne muscular dystrophy.

Authors:  Erik Landfeldt; Peter Lindgren; Christopher F Bell; Michela Guglieri; Volker Straub; Hanns Lochmüller; Katharine Bushby
Journal:  J Neurol       Date:  2016-03-10       Impact factor: 4.849

8.  Health-Related Quality of Life in Children with Duchenne Muscular Dystrophy: A Review.

Authors:  Yi Wei; Kathy Speechley; Craig Campbell
Journal:  J Neuromuscul Dis       Date:  2015-09-02

9.  Management of respiratory complications and rehabilitation in individuals with muscular dystrophies: 1st Consensus Conference report from UILDM - Italian Muscular Dystrophy Association (Milan, January 25-26, 2019).

Authors:  Fabrizio Rao; Giancarlo Garuti; Michele Vitacca; Paolo Banfi; Fabrizio Racca; Renato Cutrera; Martino Pavone; Marina Pedemonte; Matteo Schisano; Stefania Pedroni; Jacopo Casiraghi; Andrea Vianello; Valeria A Sansone
Journal:  Acta Myol       Date:  2021-03-31

10.  Reliability and validity of the Chinese version of the Pediatric Quality Of Life InventoryTM (PedsQLTM) 3.0 neuromuscular module in children with Duchenne muscular dystrophy.

Authors:  Jun Hu; Li Jiang; Siqi Hong; Li Cheng; Min Kong; Yuanzhen Ye
Journal:  Health Qual Life Outcomes       Date:  2013-03-15       Impact factor: 3.186

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