Literature DB >> 7719515

Medical and nursing problems of children with neurodegenerative disease.

A Hunt1, R Burne.   

Abstract

Little is written on the management of problems encountered by children with neurodegenerative disease. Whilst the conditions are individually rare, as a group of diseases they pose a considerable burden on the child, the family and the community. This study describes the 127 children with neurodegenerative disease who were admitted to Helen House, a hospice for children, from the time of opening in November 1982 until the end of 1993. The great majority of the conditions were genetic in origin and nearly one-third of the families had had two or more children with the same disease. Seventy-four (58%) of the children have died, with nearly half dying at home. The course of the disease was in many cases chronic and these children presented with multiple medical and nursing problems. Examination of the problems recorded in 1993 revealed that nearly all the children had no speech, or speech was impaired. Most were either totally immobile or had considerably reduced mobility. Seventy per cent of the children had feeding problems and one-quarter were fed through a nasogastric tube or gastrostomy. Thirty-five per cent of the children suffered pain on occasions, with muscle spasm being the main identifiable source of pain. Practical suggestions are made for the management of these children.

Entities:  

Mesh:

Year:  1995        PMID: 7719515     DOI: 10.1177/026921639500900104

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  7 in total

1.  Physician variability in treating pain and irritability of unknown origin in children with severe neurological impairment.

Authors:  Harold B Siden; Bruce C Carleton; Tim F Oberlander
Journal:  Pain Res Manag       Date:  2013-07-24       Impact factor: 3.037

2.  Making the White Matter Matters: Progress in Understanding Canavan's Disease and Therapeutic Interventions Through Eight Decades.

Authors:  Seemin S Ahmed; Guangping Gao
Journal:  JIMD Rep       Date:  2015-01-21

Review 3.  Designing and implementing a longitudinal study of children with neurological, genetic or metabolic conditions: charting the territory.

Authors:  Harold Siden; Rose Steele; Rollin Brant; Susan Cadell; Betty Davies; Lynn Straatman; Kimberley Widger; Gail S Andrews
Journal:  BMC Pediatr       Date:  2010-09-20       Impact factor: 2.125

4.  Variations in neurodegenerative disease across the UK: findings from the national study of Progressive Intellectual and Neurological Deterioration (PIND).

Authors:  G Devereux; L Stellitano; C M Verity; A Nicoll; R G Will; P Rogers
Journal:  Arch Dis Child       Date:  2004-01       Impact factor: 3.791

5.  Pain reporting and analgesia management in 270 children with a progressive neurologic, metabolic or chromosomally based condition with impairment of the central nervous system: cross-sectional, baseline results from an observational, longitudinal study.

Authors:  Stefan J Friedrichsdorf; Andrea C Postier; Gail S Andrews; Karen Es Hamre; Rose Steele; Harold Siden
Journal:  J Pain Res       Date:  2017-07-31       Impact factor: 3.133

6.  Quality of life and symptom burden in children with neurodegenerative diseases: using PedsQL and SProND, a new symptom-based scale.

Authors:  Annie Ting Gee Chiu; Sheila Suet Na Wong; Naomi Wing Tung Wong; Wilfred Hing Sang Wong; Winnie Wan Yee Tso; Cheuk Wing Fung
Journal:  Orphanet J Rare Dis       Date:  2022-09-02       Impact factor: 4.303

Review 7.  Detection and assessment of postoperative pain in children with cognitive impairment: A systematic literature review and meta-analysis.

Authors:  Anna Pizzinato; Ilaria Liguoro; Anna Pusiol; Paola Cogo; Alvisa Palese; Enrico Vidal
Journal:  Eur J Pain       Date:  2022-03-17       Impact factor: 3.651

  7 in total

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