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大疱性表皮松解症患者的营养管理

Nutrition management of patients with epidermolysis bullosa.

作者信息

Birge K

机构信息

Stanford University Medical Center, Department of Nutrition and Foodservice, CA 94305, USA.

出版信息

J Am Diet Assoc. 1995 May;95(5):575-9. doi: 10.1016/S0002-8223(95)00157-3.

DOI:10.1016/S0002-8223(95)00157-3
PMID:7722193
Abstract

Epidermolysis bullosa (EB), a heterogeneous group of rare, inherited disorders, is manifested by recurrent blistering of the skin induced by the slightest trauma. Little information exists regarding the nutrition management of patients with EB. This study presents information on growth, identifies potential nutrition problems, and provides guidelines for nutrition management of persons with EB. Eighty patients attending a dermatology clinic for EB patients are described. Severity of disease ranged from mild blistering of the knees, elbows, and feet to extensive blistering and scarring of the skin and entire gastrointestinal tract. Of the 18 children with EB simplex, which is a mild form of the disease, 4 (22%) were at nutritional risk. None of the 13 adults with EB simplex were underweight and 8 (62%) were overweight. Of the patients with the more severe forms of EB, 27 of the 35 (77%) children with dystrophic EB and 4 of the 7 (57%) children with junctional EB were at risk for malnutrition. Of the 7 adults with dystrophic EB, 6 (86%) were underweight. Common nutrition problems included protein-energy malnutrition, chewing and swallowing problems, constipation, anemia, and vitamin/mineral deficiencies. When nutrition care protocols address these problems, growth, development, and nutritional status can improve. For those with severe nutrition problems, gastrostomy feeding or similar nutrition therapies should be considered.

摘要

大疱性表皮松解症(EB)是一组罕见的遗传性疾病,表现为即使是最轻微的创伤也会导致皮肤反复出现水疱。关于EB患者的营养管理,现有信息较少。本研究提供了有关生长发育的信息,识别了潜在的营养问题,并为EB患者的营养管理提供了指导方针。描述了80名在皮肤科诊所就诊的EB患者。疾病严重程度从膝盖、肘部和足部的轻度水疱到皮肤和整个胃肠道的广泛水疱和瘢痕形成不等。在18名患有单纯型EB(该病的一种轻度形式)的儿童中,4名(22%)存在营养风险。13名患有单纯型EB的成年人中,没有人体重过轻,8名(62%)超重。在患有更严重形式EB的患者中,35名营养不良型EB儿童中有27名(77%)和7名交界型EB儿童中有4名(57%)存在营养不良风险。在7名患有营养不良型EB的成年人中,6名(86%)体重过轻。常见的营养问题包括蛋白质-能量营养不良、咀嚼和吞咽问题、便秘、贫血以及维生素/矿物质缺乏。当营养护理方案解决这些问题时,生长发育和营养状况可以得到改善。对于那些存在严重营养问题的患者,应考虑胃造口喂养或类似的营养治疗方法。

相似文献

1
Nutrition management of patients with epidermolysis bullosa.大疱性表皮松解症患者的营养管理
J Am Diet Assoc. 1995 May;95(5):575-9. doi: 10.1016/S0002-8223(95)00157-3.
2
Epidermolysis bullosa: management of esophageal strictures and enteric access by gastrostomy.大疱性表皮松解症:胃造口术治疗食管狭窄和肠内通路
Dermatol Clin. 2010 Apr;28(2):311-8, x. doi: 10.1016/j.det.2010.01.012.
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Gastrointestinal complications of epidermolysis bullosa in children.儿童大疱性表皮松解症的胃肠道并发症
Br J Dermatol. 2008 Jun;158(6):1308-14. doi: 10.1111/j.1365-2133.2008.08507.x. Epub 2008 Mar 20.
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Blood vitamin and trace metal levels in epidermolysis bullosa.大疱性表皮松解症患者的血液维生素和微量金属水平
Arch Dermatol. 1989 Mar;125(3):374-9.
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Eye involvement in inherited epidermolysis bullosa: experience of the National Epidermolysis Bullosa Registry.遗传性大疱性表皮松解症的眼部受累:国家大疱性表皮松解症登记处的经验
Am J Ophthalmol. 2004 Aug;138(2):254-62. doi: 10.1016/j.ajo.2004.03.034.
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Dental caries risk in hereditary epidermolysis bullosa.遗传性大疱性表皮松解症中的龋齿风险
Pediatr Dent. 1994 Nov-Dec;16(6):427-32.
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Gastrointestinal complications of inherited epidermolysis bullosa: cumulative experience of the National Epidermolysis Bullosa Registry.遗传性大疱性表皮松解症的胃肠道并发症:国家大疱性表皮松解症登记处的累积经验
J Pediatr Gastroenterol Nutr. 2008 Feb;46(2):147-58. doi: 10.1097/MPG.0b013e31812f5667.
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Tracheolaryngeal complications of inherited epidermolysis bullosa: cumulative experience of the national epidermolysis bullosa registry.遗传性大疱性表皮松解症的气管喉并发症:国家大疱性表皮松解症登记处的累积经验
Laryngoscope. 2007 Sep;117(9):1652-60. doi: 10.1097/MLG.0b013e318093ed8e.
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Quality of life in patients with epidermolysis bullosa.大疱性表皮松解症患者的生活质量。
Br J Dermatol. 2009 Oct;161(4):869-77. doi: 10.1111/j.1365-2133.2009.09306.x. Epub 2009 May 11.
10
The prevalence of epidermolysis bullosa in Scotland.苏格兰大疱性表皮松解症的患病率。
Br J Dermatol. 1997 Apr;136(4):560-4.

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An Bras Dermatol. 2015 Mar-Apr;90(2):217-23. doi: 10.1590/abd1806-4841.20153206.
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