Unilateral Multicystic Dysplastic Kidney Management: A National Survey

被引:0
|
作者
Harmer, Matthew J. [1 ,2 ,9 ]
Stewart, Douglas J. [3 ,4 ]
Prasad, Pallavi [5 ]
Veligratli, Faidra [6 ]
Pickles, Charles [7 ]
Kim, Ji Soo [6 ,8 ]
Raja, Maduri [6 ,8 ]
机构
[1] Univ Hosp Southampton NHS Fdn Trust, Southampton Childrens Hosp, Dept Paediat Nephrol, Southampton, England
[2] Univ Southampton, Southampton, England
[3] Royal Hosp Children, Dept Paediat Nephrol, NHS Greater Glasgow & Clyde, Glasgow City, Scotland
[4] Imperial Coll London, Natl Heart & Lung Inst, London, England
[5] Alder Hey Childrens NHS Fdn Trust, Alder Hey Childrens Hosp, Dept Paediat Nephrol, Liverpool, England
[6] Great Ormond St Hosp Children NHS Fdn Trust, Great Ormond St Hosp, Dept Paediat Nephrol, London, England
[7] Newcastle Tyne Hosp NHS Fdn Trust, Great North Childrens Hosp, Royal Victoria Infirm, Dept Paediat Nephrol, Victoria Wing, Newcastle Upon Tyne, England
[8] UCL, Great Ormond St Inst Child Hlth, London, England
[9] Univ Hosp Southampton NHS Fdn Trust, Southampton Childrens Hosp, Dept Paediat Nephrol, Tremona Rd, Southampton SO16 6YD, England
关键词
children; clinical practice; investigation; surveillance; multicystic dysplastic kidney;
D O I
10.1177/00099228231177808
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Risks of contralateral kidney abnormalities and chronic kidney disease necessitate follow-up for unilateral multicystic dysplastic kidneys (MCDK). A nationwide survey of senior UK pediatricians was conducted. Of the 60 responses obtained, 62% routinely perform a dimercaptosuccinic acid scan to confirm diagnosis. Eight percent routinely perform a cystogram to investigate contralateral vesicoureteric reflux. Sixty-two percent would routinely measure renal function (frequency ranging from once only to "every 2 years"). Twenty-five percent recalled MCDK nephrectomy being performed within the previous 5 years. Respondents voiced concerns that national guidance may result in an overcautious approach but could balance consensus and safe variation, and offer families choice and reassurance. The mean estimated cost of follow-up from birth to 18 years ranged from 258 pound to 3854 pound. Results demonstrate significant variation in management, highlighting the need for a clear pathway to decrease unwanted variability and to ensure those at high risk of renal sequelae are recognized early, without undue investigatory burden.
引用
收藏
页码:482 / 487
页数:6
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