The economic burden of tuberous sclerosis complex in UK patients with renal manifestations: a retrospective cohort study in the clinical practice research datalink (CPRD)

被引:11
作者
Kingswood, John C. [1 ]
Nasuti, Paola [2 ]
Patel, Keyur [2 ]
Myland, Melissa [2 ]
Siva, Vathani [3 ]
Gray, Elizabeth [3 ]
机构
[1] Royal Sussex Cty Hosp, Brighton, E Sussex, England
[2] IMS Hlth, London, England
[3] Novartis Pharmaceut UK Ltd, Frimley, England
关键词
Kidney; TSC; Healthcare resource utilization; CPRD; HES; Costs; PRACTICE RESEARCH DATABASE; MUTATIONAL ANALYSIS; KIDNEY-DISEASE; TSC2; ANGIOMYOLIPOMA; RECOMMENDATIONS; MULTICENTER; INVOLVEMENT; MANAGEMENT; EVEROLIMUS;
D O I
10.1080/13696998.2016.1202254
中图分类号
F [经济];
学科分类号
02 ;
摘要
Background: Tuberous sclerosis complex (TSC) is a multi-system genetic disorder in which renal manifestations occur in similar to 50% of children and 80% of adults. Since these often present alongside other manifestations, renal TSC is likely to incur significant costs. This study aims to quantify healthcare resource use (HCRU) and costs for renal TSC patients in the UK. Methods: TSC patients in the Clinical Practice Research Datalink (CPRD) linked to Hospital Episodes Statistics were identified from January 1987-June 2013. Clinical data were extracted over the entire history and costs were reported over the most recent 3-year period. HCRU was compared with a matched comparator cohort. Incremental costs were reported and the key cost drivers by primary manifestation category were identified by regression modeling. Results: A total of 79 renal TSC patients were identified with manifestations including chronic kidney disease stage 3-5 (with prevalence increasing with age) and renal angiomyolipoma. Renal TSC patients consistently reported greater HCRU than the comparator. Inpatient hospitalizations were more frequent for renal TSC patients (3.2 vs 1.6), but length of stay was comparable; however, 70.9% of renal TSC patients recorded no kidney-related procedures ever and averaged <1 test per year in the 3-year period. Average costs for renal TSC patients were nearly 3-fold greater than the comparator (15,162 pound vs 5672) pound. Costs increased with additional manifestation categories (3600 pound: only renal; 27,531 pound: renal with >= 4 additional manifestation categories [25% of patients]). Additional nervous system and dermatology/psychiatric manifestations significantly (p<0.028) affected costs. Conclusions: Renal TSC patients have greater HCRU than the general CPRD population, likely to result from progression of renal disease and additional manifestations; however, surveillance for disease progression appears to be deficient. Inadequate monitoring may contribute to a lack of co-ordinated care and increased healthcare-associated costs. Efforts should be made to follow the TSC guidelines to effectively monitor and treat patients.
引用
收藏
页码:1116 / 1126
页数:11
相关论文
共 42 条
[11]   Renal lesion growth in children with tuberous sclerosis complex [J].
Ewalt, DH ;
Sheffield, E ;
Sparagana, SP ;
Delgado, MR ;
Roach, ES .
JOURNAL OF UROLOGY, 1998, 160 (01) :141-145
[12]   Efficacy and safety of everolimus for subependymal giant cell astrocytomas associated with tuberous sclerosis complex (EXIST-1): a multicentre, randomised, placebo-controlled phase 3 trial [J].
Franz, David Neal ;
Belousova, Elena ;
Sparagana, Steven ;
Bebin, E. Martina ;
Frost, Michael ;
Kuperman, Rachel ;
Witt, Olaf ;
Kohrman, Michael H. ;
Flamini, J. Robert ;
Wu, Joyce Y. ;
Curatolo, Paolo ;
de Vries, Petrus J. ;
Whittemore, Vicky H. ;
Thiele, Elizabeth A. ;
Ford, James P. ;
Shah, Gaurav ;
Cauwel, Helene ;
Lebwohl, David ;
Sahmoud, Tarek ;
Jozwiak, Sergiusz .
LANCET, 2013, 381 (9861) :125-132
[13]  
Henske EP, 2006, RENAL MANIFESTATIONS
[14]   Data Resource Profile: Clinical Practice Research Datalink (CPRD) [J].
Herrett, Emily ;
Gallagher, Arlene M. ;
Bhaskaran, Krishnan ;
Forbes, Harriet ;
Mathur, Rohini ;
van Staa, Tjeerd ;
Smeeth, Liam .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2015, 44 (03) :827-836
[15]   The TSC1-TSC2 complex: a molecular switchboard controlling cell growth [J].
Huang, Jingxiang ;
Manning, Brendan D. .
BIOCHEMICAL JOURNAL, 2008, 412 :179-190
[16]   Comprehensive mutation analysis of TSC1 and TSC2 -: and phenotypic correlations in 150 families with tuberous sclerosis [J].
Jones, AC ;
Shyamsundar, MM ;
Thomas, MW ;
Maynard, J ;
Idziaszczyk, S ;
Tomkins, S ;
Sampson, JR ;
Cheadle, JP .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (05) :1305-1315
[17]   The clinical profile of tuberous sclerosis complex (TSC) in the United Kingdom: A retrospective cohort study in the Clinical Practice Research Datalink (CPRD) [J].
Kingswood, Christopher ;
Bolton, Patrick ;
Crawford, Pamela ;
Harland, Christopher ;
Johnson, Simon R. ;
Sampson, Julian R. ;
Shepherd, Charles ;
Spink, Jayne ;
Demuth, Dirk ;
Lucchese, Lara ;
Nasuti, Paola ;
Gray, Elizabeth ;
Pinnegar, Alun ;
Magestro, Matthew .
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2016, 20 (02) :296-308
[18]   Identification of 54 large deletions/duplications in TSC1 and TSC2 using MLPA, and genotype-phenotype correlations [J].
Kozlowski, Piotr ;
Roberts, Penelope ;
Dabora, Sandra ;
Franz, David ;
Bissler, John ;
Northrup, Hope ;
Au, Kit Sing ;
Lazarus, Ross ;
Domanska-Pakiela, Dorota ;
Kotulska, Katarzyna ;
Jozwiak, Sergiusz ;
Kwiatkowski, David J. .
HUMAN GENETICS, 2007, 121 (3-4) :389-400
[19]   Tuberous Sclerosis Complex Surveillance and Management: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference [J].
Krueger, Darcy A. ;
Northrup, Hope ;
Northrup, Hope ;
Krueger, Darcy A. ;
Roberds, Steven ;
Smith, Katie ;
Sampson, Julian ;
Korf, Bruce ;
Kwiatkowski, David J. ;
Mowat, David ;
Nellist, Mark ;
Northrup, Hope ;
Povey, Sue ;
de Vries, Petrus ;
Byars, Anna ;
Dunn, David ;
Ess, Kevin ;
Hook, Dena ;
Jansen, Anna ;
King, Bryan ;
Sahin, Mustafa ;
Whittemore, Vicky ;
Thiele, Elizabeth ;
Bebin, E. Martina ;
Chugani, Harry T. ;
Crino, Peter ;
Curatolo, Paolo ;
Holmes, Greg ;
Nabbout, Rima ;
O'Callaghan, Finbar ;
Wheless, James ;
Wu, Joyce ;
Darling, Thomas N. ;
Cowen, Edward W. ;
Gosnell, Elizabeth ;
Hebert, Adelaide ;
Mlynarczyk, Greg ;
Soltani, Keyomaurs ;
Teng, Joyce ;
Wataya-Kaneda, Mari ;
Witman, Patricia M. ;
Kingswood, Chris ;
Bissler, John ;
Budde, Klemens ;
Hulbert, John ;
Guay-Woodford, Lisa ;
Sampson, Julian ;
Sauter, Matthias ;
Zonneberg, Bernard ;
Jozwiak, Sergiusz .
PEDIATRIC NEUROLOGY, 2013, 49 (04) :255-265
[20]   Tuberous sclerosis and polycystic kidney disease in a 3-month-old infant [J].
Laass, MW ;
Spiegel, M ;
Jauch, A ;
Hahn, G ;
Rupprecht, E ;
Vogelberg, C ;
Bartsch, O ;
Huebner, A .
PEDIATRIC NEPHROLOGY, 2004, 19 (06) :602-608