Skip to main content
Erschienen in: Applied Health Economics and Health Policy 5/2015

01.10.2015 | Systematic Review

A Systematic Review and Narrative Synthesis of Health Economic Studies Conducted for Hereditary Haemochromatosis

verfasst von: Barbara de Graaff, Amanda Neil, Kristy Sanderson, Lei Si, Kwang Chien Yee, Andrew J. Palmer

Erschienen in: Applied Health Economics and Health Policy | Ausgabe 5/2015

Einloggen, um Zugang zu erhalten

Abstract

Background

Hereditary haemochromatosis (HH) is a common genetic condition amongst people of northern European heritage. HH is associated with increased iron absorption leading to parenchymal organ damage and multiple arthropathies. Early diagnosis and treatment prevents complications. Population screening may increase early diagnosis, but no programmes have been introduced internationally: a paucity of health economic data is often cited as a barrier.

Objective

To conduct a systematic review of all health economic studies in HH.

Methods

Studies were identified through electronic searching of economic/biomedical databases. Any study on HH with original economic component was included. Study quality was formally assessed. Health economic data were extracted and analysed through narrative synthesis.

Results

Thirty-eight studies met the inclusion criteria. The majority of papers reported on costs or cost effectiveness of screening programmes. Whilst most concluded screening was cost effective compared with no screening, methodological flaws limit the quality of these findings. Assumptions regarding clinical penetrance, effectiveness of screening, health-state utility values (HSUVs), exclusion of early symptomatology (such as fatigue, lethargy and multiple arthropathies) and quantification of costs associated with HH were identified as key limitations. Treatment studies concluded therapeutic venepuncture was the most cost-effective intervention.

Conclusions

There is a paucity of high-quality health economic studies relating to HH. The development of a comprehensive HH cost-effectiveness model utilising HSUVs is required to determine whether screening is worthwhile.
Anhänge
Nur mit Berechtigung zugänglich
Literatur
2.
Zurück zum Zitat Allen K. Hereditary haemochromatosis—diagnosis and management. Aust Fam Physician. 2010;39(12):938–41.PubMed Allen K. Hereditary haemochromatosis—diagnosis and management. Aust Fam Physician. 2010;39(12):938–41.PubMed
4.
Zurück zum Zitat Feder JN. The hereditary hemochromatosis gene (HFE): a MHC class I-like gene that functions in the regulation of iron homeostasis. Immunol Res. 1999;20(2):175–85.CrossRefPubMed Feder JN. The hereditary hemochromatosis gene (HFE): a MHC class I-like gene that functions in the regulation of iron homeostasis. Immunol Res. 1999;20(2):175–85.CrossRefPubMed
5.
Zurück zum Zitat Altes A, et al. Prevalence of the C282Y, H63D, and S65C mutations of the HFE gene in 1,146 newborns from a region of Northern Spain. Genet Test. 2004;8(4):407–10.CrossRefPubMed Altes A, et al. Prevalence of the C282Y, H63D, and S65C mutations of the HFE gene in 1,146 newborns from a region of Northern Spain. Genet Test. 2004;8(4):407–10.CrossRefPubMed
6.
Zurück zum Zitat Pedersen P, Melsen GV, Milman N. Frequencies of the haemochromatosis gene (HFE) variants C282Y, H63D and S65C in 6,020 ethnic Danish men. Ann Hematol. 2008;87(9):735–40.CrossRefPubMed Pedersen P, Melsen GV, Milman N. Frequencies of the haemochromatosis gene (HFE) variants C282Y, H63D and S65C in 6,020 ethnic Danish men. Ann Hematol. 2008;87(9):735–40.CrossRefPubMed
7.
Zurück zum Zitat Gagne G, et al. Hereditary hemochromatosis screening: effect of mutation penetrance and prevalence on cost-effectiveness of testing algorithms. Clin Genet. 2007;71(1):46–58.CrossRefPubMed Gagne G, et al. Hereditary hemochromatosis screening: effect of mutation penetrance and prevalence on cost-effectiveness of testing algorithms. Clin Genet. 2007;71(1):46–58.CrossRefPubMed
8.
Zurück zum Zitat Adams PC, Valberg LS. Screening blood donors for hereditary hemochromatosis: decision analysis model comparing genotyping to phenotyping. Am J Gastroenterol. 1999;94(6):1593–600.CrossRefPubMed Adams PC, Valberg LS. Screening blood donors for hereditary hemochromatosis: decision analysis model comparing genotyping to phenotyping. Am J Gastroenterol. 1999;94(6):1593–600.CrossRefPubMed
9.
Zurück zum Zitat Bacon BR, et al. HFE genotype in patients with hemochromatosis and other liver diseases. Ann Intern Med. 1999;130(12):953–62.CrossRefPubMed Bacon BR, et al. HFE genotype in patients with hemochromatosis and other liver diseases. Ann Intern Med. 1999;130(12):953–62.CrossRefPubMed
10.
Zurück zum Zitat Olynyk JK, et al. A population-based study of the clinical expression of the hemochromatosis gene. N Engl J Med. 1999;341(10):718–24.CrossRefPubMed Olynyk JK, et al. A population-based study of the clinical expression of the hemochromatosis gene. N Engl J Med. 1999;341(10):718–24.CrossRefPubMed
11.
Zurück zum Zitat Allen KJ, et al. Iron-overload-related disease in HFE hereditary hemochromatosis. N Engl J Med. 2008;358(3):221–30.CrossRefPubMed Allen KJ, et al. Iron-overload-related disease in HFE hereditary hemochromatosis. N Engl J Med. 2008;358(3):221–30.CrossRefPubMed
12.
Zurück zum Zitat Mclaren CE, et al. Prevalence of heterozygotes for hemochromatosis in the white-population of the United-States. Blood. 1995;86(5):2021–7.PubMed Mclaren CE, et al. Prevalence of heterozygotes for hemochromatosis in the white-population of the United-States. Blood. 1995;86(5):2021–7.PubMed
13.
Zurück zum Zitat Adams PC, et al. Hemochromatosis and iron-overload screening in a racially diverse population. N Engl J Med. 2005;352(17):1769–78.CrossRefPubMed Adams PC, et al. Hemochromatosis and iron-overload screening in a racially diverse population. N Engl J Med. 2005;352(17):1769–78.CrossRefPubMed
14.
Zurück zum Zitat Merryweather-Clarke A, et al. Geography of HFE C282Y and H63D mutations. Genet Test. 2000;4(3):183–98.CrossRefPubMed Merryweather-Clarke A, et al. Geography of HFE C282Y and H63D mutations. Genet Test. 2000;4(3):183–98.CrossRefPubMed
15.
Zurück zum Zitat Biotechnology Australia, Genetics in Family Medicine: The Australian Handbook for General Practitioners: hereditary haemochromatosis, A.G.A.B. Australia, Editor. National Health and Medical Research Council: Canberra; 2007. Biotechnology Australia, Genetics in Family Medicine: The Australian Handbook for General Practitioners: hereditary haemochromatosis, A.G.A.B. Australia, Editor. National Health and Medical Research Council: Canberra; 2007.
16.
Zurück zum Zitat Barton J, Edwards CQ. Hemochromatosis: genetics, patholphysiology, diagnosis and treatment. Cambridge: Cambridge University Press; 2000.CrossRef Barton J, Edwards CQ. Hemochromatosis: genetics, patholphysiology, diagnosis and treatment. Cambridge: Cambridge University Press; 2000.CrossRef
17.
Zurück zum Zitat Byrnes V, et al. The underdiagnosis of hereditary haemochromatosis: lack of presentation or penetration, expectations based on a study of relatives of symptomatic probands. Gastroenterology. 2000;118(4):A997. Byrnes V, et al. The underdiagnosis of hereditary haemochromatosis: lack of presentation or penetration, expectations based on a study of relatives of symptomatic probands. Gastroenterology. 2000;118(4):A997.
18.
Zurück zum Zitat Powell LW, Dixon JL, Hewett DG. Role of early case detection by screening relatives of patients with HFE-associated hereditary haemochromatosis. Best Pract Res Clin Haematol. 2005;18(2):221–34.CrossRefPubMed Powell LW, Dixon JL, Hewett DG. Role of early case detection by screening relatives of patients with HFE-associated hereditary haemochromatosis. Best Pract Res Clin Haematol. 2005;18(2):221–34.CrossRefPubMed
19.
Zurück zum Zitat McDonnell SM, et al. Screening for hemochromatosis in primary care settings. Ann Intern Med. 1998;129(11):962–70.CrossRefPubMed McDonnell SM, et al. Screening for hemochromatosis in primary care settings. Ann Intern Med. 1998;129(11):962–70.CrossRefPubMed
20.
Zurück zum Zitat Adams PC, et al. The relationship between iron overload, clinical symptoms, and age in 410 patients with genetic hemochromatosis. Hepatology. 1997;25(1):162–6.CrossRefPubMed Adams PC, et al. The relationship between iron overload, clinical symptoms, and age in 410 patients with genetic hemochromatosis. Hepatology. 1997;25(1):162–6.CrossRefPubMed
21.
Zurück zum Zitat Ajioka RS, Kushner JP. Clinical consequences of iron overload in hemochromatosis homozygotes. Blood. 2003;101(9):3351–3 (discussion 3354–8). Ajioka RS, Kushner JP. Clinical consequences of iron overload in hemochromatosis homozygotes. Blood. 2003;101(9):3351–3 (discussion 3354–8).
22.
Zurück zum Zitat Allen KJ, Warner B, Delatycki MB. Clinical haemochromatosis in HFE mutation carriers. Lancet. 2002;360(9330):412–3 (author reply 413–4). Allen KJ, Warner B, Delatycki MB. Clinical haemochromatosis in HFE mutation carriers. Lancet. 2002;360(9330):412–3 (author reply 413–4).
23.
Zurück zum Zitat Bothwell TH, MacPhail AP. Hereditary hemochromatosis: etiologic, pathologic, and clinical aspects. Semin Hematol. 1998;35(1):55–71.PubMed Bothwell TH, MacPhail AP. Hereditary hemochromatosis: etiologic, pathologic, and clinical aspects. Semin Hematol. 1998;35(1):55–71.PubMed
24.
Zurück zum Zitat Niederau C, et al. Long-term survival in patients with hereditary hemochromatosis. Gastroenterology. 1996;110(4):1107–19.CrossRefPubMed Niederau C, et al. Long-term survival in patients with hereditary hemochromatosis. Gastroenterology. 1996;110(4):1107–19.CrossRefPubMed
25.
Zurück zum Zitat European Association for the Study of the L. EASL clinical practice guidelines for HFE hemochromatosis. J Hepatol. 2010;53(1):3–22.CrossRef European Association for the Study of the L. EASL clinical practice guidelines for HFE hemochromatosis. J Hepatol. 2010;53(1):3–22.CrossRef
26.
Zurück zum Zitat Muncunill J, et al. In hereditary hemochromatosis, red cell apheresis removes excess iron twice as fast as manual whole blood phlebotomy. J Clin Apher. 2002;17(2):88–92.CrossRefPubMed Muncunill J, et al. In hereditary hemochromatosis, red cell apheresis removes excess iron twice as fast as manual whole blood phlebotomy. J Clin Apher. 2002;17(2):88–92.CrossRefPubMed
27.
Zurück zum Zitat Adams P, et al. Screening for iron overload: lessons from the hemochromatosis and iron overload screening (HEIRS) study. Can J Gastroenterol. 2009;23(11):769–72.PubMedCentralPubMed Adams P, et al. Screening for iron overload: lessons from the hemochromatosis and iron overload screening (HEIRS) study. Can J Gastroenterol. 2009;23(11):769–72.PubMedCentralPubMed
28.
Zurück zum Zitat Gasser B, et al. Hereditary hemochromatosis: presenting manifestations and diagnostic delay. Hémochromatose héréditaire: circonstances de découverte et délais diagnostiques. 2013. Gasser B, et al. Hereditary hemochromatosis: presenting manifestations and diagnostic delay. Hémochromatose héréditaire: circonstances de découverte et délais diagnostiques. 2013.
29.
Zurück zum Zitat Adams P, Brissot P, Powell L. EASL International Consensus Conference on Haemochromatosis—Part II. Expert document. J Hepatol. 2000;33(3):487–496. Adams P, Brissot P, Powell L. EASL International Consensus Conference on Haemochromatosis—Part II. Expert document. J Hepatol. 2000;33(3):487–496.
30.
Zurück zum Zitat Mundy L, Merlin T. Population genetic screening for haemochromatosis: identifying asymptomatic “at risk” homozygous individuals. Horizon scanning prioritising summary—volume 1. Adelaide Health Technology Assessment (AHTA); 2003. Mundy L, Merlin T. Population genetic screening for haemochromatosis: identifying asymptomatic “at risk” homozygous individuals. Horizon scanning prioritising summary—volume 1. Adelaide Health Technology Assessment (AHTA); 2003.
31.
Zurück zum Zitat Allen KJ. Population genetic screening for hereditary haemochromatosis: are we a step closer? Med J Aust. 2008;189(6):300–1.PubMed Allen KJ. Population genetic screening for hereditary haemochromatosis: are we a step closer? Med J Aust. 2008;189(6):300–1.PubMed
32.
Zurück zum Zitat Asberg A, et al. Benefit of population-based screening for phenotypic hemochromatosis in young men. Scand J Gastroenterol. 2002;37(10):1212–9.CrossRefPubMed Asberg A, et al. Benefit of population-based screening for phenotypic hemochromatosis in young men. Scand J Gastroenterol. 2002;37(10):1212–9.CrossRefPubMed
33.
Zurück zum Zitat Barton JC, Acton RT. Population screening for hemochromatosis: has the time finally come? Curr Gastroenterol Rep. 2000;2(1):18–26.CrossRefPubMed Barton JC, Acton RT. Population screening for hemochromatosis: has the time finally come? Curr Gastroenterol Rep. 2000;2(1):18–26.CrossRefPubMed
34.
Zurück zum Zitat Delatycki MB, et al. Use of community genetic screening to prevent HFE-associated hereditary haemochromatosis. Lancet. 2005;366(9482):314–6.CrossRefPubMed Delatycki MB, et al. Use of community genetic screening to prevent HFE-associated hereditary haemochromatosis. Lancet. 2005;366(9482):314–6.CrossRefPubMed
35.
Zurück zum Zitat Gertig DM, Hopper JL, Allen KJ. Population genetic screening for hereditary haemochromatosis. Med J Aust. 2003;179(10):517–8.PubMed Gertig DM, Hopper JL, Allen KJ. Population genetic screening for hereditary haemochromatosis. Med J Aust. 2003;179(10):517–8.PubMed
36.
Zurück zum Zitat Niederau C, et al. Screening for hemochromatosis and iron deficiency in employees and primary care patients in Western Germany. Ann Intern Med. 1998;128(5):337–45.CrossRefPubMed Niederau C, et al. Screening for hemochromatosis and iron deficiency in employees and primary care patients in Western Germany. Ann Intern Med. 1998;128(5):337–45.CrossRefPubMed
37.
Zurück zum Zitat Phatak PD, et al. Cost-effectiveness of screening for hereditary hemochromatosis. Arch Intern Med. 1994;154(7):769–76.CrossRefPubMed Phatak PD, et al. Cost-effectiveness of screening for hereditary hemochromatosis. Arch Intern Med. 1994;154(7):769–76.CrossRefPubMed
38.
Zurück zum Zitat Powell LW, et al. Screening for hemochromatosis in asymptomatic subjects with or without a family history. Arch Intern Med. 2006;166(3):294–301.CrossRefPubMed Powell LW, et al. Screening for hemochromatosis in asymptomatic subjects with or without a family history. Arch Intern Med. 2006;166(3):294–301.CrossRefPubMed
39.
Zurück zum Zitat Patch C, Roderick P, Rosenberg W. Factors affecting the uptake of screening: a randomised controlled non-inferiority trial comparing a genotypic and a phenotypic strategy for screening for haemochromatosis. J Hepatol. 2005;43(1):149–55.CrossRefPubMed Patch C, Roderick P, Rosenberg W. Factors affecting the uptake of screening: a randomised controlled non-inferiority trial comparing a genotypic and a phenotypic strategy for screening for haemochromatosis. J Hepatol. 2005;43(1):149–55.CrossRefPubMed
40.
Zurück zum Zitat Delatycki MB, et al. ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible. Eur J Hum Genet. 2012;20(5):505–9.PubMedCentralCrossRefPubMed Delatycki MB, et al. ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible. Eur J Hum Genet. 2012;20(5):505–9.PubMedCentralCrossRefPubMed
41.
Zurück zum Zitat Nisselle AE, et al. Implementation of HaemScreen, a workplace-based genetic screening program for hemochromatosis. Clin Genet. 2004;65(5):358–67.CrossRefPubMed Nisselle AE, et al. Implementation of HaemScreen, a workplace-based genetic screening program for hemochromatosis. Clin Genet. 2004;65(5):358–67.CrossRefPubMed
42.
Zurück zum Zitat Asberg A, et al. Screening for hemochromatosis: High prevalence and low morbidity in an unselected population of 65,238 persons. Scand J Gastroenterol. 2001;36(10):1108–15.CrossRefPubMed Asberg A, et al. Screening for hemochromatosis: High prevalence and low morbidity in an unselected population of 65,238 persons. Scand J Gastroenterol. 2001;36(10):1108–15.CrossRefPubMed
43.
Zurück zum Zitat Adams PC, et al. Screening for iron overload: Lessons from the HEmochromatosis and IRon Overload Screening (HEIRS) study. Can J Gastroenterol. 2009;23(11):769–72.PubMedCentralPubMed Adams PC, et al. Screening for iron overload: Lessons from the HEmochromatosis and IRon Overload Screening (HEIRS) study. Can J Gastroenterol. 2009;23(11):769–72.PubMedCentralPubMed
44.
Zurück zum Zitat Bryant J, et al. Diagnostic strategies using DNA testing for hereditary haemochromatosis in at-risk populations: a systematic review and economic evaluation. Health Technol Assess. 2009;13(23):1–126. Bryant J, et al. Diagnostic strategies using DNA testing for hereditary haemochromatosis in at-risk populations: a systematic review and economic evaluation. Health Technol Assess. 2009;13(23):1–126.
45.
Zurück zum Zitat Allen KJ, et al. Asymptomatic individuals at genetic risk of haemochromatosis take appropriate steps to prevent disease related to iron overload. Liver Int. 2008;28(3):363–9.CrossRefPubMed Allen KJ, et al. Asymptomatic individuals at genetic risk of haemochromatosis take appropriate steps to prevent disease related to iron overload. Liver Int. 2008;28(3):363–9.CrossRefPubMed
46.
Zurück zum Zitat Hicken BL, Tucker DC, Barton JC. Patient compliance with phlebotomy therapy for iron overload associated with hemochromatosis. Am J Gastroenterol. 2003;98(9):2072–7.CrossRefPubMed Hicken BL, Tucker DC, Barton JC. Patient compliance with phlebotomy therapy for iron overload associated with hemochromatosis. Am J Gastroenterol. 2003;98(9):2072–7.CrossRefPubMed
47.
Zurück zum Zitat Nadakkavukaran IM, Gan EK, Olynyk JK. Screening for hereditary haemochromatosis. Pathology. 2012;44(2):148–52.CrossRefPubMed Nadakkavukaran IM, Gan EK, Olynyk JK. Screening for hereditary haemochromatosis. Pathology. 2012;44(2):148–52.CrossRefPubMed
48.
Zurück zum Zitat Wilson JMG, Junger G. Priciples and practice of screening for disease. Geneva: Switzerland; 1968. Wilson JMG, Junger G. Priciples and practice of screening for disease. Geneva: Switzerland; 1968.
49.
Zurück zum Zitat Grosse SD, et al. Population screening for genetic disorders in the 21st century: evidence, economics, and ethics. Public Health Genomics. 2010;13(2):106–15.CrossRefPubMed Grosse SD, et al. Population screening for genetic disorders in the 21st century: evidence, economics, and ethics. Public Health Genomics. 2010;13(2):106–15.CrossRefPubMed
50.
Zurück zum Zitat Campbell and Cochrane Economics Methods GrouCampbell and Cochrane Economics Methods Group, How to add Health Economics to Cochrane Protocols. Available from http://www.c-cemg.org/. Accessed 10 Oct 2011. Campbell and Cochrane Economics Methods GrouCampbell and Cochrane Economics Methods Group, How to add Health Economics to Cochrane Protocols. Available from http://​www.​c-cemg.​org/​. Accessed 10 Oct 2011.
51.
Zurück zum Zitat Shemilt I, Mugford M, Vale L, Marsh K, Donaldson C, editors. Evidence-based decisions and economics: health care, social welfare, education and criminal justice. 2nd ed. Evidence-based medicine series. Chichester; Hoboken: Wiley-Blackwell/BMJ Books; 2010. p. 206. Shemilt I, Mugford M, Vale L, Marsh K, Donaldson C, editors. Evidence-based decisions and economics: health care, social welfare, education and criminal justice. 2nd ed. Evidence-based medicine series. Chichester; Hoboken: Wiley-Blackwell/BMJ Books; 2010. p. 206.
52.
Zurück zum Zitat Drummond MF, et al. Methods for the economic evaluation of health care programmes. Oxford: Oxford University Press; 2005. Drummond MF, et al. Methods for the economic evaluation of health care programmes. Oxford: Oxford University Press; 2005.
53.
Zurück zum Zitat Drummond MF, Jefferson TO. Guidelines for authors and peer reviewers of economic submissions to the BMJ. The BMJ Economic Evaluation Working Party. BMJ. 1996;313(7052):275–83.PubMedCentralCrossRefPubMed Drummond MF, Jefferson TO. Guidelines for authors and peer reviewers of economic submissions to the BMJ. The BMJ Economic Evaluation Working Party. BMJ. 1996;313(7052):275–83.PubMedCentralCrossRefPubMed
54.
Zurück zum Zitat Dissemination C.f.R.a. Systematic reviews: CRD’s guidance for undertaking reviews in health care. 3rd ed. York: Centre for Reviews and Dissemination; 2009. Dissemination C.f.R.a. Systematic reviews: CRD’s guidance for undertaking reviews in health care. 3rd ed. York: Centre for Reviews and Dissemination; 2009.
55.
Zurück zum Zitat Rombout-Sestrienkova E, et al. Erythrocytapheresis versus phlebotomy in the initial treatment of HFE hemochromatosis patients: results from a randomized trial. Transfusion. 2012;52(3):470–7.CrossRefPubMed Rombout-Sestrienkova E, et al. Erythrocytapheresis versus phlebotomy in the initial treatment of HFE hemochromatosis patients: results from a randomized trial. Transfusion. 2012;52(3):470–7.CrossRefPubMed
56.
Zurück zum Zitat Mariani R, et al. Erythrocytapheresis plus erythropoietin: An alternative therapy for selected patients with hemochromatosis and severe organ damage. Haematologica. 2005;90(5):717–8.PubMed Mariani R, et al. Erythrocytapheresis plus erythropoietin: An alternative therapy for selected patients with hemochromatosis and severe organ damage. Haematologica. 2005;90(5):717–8.PubMed
57.
Zurück zum Zitat Stefashyna O, et al. Pattern of care of blood donors with early-uncomplicated hereditary haemochromatosis in a Swiss blood donation centre. Vox Sang. 2014;106(2):111–7.CrossRefPubMed Stefashyna O, et al. Pattern of care of blood donors with early-uncomplicated hereditary haemochromatosis in a Swiss blood donation centre. Vox Sang. 2014;106(2):111–7.CrossRefPubMed
58.
Zurück zum Zitat Dye DE, et al. The impact of single gene and chromosomal disorders on hospital admissions in an adult population. J Community Genet. 2011;2(2):81–90.PubMedCentralCrossRefPubMed Dye DE, et al. The impact of single gene and chromosomal disorders on hospital admissions in an adult population. J Community Genet. 2011;2(2):81–90.PubMedCentralCrossRefPubMed
59.
Zurück zum Zitat Gribble D, Chaffn DJ, Bryant BJ. Cost-effectiveness of fda variance for blood collection from individuals with hereditary hemochromatosis at a 398 bed hospital-based donor center. Transfusion. 2009;49:249A. Gribble D, Chaffn DJ, Bryant BJ. Cost-effectiveness of fda variance for blood collection from individuals with hereditary hemochromatosis at a 398 bed hospital-based donor center. Transfusion. 2009;49:249A.
60.
Zurück zum Zitat Cooper K, et al. A decision analysis model for diagnostic strategies using DNA testing for hereditary haemochromatosis in at risk populations. QJM. 2008;101(8):631–41.CrossRefPubMed Cooper K, et al. A decision analysis model for diagnostic strategies using DNA testing for hereditary haemochromatosis in at risk populations. QJM. 2008;101(8):631–41.CrossRefPubMed
61.
Zurück zum Zitat Adams PC, Gregor JC, Kertesz AE, Valberg LS. Screening blood donors for hereditary hemochromatosis: decision analysis model based on a 30-year database. Gastroenterol Clin N Am. 1995;108:177–88. Adams PC, Gregor JC, Kertesz AE, Valberg LS. Screening blood donors for hereditary hemochromatosis: decision analysis model based on a 30-year database. Gastroenterol Clin N Am. 1995;108:177–88.
62.
Zurück zum Zitat Adams PC, Kertesz AE, Valberg LS. Screening for hemochromatosis in children of homozygotes: prevalence and cost-effectiveness. Hepatology (Baltimore, Md.). 1995;22(6):1720–27. Adams PC, Kertesz AE, Valberg LS. Screening for hemochromatosis in children of homozygotes: prevalence and cost-effectiveness. Hepatology (Baltimore, Md.). 1995;22(6):1720–27.
63.
Zurück zum Zitat Phatak PD, Guzman G, Woll JE, Robeson A, Phelps CE. Cost-effectiveness of screening for hereditary hemochromatosis. Arch Intern Med. 1994;154(7):769–76.CrossRefPubMed Phatak PD, Guzman G, Woll JE, Robeson A, Phelps CE. Cost-effectiveness of screening for hereditary hemochromatosis. Arch Intern Med. 1994;154(7):769–76.CrossRefPubMed
64.
Zurück zum Zitat Schoffski O, Schmidtke J, Stuhrmann M. Cost-effectiveness of population-based genetic hemochromatosis screening. Community Genet. 2000;3:2–11.CrossRef Schoffski O, Schmidtke J, Stuhrmann M. Cost-effectiveness of population-based genetic hemochromatosis screening. Community Genet. 2000;3:2–11.CrossRef
65.
Zurück zum Zitat Bassett ML, et al. Analysis of the cost of population screening for haemochromatosis using biochemical and genetic markers. J Hepatol. 1997;27(3):517–24.CrossRefPubMed Bassett ML, et al. Analysis of the cost of population screening for haemochromatosis using biochemical and genetic markers. J Hepatol. 1997;27(3):517–24.CrossRefPubMed
66.
Zurück zum Zitat El-Serag HB, Inadomi JM, Kowdley KV. Screening for hereditary hemochromatosis in siblings and children of affected patients—a cost-effectiveness analysis. Ann Intern Med. 2000;132(4):261–269. El-Serag HB, Inadomi JM, Kowdley KV. Screening for hereditary hemochromatosis in siblings and children of affected patients—a cost-effectiveness analysis. Ann Intern Med. 2000;132(4):261–269.
67.
Zurück zum Zitat Buffone GJ, Beck JR. Cost-effectiveness analysis for evaluation of screening programs—hereditary hemochromatosis. Clin Chem. 1994;40(8):1631–6.PubMed Buffone GJ, Beck JR. Cost-effectiveness analysis for evaluation of screening programs—hereditary hemochromatosis. Clin Chem. 1994;40(8):1631–6.PubMed
68.
Zurück zum Zitat Rogowski WH. The cost-effectiveness of screening for hereditary hemochromatosis in Germany: a remodeling study. Med Decis Mak. 2009;29(2):224–38.CrossRef Rogowski WH. The cost-effectiveness of screening for hereditary hemochromatosis in Germany: a remodeling study. Med Decis Mak. 2009;29(2):224–38.CrossRef
69.
Zurück zum Zitat Stuhrmann M, Strassburg C, Schmidtke J. Genotype-based screening for hereditary haemochromatosis. I: technical performance, costs and clinical relevance of a German pilot study. Eur J Hum Genet. 2005;13(1):69–78.CrossRefPubMed Stuhrmann M, Strassburg C, Schmidtke J. Genotype-based screening for hereditary haemochromatosis. I: technical performance, costs and clinical relevance of a German pilot study. Eur J Hum Genet. 2005;13(1):69–78.CrossRefPubMed
70.
Zurück zum Zitat Hickman PE, et al. Automated measurement of unsaturated iron binding capacity is an effective screening strategy for C282Y homozygous haemochromatosis. Gut. 2000;46(3):405–9.PubMedCentralCrossRefPubMed Hickman PE, et al. Automated measurement of unsaturated iron binding capacity is an effective screening strategy for C282Y homozygous haemochromatosis. Gut. 2000;46(3):405–9.PubMedCentralCrossRefPubMed
71.
Zurück zum Zitat Stave GM, et al. Evaluation of a workplace hemochromatosis screening program. Am J Prev Med. 1999;16(4):303–6.CrossRefPubMed Stave GM, et al. Evaluation of a workplace hemochromatosis screening program. Am J Prev Med. 1999;16(4):303–6.CrossRefPubMed
73.
Zurück zum Zitat Vardarli I, et al. In hospitalized patients with diabetes mellitus screening for hereditary hemochromatosis by using transferrin saturation is cost effective. Diabetologia. 2009;52(S1):S398–9. Vardarli I, et al. In hospitalized patients with diabetes mellitus screening for hereditary hemochromatosis by using transferrin saturation is cost effective. Diabetologia. 2009;52(S1):S398–9.
74.
Zurück zum Zitat Smith BN, et al. Prevalence of hereditary hemochromatosis in a Massachusetts corporation: is celtic origin a risk factor? Hepatology. 1997;25(6):1439–46.CrossRefPubMed Smith BN, et al. Prevalence of hereditary hemochromatosis in a Massachusetts corporation: is celtic origin a risk factor? Hepatology. 1997;25(6):1439–46.CrossRefPubMed
75.
Zurück zum Zitat Barton JC, et al. Hemochromatosis detection in a health screening program at an Alabama forest products mill. J Occup Environ Med. 2002;44(8):745–51.CrossRefPubMed Barton JC, et al. Hemochromatosis detection in a health screening program at an Alabama forest products mill. J Occup Environ Med. 2002;44(8):745–51.CrossRefPubMed
76.
Zurück zum Zitat Adams PC. Implications of genotyping of spouses to limit investigation of children in genetic hemochromatosis. Clin Genet. 1998;53(3):176–8.CrossRefPubMed Adams PC. Implications of genotyping of spouses to limit investigation of children in genetic hemochromatosis. Clin Genet. 1998;53(3):176–8.CrossRefPubMed
77.
Zurück zum Zitat Jacobs EM, et al. Impact of the introduction of a guideline on the targeted detection of hereditary haemochromatosis. Neth J Med. 2005;63(6):205–14.PubMed Jacobs EM, et al. Impact of the introduction of a guideline on the targeted detection of hereditary haemochromatosis. Neth J Med. 2005;63(6):205–14.PubMed
78.
79.
Zurück zum Zitat Baer DM, et al. Hemochromatosis screening in asymptomatic ambulatory men 30 years of age and older. Am J Med. 1995;98(5):464–8.CrossRefPubMed Baer DM, et al. Hemochromatosis screening in asymptomatic ambulatory men 30 years of age and older. Am J Med. 1995;98(5):464–8.CrossRefPubMed
80.
Zurück zum Zitat Adams PC, et al. Population screening for hemochromatosis: a comparison of unbound iron-binding capacity, transferrin saturation, and C282Y genotyping in 5,211 voluntary blood donors. Hepatology. 2000;31(5):1160–4.CrossRefPubMed Adams PC, et al. Population screening for hemochromatosis: a comparison of unbound iron-binding capacity, transferrin saturation, and C282Y genotyping in 5,211 voluntary blood donors. Hepatology. 2000;31(5):1160–4.CrossRefPubMed
81.
Zurück zum Zitat Balan V, et al. Screening for hemochromatosis—a cost-effectiveness study based on 12,258 patients. Gastroenterology. 1994;107(2):453–9.PubMed Balan V, et al. Screening for hemochromatosis—a cost-effectiveness study based on 12,258 patients. Gastroenterology. 1994;107(2):453–9.PubMed
82.
Zurück zum Zitat Adams PC, Kertesz AE. Human leukocyte antigen typing of siblings in hereditary hemochromatosis: a cost approach. Hepatology. 1992;15(2):263–8.CrossRefPubMed Adams PC, Kertesz AE. Human leukocyte antigen typing of siblings in hereditary hemochromatosis: a cost approach. Hepatology. 1992;15(2):263–8.CrossRefPubMed
83.
Zurück zum Zitat Beutler E, Gelbart T. Large-scale screening for HFE mutations: methodology and cost. Genet Test. 2000;4(2):131–42.CrossRefPubMed Beutler E, Gelbart T. Large-scale screening for HFE mutations: methodology and cost. Genet Test. 2000;4(2):131–42.CrossRefPubMed
84.
Zurück zum Zitat Ropert-Bouchet M, Fajardy I, Michel H. Hereditary hemochromatosis HFE: regulatory and economic aspects of diagnosis and medical management. Ann Biol Clin (Paris). 2012;70(4):405–11. Ropert-Bouchet M, Fajardy I, Michel H. Hereditary hemochromatosis HFE: regulatory and economic aspects of diagnosis and medical management. Ann Biol Clin (Paris). 2012;70(4):405–11.
86.
Zurück zum Zitat Adams PC, Kertesz AE, Valberg LS. Screening for hemochromatosis in children of homozygotes: prevalence and cost-effectiveness. Hepatology. 1995;22(6):1720–7.PubMed Adams PC, Kertesz AE, Valberg LS. Screening for hemochromatosis in children of homozygotes: prevalence and cost-effectiveness. Hepatology. 1995;22(6):1720–7.PubMed
87.
Zurück zum Zitat Schoffski O, Schmidtke J, Stuhrmann M. Cost-effectiveness of population-based genetic hemochromatosis screening. Community Genet. 2000;3(1):2–11.CrossRef Schoffski O, Schmidtke J, Stuhrmann M. Cost-effectiveness of population-based genetic hemochromatosis screening. Community Genet. 2000;3(1):2–11.CrossRef
88.
Zurück zum Zitat El-Serag HB, Inadomi JM, Kowdley KV. Screening for hereditary hemochromatosis in siblings and children of affected patients: a cost-effectiveness analysis. Ann Intern Med. 2000;132(4):261–9.CrossRefPubMed El-Serag HB, Inadomi JM, Kowdley KV. Screening for hereditary hemochromatosis in siblings and children of affected patients: a cost-effectiveness analysis. Ann Intern Med. 2000;132(4):261–9.CrossRefPubMed
89.
Zurück zum Zitat Delaveyne R, Préaubert N, Barré S. Clinical and economic assessment of screening for HFE1 haemochromatosis in 2004. L’Agence Nationale d’Accreditation d’Evaluation en Sante (ANAES) Paris; 2004. Delaveyne R, Préaubert N, Barré S. Clinical and economic assessment of screening for HFE1 haemochromatosis in 2004. L’Agence Nationale d’Accreditation d’Evaluation en Sante (ANAES) Paris; 2004.
90.
Zurück zum Zitat Higgins JPT, Green S. Cochrane handbook for systematic reviews of interventions version 5.1.0, J.P.T. Higgins, Green S, editors. The Cochrane Collaboration; 2011. Higgins JPT, Green S. Cochrane handbook for systematic reviews of interventions version 5.1.0, J.P.T. Higgins, Green S, editors. The Cochrane Collaboration; 2011.
91.
Zurück zum Zitat Popay J, et al. Guidance on the conduct of narrative synthesis in systematic reviews. UK: ESRC Methods Programme; 2006. Popay J, et al. Guidance on the conduct of narrative synthesis in systematic reviews. UK: ESRC Methods Programme; 2006.
92.
Zurück zum Zitat Balan V, et al. Screening for hemochromatosis: a cost-effectiveness study based on 12,258 patients. Gastroenterology. 1994;107(2):453–9.PubMed Balan V, et al. Screening for hemochromatosis: a cost-effectiveness study based on 12,258 patients. Gastroenterology. 1994;107(2):453–9.PubMed
93.
Zurück zum Zitat Patch C, Roderick P, Rosenberg W. Comparison of genotypic and phenotypic strategies for population screening in hemochromatosis: assessment of anxiety, depression, and perception of health. Genet Med. 2005;7(8):550–6.CrossRefPubMed Patch C, Roderick P, Rosenberg W. Comparison of genotypic and phenotypic strategies for population screening in hemochromatosis: assessment of anxiety, depression, and perception of health. Genet Med. 2005;7(8):550–6.CrossRefPubMed
94.
Zurück zum Zitat Beutler E, et al. The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic. Ann Intern Med. 2000;133(5):329–37.CrossRefPubMed Beutler E, et al. The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic. Ann Intern Med. 2000;133(5):329–37.CrossRefPubMed
95.
Zurück zum Zitat Asberg A, et al. Benefit of population-based screening for phenotypic hemochromatosis in young men. Scand J Gastroenterol. 2002;37(10):1212–9.CrossRefPubMed Asberg A, et al. Benefit of population-based screening for phenotypic hemochromatosis in young men. Scand J Gastroenterol. 2002;37(10):1212–9.CrossRefPubMed
96.
Zurück zum Zitat Uhlig T, et al. Quantification of reduced health-related quality of life in patients with rheumatoid arthritis compared to the general population. J Rheumatol. 2007;34(6):1241–7.PubMed Uhlig T, et al. Quantification of reduced health-related quality of life in patients with rheumatoid arthritis compared to the general population. J Rheumatol. 2007;34(6):1241–7.PubMed
97.
Zurück zum Zitat Dan AA, et al. Impact of chronic liver disease and cirrhosis on health utilities using SF-6D and the health utility index. Liver Transpl. 2008;14(3):321–6.CrossRefPubMed Dan AA, et al. Impact of chronic liver disease and cirrhosis on health utilities using SF-6D and the health utility index. Liver Transpl. 2008;14(3):321–6.CrossRefPubMed
98.
Zurück zum Zitat Fryback DG, et al. US norms for six generic health-related quality-of-life indexes from the National Health Measurement study. Med Care. 2007;45(12):1162–70.PubMedCentralCrossRefPubMed Fryback DG, et al. US norms for six generic health-related quality-of-life indexes from the National Health Measurement study. Med Care. 2007;45(12):1162–70.PubMedCentralCrossRefPubMed
99.
Zurück zum Zitat Adams PC, Speechley M. The effect of arthritis on the quality of life in hereditary hemochromatosis. J Rheumatol. 1996;23(4):707–10.PubMed Adams PC, Speechley M. The effect of arthritis on the quality of life in hereditary hemochromatosis. J Rheumatol. 1996;23(4):707–10.PubMed
100.
Zurück zum Zitat Rogowski W. Genetic screening by DNA technology: a systematic review of health economic evidence. Int J Technol Assess Health Care. 2006;22(3):327–37.CrossRefPubMed Rogowski W. Genetic screening by DNA technology: a systematic review of health economic evidence. Int J Technol Assess Health Care. 2006;22(3):327–37.CrossRefPubMed
101.
102.
Zurück zum Zitat Sahinbegovic E, et al. Musculoskeletal disease burden of hereditary hemochromatosis. Arthritis Rheum. 2010;62(12):3792–8.CrossRefPubMed Sahinbegovic E, et al. Musculoskeletal disease burden of hereditary hemochromatosis. Arthritis Rheum. 2010;62(12):3792–8.CrossRefPubMed
103.
Zurück zum Zitat Barton JC, et al. Characteristics of participants with self-reported hemochromatosis or iron overload at HEIRS Study initial screening. Am J Hematol. 2008;83(2):126–32.PubMedCentralCrossRefPubMed Barton JC, et al. Characteristics of participants with self-reported hemochromatosis or iron overload at HEIRS Study initial screening. Am J Hematol. 2008;83(2):126–32.PubMedCentralCrossRefPubMed
104.
Zurück zum Zitat McLaren GD, et al. Clinical manifestations of hemochromatosis in HFE C282Y homozygotes identified by screening. Can J Gastroenterol. 2008;22(11):923–30.PubMedCentralPubMed McLaren GD, et al. Clinical manifestations of hemochromatosis in HFE C282Y homozygotes identified by screening. Can J Gastroenterol. 2008;22(11):923–30.PubMedCentralPubMed
105.
Zurück zum Zitat McLernon DJ, Dillon J, Donnan PT. Health-state utilities in liver disease: a systematic review. Med Decis Mak. 2008;28(4):582–92.CrossRef McLernon DJ, Dillon J, Donnan PT. Health-state utilities in liver disease: a systematic review. Med Decis Mak. 2008;28(4):582–92.CrossRef
106.
Zurück zum Zitat Lung TW, et al. A meta-analysis of health state valuations for people with diabetes: explaining the variation across methods and implications for economic evaluation. Qual Life Res. 2011;20(10):1669–78.CrossRefPubMed Lung TW, et al. A meta-analysis of health state valuations for people with diabetes: explaining the variation across methods and implications for economic evaluation. Qual Life Res. 2011;20(10):1669–78.CrossRefPubMed
107.
Zurück zum Zitat Holland R, et al. Patients’ self-assessed functional status in heart failure by New York Heart Association class: a prognostic predictor of hospitalizations, quality of life and death. J Card Fail. 2010;16(2):150–6.PubMedCentralCrossRefPubMed Holland R, et al. Patients’ self-assessed functional status in heart failure by New York Heart Association class: a prognostic predictor of hospitalizations, quality of life and death. J Card Fail. 2010;16(2):150–6.PubMedCentralCrossRefPubMed
Metadaten
Titel
A Systematic Review and Narrative Synthesis of Health Economic Studies Conducted for Hereditary Haemochromatosis
verfasst von
Barbara de Graaff
Amanda Neil
Kristy Sanderson
Lei Si
Kwang Chien Yee
Andrew J. Palmer
Publikationsdatum
01.10.2015
Verlag
Springer International Publishing
Erschienen in
Applied Health Economics and Health Policy / Ausgabe 5/2015
Print ISSN: 1175-5652
Elektronische ISSN: 1179-1896
DOI
https://doi.org/10.1007/s40258-015-0189-y

Weitere Artikel der Ausgabe 5/2015

Applied Health Economics and Health Policy 5/2015 Zur Ausgabe