Health state utilities for beta-thalassemia : a time trade-off study
Gespeichert in:
| Autor*in: |
Martin, Antony P. [verfasserIn] Ferri Grazzi, Enrico [verfasserIn] Mighiu, Claudia [verfasserIn] Chevli, Manoj [verfasserIn] Shah, Farrukh [verfasserIn] Maher, Louise [verfasserIn] Shaikh, Anum [verfasserIn] Sagar, Aliah [verfasserIn] Hubberstey, Hayley [verfasserIn] Franks, Bethany [verfasserIn] Ramos-Goñi, Juan M. [verfasserIn] Oppe, Mark [verfasserIn] Tang, Derek [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2023 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: The European journal of health economics - Berlin : Springer, 2001, 24(2023), 1 vom: Feb., Seite 27-38 |
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| Übergeordnetes Werk: |
volume:24 ; year:2023 ; number:1 ; month:02 ; pages:27-38 |
| Links: |
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| DOI / URN: |
10.1007/s10198-022-01449-7 |
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| Katalog-ID: |
1838148116 |
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| 245 | 1 | 0 | |a Health state utilities for beta-thalassemia |b a time trade-off study |c Antony P. Martin, Enrico Ferri Grazzi, Claudia Mighiu, Manoj Chevli, Farrukh Shah, Louise Maher, Anum Shaikh, Aliah Sagar, Hayley Hubberstey, Bethany Franks, Juan M. Ramos-Goñi, Mark Oppe, Derek Tang |
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| 650 | 4 | |a Beta-thalassemia |7 (dpeaa)DE-206 | |
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| 650 | 4 | |a I12 Health Behavior |7 (dpeaa)DE-206 | |
| 650 | 4 | |a Time trade-off |7 (dpeaa)DE-206 | |
| 650 | 4 | |a Transfusion burden |7 (dpeaa)DE-206 | |
| 700 | 1 | |a Ferri Grazzi, Enrico |e verfasserin |0 (DE-588)1283571927 |0 (DE-627)1839337672 |4 aut | |
| 700 | 1 | |a Mighiu, Claudia |e verfasserin |4 aut | |
| 700 | 1 | |a Chevli, Manoj |e verfasserin |4 aut | |
| 700 | 1 | |a Shah, Farrukh |e verfasserin |4 aut | |
| 700 | 1 | |a Maher, Louise |e verfasserin |0 (DE-588)1283572265 |0 (DE-627)183933777X |4 aut | |
| 700 | 1 | |a Shaikh, Anum |e verfasserin |4 aut | |
| 700 | 1 | |a Sagar, Aliah |e verfasserin |4 aut | |
| 700 | 1 | |a Hubberstey, Hayley |e verfasserin |4 aut | |
| 700 | 1 | |a Franks, Bethany |e verfasserin |4 aut | |
| 700 | 1 | |a Ramos-Goñi, Juan M. |e verfasserin |4 aut | |
| 700 | 1 | |a Oppe, Mark |e verfasserin |4 aut | |
| 700 | 1 | |a Tang, Derek |e verfasserin |4 aut | |
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| 982 | |2 26 |1 00 |x DE-206 |b Beta-thalassemia (BT) is an inherited blood disorder characterized by reduced levels of functional hemoglobin resulting in phenotypes ranging from clinically asymptomatic to severely anemic. Patients with BT may require lifelong regular blood transfusions supported by appropriate iron chelation therapy (ICT). This study aimed to determine how the UK general population values BT health states associated with differing transfusion burden and ICT. | ||
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10.1007/s10198-022-01449-7 doi (DE-627)1838148116 (DE-599)KXP1838148116 (DE-He213)s10198-022-01449-7-e DE-627 ger DE-627 rda eng Martin, Antony P. verfasserin aut Health state utilities for beta-thalassemia a time trade-off study Antony P. Martin, Enrico Ferri Grazzi, Claudia Mighiu, Manoj Chevli, Farrukh Shah, Louise Maher, Anum Shaikh, Aliah Sagar, Hayley Hubberstey, Bethany Franks, Juan M. Ramos-Goñi, Mark Oppe, Derek Tang 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Anemia (dpeaa)DE-206 Beta-thalassemia (dpeaa)DE-206 Hemoglobin (dpeaa)DE-206 I12 Health Behavior (dpeaa)DE-206 Time trade-off (dpeaa)DE-206 Transfusion burden (dpeaa)DE-206 Ferri Grazzi, Enrico verfasserin (DE-588)1283571927 (DE-627)1839337672 aut Mighiu, Claudia verfasserin aut Chevli, Manoj verfasserin aut Shah, Farrukh verfasserin aut Maher, Louise verfasserin (DE-588)1283572265 (DE-627)183933777X aut Shaikh, Anum verfasserin aut Sagar, Aliah verfasserin aut Hubberstey, Hayley verfasserin aut Franks, Bethany verfasserin aut Ramos-Goñi, Juan M. verfasserin aut Oppe, Mark verfasserin aut Tang, Derek verfasserin aut Enthalten in The European journal of health economics Berlin : Springer, 2001 24(2023), 1 vom: Feb., Seite 27-38 Online-Ressource (DE-627)320494462 (DE-600)2011428-X (DE-576)09670425X 1618-7601 nnns volume:24 year:2023 number:1 month:02 pages:27-38 https://link.springer.com/content/pdf/10.1007/s10198-022-01449-7.pdf Verlag kostenfrei https://doi.org/10.1007/s10198-022-01449-7 Resolving-System kostenfrei GBV_USEFLAG_U GBV_ILN_26 ISIL_DE-206 SYSFLAG_1 GBV_KXP GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2941 GBV_ILN_2949 GBV_ILN_2950 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4392 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_2403 GBV_ILN_2403 ISIL_DE-LFER AR 24 2023 1 2 27-38 26 01 0206 4283228516 x1z 03-03-23 2403 01 DE-LFER 4313639462 00 --%%-- --%%-- n --%%-- l01 25-04-23 2403 01 DE-LFER https://doi.org/10.1007/s10198-022-01449-7 2403 01 DE-LFER https://link.springer.com/content/pdf/10.1007/s10198-022-01449-7.pdf 26 00 DE-206 Beta-thalassemia (BT) is an inherited blood disorder characterized by reduced levels of functional hemoglobin resulting in phenotypes ranging from clinically asymptomatic to severely anemic. Patients with BT may require lifelong regular blood transfusions supported by appropriate iron chelation therapy (ICT). This study aimed to determine how the UK general population values BT health states associated with differing transfusion burden and ICT. |
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10.1007/s10198-022-01449-7 doi (DE-627)1838148116 (DE-599)KXP1838148116 (DE-He213)s10198-022-01449-7-e DE-627 ger DE-627 rda eng Martin, Antony P. verfasserin aut Health state utilities for beta-thalassemia a time trade-off study Antony P. Martin, Enrico Ferri Grazzi, Claudia Mighiu, Manoj Chevli, Farrukh Shah, Louise Maher, Anum Shaikh, Aliah Sagar, Hayley Hubberstey, Bethany Franks, Juan M. Ramos-Goñi, Mark Oppe, Derek Tang 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Anemia (dpeaa)DE-206 Beta-thalassemia (dpeaa)DE-206 Hemoglobin (dpeaa)DE-206 I12 Health Behavior (dpeaa)DE-206 Time trade-off (dpeaa)DE-206 Transfusion burden (dpeaa)DE-206 Ferri Grazzi, Enrico verfasserin (DE-588)1283571927 (DE-627)1839337672 aut Mighiu, Claudia verfasserin aut Chevli, Manoj verfasserin aut Shah, Farrukh verfasserin aut Maher, Louise verfasserin (DE-588)1283572265 (DE-627)183933777X aut Shaikh, Anum verfasserin aut Sagar, Aliah verfasserin aut Hubberstey, Hayley verfasserin aut Franks, Bethany verfasserin aut Ramos-Goñi, Juan M. verfasserin aut Oppe, Mark verfasserin aut Tang, Derek verfasserin aut Enthalten in The European journal of health economics Berlin : Springer, 2001 24(2023), 1 vom: Feb., Seite 27-38 Online-Ressource (DE-627)320494462 (DE-600)2011428-X (DE-576)09670425X 1618-7601 nnns volume:24 year:2023 number:1 month:02 pages:27-38 https://link.springer.com/content/pdf/10.1007/s10198-022-01449-7.pdf Verlag kostenfrei https://doi.org/10.1007/s10198-022-01449-7 Resolving-System kostenfrei GBV_USEFLAG_U GBV_ILN_26 ISIL_DE-206 SYSFLAG_1 GBV_KXP GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2941 GBV_ILN_2949 GBV_ILN_2950 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4392 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_2403 GBV_ILN_2403 ISIL_DE-LFER AR 24 2023 1 2 27-38 26 01 0206 4283228516 x1z 03-03-23 2403 01 DE-LFER 4313639462 00 --%%-- --%%-- n --%%-- l01 25-04-23 2403 01 DE-LFER https://doi.org/10.1007/s10198-022-01449-7 2403 01 DE-LFER https://link.springer.com/content/pdf/10.1007/s10198-022-01449-7.pdf 26 00 DE-206 Beta-thalassemia (BT) is an inherited blood disorder characterized by reduced levels of functional hemoglobin resulting in phenotypes ranging from clinically asymptomatic to severely anemic. Patients with BT may require lifelong regular blood transfusions supported by appropriate iron chelation therapy (ICT). This study aimed to determine how the UK general population values BT health states associated with differing transfusion burden and ICT. |
| allfields_unstemmed |
10.1007/s10198-022-01449-7 doi (DE-627)1838148116 (DE-599)KXP1838148116 (DE-He213)s10198-022-01449-7-e DE-627 ger DE-627 rda eng Martin, Antony P. verfasserin aut Health state utilities for beta-thalassemia a time trade-off study Antony P. Martin, Enrico Ferri Grazzi, Claudia Mighiu, Manoj Chevli, Farrukh Shah, Louise Maher, Anum Shaikh, Aliah Sagar, Hayley Hubberstey, Bethany Franks, Juan M. Ramos-Goñi, Mark Oppe, Derek Tang 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Anemia (dpeaa)DE-206 Beta-thalassemia (dpeaa)DE-206 Hemoglobin (dpeaa)DE-206 I12 Health Behavior (dpeaa)DE-206 Time trade-off (dpeaa)DE-206 Transfusion burden (dpeaa)DE-206 Ferri Grazzi, Enrico verfasserin (DE-588)1283571927 (DE-627)1839337672 aut Mighiu, Claudia verfasserin aut Chevli, Manoj verfasserin aut Shah, Farrukh verfasserin aut Maher, Louise verfasserin (DE-588)1283572265 (DE-627)183933777X aut Shaikh, Anum verfasserin aut Sagar, Aliah verfasserin aut Hubberstey, Hayley verfasserin aut Franks, Bethany verfasserin aut Ramos-Goñi, Juan M. verfasserin aut Oppe, Mark verfasserin aut Tang, Derek verfasserin aut Enthalten in The European journal of health economics Berlin : Springer, 2001 24(2023), 1 vom: Feb., Seite 27-38 Online-Ressource (DE-627)320494462 (DE-600)2011428-X (DE-576)09670425X 1618-7601 nnns volume:24 year:2023 number:1 month:02 pages:27-38 https://link.springer.com/content/pdf/10.1007/s10198-022-01449-7.pdf Verlag kostenfrei https://doi.org/10.1007/s10198-022-01449-7 Resolving-System kostenfrei GBV_USEFLAG_U GBV_ILN_26 ISIL_DE-206 SYSFLAG_1 GBV_KXP GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2941 GBV_ILN_2949 GBV_ILN_2950 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4392 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_2403 GBV_ILN_2403 ISIL_DE-LFER AR 24 2023 1 2 27-38 26 01 0206 4283228516 x1z 03-03-23 2403 01 DE-LFER 4313639462 00 --%%-- --%%-- n --%%-- l01 25-04-23 2403 01 DE-LFER https://doi.org/10.1007/s10198-022-01449-7 2403 01 DE-LFER https://link.springer.com/content/pdf/10.1007/s10198-022-01449-7.pdf 26 00 DE-206 Beta-thalassemia (BT) is an inherited blood disorder characterized by reduced levels of functional hemoglobin resulting in phenotypes ranging from clinically asymptomatic to severely anemic. Patients with BT may require lifelong regular blood transfusions supported by appropriate iron chelation therapy (ICT). This study aimed to determine how the UK general population values BT health states associated with differing transfusion burden and ICT. |
| allfieldsGer |
10.1007/s10198-022-01449-7 doi (DE-627)1838148116 (DE-599)KXP1838148116 (DE-He213)s10198-022-01449-7-e DE-627 ger DE-627 rda eng Martin, Antony P. verfasserin aut Health state utilities for beta-thalassemia a time trade-off study Antony P. Martin, Enrico Ferri Grazzi, Claudia Mighiu, Manoj Chevli, Farrukh Shah, Louise Maher, Anum Shaikh, Aliah Sagar, Hayley Hubberstey, Bethany Franks, Juan M. Ramos-Goñi, Mark Oppe, Derek Tang 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Anemia (dpeaa)DE-206 Beta-thalassemia (dpeaa)DE-206 Hemoglobin (dpeaa)DE-206 I12 Health Behavior (dpeaa)DE-206 Time trade-off (dpeaa)DE-206 Transfusion burden (dpeaa)DE-206 Ferri Grazzi, Enrico verfasserin (DE-588)1283571927 (DE-627)1839337672 aut Mighiu, Claudia verfasserin aut Chevli, Manoj verfasserin aut Shah, Farrukh verfasserin aut Maher, Louise verfasserin (DE-588)1283572265 (DE-627)183933777X aut Shaikh, Anum verfasserin aut Sagar, Aliah verfasserin aut Hubberstey, Hayley verfasserin aut Franks, Bethany verfasserin aut Ramos-Goñi, Juan M. verfasserin aut Oppe, Mark verfasserin aut Tang, Derek verfasserin aut Enthalten in The European journal of health economics Berlin : Springer, 2001 24(2023), 1 vom: Feb., Seite 27-38 Online-Ressource (DE-627)320494462 (DE-600)2011428-X (DE-576)09670425X 1618-7601 nnns volume:24 year:2023 number:1 month:02 pages:27-38 https://link.springer.com/content/pdf/10.1007/s10198-022-01449-7.pdf Verlag kostenfrei https://doi.org/10.1007/s10198-022-01449-7 Resolving-System kostenfrei GBV_USEFLAG_U GBV_ILN_26 ISIL_DE-206 SYSFLAG_1 GBV_KXP GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2018 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2941 GBV_ILN_2949 GBV_ILN_2950 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4392 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_2403 GBV_ILN_2403 ISIL_DE-LFER AR 24 2023 1 2 27-38 26 01 0206 4283228516 x1z 03-03-23 2403 01 DE-LFER 4313639462 00 --%%-- --%%-- n --%%-- l01 25-04-23 2403 01 DE-LFER https://doi.org/10.1007/s10198-022-01449-7 2403 01 DE-LFER https://link.springer.com/content/pdf/10.1007/s10198-022-01449-7.pdf 26 00 DE-206 Beta-thalassemia (BT) is an inherited blood disorder characterized by reduced levels of functional hemoglobin resulting in phenotypes ranging from clinically asymptomatic to severely anemic. Patients with BT may require lifelong regular blood transfusions supported by appropriate iron chelation therapy (ICT). This study aimed to determine how the UK general population values BT health states associated with differing transfusion burden and ICT. |
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Enthalten in The European journal of health economics 24(2023), 1 vom: Feb., Seite 27-38 volume:24 year:2023 number:1 month:02 pages:27-38 |
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26 00 DE-206 Beta-thalassemia (BT) is an inherited blood disorder characterized by reduced levels of functional hemoglobin resulting in phenotypes ranging from clinically asymptomatic to severely anemic. Patients with BT may require lifelong regular blood transfusions supported by appropriate iron chelation therapy (ICT). This study aimed to determine how the UK general population values BT health states associated with differing transfusion burden and ICT Health state utilities for beta-thalassemia a time trade-off study Antony P. Martin, Enrico Ferri Grazzi, Claudia Mighiu, Manoj Chevli, Farrukh Shah, Louise Maher, Anum Shaikh, Aliah Sagar, Hayley Hubberstey, Bethany Franks, Juan M. Ramos-Goñi, Mark Oppe, Derek Tang Anemia (dpeaa)DE-206 Beta-thalassemia (dpeaa)DE-206 Hemoglobin (dpeaa)DE-206 I12 Health Behavior (dpeaa)DE-206 Time trade-off (dpeaa)DE-206 Transfusion burden (dpeaa)DE-206 |
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Ferri Grazzi, Enrico Mighiu, Claudia Chevli, Manoj Shah, Farrukh Maher, Louise Shaikh, Anum Sagar, Aliah Hubberstey, Hayley Franks, Bethany Ramos-Goñi, Juan M. Oppe, Mark Tang, Derek |
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Grazzi, Enrico Ferri Ferri Grazzi, Enrico Maher, L. Maher, Louise |
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Grazzi, Enrico Ferri Ferri Grazzi, Enrico Maher, L. Maher, Louise |
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Grazzi, Enrico Ferri Ferri Grazzi, Enrico Maher, L. Maher, Louise |
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10.1007/s10198-022-01449-7 |
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2024-07-04T19:00:53.205Z |
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"><subfield code="d">24</subfield><subfield code="j">2023</subfield><subfield code="e">1</subfield><subfield code="c">2</subfield><subfield code="h">27-38</subfield></datafield><datafield tag="980" ind1=" " ind2=" "><subfield code="2">26</subfield><subfield code="1">01</subfield><subfield code="x">0206</subfield><subfield code="b">4283228516</subfield><subfield code="y">x1z</subfield><subfield code="z">03-03-23</subfield></datafield><datafield tag="980" ind1=" " ind2=" "><subfield code="2">2403</subfield><subfield code="1">01</subfield><subfield code="x">DE-LFER</subfield><subfield code="b">4313639462</subfield><subfield code="c">00</subfield><subfield code="f">--%%--</subfield><subfield code="d">--%%--</subfield><subfield code="e">n</subfield><subfield code="j">--%%--</subfield><subfield code="y">l01</subfield><subfield code="z">25-04-23</subfield></datafield><datafield tag="981" ind1=" " ind2=" "><subfield code="2">2403</subfield><subfield code="1">01</subfield><subfield code="x">DE-LFER</subfield><subfield code="r">https://doi.org/10.1007/s10198-022-01449-7</subfield></datafield><datafield tag="981" ind1=" " ind2=" "><subfield code="2">2403</subfield><subfield code="1">01</subfield><subfield code="x">DE-LFER</subfield><subfield code="r">https://link.springer.com/content/pdf/10.1007/s10198-022-01449-7.pdf</subfield></datafield><datafield tag="982" ind1=" " ind2=" "><subfield code="2">26</subfield><subfield code="1">00</subfield><subfield code="x">DE-206</subfield><subfield code="b">Beta-thalassemia (BT) is an inherited blood disorder characterized by reduced levels of functional hemoglobin resulting in phenotypes ranging from clinically asymptomatic to severely anemic. Patients with BT may require lifelong regular blood transfusions supported by appropriate iron chelation therapy (ICT). This study aimed to determine how the UK general population values BT health states associated with differing transfusion burden and ICT.</subfield></datafield></record></collection>
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7.399473 |