Literature DB >> 26157182

Cost-Consequence Analysis of Nitisinone for Treatment of Tyrosinemia Type I.

Mariève Simoncelli1, Johanne Samson2, Jean-François Bussières3, Jacques Lacroix4, Marc Dorais5, Renaldo Battista6, Sylvie Perreault7.   

Abstract

BACKGROUND: Tyrosinemia type I is a rare but severe genetic metabolic disorder. Nitisinone combined with a diet low in tyrosine and phenylalanine became first-line therapy in 1994.
OBJECTIVES: To estimate the direct medical costs of health care services related to the treatment of tyrosinemia type I, taking into consideration the real-life efficacy of nitisinone.
METHODS: A cost-consequence analysis was performed for all children with a confirmed diagnosis of tyrosinemia type I who were treated in Quebec between January 1, 1984, and January 1, 2009. The costs of care were compared for 3 consecutive historical groups: no nitisinone (1984 to 1994), late intervention with nitisinone (first dose received between 1994 and 1997), and early intervention with nitisinone (first dose received between 1997 and 2008). Data were derived from patient charts, hospital databases, and the Régie de l'assurance maladie du Québec and MED-ÉCHO administrative databases. Costs were reported in 2008 Canadian dollars.
RESULTS: Nitisinone treatment was associated with significant reductions in the number and duration of hospital admissions, the number of admissions to a pediatric intensive care unit, and the number of liver transplants. The cost of hospitalization per person-year was significantly lower in the 2 groups treated with nitisinone: $673 and $5 590 for the early-intervention and late-intervention groups, respectively, as compared to $12 980 for the no-nitisinone group (p < 0.001). Hospital costs per person-year for liver transplant were $3 198 for the late-intervention group and $5 044 for the no-nitisinone group: there were no transplants in the early-intervention group. The cost of nitisinone per person-year was $51 493 for the early-intervention group and $64 895 for the late-intervention group.
CONCLUSIONS: Nitisinone treatment significantly improved the outcomes of patients with tyrosinemia type I, while decreasing utilization of health care resources, liver transplants, and associated costs.

Entities:  

Keywords:  NTBC [2-(2-nitro-4-trifluoromethyl-benzoyl)-1,3-cyclohexanedione]; cost–consequence analysis; genetic disease; health technology assessment; hereditary tyrosinemia type I; metabolic disorder; nitisinone; pharmacotherapy; rare diseases; tyrosinemia

Year:  2015        PMID: 26157182      PMCID: PMC4485508     

Source DB:  PubMed          Journal:  Can J Hosp Pharm        ISSN: 0008-4123


  9 in total

1.  Renal function in tyrosinaemia type I after liver transplantation: a long-term follow-up.

Authors:  L J W M Pierik; F J van Spronsen; C M A Bijleveld; C M L van Dael
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.982

Review 2.  Nontransplant treatment of tyrosinemia.

Authors:  E Holme; S Lindstedt
Journal:  Clin Liver Dis       Date:  2000-11       Impact factor: 6.126

Review 3.  The pathophysiology and treatment of hereditary tyrosinemia type 1.

Authors:  M Grompe
Journal:  Semin Liver Dis       Date:  2001-11       Impact factor: 6.115

Review 4.  Tyrosinemia: the Quebec experience.

Authors:  K Paradis
Journal:  Clin Invest Med       Date:  1996-10       Impact factor: 0.825

5.  Hereditary tyrosinemia type I: a new clinical classification with difference in prognosis on dietary treatment.

Authors:  F J van Spronsen; Y Thomasse; G P Smit; J V Leonard; P T Clayton; V Fidler; R Berger; H S Heymans
Journal:  Hepatology       Date:  1994-11       Impact factor: 17.425

6.  Effect of nitisinone (NTBC) treatment on the clinical course of hepatorenal tyrosinemia in Québec.

Authors:  Jean Larochelle; Fernando Alvarez; Jean-François Bussières; Isabelle Chevalier; Louis Dallaire; Josée Dubois; Frédéric Faucher; Daphna Fenyves; Paul Goodyer; André Grenier; Elisabeth Holme; Rachel Laframboise; Marie Lambert; Sven Lindstedt; Bruno Maranda; Serge Melançon; Aicha Merouani; John Mitchell; Guy Parizeault; Luc Pelletier; Véronique Phan; Piero Rinaldo; C Ronald Scott; Charles Scriver; Grant A Mitchell
Journal:  Mol Genet Metab       Date:  2012-07-13       Impact factor: 4.797

7.  NTBC treatment in tyrosinaemia type I: long-term outcome in French patients.

Authors:  A Masurel-Paulet; J Poggi-Bach; M-O Rolland; O Bernard; N Guffon; D Dobbelaere; J Sarles; H Ogier de Baulny; G Touati
Journal:  J Inherit Metab Dis       Date:  2008-01-25       Impact factor: 4.982

8.  Validation of diagnostic codes within medical services claims.

Authors:  Machelle Wilchesky; Robyn M Tamblyn; Allen Huang
Journal:  J Clin Epidemiol       Date:  2004-02       Impact factor: 6.437

9.  The use of prescription claims databases in pharmacoepidemiological research: the accuracy and comprehensiveness of the prescription claims database in Québec.

Authors:  R Tamblyn; G Lavoie; L Petrella; J Monette
Journal:  J Clin Epidemiol       Date:  1995-08       Impact factor: 6.437

  9 in total
  8 in total

1.  Competitive rational inhibitor design to 4-maleylaceto-acetate isomerase.

Authors:  Narges Zolfaghari
Journal:  Bioinformation       Date:  2017-05-31

2.  Liver Transplantation: A Safe and Definitive Alternative to Lifelong Nitisinone for Tyrosinemia Type 1.

Authors:  Jagadeesh Menon; Naresh Shanmugam; Joseph J Valamparampil; Abdul Hakeem; Mukul Vij; Anil Jalan; Mettu Srinivas Reddy; Mohamed Rela
Journal:  Indian J Pediatr       Date:  2021-08-16       Impact factor: 1.967

3.  Curative Ex Vivo Hepatocyte-Directed Gene Editing in a Mouse Model of Hereditary Tyrosinemia Type 1.

Authors:  Caitlin VanLith; Rebekah Guthman; Clara T Nicolas; Kari Allen; Zeji Du; Dong Jin Joo; Scott L Nyberg; Joseph B Lillegard; Raymond D Hickey
Journal:  Hum Gene Ther       Date:  2018-06-22       Impact factor: 5.695

4.  Mildly elevated succinylacetone and normal liver function in compound heterozygotes with pathogenic and pseudodeficient FAH alleles.

Authors:  Hao Yang; Francis Rossignol; Denis Cyr; Rachel Laframboise; Shu Pei Wang; Jean-François Soucy; Marie-Thérèse Berthier; Yves Giguère; Paula J Waters; Grant A Mitchell
Journal:  Mol Genet Metab Rep       Date:  2017-12-27

5.  Autologous Gene and Cell Therapy Provides Safe and Long-Term Curative Therapy in A Large Pig Model of Hereditary Tyrosinemia Type 1.

Authors:  Raymond D Hickey; Clara T Nicolas; Kari Allen; Shennen Mao; Faysal Elgilani; Jaime Glorioso; Bruce Amiot; Caitlin VanLith; Rebekah Guthman; Zeji Du; Harvey Chen; Cary O Harding; Robert A Kaiser; Scott L Nyberg; Joseph B Lillegard
Journal:  Cell Transplant       Date:  2018-11-26       Impact factor: 4.064

6.  Clinical and genetic characteristics of two patients with tyrosinemia type 1 in Slovenia - A novel fumarylacetoacetate hydrolase (FAH) intronic disease-causing variant.

Authors:  Jaka Sikonja; Jernej Brecelj; Mojca Zerjav Tansek; Barbka Repic Lampret; Ana Drole Torkar; Simona Klemencic; Neza Lipovec; Valentina Stefanova Kralj; Sara Bertok; Jernej Kovac; Barbara Faganel Kotnik; Marketa Tesarova; Ziga Iztok Remec; Marusa Debeljak; Tadej Battelino; Urh Groselj
Journal:  Mol Genet Metab Rep       Date:  2021-12-16

7.  mRNA-based therapy proves superior to the standard of care for treating hereditary tyrosinemia 1 in a mouse model.

Authors:  Maximiliano L Cacicedo; Christine Weinl-Tenbruck; Daniel Frank; Sebastian Wirsching; Beate K Straub; Jana Hauke; Jürgen G Okun; Nigel Horscroft; Julia B Hennermann; Fred Zepp; Frédéric Chevessier-Tünnesen; Stephan Gehring
Journal:  Mol Ther Methods Clin Dev       Date:  2022-07-15       Impact factor: 5.849

Review 8.  Evaluation of pre-symptomatic nitisinone treatment on long-term outcomes in Tyrosinemia type 1 patients: a systematic review.

Authors:  Julia Geppert; Chris Stinton; Karoline Freeman; Hannah Fraser; Aileen Clarke; Samantha Johnson; Paul Sutcliffe; Sian Taylor-Phillips
Journal:  Orphanet J Rare Dis       Date:  2017-09-11       Impact factor: 4.123

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.