Biological drugs for the treatment of psoriasis in a public health system

被引:10
作者
Lopes, Luciane Cruz [1 ]
do Nascimento Silveira, Miriam Sanches [1 ]
de Camargo, Iara Alves [1 ,2 ]
Barberato-Filho, Silvio [1 ]
Del Fioli, Fernando de Sa [1 ]
Serpa Osorio-de-Castro, Claudia Garcia [3 ]
机构
[1] Univ Sorocaba, Programa Posgrad Ciencias Farmaceut, Sorocaba, SP, Brazil
[2] Secretaria Estadual Saude Sao Paulo, Coordenacao Demandas Estrateg Sistema Unico Saude, Sao Paulo, Brazil
[3] Fundacao Oswaldo Cruz, Escola Nacl Saude Publ Sergio Arouca, Nucleo Assistencia Farmaceut, Rio De Janeiro, RJ, Brazil
来源
REVISTA DE SAUDE PUBLICA | 2014年 / 48卷 / 04期
基金
巴西圣保罗研究基金会;
关键词
Psoriasis; Antibodies; Monoclonal; therapeutic use; Pharmaceutical Services; legislation; jurisprudence; Judicial Decisions; Equity in Access; SEVERE PLAQUE PSORIASIS; MODERATE; SAFETY; AGENTS; METAANALYSIS; ARTHRITIS; EFFICACY;
D O I
10.1590/S0034-8910.2014048005109
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
OBJECTIVE: To analyze the access and utilization profile of biological medications for psoriasis provided by the judicial system in Brazil. METHODS: This is a cross-sectional study. We interviewed a total of 203 patients with psoriasis who were on biological medications obtained by the judicial system of the State of Sao Paulo, from 2004 to 2010. Sociodemographics, medical, and political-administrative characteristics were complemented with data obtained from dispensation orders that included biological medications to treat psoriasis and the legal actions involved. The data was analyzed using an electronic data base and shown as simple variable frequencies. The prescriptions contained in the lawsuits were analyzed according to legal provisions. RESULTS: A total of 190 lawsuits requesting several biological drugs (adalimumab, efalizumab, etanercept, and infliximab) were analyzed. Patients obtained these medications as a result of injunctions (59.5%) or without having ever demanded biological medication from any health institution (86.2%), i.e., public or private health services. They used the prerogative of free legal aid (72.6%), even though they were represented by private lawyers (91.1%) and treated in private facilities (69.5%). Most of the patients used a biological medication for more than 13 months (66.0%), and some patients were undergoing treatment with this medication when interviewed (44.9%). Approximately one third of the patients discontinued treatment due to worsening of their illness (26.6%), adverse drug reactions (20.5%), lack of efficacy, or because the doctor discontinued this medication (13.8%). None of the analyzed medical prescriptions matched the legal prescribing requirements. Clinical monitoring results showed that 70.3% of the patients had not undergone laboratory examinations (blood work, liver and kidney function tests) for treatment control purposes. CONCLUSIONS: The plaintiffs resorted to legal action to get access to biological medications because they were either unaware or had difficulty in accessing them through institutional public health system procedures. Access by means of legal action facilitated long-term use of this type of medication through irregular prescriptions and led to a high rate of adverse drug reactions as well as inappropriate clinical monitoring.
引用
收藏
页码:651 / 661
页数:11
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