药物使用和药物坚持治疗牛皮关节炎:一项意大利研究
Fiorenzo Santoleri1, Paolo Abrate2, Laura Pestrin3
1Pescara General Hospital, Pescara - Italy.
Global & regional health technology assessment
|October 14, 2024
概括
生物和向合成修饰疾病的抗风湿药物 (b/tsDMARDs) 在牛皮关节炎 (PsA) 中表现出可变的持久性. 与原始药物相比,生物类药物,特别是乙素,表现出更好的坚持性和显著的成本节省.
科学领域:
- 类风湿病学 类风湿病学
- 药物经济学 药物经济学
- 药物开发 药物开发
背景情况:
- 牛皮关节炎 (PsA) 管理涉及生物和向合成修饰疾病的抗风湿药物 (b/tsDMARDs).
- 治疗的持续性和坚持性对于PsA的最佳临床结果至关重要.
- 了解药物成本和生物类似药的作用对于医疗保健资源优化至关重要.
研究的目的:
- 评估b/tsDMARDs在意大利的PsA患者的持续性,治疗坚持性和药物成本.
- 为了比较原始药和生物类似药的实际有效性和成本效益.
- 评估生物类似药物使用对医疗保健支出的影响.
主要方法:
- 意大利八家医院药房的回顾性观察研究 (2017年1月 - 2020年12月).
- 包括生物/向合成的先前没有使用DMARD的PsA患者,12个月的随访.
- 使用覆盖日数比例 (PDC) 评估持久性和坚持性;原始剂与生物类似的阿达利穆马布和埃坦塞普特的比较.
主要成果:
- 整体1年持久率为48.6%;47.6%的患者坚持 (PDC≥0.8).
- 阿达利穆马布原始剂和生物类似剂显示出类似的持久性和粘附性.
- 与其原始物相比,etanercept生物类似物表现出更好的持久性和坚持性,可节省大量成本 (>每年每患者2,500欧元).
结论:
- 药物坚持不良会对PsA的临床结果产生负面影响.
- 生物相似的乙坦塞普特提供了比原始药物更好的持久性和粘附性.
- 使用生物类似药物支持医疗保健资源优化和PSA管理的成本效益.
相关概念视频
Drug Therapy
39
The advent of drug therapy has profoundly shaped modern mental health care, providing targeted treatments for a range of psychological disorders. Psychotherapeutic drugs, classified into antianxiety, antidepressant, and antipsychotic medications, address symptoms across anxiety disorders, mood disorders, and schizophrenia. While these medications have transformed patient outcomes, they require careful management due to their potential side effects and limitations.
Antianxiety Medications
Antianxiety Medications
39
Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents
143
Crohn's disease is an inflammatory bowel disorder marked by chronic inflammation of the GI tract. Various treatment strategies for Crohn's disease are employed, such as immunomodulatory agents, glucocorticoids, and biologics or anti-TNF therapy. Azathioprine (Imuran), a commonly used immunomodulatory drug for Crohn's disease, is converted in the body to mercaptopurine, which inhibits purine biosynthesis and cell proliferation. Both are utilized in severe cases of Inflammatory Bowel...
143
Drugs for Treatment of Ulcerative Colitis in IBD
126
Ulcerative colitis is a chronic inflammatory condition primarily affecting the colon and rectum. The primary drugs used in the treatment of ulcerative colitis are aminosalicylates. They exhibit anti-inflammatory and immunosuppressive properties. They modulate inflammatory mediators and inhibit the activity of nuclear factor κB (NF-κB). Aminosalicylates also reduce inflammation by inhibiting prostaglandin and leukotriene production and decreasing neutrophil chemotaxis and superoxide...
126
Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF
117
Tumor Necrosis Factor (TNF), a proinflammatory cytokine, contributes significantly to the inflammation seen in Crohn's disease. It exists as soluble TNF and membrane-bound TNF, with actions mediated through TNF receptors (TNFR). TNFR activation leads to the release of proinflammatory cytokines, T-cell activation, collagen production, and leukocyte migration, all contributing to inflammation in Crohn's disease. Anti-TNF monoclonal antibodies, namely infliximab (Remicade), adalimumab...
117
Psychosis: Goals of Pharmacotherapy
109
Antipsychotic drugs are a crucial treatment method for acute and chronic psychoses, bipolar illness, and behavioral disorders. The selection of these drugs depends on several factors, including the state of the disease, clinical judgment, possible drug interactions, and the patient's sensitivity to adverse effects. In immediate scenarios, such as delirium and dementia, short-term treatment with low doses of high-potency typical or atypical agents can effectively manage symptom exacerbation.
109
Drugs for Treatment of Crohn's Disease in IBD Using Glucocorticoids
97
Glucocorticoids, a class of anti-inflammatory drugs, are pivotal in treating moderate to severe Crohn's disease by inducing remission. They exhibit their anti-inflammatory action by inhibiting the production of inflammatory cytokines such as tumor necrosis factor (TNF)-α, interleukin (IL)-1, and chemokines like IL-8. In addition, they reduce the expression of inflammatory cell adhesion molecules and inhibit gene transcription of nitric oxide synthase, phospholipase A2, cyclooxygenase-2...
97


