医学
治疗药物监测
炎症性肠病
加药
药品
重症监护医学
疾病
临床终点
药物反应
治疗效果
治疗方法
生物标志物
精密医学
内科学
药理学
临床试验
病理
生物化学
化学
作者
Anam Fahad,Somia Jamal Sheikh,Mishaal Munir,Asfand Yar Cheema,Muhammad Ali Khan,Hira Tahir,Rahimeen Rajpar,Ahmad Kasem,Sarayu Bhogoju,Hammad Qureshi,Syed Adeel Hassan
出处
期刊:IntechOpen eBooks
[IntechOpen]
日期:2023-07-12
被引量:1
标识
DOI:10.5772/intechopen.1002197
摘要
Decades of cutting edge innovation in Inflammatory bowel disease (IBD) has yielded a diverse therapeutic armamentarium and warranted a shift in desired clinical endpoint (CE) from symptomatic management towards mucosal healing, histologic outcomes, serial biomarker trends and endoscopic remission. Despite these advancements, disease remission and therapeutic response rates remain suboptimal. This is due to failure to respond to therapy during the induction period (primary non-responder) or a subsequent loss of response (secondary non-responder). To address this area of unmet need, therapeutic drug monitoring (TDM) provides an opportunity to optimize dosing and therapeutic drug concentrations as per desired end clinical targets to improve response rates and offset aggressive disease complications. This further provides a platform for IBD therapeutic stratification based on patient, non-patient related factors and desired CE. In this chapter we aim to discuss a background regarding current TDM applications for various Food and Drug Administration (FDA)-approved IBD therapies and pinpoint deficiencies to enhance its smooth clinical implementation with a view to elucidating precision medicine as a novel therapeutic avenue in IBD.
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