治疗癌症患者慢性疼痛:他法algin的使用经验。病例报告

Q4 Medicine
N. Ognerubov
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引用次数: 0

摘要

背景。慢性疼痛是与癌症相关的最常见和最严重的疾病,引起外周和中枢神经系统疾病,疼痛控制不足可能具有破坏性,并对患者的生活质量和日常活动产生负面影响。因此,开发在抗肿瘤治疗和姑息治疗中完全控制疼痛的新药是现代肿瘤学迫切需要解决的问题。其中一个方向是寻找与1-阿片受体相互作用的选择性分子,而不会产生阿片样物质的许多副作用。的目标。评价一种新的选择性1-阿片类镇痛药他法algin治疗胰腺癌患者慢性疼痛的疗效。材料和方法。1例60岁IV期胰腺癌患者,pT2 N0M1伴肝转移,多次化疗10个周期后的状态,远端胰腺次全切除伴脾切除术,2022年10月进展,肝转移;多化疗4个周期后状态,重度慢性疼痛。结果。使用视觉模拟量表评估初始疼痛严重程度:休息时7分,用力时9分。患者在FOLFIRINOX复合化疗期间出现疼痛,为此他接受了曲马多,每日剂量为400mg,与扑热息痛联合使用,效果为1.5个月。疼痛程度随突破疼痛而增加。给予长效吗啡60mg /d,效果良好。然而,患者感到恶心和呕吐。吗啡剂量减少至20mg,消除了副作用,降低了疗效。他法algin给药剂量为4mg TID。疼痛程度降至11.2分。无不良事件报告。病人已经服药52天了。他的睡眠和食欲有所改善,体力活动有所增加,体重也没有下降。结论。当病人改用他法金时,持续适当的疼痛控制得以维持,并不逊于吗啡。他法尔金具有良好的安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapy of chronic pain in cancer patients: Tafalgin use experience. Case report
Background. Chronic pain is the most common and severe condition associated with cancer, causing peripheral and central nervous system disorders Inadequate pain control can be destructive and negatively affect patients' quality of life and daily activity. Therefore, developing new drugs for complete pain control during antitumor therapy and palliative care is an urgent problem in modern oncology. One of these directions is the search for selective molecules that interact with 1-opioid receptors without many side effects of opioids. Aim. To evaluate the effectiveness of a new selective 1-opioid analgesic, Tafalgin, in treating chronic pain in a patient with pancreatic cancer. Materials and methods. Tafalgin was used to control chronic pain in a 60-year-old patient with stage IV pancreatic cancer, pT2 N0M1, with liver metastases, state after 10 cycles of polychemotherapy, and distal subtotal resection of the pancreas with splenectomy, progression in October 2022, liver metastases; state after 4 cycles of polychemotherapy, severe chronic pain. Results. The initial pain severity was evaluated using a visual analog scale: 7 points at rest and 9 points on exertion. The patient developed pain during FOLFIRINOX polychemotherapy, for which he received tramadol at a daily dose of 400 mg in combination with paracetamol, with an effect for 1.5 months. The pain severity increased with breakthrough pain. The patient was prescribed long-acting morphine at 60 mg/day, with good effect. However, the patient experienced nausea and vomiting. The morphine dose was reduced to 20 mg, thus resolving side effects and decreasing the effectiveness. Tafalgin was administered at a dose of 4 mg TID. The pain severity decreased to 11.2 points. No adverse events were reported. The patient has been receiving the drug for 52 days. His sleep and appetite have improved, physical activity has increased, and no weight loss has been reported. Conclusion. When switching a patient to Tafalgin, continuous adequate pain control is maintained, not inferior to morphine. Tafalgin is associated with a favorable safety profile.
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来源期刊
Journal of Modern Oncology
Journal of Modern Oncology Medicine-Oncology
CiteScore
0.50
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