1例卵巢癌伴淋巴结核规律血透患者复杂药物治疗的药学干预

周雪,, 陈杰*, 高翔

中国药学杂志 ›› 2015, Vol. 50 ›› Issue (7) : 646-649.

PDF(709 KB)
PDF(709 KB)
中国药学杂志 ›› 2015, Vol. 50 ›› Issue (7) : 646-649. DOI: 10.11669/cpj.2015.07.017
药物与临床

1例卵巢癌伴淋巴结核规律血透患者复杂药物治疗的药学干预

  • 周雪1,2, 陈杰1*, 高翔1
作者信息 +

Pharmaceutical Intervention on a Complicated Patient with Oophoroma, Lymphatic Tuberculosis and Regular Hemodialysis

  • ZHOU Xue1,2, CHEN Jie1*, GAO Xiang1
Author information +
文章历史 +

摘要

目的 临床药师通过对1例国内外罕见报道的卵巢癌术后复发伴淋巴结核血透患者的抗结核和化疗方案进行药学干预,达到了较好的治疗效果。方法 临床药师在血液透析患者化疗与抗结核治疗的复杂情况下,利用自己药学专业知识,查阅国内外相关资料,确定患者的抗结核及化疗方案,优化卡铂剂量,并对患者进行游离铂的浓度测定及不良反应等药学监护,计算AUC,优化下一次给药方案。结果 全院会诊建议患者先进行抗结核治疗,待淋巴结结核有所控制后再进行卵巢癌化疗。临床药师在医师会诊讨论基础上优化治疗方案为:利福平0.45 g,1日1次,晨空腹服;异烟肼,0.3 g,1日1次,透析当日在透析后给药;乙胺丁醇0.75 g,每周一、三、五透析后给药;根据Calvert公式计算卡铂0.15 g,并予以紫杉醇0.15 g·m-2化疗。给药结束24 h后进行血液透析,血液透析维持3 h,游离铂的浓度测定,化疗第2~4疗程方案为紫杉醇0.15 g·m-2,卡铂0.166 g,给药方式同第一疗程。在整个化疗过程中,患者无明显不良反应,抗结核治疗和化疗均取得较好疗效,且患者耐受性良好。结论 临床药师根据药物的药动学和药效学特点,结合患者病理生理情况,为患者设计最佳治疗方案、预防不良反应、监测治疗效果,使患者获得最佳治疗。

Abstract

OBJECTIVE To carry out pharmaceutical intervention on a complicated patient with oophoroma, lymphatic tuberculosis and regular hemodialysis to achieve better therapeutic effect.METHODS Clinical pharmacists developed anti-tuberculosis and anti-tumor schemes, optimized carboplatin dosage, determined free platinum concentrations, calculated AUC of platinum and monitored adverse drug effect by using their pharmaceutical expertise.RESULTS Hospital-wide consultation recommended this patient with prior anti-TB treatment, and continue with ovarian cancer chemotherapy after somewhat lymphatic tuberculosis is controlled. The final anti-TB treatment scheme is rifampicin 0.45 g, once daily, morning empty stomach; isoniazid, 0.3 g, once daily, administrated after dialysis on dialysis day; ethambutol, 0.75 g, administrated after each dialysis. The first course of anti-tumor schemes is paclitaxel 0.15 g穖-2 and carboplatin 0.15 g calculated according to Calvert formula, dialysis was carried 24 h later and kept 3 h. Then determined free platinum concentrations, and calculated out the following 2nd-4th courses of anti-tumor treatment, which is paclitaxel 0.15 g穖-2 and carboplatin 0.166 g. The patient had no significant adverse reactions throughout the course of therapy, and anti-tuberculosis and anti-tumor treatment achieved good effect and well tolerance by patients.CONCLUSIONS According to pharmacokinetic and pharmacodynamic characteristics of the drug combined with patient pathophysiological conditions, clinical pharmacist designs the best treatment schemes for patients, prevents adverse reactions and held treatment monitoring.This patient can get the best treatment as a result.

关键词

临床药师 / 抗结核治疗 / 卵巢癌化疗 / 血液透析 / 药学干预

Key words

clinical pharmacist / anti-tuberculosis / anti-ovarian cancer chemotherapy / hemodialysis / pharmaceutical intervention

引用本文

导出引用
周雪,, 陈杰*, 高翔. 1例卵巢癌伴淋巴结核规律血透患者复杂药物治疗的药学干预[J]. 中国药学杂志, 2015, 50(7): 646-649 https://doi.org/10.11669/cpj.2015.07.017
ZHOU Xue,, CHEN Jie*, GAO Xiang. Pharmaceutical Intervention on a Complicated Patient with Oophoroma, Lymphatic Tuberculosis and Regular Hemodialysis[J]. Chinese Pharmaceutical Journal, 2015, 50(7): 646-649 https://doi.org/10.11669/cpj.2015.07.017
中图分类号: R969.3   

参考文献

[1] VINCENT L V, HASSANE I, GILBERT D. Pharmacokinetic considerations in the treatment of tuberculosis in patients with renal failure. Clin Pharmacokinet,2005,44(3):221-235. [2] LEUNG G K Y, TAM P Y W, TING R H. Isoniazid toxicity in hemodialysis patients . Am Soc Nephrol, 2002,13(Suppl 1):464A. [3] ALTIPARMAK M R, PAMUK O N, PAMUK G E, et al. Is isoniazid ototoxic in patients undergoing hemodialysis. Nephron, 2002,92(2):478-480. [4] MAGDI M H, JAAP M M, HAYSAM R. Tuberculosis and chronic renal disease . Seminars in Dialysis,2003, 16(1):38-44. [5] LIU Z W, HU Z H, CAI Y Y. The combined effect of isoniazid and rifampicin on the activities of CYP4501A2 and CYP4503A4 in primary hepatocytes from healthy human adults . Chin J Tuberc Respir Dis, 28(11):785-788. [6] BENNETT W M. Guide to drug dosage in renal failure. Clin Pharmacokinet, 1988,15(5):326-354. [7] MALONE R S, FISH D N, SPIEGEL D M, et al. The effect of hemodialysis on isoniazid, rifampin, pyrazinamide, and ethambutol . Am J Respir Crit Care Med, 1999,159(5):1580-1584. [8] YOSHIDA H, SUMI T, ABE K,et al. Pharmacokinetics of paclitaxel and carboplatin in a hemodialysis patient with advanced ovarian cancer. Eur J Gynaecol Oncol,2009,30(5):583-585. [9] YOKOYAMA Y, FUTAGAMI M, HIGUCHI T, et al. Pharmacokinetic analysis of paclitaxel and carboplatin in a patient with advanced ovarian cancer during hemodialysis--case report. Eur J Gynaecol Oncol, 2006, 27(4):437-439. [10] CALVERT A H, NEWELL D R, GUMBRELL L A, et al. Carboplatin dosage:Prospective evaluation of a simple formula based on renal function. J Clin Oncol,1989,7(11):1748-1756. [11] KODAMA J, SASAKI A, MASAHIRO S,et al. Pharmacokinetics of combination chemotherapy with paclitaxel and carboplatin in a patient with advanced epithelial ovarian cancer undergoing hemodialysis. Oncol Lett,2010, 1(3):511-513. [12] WATANABE M, AOKI Y, TOMITA M,et al. Paclitaxel and carboplatin combination chemotherapy in a hemodialysis patient with advanced ovarian cancer. Gynecol Oncol,2002, 84(2):335-338. [13] JEYABALAN N, HIRTE H W, MOENS F. Treatment of advanced ovarian carcinoma with carboplatin and paclitaxel in a patient with renal failure . Int J Gynecol Cancer, 2000, 10(6):463-468. [14] CHATELUT E, ROSTAING L, GUALANO V, et al. Pharmacokinetics of carboplatin in a patient suffering from advanced ovarian carcinoma with hemodialysis-dependent renal insufficiency. Nephron, 1994, 66(2):157-161. [15] OGURI T, SHIMOKATA T, INADA M,et al. Pharmacokinetic analysis of carboplatin in patients with cancer who are undergoing hemodialysis. Cancer Chemother Pharmacol,2010, 66(4):813-817.
PDF(709 KB)

60

Accesses

0

Citation

Detail

段落导航
相关文章

/