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find Keyword "毒性反应" 5 results
  • 氟尿嘧啶所致心脏毒性反应的临床观察及护理

    目的探讨氟尿嘧啶(5-FU)所致心脏毒性反应的观察及护理。 方法对2012年3月-2013年12月住院期间使用奥沙利铂+亚叶酸钙+5-FU(FOLFIRI)方案或者伊立替康+亚叶酸钙+5-FU(FOLFOX)方案的患者中,输注5-FU时发生心脏毒性反应23例,总结其临床表现期护理干预措施。 结果23例患者中出现胸闷心悸15例,心律失常6例,肌酸磷酸激酶增高2例。给予积极的护理干预和对症处理等措施,23例者均得到有效控制,未发生严重并发症。 结论5-FU对心脏有一定损伤,可出现不同程度的心脏毒性反应,输注过程中需密切观察,发现异常及时处理,并做好相应的护理,避免引起不可逆的心脏毒性反应的发生。

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  • 体外循环心内直视手术中鱼精蛋白致严重循环抑制的治疗

    目的 总结体外循环心内直视手术中鱼精蛋白所致严重循环抑制的救治经验。 方法 回顾性分析 2016 年 6 月至 2017 年 7 月我中心体外循环心内直视手术中给予鱼精蛋白中和肝素后出现严重循环抑制 9 例患者的临床资料,其中男 7 例,女 2 例,年龄 62.3(36~78)岁。7 例为左心室肥厚者。分析其临床特点及处理方法。 结果 1 例因反复给予鱼精蛋白而循环衰竭死亡,1 例因非鱼精蛋白原因死亡,余 7 例经肝素化转机和/或垂体后叶素等血管活性药抢救后好转。 结论 鱼精蛋白毒性反应所导致的严重循环抑制为突发事件且往往危及生命,果断肝素化转机和垂体后叶素的及时应用是成功挽救患者生命的重要环节。

    Release date:2018-06-26 05:41 Export PDF Favorites Scan
  • Progress of stereotactic radiotherapy in the treatment of brain metastatic tumor

    Patients with brain metastases are more prone to developing life-threatening neurological symptoms. Initial therapies include surgery, whole brain radiotherapy (WBRT), and stereotactic radiotherapy. With the progress of stereotactic radiotherapy, the indication of stereotactic radiosurgery (SRS) is gradually expanding, and the indications for surgery and WBRT gradually narrowed. The existing studies have shown that SRS can significantly benefit patients who are <50 years old with single brain metastasis, but the specific scope of the application with SRS is still controversial, and a large number of the phase Ⅲ randomized multicenter trials designed around the controversies are also developing. This review summarizes the results of clinical research and came to the conclusion. Firstly, postoperative adjuvant SRS in the treatment of brain metastases is superior to postoperative adjuvant WBRT. Secondly, using SRS in the elderly patients with multiple brain metastases are safe and effective. Thirdly, the use of targeted therapy in patients with brain metastases thereby delaying SRS may lead to poor prognosis. The focus of future research include selection of optimal timing for adjuvant targeted therapy after SRS and the appropriate patient population, as well as prevention of recurrence and metastasis after lacal treatment.

    Release date:2018-04-23 05:00 Export PDF Favorites Scan
  • Biocompatibility of bioprosthetic heart valve materials with a non-glutaraldehyde-based chemical treatment

    ObjectiveTo study the biocompatibility of bioprosthetic heart valve material with a non-glutaraldehyde-based treatment, and to provide the safety data for the clinical application. MethodsAll the tests were conducted according to GB/T16886 standards. The in vitro cytotoxicity was determined by methyl thiazolyl tetrazolium assay. Fifteen guinea pigs were divided into a test group (n=10) and a control group (n=5) in the skin sensitization test. Three New Zealand white rabbits were used in the intradermal reactivity test. Five sites on both sides of the rabbit back were set as test sites and control sites, respectively. In the acute systemic toxicity test, a total of 20 ICR mice were randomly assigned to 4 groups: a test group (polar medium), a control group (polar medium), a test group (non-polar medium) and a control group (non-polar medium), 5 in each group. Forty SD rats were divided into a test group (n=20) and a control group (n=20) in the subchronic systemic toxicity test. ResultsThe viability of the 100% extracts of the bioprosthetic heart valve material with a non-glutaraldehyde-based treatment was 75.2%. The rate of positive reaction was 0.0%. The total intradermal reactivity test score was 0. There was no statistical difference in the body weight between the test group and control group in the acute systemic toxicity test. There was no statistical difference in the body weight, organ weight, organ weight/body weight ratio, blood routine test or blood biochemistry between the test group and control group in the subchronic systemic toxicity test. ConclusionThe bioprosthetic heart valve material with a non-glutaraldehyde-based treatment has satisfying biocompatibility, which conforms to relevant national standards. The material might be a promising material for application in valve replacement.

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  • Progress in the prevention and treatment of chemotherapy-induced mucositis

    Chemotherapy-induced mucositis, one of the most common complications of chemotherapy, can be subdivided in oral and gastrointestinal mucositis. The patients always suffer from oral pain and ulcers, nausea, vomiting, abdominal pain and diarrhea. 5-Fluorouracil- and irinotecan-based regimens are frequently associated with a higher risk and more severe grade of mucositis. The onset of mucositis is also influenced by the patient’s characteristics including age, sex, genetic polymorphisms, systemic comorbidities. At present, the diagnosis of chemotherapy-induced mucositis is mainly based on medical history, physical examination and gastroenteroscopy, lack of reliable biomarkers for early diagnosis. The principles of diagnosis and treatment mainly refer to the clinical practice guidelines issued. Therefore, this article will review the mechanism, diagnosis, latest preventive and treatment strategies of chemotherapy-induced mucositis for helping clinicians to further correctly understand and deal with the adverse reactions.

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