Patients with advanced cancer Efficacy of intravenous analgesia PCIA.doc

Patients with advanced cancer Efficacy of intravenous analgesia PCIA.doc

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Patients with advanced cancer Efficacy of intravenous analgesia PCIA

 PAGE \* MERGEFORMAT 11 Patients with advanced cancer Efficacy of intravenous analgesia PCIA Of: Meiju Xiang, Wang Ying, Zhou Quanhua, Tao Ying [Abstract] Objective To observe the advanced cancer patient-controlled analgesia PCIA clinical effect. Methods 60 cases of advanced cancer patients, the use of PCIA infusion: pain formula lornoxicam 32 mg plus fentanyl 0.5 mg, droperidol alcohol 5 mg, tropisetron hydrochloride 5 mg, dexamethasone 5 mg diluted to 100 ml normal saline mixture. observed analgesia, sleep quality, pain before and after the complications. Results 97.5% rate of effective analgesia complications reduced, the patient sleep and quality of life improved significantly. Conclusions lornoxicam PCIA fentanyl analgesia sustainable and effective pain control of advanced cancer patients, improve patient quality of life. [Keywords:] advanced cancer; PCIA; lornoxicam; fentanyl; intravenous infusion Pain and cancer are not synonymous, at least 2 / 3 of the patients in the disease process will feel the pain, most patients require the use of opioid analgesics [1]. Advanced cancer patients are often associated with difficult to control the pain, seriously affect the quality of life of patients. In addition, most patients with cancer pain or symptoms of fear. proper application of analgesic drugs (especially opioids) can effectively control the vast majority of patients with cancer pain, because these drugs often cause nausea , vomiting, respiratory depression, excessive sedation and other adverse reactions [1 3], so the search for good pain relief method is particularly important in the treatment of cancer pain .2007 October to April 2009, we adopted a continuous intravenous infusion of PCIA analgesic drugs for 60 patients with advanced cancer pain, clinical results were satisfactory, are as follows. Subjects and Methods 1. General information open trial with no control, select the VAS score from 8 to 10 minutes 60 cases of advanced cancer pa

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