目的:探讨临床药师主导的慢病管理在出院老年精神病患者用药错误防范中的作用。方法:研究对象选自2019年3月至2020年9月在衢州市第三医院老年精神科住院、年龄60~85岁的精神病患者。在入院时对患者进行遴选,记录入组患者的基本信息,包括性别、年龄、支付方式、文化水平、职业、合并慢性病种及通讯信息。入组患者在住院期间由老年科临床药师对其进行同质化药学服务,出院时被随机分为干预组和对照组,出院后均接受为期24周的随访。干预组患者出院后第1~12周每2周随访1次,第13~24周每4周随访1次;对照组患者在出院后第12和24周末各随访1次。随访内容包括体重、血清泌乳素水平、血压、血糖、血脂、心肝肾功能、血药浓度等指标的检测结果,所应用药物的名称及用法用量,是否按时服药,有无药物不良反应,以及生活环境或监护人有无改变等。若发现患者出现用药错误,用专用表格记录用药错误的发现时间、内容、级别、次数及涉及药品的分类。临床药师在随访过程中对患者及其家属进行个体化用药指导,发现用药错误后及时进行干预、纠正。结果:干预组纳入患者54例,对照组54例,患者基本信息的差异均无统计学意义(均P ≥ 0.05)。24周随访期内,发现干预组有15例、对照组有10例患者出现用药错误,2组用药错误发现率差异有统计学意义[27.78% (15/54)比18.52% (10, 54, χ2 = 0.043, P = 0.032]。2组患者共发现用药错误44例,干预组30例次(68.18%),对照组14例次(31.82%);随访12周内,由药师发现的干预组和对照组的用药错误分别为28例次(93.33%)和12例次(85.71%),差异有统计学意义(P = 0.002)。2组患者出现不同用药错误内容占比的差异无统计学意义(P > 0.05),2组患者出现不同用药错误内容占比的差异无统计学意义(P > 0.05),干预组以给药时间错误占比最高[干预组40.0% (12/30),对照组以用药频次错误占比最高21.43% (3/14)]。在44例次用药错误中,43例次(97.73%)属于第2层级错误(有错误无伤害),包括32例次C级错误和11例次D级错误;1例次(2.27%)属于第3层级错误(有错误有伤害),为F级错误。经临床药师干预,第2层级错误均被纠正,第3层级错误导致患者再次入院治疗,经药师与主管医生再次向患者家属强调重复用药的危害性,遵医嘱用药的重要性后,患者未再出现用药错误。用药错误涉及的药品共8类(抗精神分裂症药、抗抑郁药、抗焦虑药、抗癫痫药(主要作心境稳定剂)、抗痴呆药、降糖药、抗心律失常药以及抗胆碱能药物)。结论:临床药师主导的精神病慢病管理有助于及时发现和纠正出院老年精神病患者的用药错误。 Objective: To explore the role of chronic disease management led by clinical pharmacists in the prevention of medication errors in discharged elderly psychiatric patients. Methods: The subjects were psychiatric patients aged 60~85 years old who were hospitalized in the Department of Geriat-ric Psychiatry of Quzhou Third Hospital from March 2019 to September 2020. The patients were selected at the time of admission, and the basic information of the enrolled patients was recorded, including gender, age, payment method, educational level, occupation, combined chronic diseases and communication information. The patients in the group received homogenized pharmaceutical care by the clinical pharmacist of geriatrics during hospitalization. They were randomly divided in-to intervention group and control group at discharge. They were followed up for 24 weeks after discharge. The patients in the intervention group were followed up every 2 weeks from the 1st week to the 12th week after discharge, and every 4 weeks from the 13th week to the 24th week; the patients in the control group were followed up once at the 12th and 24th weekend after discharge. The follow-up contents include the test results of body weight, serum prolactin level, blood pressure, blood glucose, blood lipid, heart, liver and kidney function, blood drug concentration and other indicators, the name, usage and dosage of the drugs used, whether the drugs are taken on time, whether there are adverse drug reactions, and whether the living environment or guardians have changed. If the patient is found to have medication errors, use a special form to record the discovery time, content, level, times of medication errors and the classification of drugs involved. Clinical pharmacists provide individualized medication guidance to patients and their families during follow-up, and timely intervene and correct medication errors. Results: There were 54 patients in the intervention group and 54 patients in the control group. There was no significant difference in the basic information of patients (all P ≥ 0.05). During the follow-up period of 24 weeks, it was found that 15 patients in the intervention group and 10 patients in the control group had medication errors. The difference in medication error detection rate between the two groups was statistically significant [27.78% (15/54) vs. 18.52% (10/54), χ 2 = 0.043, P = 0.032]. 44 cases of medication errors were found in the two groups, 30 cases in the intervention group (68.18%) and 14 cases in the control group (31.82%); within 12 weeks of follow-up, the medication errors found by pharmacists in the intervention group and the control group were 28 cases (93.33%) and 12 cases (85.71%) respectively, with significant difference (P = 0.002). There was no significant difference in the proportion of different medication errors between the two groups (P > 0.05), and there was no significant difference in the proportion of different medication errors between the two groups (P > 0.05). The proportion of medication time errors in the intervention group was the highest [40.0% (12/30) in the intervention group, and 21.43% (3/14) in the control group]. Among 44 medication errors, 43 (97.73%) belonged to level 2 errors (with errors and no harm), including 32 Level C errors and 11 level D errors; one case (2.27%) belongs to level 3 error (with error and injury), which is level F error. After the intervention of the clinical pharmacist, the level 2 errors were corrected, and the level 3 errors led to the patient’s readmission for treatment. After the pharmacist and the competent doctor again emphasized the harm of repeated medication to the patient’s family members and the importance of medication according to the doctor’s advice, the patient did not have medication errors again. There are 8 types of drugs involved in medication errors (anti schizophrenic drugs, antidepressants, anti anxiety drugs, anti epileptic drugs (mainly used as mood stabilizer), anti dementia drugs, hypoglycemic drugs, antiarrhythmic drugs and anticholinergic drugs). Conclusion: Clinical pharmacist led chronic psychiatric disease management is helpful to find and correct the medication errors of discharged elderly psychiatric patients in time.
目的:探讨临床药师主导的慢病管理在出院老年精神病患者用药错误防范中的作用。方法:研究对象选自2019年3月至2020年9月在衢州市第三医院老年精神科住院、年龄60~85岁的精神病患者。在入院时对患者进行遴选,记录入组患者的基本信息,包括性别、年龄、支付方式、文化水平、职业、合并慢性病种及通讯信息。入组患者在住院期间由老年科临床药师对其进行同质化药学服务,出院时被随机分为干预组和对照组,出院后均接受为期24周的随访。干预组患者出院后第1~12周每2周随访1次,第13~24周每4周随访1次;对照组患者在出院后第12和24周末各随访1次。随访内容包括体重、血清泌乳素水平、血压、血糖、血脂、心肝肾功能、血药浓度等指标的检测结果,所应用药物的名称及用法用量,是否按时服药,有无药物不良反应,以及生活环境或监护人有无改变等。若发现患者出现用药错误,用专用表格记录用药错误的发现时间、内容、级别、次数及涉及药品的分类。临床药师在随访过程中对患者及其家属进行个体化用药指导,发现用药错误后及时进行干预、纠正。结果:干预组纳入患者54例,对照组54例,患者基本信息的差异均无统计学意义(均P ≥ 0.05)。24周随访期内,发现干预组有15例、对照组有10例患者出现用药错误,2组用药错误发现率差异有统计学意义[27.78% (15/54)比18.52% (10, 54, χ2 = 0.043, P = 0.032]。2组患者共发现用药错误44例,干预组30例次(68.18%),对照组14例次(31.82%);随访12周内,由药师发现的干预组和对照组的用药错误分别为28例次(93.33%)和12例次(85.71%),差异有统计学意义(P = 0.002)。2组患者出现不同用药错误内容占比的差异无统计学意义(P > 0.05),2组患者出现不同用药错误内容占比的差异无统计学意义(P > 0.05),干预组以给药时间错误占比最高[干预组40.0% (12/30),对照组以用药频次错误占比最高21.43% (3/14)]。在44例次用药错误中,43例次(97.73%)属于第2层级错误(有错误无伤害),包括32例次C级错误和11例次D级错误;1例次(2.27%)属于第3层级错误(有错误有伤害),为F级错误。经临床药师干预,第2层级错误均被纠正,第3层级错误导致患者再次入院治疗,经药师与主管医生再次向患者家属强调重复用药的危害性,遵医嘱用药的重要性后,患者未再出现用药错误。用药错误涉及的药品共8类(抗精神分裂症药、抗抑郁药、抗焦虑药、抗癫痫药(主要作心境稳定剂)、抗痴呆药、降糖药、抗心律失常药以及抗胆碱能药物)。结论:临床药师主导的精神病慢病管理有助于及时发现和纠正出院老年精神病患者的用药错误。
药师,老年人,精神病,病人出院,随访研究,用药错误
Zhizhen Hua, Haiyan Xie, Yunyu Chen, Shouya Zhang
Clinical Pharmacy Department of the Third Hospital of Quzhou City, Quzhou Zhejiang
Received: Jan. 27th, 2022; accepted: Mar. 16th, 2022; published: Mar. 23rd, 2022
Objective: To explore the role of chronic disease management led by clinical pharmacists in the prevention of medication errors in discharged elderly psychiatric patients. Methods: The subjects were psychiatric patients aged 60~85 years old who were hospitalized in the Department of Geriatric Psychiatry of Quzhou Third Hospital from March 2019 to September 2020. The patients were selected at the time of admission, and the basic information of the enrolled patients was recorded, including gender, age, payment method, educational level, occupation, combined chronic diseases and communication information. The patients in the group received homogenized pharmaceutical care by the clinical pharmacist of geriatrics during hospitalization. They were randomly divided into intervention group and control group at discharge. They were followed up for 24 weeks after discharge. The patients in the intervention group were followed up every 2 weeks from the 1st week to the 12th week after discharge, and every 4 weeks from the 13th week to the 24th week; the patients in the control group were followed up once at the 12th and 24th weekend after discharge. The follow-up contents include the test results of body weight, serum prolactin level, blood pressure, blood glucose, blood lipid, heart, liver and kidney function, blood drug concentration and other indicators, the name, usage and dosage of the drugs used, whether the drugs are taken on time, whether there are adverse drug reactions, and whether the living environment or guardians have changed. If the patient is found to have medication errors, use a special form to record the discovery time, content, level, times of medication errors and the classification of drugs involved. Clinical pharmacists provide individualized medication guidance to patients and their families during follow-up, and timely intervene and correct medication errors. Results: There were 54 patients in the intervention group and 54 patients in the control group. There was no significant difference in the basic information of patients (all P ≥ 0.05). During the follow-up period of 24 weeks, it was found that 15 patients in the intervention group and 10 patients in the control group had medication errors. The difference in medication error detection rate between the two groups was statistically significant [27.78% (15/54) vs. 18.52% (10/54), χ 2 = 0.043, P = 0.032]. 44 cases of medication errors were found in the two groups, 30 cases in the intervention group (68.18%) and 14 cases in the control group (31.82%); within 12 weeks of follow-up, the medication errors found by pharmacists in the intervention group and the control group were 28 cases (93.33%) and 12 cases (85.71%) respectively, with significant difference (P = 0.002). There was no significant difference in the proportion of different medication errors between the two groups (P > 0.05), and there was no significant difference in the proportion of different medication errors between the two groups (P > 0.05). The proportion of medication time errors in the intervention group was the highest [40.0% (12/30) in the intervention group, and 21.43% (3/14) in the control group]. Among 44 medication errors, 43 (97.73%) belonged to level 2 errors (with errors and no harm), including 32 Level C errors and 11 level D errors; one case (2.27%) belongs to level 3 error (with error and injury), which is level F error. After the intervention of the clinical pharmacist, the level 2 errors were corrected, and the level 3 errors led to the patient’s readmission for treatment. After the pharmacist and the competent doctor again emphasized the harm of repeated medication to the patient’s family members and the importance of medication according to the doctor’s advice, the patient did not have medication errors again. There are 8 types of drugs involved in medication errors (anti schizophrenic drugs, antidepressants, anti anxiety drugs, anti epileptic drugs (mainly used as mood stabilizer), anti dementia drugs, hypoglycemic drugs, antiarrhythmic drugs and anticholinergic drugs). Conclusion: Clinical pharmacist led chronic psychiatric disease management is helpful to find and correct the medication errors of discharged elderly psychiatric patients in time.
Keywords:Pharmacist, The Aged, Mental Disease, Patient Discharge, Follow-Up Study, Medication Error
Copyright © 2022 by author(s) and beplay安卓登录
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精神分裂症是一组原因未明的重型精神病,通常病情迁延,治疗周期较长,并且容易反复发作甚至逐渐加重,目前临床上以药物治疗为主 [
国务院《中国防治慢性病中长期规划(2017~2025年)》中指出,慢性病是严重威胁我国居民健康的一类疾病,已成为影响国家经济社会发展的重大公共卫生问题。规划中提出计划至2020年,65岁以上老年人中医药健康管理率达到65%,2025年达到80% [
2019年7月至2019年12月衢州市第三医院老年精神科病房收治的符合入组标准的老年精神病出院患者共108例(男34例,女74例)。
入组标准:① 精神分裂症诊断符合国际疾病分类第10版《ICD-10》的诊断标准;② 患者年龄60~85岁;③ BMI ≤ 30 kg/m2;④ 患者或及其家属了解本研究内容,自愿接受24周随访,能与本研究组保持稳定联系,本人或家属签署知情同意书。
① 无法与本研究组保持稳定联系者;② 难以沟通的患者。退出标准:① 不能坚持整个随访过程的患者;② 随访期间出现排除标准所列条件的患者。
出院时,依据事先制定的随机数字表,根据入组序号将纳入的患者分为对照组和干预组。
患者住院期间,由老年精神科临床药师对2组患者进行同质化药学服务,住院当日对患者进行药学评估,填写住院患者药物使用信息及依从性评估表;向患者及家属介绍用药方案、注意事项、常见不良反应的预防及处理;核查患者是否按照正确的方法使用药物。患者出院后由老年科临床药师主导对2组出院患者进行随访。随访方式包括电话、微信或面对面随访,嘱患者及其家属随访期间若出现用药相关问题,可随时与临床药师联系。随访时间为24周。对照组患者出院后慢病管理随访常规进行,干预组患者出院后的慢病管理随访由临床药师主导并进行用药错误干预。第2~24周每2周随访1次,第25~48周每4周随访1次;第24和48周末各随访1次。每次随访时间为10~30 min。随访时逐项询问本研究组自行制定的《出院老年精神病患者管理随访登记表》的内容,主要包括患者基本信息;共病信息;心、肝、肾功能以及血压、血糖、血脂、药物浓度等指标的检测结果,目前应用药物的名称及用法用量,是否按时服药,有无药物不良反应史,以及生活方式有无改变(吸烟、饮酒、饮食及运动情况)等,并对患者及其家属进行疾病知识宣教、个体化用药指导、对家属实施如药物监管方式、方法的相关培训以及药物可能出现副作用方面的知识宣教。若涉及药物调整问题,由临床药师与患者的主管医师沟通,达成一致后予以实施。随访过程中若发现患者出现用药错误,须做详细记录,包括用药错误的发现时间、内容、次数、级别及所涉及药品的分类,及时提出相对应的个体化处理方式或改进措施,用药错误内容分类和错误分级均参照《中国用药错误管理专家共识》推荐的相关标准。
本研究方案经我院医学伦理委员会审核批准(2020-18)。
全部资料由专门统计人员录入电脑,采用SPSS 26.0统计软件进行数据处理和分析。计数资料用率(%)表示,组间比较采用χ2检验或Fisher精确检验,设定P < 0.05差异有统计学意义。
按照纳入标准和排除标准,共纳入110例患者,两组各55例。其中干预组有1例失访,对照组有1例由其家属送往其他医院住院治疗,最终各54例进入数据统计。两组患者基本信息如性别、年龄、受教育程度、职业、缴费方式以及共患慢病种类等方面,经比较,差异无统计学意义(均P ≥ 0.05)。结果见表1。
特征 | 干预组(n = 54) | 对照组(n = 54) | χ2值 | P值 |
---|---|---|---|---|
性别 | 0.172 | 0.679 | ||
男性 | 16 (29.6) | 18 (33.3) | ||
女性 | 38 (70.4) | 36 (66.7) | ||
年龄 | 0.156 | 0.693 | ||
60~70岁 | 34 (63.0) | 32 (59.3) | ||
71~80岁 | 20 (37.0) | 22 (40.7) | ||
文化程度 | 0.561 | 0.755 | ||
文盲 | 16 (29.6) | 16 (29.6) | ||
小学 | 28 (51.9) | 25 (46.3) | ||
初中以上 | 10 (18.5) | 13 (24.1) | ||
职业 | 1.608 | 1.000 | ||
机关、企事业单位工作人员 | 2 (3.7) | 2 (3.7) | ||
商业及服务行业从业者 | 0 | 1 (1.9) | ||
农林牧渔业从业者 | 52 (96.3) | 51 (94.4) | ||
缴费类型 | 0.000 | 1.000 | ||
医保 | 2 (3.7) | 1 (1.9) | ||
新农合 | 52 (96.3) | 53 (98.1) | ||
共患慢病种类 | 3.315 | 0.610 | ||
1 | 5 (9.3) | 9 (16.6) | ||
2 | 21 (38.9) | 25 (46.3) | ||
3 | 24 (44.4) | 18 (33.3) | ||
4 | 2 (3.7) | 1 (1.9) | ||
5 | 2 (3.7) | 1 (1.9) |
表1. 2组出院老年精神病患者的基本特征比较[例数(%)]
1) 用药错误发现率24周随访期内,临床药师发现用药错误干预组15例、对照组10例,2组用药错误发现率的差异有统计学意义[27.78% (15/54)比18.52% (10/54, χ2 = 0.043, P = 0.032]。2组患者12周内发现用药错误共44例次,干预组30例次(68.18%),对照组14例次(31.82%)。
2)用药错误发现时间干预组30例次用药错误中有28例次,发现时间为出院后2、4、6、8、12、16和24周,其中有25例次(89.29%)在随访的12周内由药师发现。对照组14例次用药错误中,发现时间为2、4、12、16、20和24周,其中12例次在出院12周末由药师发现。两组患者在12周内由药师发现的用药错误发现率的差异有统计学意义(χ2 = 9.818, P = 0.002)。
3) 用药错误类型干预组患者30例次用药错误中12例次(60.0%)为用量错误,包括剂量错误、给药频次错误、给药时间错误;6例次(20.0%)为品种错误;5例次(16.7%)用法错误,包括漏服药物、用药技术错误、重复用药;1例(3.3%)管理错误,即监测错误。对照组患者14例次用药错误中用量错误有9例次(64.3%),包括剂量错误、给药频次错误、给药时间错误和疗程错误;用法错误2例次(14.3%),包括漏服药物、用药技术错误;2例次(14.3%)管理错误,即监测错误;1例次(7.1%)品种错误。两组患者用药错误内容差异无统计学意义(均P > 0.005)。见表2。
用药错误类型 | 干预组30 (例次) | 对照组14 (例次) | χ2值 | P值 |
---|---|---|---|---|
品种 | 无 | 0.401 | ||
品种错误 | 6 (20.0) | 1 (7.1) | ||
用法 | 无 | 1.000 | ||
漏服药物 | 2 (6.7) | 1 (7.1) | ||
用药技术错误 | 1 (3.3) | 1 (7.1) | ||
重复用药 | 2 (6.7) | 0 | ||
用量 | 0.074 | 0.786 | ||
剂量错误 | 2 (6.7) | 1 (7.1) | ||
用药频次错误 | 4 (13.3) | 3 (21.5) | ||
用药时间/时机错误 | 12 (40.0) | 2 (14.3) | ||
疗程错误 | 0 | 3 (21.5) | ||
管理错误 | 无 | 0.234 | ||
监测错误 | 1 (3.3) | 2 (14.3) |
表2. 2组用药错误类型比较[例数(%)] (随访12周)
注:干预组患者出院后第1~12周每2周、第13周~24周每4周随访1次,对照组患者出院后第12、24周末各随访1次。
2例次重复用药错误均发生在干预组,包括氯氮平片与氯氮平口腔崩解片的重复用药1例次,奥氮平片与氯氮平片的联合用药1次。前者是因为4 + 7带量采购问题,氯氮平口腔崩解片由氯氮平片所替代,患者家属自认为是2种药物,故造成同时服用2种药物,药师在随访的12周内发现,经药师反复对比药物的实物及耐心解释,患者家属同意药师的提议停用氯氮平口腔崩解片,单用氯氮平片治疗,同时建议临床医生予患者进行氯氮平血药浓度测定,避免药物中毒。奥氮平片与氯氮平片的联合使用,药师与临床医生沟通,因患者是慢性难治性精神分裂症,2药合用患者目前病情控制尚可,故未换药,采取减量的方式维持治疗。
药品 | 例次 | 构成比(%) |
---|---|---|
抗精神分裂症药 | ||
富马酸喹硫平 | 8 | 13.2 |
奥氮平 | 8 | 13.2 |
利培酮 | 6 | 10.0 |
氯氮平 | 4 | 6.6 |
癸酸氟哌啶醇注射液 | 3 | 5.0 |
舒必利 | 1 | 1.7 |
氨磺必利 | 1 | 1.7 |
齐拉西酮 | 1 | 1.7 |
抗焦虑药 | ||
阿普唑仑片 | 5 | 8.3 |
劳拉西泮片 | 3 | 5.0 |
佐匹克隆 | 2 | 3.3 |
氯硝西泮 | 1 | 1.7 |
氟哌噻吨美利曲辛片 | 1 | 1.7 |
抗癫痫药 | ||
丙戊酸钠缓释片 | 3 | 5.0 |
碳酸锂片/缓释片 | 3 | 5.0 |
丙戊酸镁缓释片 | 1 | 1.7 |
抗抑郁药 | ||
米氮平 | 1 | 1.7 |
舍曲林 | 1 | 1.7 |
米安色林 | 1 | 1.7 |
抗胆碱药 | ||
苯海索 | 1 | 1.7 |
抗痴呆药 | ||
多奈哌齐 | 1 | 1.7 |
降糖药 | ||
二甲双胍 | 2 | 3.3 |
阿卡波糖 | 1 | 1.7 |
抗心律失常药 | ||
酒石酸美托洛尔 | 1 | 1.7 |
合计 | 60 | 100.0 |
表3. 44例次用药错误涉及的药品排名
4) 用药错误分级在2组患者共发现的44例次用药错误中,有43例次(97.73%)属于第2层级错误(有错误无伤害),包括32例次C级错误和11例次D级错误;1例次(2.27%)属于第3层级错误(有错误有伤害),为F级错误。经临床药师干预,第2层级错误均被纠正,第3层级错误导致患者再次入院治疗,经药师与主管医生再次向患者家属强调重复用药的危害性,遵医嘱用药的重要性后,患者未再出现用药错误。
5) 用药错误涉及药物分析2组108例患者出现的用药错误44例,涉及药物共8类(抗精神分裂症药、抗抑郁药、抗焦虑药、抗癫痫药(主要作心境稳定剂)、抗痴呆药、降糖药、抗心律失常药以及抗胆碱能药物) 24种,包括抗精神病药物8种,抗焦虑药5种,抗癫痫药(心境稳定剂) 3种,抗抑郁药3种,抗痴呆药1种,抗胆碱药1种,降糖药2种以及抗心律失常药1种,见表3。
据报道美国每年至少有150万人发生用药错误,导致每年增加3.5亿美元的住院费用,成为第8位死亡原因 [
据报道,90%老年患者的用药错误是可以预防的 [
王雅葳等研究结果显示引发老年患者用药错误的主要人员为医师和药师,其中医师引发的ME主要发生在处方环节,主要发生在给药剂量、用药频次、给药途径和相互作用等方面,可能与其药学知识欠缺有关。处方审核是用药错误防范策略中技术策略第4级 [
老年精神病患者对于使用特殊药品,比如吸入装置的使用方法、分散片与肠溶片、缓控释片的服用方法普遍掌握较差,因此药师应主动向患者及其监护人提供标准化的用药指导以减少患者的用药错误;药师还可以利用互联网技术对病人进行在线用药咨询。本研究结果显示,互联网用药咨询服务可以帮助患者及家长更详细了解治疗药物的用药信息,促进合理用药,以减少患者的用药错误。
本研究结果显示药师是用药错误监测小组核心成员,未避免药物不良反应的发生,利用医院检验科优势,建议临床医生定期对患者所服的抗精神病药物进行血药浓度监测。因患者服用药物的特殊性,尤其是BZDs药物的使用,予患者及其家属实施防跌倒宣教,不良反应监测如定期监测肝肾功能、心电图检查等,减免药物不良反应或事件的发生。本研究结果显示用药错误大部分来源于药师上报,反应了医护重视不够,药师可以定期总结分享用药错误案例,组织全体医护人员共同分析和探讨,提升用药错误分享意识,以减少用药错误的发生。
本研究结果显示,以临床药师为主导的慢病管理有助于及时发现并纠正出院老年精神病患者的用药错误,对出院老年患者的用药安全具有积极意义。本研究也设计方案存在不足之处,导致2组入组研究人数偏少,对试验结论的说服力产生一定影响。因此,我们需要改进研究方案,设计多中心、大样本的研究。尽管住院期间和出院时对老年患者做了详细的用药指导,出院后随访时仍能发现患者出现用药错误。这提示药师用药安全教育工作不完全到位。今后对老年慢病患者进行用药安全管理时应缩短随访间隔,与老年患者沟通时,注意放慢语速,重要的内容应重复讲解,必要时可让老年患者重复药师强调的重点,给患者提供易于理解的用药宣传材料。同时,在老年患者住院、出院和随访时应尽可能对患者、家属或监护人同时进行用药指导。
衢州市指导性科技计划项目(2020116)。
华志珍,谢海燕,陈云郁,张守亚. 临床药师主导的慢病管理在出院老年精神病患者用药错误防范中的作用The Role of Chronic Disease Management Led by Clinical Pharmacists in the Prevention of Medication Errors in Discharged Elderly Psychiatric Patients[J]. 医学诊断, 2022, 12(01): 50-59. https://doi.org/10.12677/MD.2022.121009
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