Kunac Desireé L, Kennedy Julia, Austin Nicola, Reith David
School of Pharmacy, University of Otago, Dunedin, New Zealand.
Paediatr Drugs. 2009;11(2):153-60. doi: 10.2165/00148581-200911020-00005.
Adverse drug events (ADEs) are an important problem in all hospitalized patients as these events represent medication-related patient harm. Few epidemiologic data exist regarding ADEs in the pediatric inpatient setting and, in particular, the economic impact of such ADEs upon the healthcare sector. To evaluate the incidence, preventability, and seriousness of ADEs and potential ADEs occurring in hospitalized children and to examine the cost implications of these ADEs. This was a prospective observational cohort study conducted in the pediatric, neonatal intensive care unit (NICU), and postnatal wards of a university-affiliated urban general hospital in Dunedin, New Zealand (NZ). The study population was all patients admitted to these wards for >24 hours over a 12-week period from 18 March 2002 to 9 June 2002. Medication-related events were identified by chart review, attendance at multidisciplinary clinical meetings, parent/carer/child interviews, and voluntary and verbally solicited reports from staff. All suspected medication-related events were reviewed by a panel of three health professionals who independently categorized the events and rated them for seriousness, preventability, and causality, using a standardized reviewer form. Costs attributable to ADEs were calculated using both the average cost of a bed day, and specific costs for diagnostic groupings. The main outcome measures of the study were ADEs and potential ADEs. There were 495 eligible study patients, who had a total of 520 admissions and 3037 patient-days of admission, during which 3160 prescription episodes were written. There were 67 ADEs, of which 38 (56.7%) were classified as preventable, and 77 potential ADEs. ADEs occurred at a rate of 2.1 per 100 prescription episodes, 12.9 per 100 admissions, and 22.1 per 1000 patient-days. Potential ADEs occurred at a rate of 2.4 per 100 prescription episodes, 14.6 per 100 admissions, and 25 per 1000 patient-days. Although the greatest number (and rate per 100 admissions) of ADEs occurred in NICU patients, surgical pediatric ward patients had the greatest rate of ADEs per 1000 patient-days. Few events occurred in postnatal patients. Forty-six percent of ADEs were classified as being serious; 15% were deemed to result in persistent disability or were classified as life threatening. Potential ADEs were deemed more likely to be serious with 82% classified as potentially serious events; 33% were deemed as having the potential to result in persistent disability, or the potential to cause a life-threatening event. Fifteen ADEs were judged to have caused the hospital admission or to have prolonged hospital stay. The total number of days attributed to ADEs was 92 (range 1-26 days); of these, 58 were deemed preventable days and 34 non-preventable days. This extrapolates to a total annual cost of $NZ235 214 (2002 values) to the pediatric service, subdivided into $NZ148 287 for preventable ADEs and $NZ86 927 for non-preventable ADEs. ADEs and potential ADEs represent a considerable hazard for the pediatric inpatient population and ADEs represent a large cost imposition upon the healthcare sector. Over half of the ADEs were deemed preventable. This highlights the importance of developing strategies to prevent and ameliorate ADEs both to improve the quality of patient care and to reduce healthcare costs.
药物不良事件(ADEs)是所有住院患者面临的一个重要问题,因为这些事件意味着与用药相关的患者伤害。关于儿科住院患者的药物不良事件,尤其是此类药物不良事件对医疗保健部门的经济影响,现有的流行病学数据很少。为了评估住院儿童中发生的药物不良事件和潜在药物不良事件的发生率、可预防性和严重性,并研究这些药物不良事件的成本影响。这是一项前瞻性观察队列研究,在新西兰达尼丁市一家大学附属城市综合医院的儿科、新生儿重症监护病房(NICU)和产后病房进行。研究人群为2002年3月18日至2002年6月9日这12周期间入住这些病房超过24小时的所有患者。通过病历审查、参加多学科临床会议、与家长/护理人员/儿童面谈以及工作人员主动提供和口头征求的报告来识别与用药相关的事件。所有疑似与用药相关的事件均由三名卫生专业人员组成的小组进行审查,他们使用标准化的审查表对事件进行独立分类,并对其严重性、可预防性和因果关系进行评级。使用每日床位平均成本和诊断分组的特定成本来计算药物不良事件的归因成本。该研究的主要结局指标为药物不良事件和潜在药物不良事件。共有495名符合条件的研究患者,共入院520次,住院天数达3037天,在此期间开出了3160次处方。发生了67起药物不良事件,其中38起(56.7%)被归类为可预防的,还有77起潜在药物不良事件。药物不良事件的发生率为每100次处方事件2.1起、每100次入院12.9起、每1000个住院日22.1起。潜在药物不良事件的发生率为每100次处方事件2.4起、每100次入院14.6起、每1000个住院日25起。虽然药物不良事件数量最多(以及每100次入院的发生率)的是NICU患者,但儿科外科病房患者每1000个住院日的药物不良事件发生率最高。产后患者发生的事件很少。46%的药物不良事件被归类为严重;15%被认为导致持续残疾或被归类为危及生命。潜在药物不良事件被认为更有可能是严重的,82%被归类为潜在严重事件;33%被认为有可能导致持续残疾或有可能引发危及生命的事件。15起药物不良事件被判定导致了住院或延长了住院时间。归因于药物不良事件的总天数为92天(范围为1 - 26天);其中,58天被视为可预防天数,34天为不可预防天数。这推算出儿科服务每年的总成本为235214新西兰元(2002年价值),细分为可预防药物不良事件的148287新西兰元和不可预防药物不良事件的86927新西兰元。药物不良事件和潜在药物不良事件对儿科住院患者构成了相当大的危害,药物不良事件给医疗保健部门带来了巨大的成本负担。超过一半的药物不良事件被认为是可预防的。这凸显了制定预防和改善药物不良事件策略的重要性,以提高患者护理质量并降低医疗保健成本。