Drug-Related Problems in Hospitalised Parkinson's Disease Patients in China

Drug-Related Problems in Hospitalised Parkinson's Disease Patients in China

Eur J Hosp Pharm: first published as 10.1136/ejhpharm-2020-002356 on 30 October 2020. Downloaded from Original research Drug- related problems in hospitalised Parkinson’s disease patients in China Hui Liu ,1 Yixuan Zhong,1 Zhaohao Zeng,2 Wei Bi,2 Huiting Zhong,1 Lianfang Xue,1 Suishan Qiu1 1Department of Pharmacy, The ABSTRACT hypertension, type 2 diabetes mellitus and hyper- First Affiliated Hospital of Jinan Background There has been a lack of studies on the lipidaemia.3 These patients are at particular risk University, Guangzhou, China 2 of experiencing drug- related problems (DRPs), Department of Neurology, The types and severity of drug-related problems (DRPs) in First Affiliated Hospital of Jinan hospitalised patients with Parkinson’s disease (PD) in including both complications arising from the drug University, Guangzhou, China China until now. itself, such as adverse drug reactions, and those Objective To investigate the types and causes of DRPs, attributable to the prescribing physician. Correspondence to and to assess the severity of these DRPs in PD patients in DRPs are defined as events or circumstances Lianfang Xue, Guangzhou, neurology wards. involving drug therapy that actually or potentially China; xlf18666@ 163. com 4 Methods A retrospective study involving 209 PD interfere with desired health outcomes. Optimisa- Received 7 May 2020 inpatients was conducted at a tertiary hospital in tion of drug therapy to address and prevent DRPs Revised 31 August 2020 China from January 2017 to December 2018. The can potentially shorten the length of hospital stays, Accepted 5 October 2020 identification and assessment of DRPs were based on save lives, and enhance patient quality of life. This EAHP Statement 4: Clinical the Pharmaceutical Care Network Europe (PCNE) tool study of DRPs is a complex process and a new chal- 5 Pharmacy Services. version 8.03. The severity ratings of these DRPs was lenge for clinical pharmacists. Recently published assessed based on the National Coordinating Council for studies assessing clinical pharmacists’ interventions Medication Error Reporting and Prevention (NCC MERP) showed they assisted in the early detection of DRPs classification. and helped prevent consequent patient harms in Results A total of 274 DRPs with an average of hospitalised patients with neurological diseases.6 7 1.31±1.00 problems per patient were identified, in Further, Schröder et al examined the role commu- which 83.3% of the population had at least one DRP. nity pharmacists play in identifying DRPs in PD Using the PCNE classification system, the most common outpatients, verifying 331 DRPs in 113 PD outpa- domain of DRPs was “Other, P3” (62.8%), followed by tients.8 Similarly, Hsu et al, studying outpatient “Treatment effectiveness, P1” (19.3%) and “Treatment care of heart disease patients, found that only safety, P2” (17.9%). A total of 88.7% of the DRPs 74.6% of patients received correct drug admin- were rated at severity categories B to D (causing no istration during the first 2 days post-admission. 9 or potential harm), whereas 11.3% were rated as However, there is still a lack of studies on DRPs in categories E to H (causing actual harm). hospitalised PD patients, both locally and globally, Conclusions These data indicate that the prevalence which limits the comparisons which can be drawn of DRPs is high among PD patients. The identification of between current and prior research. Therefore, this http://ejhp.bmj.com/ different subtypes of DRPs may facilitate risk reduction study aims to investigate DRPs in PD patients in for PD patients. neurology wards of The First Affiliated Hospital of Jinan University. The findings from this study can help to determine the incidence rates and character- istics of DRPs among the PD population and can be INTRODUCTION used as preliminary data for future studies. Parkinson’s disease (PD) is a progressive neurode- on September 25, 2021 by guest. Protected copyright. generative disease that afflicts 1.7% of residents 1 METHODS aged 65 years or older in China. The incidence of PD is estimated to double to 8.7 million world- Study design and setting wide by 2030.2 Impaired motor functions, such as This was a retrospective study conducted at the bradykinesia, rigidity and muscle stiffness, tremor, neurology department at The First Affiliated gait disturbance and postural instability, are the Hospital of Jinan University in China, which is a disease’s primary signs and symptoms. As the tertiary public general teaching hospital with 1900 condition progresses, other non- motor symptoms beds. © European Association of may include disturbances in gastrointestinal func- Hospital Pharmacists 2020. tion, sleep, blood pressure, or cognition, as well as Study population and sampling sizes Re-use permitted under CC psychological distress. The primary goals of therapy The study included patients with idiopathic PD who BY-NC . No commercial re-use . Published by BMJ. for patients with PD are to minimise their symp- were admitted as inpatients between 1 January 2017 toms and to improve their quality of life with medi- and 31 December 2018. The two inclusion criteria To cite: Liu H, Zhong Y, cations and surgery. were: a diagnosis of idiopathic PD by a neurology Zeng Z, et al. Because of the broad spectrum of symptoms, specialist fulfilling ICD-10 classification according Eur J Hosp Pharm Epub ahead of print: [please treatment frequently consists of complicated medi- to Diagnostic Criteria for Parkinson’s Disease in include Day Month Year]. cation regimens. Moreover, the majority of PD China (2016 edition) and at least one anti-PD medi- doi:10.1136/ patients are elderly and most of them experience cation taken daily. Patients were excluded from the ejhpharm-2020-002356 comorbidities, including coronary heart disease, analyses if they exhibited atypical parkinsonian Liu H, et al. Eur J Hosp Pharm 2020;0:1–5. doi:10.1136/ejhpharm-2020-002356 1 Eur J Hosp Pharm: first published as 10.1136/ejhpharm-2020-002356 on 30 October 2020. Downloaded from Original research syndromes or secondary parkinsonism, had uncertain diagnoses, references— such as UpToDate (version 21.2, Wolters Kluwer, had hospitalisations with a duration <48 hours, or if relevant Netherlands), Martindale: The Complete Drug Reference,16 data were missing. or New Materia Medica.17 The authors, either clinical phar- The sample size was determined using the Raosoft sample macists (H Liu, Y Zhong, L Xue) or neurologists (Z Zheng, W size calculator, which indicated a minimum of 197 patients Bi), were involved in determining the presence of DRPs. The were needed to achieve a 95% confidence level with a 5% National Coordinating Council for Medication Error Reporting margin of error and a conservative assumption of 50% response and Prevention (NCC MERP) Index for categorising the DRP distribution.10 algorithm was used to determine the severity of the DRPs.18 19 This classification consists of five categories based on Data collection ascending severity of the patient outcome: (1) circumstances or The data were retrieved by the authors, who are pharmacists, events that had the capacity to cause error (potential errors, cate- from Electronic Medical Records and the Hospital Information gory A); (2) medication errors (MEs) occurred without posing System. Demographic and clinical characteristics such as age, harm to patients (categories B and C); (3) MEs caused potential gender, duration of hospital stay, duration of PD, past medical harm to patients (category D); (4) MEs caused harm to patients history, and concurrent medications were also collected. (of increasing severity, categories E, F, G, and H); (5) MEs resulted in a patient’s death (category I). The assessment of DRPs Classification, identification, and assessment of DRPs and severity ratings were performed by two pharmacists inde- The Pharmaceutical Care Network Europe (PCNE) classification pendently, and discrepancies were resolved through discussions. version 8.03, the most recent version during the study period, 11 was used to categorise the DRPs. All DRPs were identified by Statistical analyses clinical pharmacists with neurology training, then confirmed by All the data collected and extracted in this study were analysed a specialist physician in neurology. using SPSS version 20 (IBM Corp). Individual-level and problem- The PCNE creates guidelines and classifications to describe level analyses were performed separately because many patients DRPs uniformly and serves as a process indicator in studies 12 exhibited more than one DRP. Between- group differences were of pharmaceutical care outcomes. The classification system, analysed using the χ2 test, with Fisher’s exact adjustment where which is validated and updated regularly, has been used exten- appropriate for categorical variables, and the t-test for contin- sively by many recent studies.9 13 14 The advantage of this system 15 uous variables was used to compare means between groups. is that DRP causes are classified into separate categories. The Mean age was analysed using the Mann- Whitney U test. Statis- basic classification now has three primary domains for problems, tical significance was set at p<0.05. All tests were two-tailed. nine primary domains for causes, and five primary domains for interventions.11 Because clinical pharmacists did not provide a medication appraisal to prescribers nor directly contact patients RESULTS during the review of DRP, the medication compliance of patients Demographic characteristics could not be comprehensively identified. Therefore, DRP cause A total of 209 PD patients fulfilled the inclusion criteria for this codes such as “Dispensing”, “Drug use process” and “Patient study, the demographics and clinical characteristics of which related” were excluded. are listed in table 1. Males composed 51.0% (107/209) of the The identified DRPs included adverse reactions, drug choice subjects. The minimum and maximum age of the patients were problems, dosing problems, drug use problems, and possible drug 43 and 88 years, respectively, with a mean of 69.1±10.32 years; http://ejhp.bmj.com/ interactions.

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