Research Article |
Corresponding author: Julio Campos-Florián ( jcamposf@unitru.edu.pe ) Academic editor: Maria Kamusheva
© 2024 Mónica Bazán-Vásquez, Gladys Galliani-Huamanchumo, Alessandra Campos-Bazán, Haydee Villafana-Medina, Kelyn Requejo-Torres, Julio Campos-Florián.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Bazán-Vásquez M, Galliani-Huamanchumo G, Campos-Bazán A, Villafana-Medina H, Requejo-Torres K, Campos-Florián J (2024) Potentially inappropriate prescription of medications to older adults who access a community pharmacy in Peru. Pharmacia 71: 1-11. https://doi.org/10.3897/pharmacia.71.e127723
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Polypharmacy in older adults is associated with a higher incidence of medication-related problems, such as pharmacological interactions, adverse reactions, and medication errors. This study aimed to identify and evaluate potentially inappropriate prescription of medications (PIP) using the screening tool of older persons’ prescriptions/screening tool to alert doctors to right treatment (STOPP/START) criteria in a representative community pharmacy in Trujillo, Peru. The population sample consisted of 158 subjects, with 66.5% between 65 and 69 years old, 53.8% male, and 77.9% receiving between 3 and 4 medications. Medical prescriptions were analyzed using the explicit STOPP/START version 2 criteria, revealing that 93.7% of patients presented STOPP criteria (to stop medication) and 53.8% presented START criteria (to start medication). The most frequently identified STOPP criterion was the gradual withdrawal of benzodiazepines, while the most frequently identified START criterion was the initiation of antihypertensive treatment in patients with systolic blood pressure > 160 mmHg and diastolic blood pressure > 90 mmHg. Principal component analysis showed that the high prevalence of PIP was significantly associated (p < 0.05) with the number of prescribed medications and as age decreases, the number of medical diagnoses also decreases. It is concluded that there is a high prevalence of PIP in the studied population, posing a greater challenge in older adults, highlighting the importance of addressing prescribing practices with greater involvement of community pharmacists.
medications, older adults, polypharmacy, potentially inappropriate medication
Globally, significant demographic changes have been observed in recent decades, characterized by an increase in life expectancy and shifts in physical and social factors. According to the
This increase in the population of older adults is accompanied by a rise in demand for healthcare services, as this demographic is characterized by vulnerability, multimorbidity, and polypharmacy, resulting from age-related physiological changes (
Polypharmacy is a common characteristic among older adults, defined as the concurrent use of five or more medications by an individual, with the use of ten or more medications considered excessive polypharmacy (
The trend toward polypharmacy in older adults leads to high rates of medication-related problems (MRPs), including medication errors and potentially inappropriate prescriptions (PIP) (
Currently, tools and methods have been developed to assess the quality of medication prescription and use in older adults, which are classified into implicit and explicit methods (
The most widely used explicit methods are the Beers criteria, the McLeod criteria, the START, and the STOPP. The Beers criteria were among the first to be published and have been updated over time; however, they have limitations, such as failing to consider certain pharmacological interactions, therapeutic duplication, and omission of prescribed medications (
It has been shown that the application of the STOPP/START criteria is effective in optimizing prescribing and reducing the risk of morbidity in geriatric patients (
This observational, prospective, and cross-sectional study was conducted in four phases between October 2019 and January 2020. For the selection of the pharmacy, the following criteria were considered: implementation of community pharmaceutical care, management by a qualified clinical pharmacist, and a minimum of 2000 prescriptions attended per month to ensure representativeness (see Scheme 1).
Flow chart of the selection of the community pharmacy establishment. * https://serviciosweb-digemid.minsa.gob.pe/Consultas/Establecimientos.
Users were selected based on inclusion criteria (age over 65 years, users who visited the pharmacy establishment with a medical prescription containing three or more prescribed medications), and exclusion criteria (users with communication and cognitive difficulties that hindered data collection, users with illegible medical prescriptions, or those containing vitamins or dietary supplements). The selection of community members who made up the sample was performed using non-probabilistic sampling until saturation (
The sample consisted of clients who visited the pharmacy establishment and met the inclusion criteria and agreed to participate in the study. At the time of admission, they were asked to sign the informed consent form, and their age and sex were recorded, along with clinical data such as prescribed medications, registered through the international nonproprietary names (INN) and included in The Prescription Drug List, and the patients diagnoses as listed in the “International Statistical Classification of Diseases and Related Health Problems,” 10th Revision (ICD-10) (https://icd.who.int/browse10/2019/en).
Medical prescriptions were analyzed, and the prescribed and dispensed medications were entered into the website stoppstart.free.fr/index.php. This tool allows for entering medications from a specific prescription as well as medical diagnoses, automatically generating potentially inappropriate prescriptions (PIP). Validation of PIP was performed by the clinical pharmacist, taking into account the STOPP/START criteria, version 2 (
The identified PIPs were systematically classified according to the STOPP criteria, consisting of 80 indications, and START criteria, consisting of 34 indications. Additionally, the pharmacological groups associated with the PIPs, number of medications, and diagnosis (ICD-10) were determined (
Data on potentially inappropriate prescriptions in polymedicated elderly patients were processed considering the study variables. For the association of variables, bivariate statistics using Chi2 were used, while to reduce dimensionality and verify the re-grouping of variables into clusters, principal component analysis (PCA) with Varimax rotation and Kaiser normalization was used to understand the variance disposition (
Participant confidentiality was maintained throughout the study, and their decision to decline participation or withdraw at any time was respected. The ethical regulations of the National University of Trujillo were considered (
This study recruited a total of 158 elderly adults (85 men and 73 women) who visited the pharmacy establishment with a medical prescription and met the previously established criteria. The largest proportion of individuals were between 65 and 69 years old (66.5%), who are individuals who are still able to care for themselves and obtain their medications. Regarding the number of medications, 77.9% had between 3 and 4 medications in their prescriptions. Notably, 22.1% of elderly adults had 5 or more medications in their prescriptions (Table
Variables | Frequency | % | |
---|---|---|---|
Age (years) | 65–69 | 105 | 66.5 |
70–74 | 40 | 25.3 | |
75–79 | 10 | 6.3 | |
80–84 | 3 | 1.9 | |
≥ 85 | 0 | 0.0 | |
Sex | Male | 85 | 53.8 |
Female | 73 | 46.2 | |
Number of medications | < 5 | 123 | 77.9 |
5–9 | 34 | 21.5 | |
> 10 | 1 | 0.6 |
In Fig.
Table
Potentially inappropriate prescription (PIP) according to STOPP and START indicators.
Variables | STOPP Indicators | START Indicators | ||
---|---|---|---|---|
ni/n (%) = 148/158 (93.7) | ni/n (%) = 85/158 (53.8) | |||
Sex | ||||
Male | 80/85 (94.1) | p > 0.05 | 46/85 (54.1) | p > 0.05 |
Female | 68/73 (93.1) | 39/73 (53.4) | ||
Age | ||||
65–69 | 96/105 (91.4) | p > 0.05 | 55/105 (52.4) | p > 0.05 |
70–74 | 39/40 (97.5) | 21/40 (52.5) | ||
75–79 | 10/10 (100.0) | 7/10 (70.0) | ||
80–84 | 3/3 (100.0) | 2/3 (66.7) | ||
≥ 85 | 0/0 (0.0) | 0/0 (0.0) | ||
Number of Medications | ||||
< 5 | 113/123 (91.9) | p < 0.05 | 59/123 (48.0) | p < 0.05 |
5–9 | 34/34 (100.0) | 25/34 (73.5) | ||
> 10 | 1/1 (100.0) | 1/1 (100.0) |
Fig.
The study provides details of the PIP in accordance with the STOPP/START criteria classification outlined in Table
STOPP Criteria | n = 733 (%) |
А. Medical Indications | |
A3 Duplication of prescription of a class of drugs (benzodiazepines, NSAIDs, SSRIs, loop diuretics, ACE inhibitors, beta-blockers, anticoagulants) | 10 (1.3) |
B. Cardiovascular system | |
B4 A beta blocker in the presence of bradycardia (heart rate < 50 bpm), second, or third degree atrioventricular block | 4 (0.5) |
B6 A loop diuretic for high blood pressure | 4 (0.5) |
B7 A loop diuretic for lower extremity edema of peripheral origin | 4 (0.5) |
B8 A thiazide diuretic in the presence of hypokalemia (K+ < 3.5 mmol/L), hyponatremia (Na+ < 130 mmol/L), hypercalcemia (corrected Ca++ > 2.65 mmol/L or > 10.6 mg/dL), or a history of microcrystalline arthritis (gout or chondrocalcinosis). | 5 (0.7) |
B9 Loop diuretic for hypertension in the presence of urinary incontinence. | 4 (0.5) |
B11 An ACE inhibitor or ARB with a history of hyperkalemia | 21 (2.9) |
B12 An aldosterone antagonist (spironolactone, splerenone) in the absence of potassium monitoring when this antagonist is associated with a potassium-sparing drug. | 1 (0.1) |
C. Antiplatelets/Anticoagulants | |
C1 Long-term aspirin at doses > 160 mg/day (increased risk of bleeding) | 4 (0.5) |
C2 Aspirin in a history of peptic ulcer without a prescription of a PPI | 1 (0.1) |
C3 Antiplatelet (aspirin, clopidogrel) or an oral anticoagulant (vitamin K antagonist, direct thrombin inhibitors, or Factor Xa) in the presence of a significant bleeding risk | 9 (1.2) |
C11 NSAID in the presence of an antiplatelet agent, without preventive treatment with PPI. | 3 (0.4) |
D. Central nervous system and psychotropics | |
D1 A tricyclic antidepressant in the presence of dementia, acute angle glaucoma, cardiac conduction disorder, prostatism, dysuria, or a history of acute urinary retention. | 10 (1.4) |
D2 A tricyclic antidepressant as a first-line treatment for depression. | 10 (1.4) |
D3 A neuroleptic with anticholinergic effect (chlorpromazine, clozapine, pipotiazine, promazine) in the presence of prostatism or a history of urinary retention. | 2 (0.3) |
D4 SSRI with concomitant or recent hyponatremia (Na+ <130 mmol/l) | 24 (3.3) |
D5 A benzodiazepine for more than four weeks; risks of sedation, confusion, loss of balance, falls, and/or accidents. After four weeks, all benzodiazepine consumption should be tapered off. | 84 (11.5) |
D6 A neuroleptic in the presence of parkinsonism or dementia | 5 (0.7) |
D7 An anticholinergic/antimuscarinic drug for the treatment of extrapyramidal effects induced by a neuroleptic. | 6 (0.8) |
D8 A drug with anticholinergic effect in the presence of dementia and/or delirium. | 3 (0.4) |
D9 A neuroleptic in psycho-behavioral symptoms associated with dementia. | 29 (4.0) |
D10 A neuroleptic for insomnia | 29 (4.0) |
D12 Phenothiazine as a first-line antipsychotic. | 2 (0.3) |
D13 Levodopa or a dopamine agonist for benign essential tremor. | 2 (0.3) |
F. Gastrointestinal system | |
F1 Prochlorperazine or metoclopramide in the presence of extrapyramidal symptoms. | 3 (0.4) |
F2 A PPI for more than eight weeks for peptic esophagitis or peptic ulcer. | 9 (1.2) |
F3 An astringent medication (anticholinergics, oral iron, opiates, verapamil, aluminum-based antacids) in the presence of chronic constipation when alternatives exist. | 46 (6.3) |
F4 Elemental iron dose > 200 mg/day orally (iron fumarate > 600 mg/day, iron sulfate > 600 mg/day, iron gluconate > 1800 mg/day) | 1 (0.1) |
G. Respiratory system | |
G2 Systemic rather than inhaled corticosteroids for the long-term treatment of moderate to severe COPD. | 24 (3.3) |
G3 Anticholinergic bronchodilators (ipratropium, tiotropium) in the presence of acute angle glaucoma. | 1 (0.1) |
G5 A benzodiazepine in the presence of acute or chronic respiratory failure | 1 (0.1) |
H. Musculoskeletal system | |
H1 An NSAID (non-cox-2 selective) in the presence of a history of peptic ulcer or gastrointestinal bleeding, without gastroprotective treatment with PPI or antiH2. | 32 (4.4) |
H2 NSAIDs in the presence of severe hypertension or severe heart failure. | 3 (0.4) |
H3 A long-term NSAID (> 3 months) as first line for pain in osteoarthritis (paracetamol is effective in controlling moderate osteoarthritis pain). | 40 (5.5) |
H4 Long-term (>3 months) corticosteroid therapy for rheumatoid arthritis as monotherapy (risk of side effects). | 24 (3.3) |
H5 Corticosteroids for osteoarthritis pain, oral or local. | 23 (3.1) |
H7 NSAID or selective COX-2 inhibitor in the presence of uncontrolled cardiovascular disease (angina pectoris, severe hypertension). | 3 (0.4) |
H8 An NSAID in the presence of corticosteroids without preventive treatment with PPIs. | 10 (1.4) |
I. Urogenital system | |
I1 A drug anticholinergic effects in the presence of dementia, chronic cognitive impairment (risk of increased confusion, agitation), narrow-angle glaucoma (risk of glaucoma exacerbation), or persistent prostatism. | 19 (2.6) |
STOPP Criteria (Continued) | n = 733 (%) |
J. Endocrine system | |
J1 Long-acting sulfonylureas (glibenclamide, chlorpropamide, glimepiride, glycolazide extended release) in patients with type 2 diabetes mellitus. | 1 (0.1) |
J6 Androgens in the absence of confirmed hypogonadism (risk of androgen toxicity, lack of proven benefit outside of hypogonadism). | 1 (0.1) |
K. Drugs that predictably increase the risk of falls in older people | |
K1 A benzodiazepine in all cases (sedative effect, may reduce level of consciousness, impair balance). | 84 (11.5) |
K2 A neuroleptic in all cases (sedative effect, gait dyspraxia, extrapyramidal symptoms). | 28 (3.8) |
K3 A vasodilator (alpha1-adrenergic blockers, calcium antagonists, long-acting nitrates, ACEI, ARB) in the presence of persistent orthostatic hypotension (risk of syncope, falls). | 22 (3.0) |
K4 Hypnotic-Z (zopiclone, zolpidem, zaleplon) (risk of prolonged daytime sedation, ataxia). | 2 (0.3) |
L. Painkillers | |
L1 Use of strong oral or transdermal opioids (morphine, oxycodone, fentanyl, buprenorphine, diamorphine, methadone, tramadol, pethidine, pentazocine) as first-line treatment for mild pain. | 26 (3.5) |
L2 A maintenance treatment with opiates without the concomitant prescription of a treatment with laxatives (risk of severe constipation). | 26 (3.5) |
L3 Long-acting opioids without rapid-acting opioids for breakthrough pain (risk of persistent pain). | 26 (3.5) |
N. Anticholinergics | |
N1 Concomitant use of 2 or more antimuscarinic/anticholinergic drugs (antispasmodics, first generation antihistamines). | 2 (0.3) |
START Criteria | n = 140 (%) |
A. Cardiovascular system | |
A3 Antiplatelets (aspirin or clopidogrel or prasugrel or ticagrelor) in the presence of coronary artery disease (angina pectoris, stent, or history of MI), history of stroke, or peripheral arterial disease. | 1 (0.7) |
A4 An antihypertensive drug, in the presence of persistent hypertension, treated or not (systolic > 160 mmHg and/or diastolic > 90 mmHg). For diabetic patients, thresholds of 140 mmHg for systolic and 90 mmHg for diastolic are preferred. | 20 (14.3) |
A5 A statin, in the presence of coronary artery disease or a history of peripheral arterial disease or stroke, unless the patient is at the end of life or over 85 years of age. | 1 (0.7) |
B. Respiratory system | |
B1 An inhaled beta2-adrenergic agonist or antimuscarinic bronchodilator (ipratropium, tiotropium) in the presence of mild to moderate asthma or COPD | 1 (0.7) |
B2 Taking an inhaled corticosteroid in the presence of moderate to severe asthma or COPD when the forced expiratory volume (FEV1) < 50% or when there are frequent exacerbations that require oral corticosteroids. | 2 (1.4) |
C. Central nervous system and visual apparatus | |
C1. Levodopa or dopamine agonist, in the presence of confirmed idiopathic Parkinson’s disease, with significant functional repercussions. | 5 (3.6) |
C2. A non-tricyclic antidepressant in the presence of major depressive symptoms. | 12 (8.6) |
C3. Acetylcholinesterase inhibitor in mild to moderate Alzheimer’s (donepezil, rivastigmine, galantamine) or Lewy body disease (rivastigmine). | 5 (3.6) |
C5. In severe persistent anxiety, an SSRI. In cases of SSRI contraindication, a serotonin and norepinephrine reuptake inhibitor, or pregabalin. | 7 (5.0) |
D Gastrointestinal tract | |
D1 Proton pump inhibitor, in the presence of severe gastroesophageal reflux or peptic stricture requiring dilation. | 3 (2.1) |
D2 Fiber supplements (bran, methylcellulose) in the presence of diverticular disease associated with a chronic history of constipation. | 1 (0.7) |
E Musculoskeletal system | |
E1 Disease-modifying antirheumatic drugs in disabling rheumatoid arthritis (methotrexate, hydroxychloroquinine, minocycline, tocilizumab, etanercept, adalimumab, infliximab, rituximab, and certolizumab). | 3 (2.1) |
E3 In patients with osteoporosis or a history of fragility fracture, a supplement of vitamin D (cholecalciferol 800–1000 IU/day) and calcium (1–1.2 g/day). | 1 (0.7) |
E4 In the presence of confirmed osteoporosis or history of fragility fracture, a bone resorption inhibitor treatment (e.g., bisphosphonates, strontium ranelate, teriparatide, denosumab). | 1 (0.7) |
E5 In older patients who do not leave home, who suffer falls or have osteopenia, vitamin D supplements (cholecalciferol 800–1000 IU/day). | 1 (0.7) |
F Endocrine system | |
F1 ACE inhibitors or ARA-II in the presence of diabetic nephropathy, overt proteinuria, or microalbuminuria (> 30 mg/24 h) with or without renal failure. | 4 (2.9) |
H Analgesics | |
H1 In moderate to severe pain, propose opioid agonists when paracetamol, NSAIDs, or weak opioids are not appropriate. | 35 (25,0) |
H2 Laxatives in patients taking opioids regularly. | 25 (17,9) |
I Vaccines | |
I2 Pneumococcal vaccine at least once after age 65, according to national recommendations. | 12 (8,6) |
Factorial analysis was performed using Principal Component Analysis (PCA) (Table
Distribution of potentially inappropriate prescriptions in components*, according to factor analysis**.
Variables | Components | |
---|---|---|
1 | 2 | |
Age | 0.155 | -0.552 |
Sex | 0.159 | 0.742 |
Diagnosis | 0.013 | 0.650 |
Number of Medications | 0.841 | -0.063 |
Number of STOPP Criteria | 0.693 | 0.128 |
Number of START Criteria | 0.712 | -0.080 |
Polypharmacy is a public health issue present in patients with multiple chronic diseases and becomes one of the main causes of multimorbidity, especially in vulnerable older adults from a pharmacological context. This can be attributed to the use of potentially inappropriate medications and adverse drug reactions due to changes in physiological functions and pharmacokinetic and pharmacodynamic characteristics that occur with aging (
In the present study, a high consumption of psychotropic, neurological, and pain medication was found, which is due to the fact that neurodegenerative problems are prominent in this age group (
Benzodiazepines, which have shown high consumption in this study, are associated with confusion, dizziness, and risk of falls in older adults, mainly those with prolonged action. In that sense, polypharmacy that includes benzodiazepines along with other central depressants should be avoided because it potentiates the effects, increasing the risk of morbidity and mortality (
Initially, the determination of PPI in older adults using the STOPP-START criteria was performed in a European context, with STOPP prevalence ranging from 35% to 77% and START from 51% to 73% (
In the OPERAM trial, a pharmacotherapy team decided to determine the frequency of STOPP/START criteria in a European hospital setting, finding that 99% of patients presented a STOPP or START criterion. Medications prescribed without evidence-based clinical indication, duplicate prescriptions, and the criterion with the highest prevalence were related to the use of benzodiazepines for more than four weeks (
In Mexico and Brazil, potentially inappropriate prescriptions were also evaluated in hospitalized older adults. In the study conducted in Mexico, a PIP prevalence of 67% was found according to the STOPP/START criteria, and in Brazil, a high number of STOPP criteria corresponding to the central nervous system (24.8%) was identified. The START criteria that stand out are errors due to omission of medications (59.9%); however, when identified at hospital admission, the percentages were significantly reduced (
In Lima, Peru, prescriptions filled at pharmacies and drugstores were also evaluated according to the Beers criteria, finding that 69.2% of older adults had potentially inappropriate prescriptions due to the consumption of anxiolytics, with a higher incidence in women (61.6%) (
In the context of community pharmacy, a study was conducted in Bulgaria that identified PIP in a single pharmacy using the EU(7)-PIM List criteria, finding that 67% of the polymedicated population had at least one PIP (
The application of the STOPP START criteria in public and private health services would allow for a reduction in the incidence of adverse effects and optimization of treatments received by older adults in general. While the STOPP/START criteria constitute a good tool for identifying problems with medication in older adults, it is also true that, in a global context, these criteria may have limitations, as indicated by Verdoorn et al. (
Our study also reflects the need for clinical pharmacists in the community context, with the necessary competencies to identify and resolve, within their competence, potential problems associated with medications in older adult users who attend pharmacies, or, if necessary, refer or recommend patients to medical attention.
A limitation of the present study is that it was based on patients’ prescriptions, and complete access to the medical history of the participants was not available. Additionally, being a cross-sectional study, it was not possible to establish follow-up and have more precise exposure to medication; perhaps many of them are not entirely adherent to the medications they purchased at the pharmacy. Although we are detecting a high prevalence of PIP, the clinical relevance of these PIP is not being considered, which can be addressed in future multidisciplinary studies.
Polypharmacy is a common problem in the elderly due to the physiological changes they experience and is directly associated with the incidence of PIP. According to the criteria used in the study, a high prevalence of STOPP and START criteria was found in the analyzed prescriptions. Additionally, a significant association was identified through component analysis: with a higher number of prescribed medications, there is a higher probability of PIP occurrence. It is necessary for community pharmacies to implement systems for detecting PIPs in the geriatric population, which, along with other strategies, allow for the optimization of pharmacotherapy in older adult users. However, this constitutes a challenge for the healthcare systems of countries where there is a lack of better articulation of primary care processes.
Conceptualization (MBV, JCF), Methodology (MBV, GGH, JCF), Software (GGH, ACB, KRT, HVM), Validation (MBV, JCF, HVM), Formal analysis (MBV, GGH), Investigation (MBV, ACB, HVM, KRT), Resources (MBV, GGH, HVM, KRT, JCF), Data Curation (GGH, ACB, JCF), Writing – Original draft, Writing – Review and Editing (GGH, JCF, ACB), Visualization (ACB, KRT), Supervision (JCF), Project administration (MBV).
All authors have read and agreed to the published version of the manuscript.
No potential conflict of interest was reported by the authors.