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Open AccessJournal ArticleDOI

Predicting risk of adverse drug reactions in older adults

TLDR
Good clinical practice for detecting and predicting ADRs in vulnerable patients includes detailed documentation and regular review of prescribed and over-the-counter medications through standardized medication reconciliation.
Abstract
Adverse drug reactions (ADRs) are common in older adults, with falls, orthostatic hypotension, delirium, renal failure, gastrointestinal and intracranial bleeding being amongst the most common clinical manifestations. ADR risk increases with age-related changes in pharmacokinetics and pharmacodynamics, increasing burden of comorbidity, polypharmacy, inappropriate prescribing and suboptimal monitoring of drugs. ADRs are a preventable cause of harm to patients and an unnecessary waste of healthcare resources. Several ADR risk tools exist but none has sufficient predictive value for clinical practice. Good clinical practice for detecting and predicting ADRs in vulnerable patients includes detailed documentation and regular review of prescribed and over-the-counter medications through standardized medication reconciliation. New medications should be prescribed cautiously with clear therapeutic goals and recognition of the impact a drug can have on multiple organ systems. Prescribers should regularly review medication efficacy and be vigilant for ADRs and their contributory risk factors. Deprescribing should occur at an individual level when drugs are no longer efficacious or beneficial or when safer alternatives exist. Inappropriate prescribing and unnecessary polypharmacy should be minimized. Comprehensive geriatric assessment and the use of explicit prescribing criteria can be useful in this regard.

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Association of Sex, Age, and Comorbidities with Mortality in COVID-19 Patients: A Systematic Review and Meta-Analysis.

TL;DR: Implementing adequate protection and interventions for COVID-19 patients in general and in particular male patients with age ≥50 years having comorbidities may significantly reduce risk of mortality associated with CO VID-19.
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Current and future perspectives on the management of polypharmacy

TL;DR: There is considerable scope to improve the quality of prescribing and reduce risks from poly-pharmacy using non-medical groups such as pharmacists, specialist nurses and physician assistants, and developments such as the introduction of artificial intelligence and clinical decision support systems also have the potential to improve prescribing and minimise the risks.
Journal ArticleDOI

Facilitating the ethical use of health data for the benefit of society: electronic health records, consent and the duty of easy rescue.

TL;DR: It is argued that the duty of easy rescue—the principle that persons should benefit others when this can be done at no or minimal risk to themselves—grounds the removal of consent requirements for minimally risky records-based research.
Journal ArticleDOI

Prediction of Hospitalization due to Adverse Drug Reactions in Elderly Community-Dwelling Patients (The PADR-EC Score).

TL;DR: The number of antihypertensives was the strongest predictor of an ADR followed by presence of dementia, renal failure, drug changes in the preceding 3 months and use of anticholinergic medications; these variables were used to derive the ADR prediction score.
Journal ArticleDOI

Explicit criteria as clinical tools to minimize inappropriate medication use and its consequences.

TL;DR: The most widely used sets of explicit PIM criteria to address inappropriate polypharmacy are described with particular focus on STOPP/START criteria and FORTA criteria which have been associated with positive patient-related outcomes when used as interventions in recent randomized controlled trials.
References
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Journal ArticleDOI

Potentially Inappropriate Medications Defined by STOPP Criteria and the Risk of Adverse Drug Events in Older Hospitalized Patients

TL;DR: STOPP criteria PIMs, unlike Beers criteria Pims, are significantly associated with avoidable ADEs in older people that cause or contribute to urgent hospitalization.
Journal ArticleDOI

Proposal for a New Tool to Evaluate Drug Interaction Cases

TL;DR: The Drug Interaction Probability Scale (DIPS) was developed to provide a guide to evaluating drug interaction causation in a specific patient and can serve as a guide in the preparation of articles describing case reports of drug interactions, as well as in the evaluation of published case reports.
Journal ArticleDOI

Inappropriate drug prescribing for the community-dwelling elderly.

TL;DR: Physicians prescribe potentially inappropriate medications for nearly a quarter of all older people living in the community, placing them at risk of drug adverse effects such as cognitive impairment and sedation.
Journal ArticleDOI

Polypharmacy as commonly defined is an indicator of limited value in the assessment of drug-related problems

TL;DR: The number of DRPs per patient was linearly related to the number of drugs used on admission, and to set a strict cut-off to identify polypharmacy and declare that using more than this number of drug represents a potential risk for occurrence ofDRPs, is of limited value when assessing DRPs in a clinical setting.
Journal ArticleDOI

Development and Validation of a Clinical Scale for the Diagnosis of Drug-Induced Hepatitis

TL;DR: The clinical scale was shown to have a high‐level of validity and inter‐rater reliability as well as a good discriminatory capacity between different levels of probability, suggesting that the scale is suitable for use in clinical practice and may contribute to overcome the difficulties in the process of causality assessment in DILI.
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