Copyright
©The Author(s) 2015.
World J Pharmacol. Jun 9, 2015; 4(2): 193-209
Published online Jun 9, 2015. doi: 10.5497/wjp.v4.i2.193
Published online Jun 9, 2015. doi: 10.5497/wjp.v4.i2.193
Absorption | ↓ amount of saliva |
↑ gastric pH | |
↓ gastric acid secretion | |
↑ gastric emptying time | |
↓ gastric surface area | |
↓ gastrointestinal motility | |
↓ active transport mechanisms | |
Distribution | ↓ cardiac output |
↑ peripheral vascular resistance | |
↓ renal blood flow | |
↓ hepatic blood flow | |
↓ body water | |
↑ body fat tissue | |
↓ serum albumin levels | |
↑ for lipid soluble and decrease for water soluble drugs | |
Metabolic | ↓ microsomal hepatic oxidation |
↓ clearance | |
↑ steady state levels | |
↑ half lives | |
↑ levels of active metabolites | |
↓ first pass metabolism due to reduced ↓ blood flow | |
Excretion | ↓ in renal perfusion |
↓ in renal size | |
↓ in glomerular filtration rate | |
↓ tubular secretion | |
↓ in tubular reabsorption |
Enzyme inhibitors | Enzyme inducers |
Amiodarone | Carbamazepine |
Allopurinol | Ethanol |
Cimetidine | Isoniazid |
Citalopram, sertraline | Phenytoin |
Ciprofloxacin | Phenobarbital |
Diltiazem, verapamil | Rifampcin |
Fluxetine, paroxetine | St. Johns Wort |
Erythromycin, clarithromycin | |
Fluconazole, ketoconazole | |
Omeprazole | |
Sulphonamides | |
Grapefruit Juice |
Drug class | Adjust dose in CKD stage 1-3 | Avoid in CKD stages 4 and 5 |
ACE-inhibitors and Angiotensin 2 receptor blockers | All ACE inhibitors | Olmesartan |
Diuretics | Potassium-sparing and thiazide diuretics | Potassium-sparing and thiazide diuretics |
Beta-blockers | Acebutolol, atenolol, bisoprolol, nadolol, sotalol | Sotalol |
Lipid lowering agents | Pravastatin, rosuvastatin, fibrates | Glyburide, metformin, exanitide |
Hypoglycaemic agents | Gliclazide, acarbose, insulin, gliptins | |
Analgesia (NSAIDs and opioids) | Codeine, tramadol, morphine, oxycodone, | All NSAIDs, pethidine |
Psychotropic agents | Lithium, gabapentin, pregabalin, topiramate, vigabatrin, bupropion, duloxetine, paroxetine, venlafaxine | |
Miscellaneous | Allopurinol, colchicine, digoxin | Dabigatran Rivaroxaban (CI stage 5, dose adjust in stage 4 CKD) Apixaban (CI stage 5, dose adjust in stage 4) |
Drug type | Specific drug | Pharmacodynamic response in older people | Potential clinical consequence |
Analgesia | Morphine | ↑ | Excessive sedation, confusion, constipation, respiratory depression |
Anticoagulant | Warfarin Dabigatran in those ≥ 75 yr with a body weight of < 50 kg) | ↑ | Increased bleeding risk |
Cardiovascular system drugs | Angiotensin II receptor blockers | ↑ | Hypotension |
Diltiazem | ↑ | ||
Enalapril | ↑ | ||
Verapamil | ↑ | ||
Propranolol | ↓ | ||
Diuretics | Frusemide | ↓ | Reduced diuretic effect at standard doses |
Bumetanide | ↑ | ||
Psychoactive drugs | Diazepam | ↑ | Excessive sedation, confusion, postural sway, falls |
Midazolam | ↑ | ||
Temazepam | ↑ | ||
Haloperidol | ↑ | ||
Traizolam | ↑ | ||
Others | Levodopamine | ↑ | Dyskinesia, confusion, hallucinations |
Drug | Typical dose in younger patient (< 65 yr) | Typical dose in older patient (≥65 yr) | Reason for different dose in the elderly |
Anti-arrhythmics | |||
Digoxin | Loading dose is 1-1.5 mg in divided doses over 24 h Maintenance dose 125-250 mcg OD | Loading dose is 1 mg in divided doses over 24 h Maintenance dose 62.5-125 mcg OD | Water soluble contributing to increased plasma levels in the elderly |
Anti-coagulants | |||
Warfarin | Standard initiation dose, e.g., 10 mg daily for two days | Lower initiation dose, e.g., 5 mg daily for two days | Increased sensitivity to anticoagulant effect |
Dabigatran | 150 mg BD | Patient > 80 yr 110 mg BD Patient 75-80 yr 150 mg BD in setting or normal eGFR | Increased sensitivity to anticoagulant effect |
Anti-hypertensive | |||
Ramipril | Initiation dose 2.5 mg | Initiation dose 1.25 mg | Lower initial dose and gradual dose titration required (higher risk of ADE in the elderly) |
Psychoactive drugs | |||
Diazepam | 2 mg TDS | 1 mg BD | Lipid soluble with higher volume of distribution in older people thus contributing to a prolonged duration of effect |
Drug | Drug | Interaction | Effect |
Anti- hypertensive agents | NSAID | NSAID antagonizes hypotensive effect | ↓ antihypertensive effect |
Aspirin | NSAID, oral corticosteroids | ↑ risk of peptic ulceration | Peptic ulceration |
Calcium channel blockers | Enzyme inducers | ↑ clearance of calcium channel blocker | ↓ anti-hypertensive effect |
Digoxin | Diuretics | Diuretic-induced hypokalaemia | ↑ effect of digoxin (arrhythmia, toxicity) |
Digoxin | Amiodarone, Ditiazem, Verapamil | ↓ clearance of digoxin | ↑ effect of digoxin (arrhythmia, toxicity) |
TCA | Enzyme inhibitors | ↓ clearance of TCA | Arrhythmia, confusion, orthostatic hypotension, falls |
Phenytoin | Enzyme inhibitors | ↓ clearance of phenytoin | ↑ effect of phenytoin, toxicity |
Thyroxine | Enzyme inducers | ↑ clearance of thyroxine | ↓ effect of thyroxine |
Use non-pharmacological treatment whenever possible |
Include the patient (and carer where appropriate) in prescribing decisions |
Ensure each medication has an appropriate indication and a clear therapeutic goal (this involves careful clinical assessment and appreciation of time to obtain treatment effect and life expectancy) |
Start at the smallest dose and titrate slowly according to response and efficacy |
Use the simplest dosing regimen (e.g., once a day preferable to three times per day) and most appropriate formulation |
Provide verbal and written instructions on indication, time and route of administration and potential adverse effects of each medication |
Regularly review prescriptions in the context of co-exiting disease states, concurrent medications, functional and cognitive status and therapeutic expectation |
Be aware that new presenting symptoms may be due to an existing medication, drug-drug interaction or drug-disease interaction (avoid prescribing cascade) |
When stopping a medication check that it can be stopped abruptly or whether it needs to be tapered, e.g., long-term steroids, benzodiazepines |
An 80-year-old lady is referred with a four day history of general malaise, nausea, vomiting and recurrent falls. Her past medical history includes paroxysmal atrial fibrillation, non-obstructive coronary artery disease, hypertension, recurrent episodes of acute gout, dependent lower limb edema and “vertigo/dizziness”. Prior to this episode she was functionally independent and had normal cognition | |||
Her medications were as follows: Simvastatin 40 mg daily; Verapamil 240 mg daily; Quinine Sulphate 300 mg daily, Perindopril 5 mg/Indapamide 1.5 mg daily; Digoxin 250 mcg daily; Diclofenac 75 mg twice daily; Frusemide 40 mg daily; Betahistine 16 g three times per day; Paracetamol 1 g as required; Warfarin as per INR (target INR 2-3); Flurazepam 30 mg nocte. She was not taking OTC medications | |||
On assessment she was pale and tired. Supine blood pressure was 122/70 mmHg; erect blood pressure after one minute was 92/62 mmHg | |||
Pulse was 52 beats per minute. She had no clinical signs of congestive cardiac failure. She scored 9/10 on a short mental test score | |||
Investigations showed a eGFR of 38 mL/min, serum potassium 2.8 mmol/L (low) and serum sodium 126 mmol/L (low). Haemoglobin was 10.2 g/dL with MCV 72fl (hypochromic microcytic anemia) | |||
When evaluating the appropriateness of an older person’s prescription medications it is important to consider the following two questions: | |||
1 Is there a clinical indication for the drug? | |||
2 Could the drug be contributing to the presenting symptoms? | |||
Using this approach each medication should be evaluated in turn and corrective action implemented | |||
Medication | Clinical indication? | Contributing to presenting symptoms? | Action taken? |
Simvastatin 40 mg | Yes (hyperlipidaemia, high cardiovascular risk) | Could cause muscle cramps and myopathy which could lead to falls (note patient prescribed quinine) | Check fasting lipid profile and creatine phosphokinase. Revise dose according to target lipid levels |
Verapamil 240 mg | Yes (hypertension, arrhythmia) | Could cause hypotension and bradycardia. Increased risk of myopathy when prescribed with simvastatin | Consider discontinuation. Beta-blocker may be more appropriate choice as rate controlling agent |
Quinine 300 mg | No clear indication | No | Muscle cramps may be due to statin. Review choice of statin. Discontinue Quinine |
Perindopril 5 mg | Yes (hypertension) | Could contribute to postural hypotension and acute renal injury | Consider temporary withdrawal while investigating cause of renal dysfunction |
Indapamide 1.5 mg | Yes (hypertension) | Could contribute to postural hypotension, acute renal injury, hyponatraemia and hypokalaemia. Can precipitate digoxin toxicity, hyperuricaemia and recurrent episodes of gout | Discontinue |
Digoxin 250 mcg | Yes (atrial fibrillation) | Symptoms of digoxin toxicity. Dose too high given level of renal dysfunction | Discontinue. Beta-blocker may be more appropriate choice of rate controlling agent |
Diclofenac 75 mg | Yes (acute gout) | Yes. Diclofenac may be causing renal impairment. Gastritis/peptic ulcer disease should also be considered because of nausea, vomiting and microcytic anemia. NSAIDs should not be prescribed with warfarin because of significantly increased risk of bleeding | Discontinue. Consider addition of allopurinol for gout prophylaxis |
Frusemide 40 mg | Yes (hypertension) | Yes (hypotension, hyponatraemia, hypokalaemia, renal impairment) | Frusemide is not required as an anti-hypertensive in this patient. It has been prescribed to treat dependent lower limb edema. Leg elevation and compression stockings would be more appropriate |
Betahistine 16 mg | No (prescribed for dizziness which is actually related to orthostatic hypotension) | No | Discontinue. No indication |
Paracetamol 1 g | Yes (pain) | No | Continue |
Warfarin | Yes (atrial fibrillation embolic prophylaxis) | May be contributing to anemia. Should not be co-prescribed with diclofenac as there is an increased risk of bleeding | Investigate cause of anemia. Consider future suitability for anticoagulation if high falls risk persists |
Flurazepam 30 mg | No | Yes (falls, malaise) | Contact GP and pharmacy for prescription history. Do not suddenly discontinue because of risk of benzodiazepine withdrawal |
Explicit criteria | Advantages | Disadvantages |
Beers criteria[70] | Assesses prescribing quality Useful for education | Several drugs unavailable outside United States Does not include underuse of drugs, drug-drug interactions or duplicate drugs No under-prescribing indicators |
Beers criteria[71] | Concise explanation of inappropriateness Severity ratings of adverse outcomes Assesses prescribing quality Useful for education | Several drugs unavailable outside United States Does not include underuse of drugs, drug-drug interactions or duplicate drugs No under-prescribing indicators |
Beers criteria[72] | Concise explanation of inappropriateness Severity ratings of adverse outcomes Can be used by computerized clinical information systems | Several drugs unavailable outside the United States Controversy over some drugs labeled as inappropriate No drug to drug interaction No drug disease interactions No under prescribing |
Beers criteria[73] | Concise explanation of inappropriateness Structured according to therapeutic classes and organ systems Drug disease interactions | Several drugs unavailable outside United States No drug-drug interaction No under prescribing |
STOPP/START[74] | Organised by physiological system Concise list on inappropriate medications Includes drug and disease interactions, therapeutic duplications and prescribing omissions | Does not suggest safer alternatives Does not address certain domains of prescribing, e.g., indication |
McLeod criteria[113] | Concise list of inappropriate medications with safer alternatives suggested Useful for education | Obsolete indicators, e.g., beta blockers in heart failure No under-prescribing indicators Several drugs unavailable outside United States |
IPET 2000 (Improved prescribing in the elderly tool)[114] | Concise Useful for education | Not comprehensive Predominantly cardiovascular and psychotropic drugs No under-prescribing indicators |
Zhans criteria[115] | Less restrictive than previous criteria | Several drugs unavailable outside United States No drug to drug interaction No drug disease interactions No under-prescribing indicators |
French Consensus Panel List[116] | Concise explanation of inappropriateness Includes drug duplications Safer alternatives suggested | No clinical studies to date No under prescribing |
Rancourt[117] | 26 Drug drug interactions 10 drug duplications | Large number of criteria to get through in clinical practice Data only on long term care setting |
Australian Prescribing Indicators Tool[118] | Includes drug duplication Includes under-prescribing | Not validated and time consuming Derived from Australian data sources limiting international applicability |
Norwegian General Practice (NORGEP) Criteria[119] | Can be applied to medication list with no clinical information | No drug prescribing No drug-disease interactions No studies to date outside Norway |
Priscus List[120] | Provides therapeutic alternatives Recommendations on dose adjusting and monitoring | No studies to date published outside Germany |
Thailand Criteria[121] | Drug interactions Drug disease interactions | No studies to date outside country of origin |
- Citation: Lavan AH, O’Grady J, Gallagher PF. Appropriate prescribing in the elderly: Current perspectives. World J Pharmacol 2015; 4(2): 193-209
- URL: https://www.wjgnet.com/2220-3192/full/v4/i2/193.htm
- DOI: https://dx.doi.org/10.5497/wjp.v4.i2.193