Physiological changes in the elderly
With increasing age, many physiological changes may alter pharmacokinetics. These include:
- Increased gastric motility
- Reduced intestinal blood flow
- Lower body weight and lean body mass
- Higher proportion of body fat
- Lower hepatic and renal blood flow (and thus glomerular filtration rate)
- Change in immune response
All these factors alter pharmacokinetics:
- Absorption of most drugs remains the same except for reduction in iron, calcium and thiamine absorption
- Lower concentration of fat-soluble drugs
- Higher concentration of water-soluble drugs
- Lower rate of drug metabolism and hepatic clearance
- Less efficient renal drug excretion
Pharmacodynamic changes that also occur simultaneously are as follows:
- Central nervous system becomes more sensitive to sedative medications
- Less effective homeostatic mechanisms and less able to compensate for side effects (especially postural hypotension)
- Reduced clotting factor synthesis
- Increased risk of adverse and allergic reactions
Together with the fact that polypharmacy is more prevalent in the elderly, up to 97% in hospitalised patients, they are also more likely to experience side effects secondary to drug interactions.
| Fat-soluble (lipophilic) | Water-soluble (hydrophilic) |
|---|---|
| Diazepam | Digoxin |
| Fentanyl | Verapamil |
| Naproxen | Paracetamol |
| Propranolol | Penicillin |
Table 1. Common fat-soluble and water-soluble drugs
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