Psychopharmacological Treatment in Older People: Avoiding Drug Interactions and Polypharmacy
Avoiding drug interactions and polypharmacy
Background: As the elderly population increases, so, too, does the number of multimorbid patients and the risk of polypharmacy. The consequences include drug interactions, undesired side effects of medication, health impairment, and the need for hospitalization. 5–10% of hospital admissions among the elderly are attributable to undesired side effects of medication.
Methods: This review is based on publications retrieved by a selective search in PubMed and the Cochrane Library that employed the search terms “drug interaction,” “undesired side effect,” “polypharmacy,” “pharmacokinetics,” and “pharmacodynamics.”
Results: Elderly patients are particularly at risk of polypharmacy, both because of the prevalence of multimorbidity in old age and because of physicians’ uncritical implementation of guidelines. The more drugs a person takes, the greater the risk of drug interactions and undesired side effects. Age-associated changes in pharmacokinetics and pharmacodynamics elevate this risk as well. Physicians prescribing drugs for elderly patients need to know about the drugs’ catabolic pathways, protein binding, and inductive and inhibitory effects on cytochrome P450 in order to avoid drug interactions and polypharmacy.
Conclusion: Multiple aids and instruments are available to ensure practical and reasonable drug monitoring, so that the risks of drug interactions and undesired side effects can be detected early and avoided.
The elderly are making up an ever-increasing percentage of the overall population as part of an ongoing demographic development. There are already more than 6 million persons over age 80 in Germany now; by 2050, there will be approximately 10 million (1). Because of the growing elderly population, there are more multimorbid persons than ever before, and thus more patients who need to take multiple drugs (2). Polypharmacy, which is defined as the simultaneous use of five or more drugs, is a particular problem among persons aged 75 to 85 (2).
Polypharmacy leads to an increasing frequency of drug interactions, undesired side effects of medication (“adverse drug effects,” ADE), impaired health, and hospitalization (e1). Drug interactions can lead to toxicity or to diminished therapeutic efficacy via inhibitory or inductive effects on cytochrome P450 (CYP). ADE cause increased costs in the health care system and are responsible for 5–10% of hospital admissions of elderly patients (3–6, e2). The elderly are also at higher risk of rehospitalization because of severe ADE (e3). Drugs that often cause ADE in old age include antihypertensive drugs (36%), non-steroidal anti-inflammatory drugs (NSAID) (17.8%), insulin preparations (13.9%), anticoagulants (33.3%), and psychoactive drugs (24.8%) (7, e1, e4, e5).
The uncritical use of psychoactive drugs in elderly patients, along with the altered pharmacokinetics and pharmacodynamics of drugs in old age, can also increase the rate of undesired side effects. Anticholinergic drugs and sedating psychoactive drugs are risky. ADE are often hard to tell apart from manifestations of the known underlying disease or a new disease (8, 9). Undesired effects of psychoactive drugs in the elderly can have dramatic consequences: falls due to drug overdose or parkinsonoid effect; delirium, syncope, and cognitive dysfunction caused by anticholinergic drugs; bradycardia due to cardiac side effects; decompensated diabetes and heart attack or stroke due to metabolic side effects.
The rigid application of guidelines in patients suffering from multiple chronic diseases markedly increases the risk of polypharmacy and the likelihood of potentially dangerous drug interactions and ADE (10, 11). The failure to adjust drug doses because of a lack of knowledge of the pharmacokinetics and pharmacodynamics of psychoactive drugs in old age is a common cause of drug interactions and ADE (11).
The treatment of elderly patients with psychoactive drugs is important; it may be needed to sustain a good quality of life. A proper knowledge of the specific changes of pharmacodynamics and pharmacokinetics in old age can help limit the frequency of drug interactions and polypharmacy (e6). This knowledge is necessary, simple, and easily acquired. In one study, training of intensive care unit staff in this matter lowered the frequency of drug interactions from 66% to 54% and of ADE from 44% to 25% (12).
This review is based on publications retrieved by a selective search in PubMed and publicly available databases.
Readers of this article should acquire
- an understanding of the special aspects of the pharmacokinetics and pharmacodynamics of psychoactive drugs in the elderly,
- an acquaintance with age-associated aspects of drug resorption, distribution, elimination, and biotransformation, and
- knowledge of how to avoid polypharmacy and undesired side effects when prescribing psychoactive drugs to elderly patients who need them.
Pharmacokinetic interactions affect the bioavailability of a drug either indirectly (through the induction or inhibition of CYP) or directly. Pharmacokinetic changes in old age include altered resorption (through the gastrointestinal tract and across the blood-brain barrier), distribution, protein binding, renal elimination, and biotransformation (CYP) (13, e7).
Age-associated changes include lower fluid volume, organ perfusion, muscle mass, and serum albumin concentration, and an increase in body fat (14). The consequences include altered serum concentrations, longer persistence of drugs in the body, stronger drug effects at lower doses, and increased side effects and toxicity.
The increased body fat resulting from the ongoing conversion of muscle mass to fat and connective tissue in old age leads to an increased concentration and uncontrolled deposition of lipophilic drugs in the fat depots of the body. Thus, the half-life of diazepam, a highly lipophilic drug, is twice as long in the elderly even if there is no change in creatinine clearance, and the use of diazepam in elderly patients should be viewed critically (15). Oxazepam and lorazepam are not lipophilic, do not have a prolonged half-life in the elderly, and should be used in preference to diazepam.
The serum albumin concentration is normally lower in old age (15, 16, e8). Drugs, however, bind to albumin, and only the free drug, not the bound drug, is pharmacologically active. Drug doses must, therefore, be adjusted to avoid excessive concentrations of free drug leading to undesired side effects or toxicity. Psychoactive drugs with high protein binding (> 90%), a steep dose-response curve, and a narrow therapeutic window are affected. Such situations, though uncommon, can be problematic, for example, when acetylsalicyic acid (ASA) and valproic acid are given together (interactions, bleeding tendency). ASA—e.g., given for secondary prophylaxis after stroke—can displace valproic acid from protein, leading to a rise in the serum valproic acid concentration. Agitation, confusion, or, rarely, valproic acid encephalopathy may ensue.
Age-associated changes in renal elimination may be present on an individual basis. Renal perfusion, the number of nephrons, and the glomerular filtration rate (GFR) all decline with age. The GFR falls by as much as 1 mL/min per year, and tubular function diminishes by 1% per year after age 50 (16, 17). There may be delayed elimination of renally excreted drugs such as gyrase inhibitors and digoxin. Blood levels of drugs should, therefore, be checked more frequently in elderly patients, and drugs should be preferred that are catabolized in more than one pathway. For example, digoxin (which is renally eliminated) can be switched to digitoxin (which is eliminated via the kidneys and the liver).
Biotransformation and CYP
Biotransformation is especially important in old age. In the elderly, the liver is up to 40% smaller, its perfusion is reduced by as much as 30%, the enzymatic activity of the CYP-dependent phase I reaction is lower, and there is greater bioavailability and slower elimination of hepatically eliminated drugs, including propranolol, metoprolol, verapamil, and nifedipine (e9).
CYP plays an essential role, because it participates in oxidation and hydrolysis in the phase I reaction of the liver. Phase I is subject to age-associated changes, while phase II (glucuronidation) is generally unchanged in old age. Particularly important isoenzymes in the treatment of elderly patients with psychoactive drugs include 1A2, 3A4, 2D6, 2C19, 2B6 and 2C9 (eFigure).
When multiple hepatically catabolized drugs are given simultaneously, the blood levels of these drugs can be either elevated or decreased. A drug combination can lead to a relevant pharmacokinetic interaction if one of the administered drugs inhibits or induces a CYP enzyme (“perpetrator drug”) while another one of them is preferentially catabolized by the inhibited or induced enzyme (“victim drug”). It is thus important to know how the various drugs being taken by a patient are catabolized, and whether they can inhibit or induce a CYP enzyme.
Inhibition of cytochrome P450 enzymes
The physician prescribing a psychoactive drug to an elderly patient must consider possible inhibition of isoenzyme 2D6, which plays a role in the catabolism of many drugs used in internal medicine as well as that of certain psychoactive drugs. Inhibiting it can lead to serious drug interactions and ADE. The antidepressant drugs paroxetine and fluoxetine are potent inhibitors. Paroxetine combined with either nebivolol or metoprolol (two antihypertensive agents) can cause severe bradyarrhythmia (18) by inhibiting the catabolism of the antihypertensive drug and thereby raising its blood level. The plasma concentration of aripiprazole also rises when a 2D6 inhibitor is given (19, 20).
Tramadol, an analgesic drug, and tamoxifen, a drug used for the hormonal treatment of breast cancer, are both given as inactive precursor stages (prodrugs) that are converted to their active forms through the activity of isoenzyme 2D6 (21). If either of these drugs is taken in combination with a strong 2D6 inhibitor, such as paroxetine, fluoxetine, bupropion, or melperone (doses >50 mg/day), its efficacy can be markedly impaired (21). In the case of tamoxifen, this can increase the mortality from breast cancer (e10).
2C19 is another relevant isoenzyme. The combination of sertraline with omeprazole can lead to ADE and serious drug interactions (22). A serotonergic syndrome can arise, because sertraline is catabolized through the activity of isoenzyme 2C19, which omeprazole inhibits. Pantoprazole, which does not inhibit isoenzyme 2C19, is therefore to be preferred. In elderly patients, citalopram, venlafaxine, and mirtazapine should be used instead of sertraline. Paroxetine and fluoxetine should be avoided (Table 1).
Inhibition of the effect of isoenzyme 3A4 must also be borne in mind in the pharmacotherapy of elderly patients. Drugs that are catabolized through its activity can have an elevated plasma concentration and exert toxic effects. The antibiotics clarithromycin and erythromycin potently inhibit isoenzyme 3A4 (23, e11), and their use in combination with drugs catabolized via isoenzyme 3A4, such as quetiapine and aripiprazole, is problematic, as the plasma levels of the latter will rise (19, 20 24).
Not only psychoactive drugs, but even grapefruit juice (25) can inhibit hepatic drug catabolism, particularly via isoenzyme 3A4. Grapefruit juice can elevate the bioavailability of psychoactive drugs such as quetiapine, comipramine, carbamazepine, and buspiron three- to fivefold (25). Patients should be informed of this and instructed to avoid grapefruit juice.
Induction of cytochrome P450 enzymes
CYP induction can cause major problems in the pharmacotherapy of the elderly (Table 2).
Carbamazepine and St. John’s wort are both potent inductors of multiple CYP isoenzymes (e.g., 1A2, 2C9, 2C19, 3A4) (26–29). Thus, the concomitant administration of either of these drugs can markedly lower the plasma level of quetiapine through the induction of isoenzyme 3A4 (19, 20).
St. John’s wort is a popular mild antidepressant. If given together with a phenprocoumone, it can counteract the effect of the latter (29) by inducing isoenzyme 3A4, through which it is catabolized. The consequences can include thrombosis, heart attack, and stroke. The inducing effect of St. John’s wort can also be seen when it is given concomitantly with theophylline, cyclosporines, carbamazepine, anti-infectious drugs (e.g., antiretroviral drugs against HIV), tricyclic antidepressants (TCA, e.g., amitriptyline), and oral contraceptives (29, 30).
Carbamazepine potently induces isoenzymes 1A2, 2C9, and 3A4, stimulating the catabolism of certain neuroleptic drugs, coumarins, cyclosporines, anti-infectious drugs, and oral contraceptives (31, 32).
Ginkgo biloba can induce CYP as well. Some preparations (25) accelerate the metabolism via isoenzyme 2C19, leading to a 50–60% drop in the plasma level of, for example, citalopram, escitalopram, TCA, pantoprazole, and omeprazole (30, 33). Ginkgo biloba may also induce isoenzyme 2C9, an important isoenzyme in the catabolism of phenprocoumones and warfarins. Thus, the use of St. John’s Wort, carbamazepine, and ginkgo biloba in elderly patients should be critically reassessed.
Various foods, as well as cigarette smoking, can also lead to enzymatic induction. Smoking, meat grilled over wood charcoal, and broccoli can all induce isoenzyme 1A2, through whose activity olanzapine and clozapine, among other drugs, are catabolized (34).
In a pharmacodynamic interaction, two drugs that exert their effects on a single organ or regulatory circuit interact either directly (by competition) or indirectly (by antagonism or synergism).
Altered pharmacodynamics in old age can promote drug interactions and adverse drug effects. A decline in neuronal density, lower receptor density, reduced transmitter synthesis, and receptor hypersensitivity all need to be taken into account. Clinical consequences can be seen in the dopaminergic, serotonergic, and cholinergic systems, including (respectively) an increased tendency to exhibit extrapyramidal motor symptoms and signs (EPMS); an elevated risk of agitation and sexual dysfunction; and a tendency toward anticholinergic side effects, such as urinary retention, glaucoma, and delirium (35, e7).
The serotonergic syndrome
This syndrome is due to heightened central and peripheral synaptic effects of serotonin, as seen, for example, in patients taking a selective serotonin reuptake inhibitor (SSRI) combined with a monoamine oxidase inhibitor (MAOI). Its main manifestations are fever, neuromuscular manifestations (tremor, hyperreflexia, myoclonus, hyperrigidity), and mental disturbances including disorientation, confusion, agitation, or euphoria, as well as vegetative manifestations (e.g., nausea, vomiting, diarrhea, hyperhidrosis, tachycardia). Combinations of substances working via different pathways to stimulate the secretion of the same active metabolite are problematic. For example, SSRI combined with triptans can induce a serotonergic syndrome (e12).
Drugs that increase the risk of falling
These include antihypertensive drugs, muscle relaxants, benzodiazepines (sedation and diminution of muscle tone), antipsychotic drugs, and antidepressants with an alpha-antagonistic and therefore blood-pressure-lowering effect. Diuretic drugs can also increase the risk of falling by lowering the blood pressure and by disturbing renal function and electrolyte homeostasis (e13). There is evidence that SSRI increase the risk of falling in demented patients in dose-dependent fashion (e14). Caution should be exercised when combining two drugs with similar receptor-binding profiles. Tricyclic antidepressants, such as amitriptyline, and neuroleptic drugs, such as promethazine and quetiapine, can cause a drop in blood pressure if combined with an antihypertensive drug. Benzodiazepines should be used with caution in elderly patients, as they may be depressiogenic, in addition to their other known risks, i.e., sedation, falls, and drug dependence. The uncritical use of benzodiazepines in demented patients can cause organo-affective disturbances (36) that manifest themselves as behavioral abnormalities (37). Benzodiazepines can destroy the normal architecture of sleep and worsen any sleep disorder that the patient may already have.
Drugs with anticholinergic effects and an increased risk of delirium
Drugs that exert anticholinergic effects are problematic, as the elderly are more susceptible to anticholinergic side effects. The drugs listed in the Box as members of this group should not be given to elderly patients if this can be avoided. If these drugs need to be given and rapid cognitive worsening or delirium ensues, they must be discontinued or switched to another drug. A lack of understanding of such events often leads to the non-recognition of adverse drug effects as such, so that they are treated symptomatically with yet more medication.
The simultaneous use of multiple drugs with anticholinergic effects, such as low-potency neuroleptic drugs and eyedrops that contain atropine, should be avoided. Antiparkinsonian drugs and tricyclic antidepressants (anticholinergic effect) or neuroleptic drugs (such as olanzapine or quetiapine) can cause a central anticholinergic syndrome or delirium. Drugs given in internal medicine, such as cortisone, antiemetics (e.g., dimenhydrinate), and calcium antagonists, can also have anticholinergic effects. Urological drugs can as well.
Combinations of drugs that simultaneously affect electrolyte metabolism should be critically reassessed. The combination of an ACE inhibitor with a potassium-sparing diuretic can lead to hyperkalemia and delirium. Serotonergic drugs, such as citalopram, can cause hyponatremia by inducing SIADH (the syndrome of inappropriate antidiuretic hormone secretion: elevated ADH secretion by the pituitary gland leads to fluid retention, with hypervolemia and dilutional hyponatremia), which can present with delirium or a dementia-like syndrome. The simultaneous administration of a diuretic drug (particularly a thiazide diuretic) and a serotonergic drug elevates the risk for hyponatremia as well.
Drugs that can prolong the QTc interval
Drugs that can prolong the QTc interval should be avoided in the elderly and should not be combined. Critical drugs in this category include tricyclic antidepressants and neuroleptic drugs such as haloperidol, ziprasidone, quetiapine, and sulpiride. Caution must also be exercised in combining these drugs with other drugs that prolong the QTc interval, such as amantadine (19, 20, e15) (Table 3).
Drugs that increase the risk of bleeding
Serotonergic drugs increase the risk of bleeding when given in combination with platelet aggregation inhibitors, newer oral anticoagulant drugs (NOAC), or phenprocoumones (e16). Serotonin increases platelet aggregation. SSRI lessen the reuptake of serotonin from the blood into the platelets and thereby leads to a bleeding tendency (e17). Gingko preparations can also increase the risk of bleeding when given in combination with SSRI, platelet aggregation inhibitors, NOAC, or phenprocoumones (e18). Valproic acid in combination with either ASA or an anticoagulant drug increases the risk of bleeding as well (19, 20).
Interactions with lithium
Lithium, a drug with a narrow therapeutic spectrum, plays an important role in modern psychiatric pharmacotherapy, in the elderly just as in younger patients. Nonetheless, its use for phase prophylaxis, mood stabilization, and treatment of suicidality requires a thorough knowledge of its potential drug interactions (eTable 1).
To avoid lithium intoxication, lithium should not be combined with thiazide or loop diuretics, non-steroidal anti-inflammatory agents, ACE inhibitors, or calcium antagonists (19, 20, 38, e19). The treating psychiatrists and somatic physicians must collaborate to ensure that this does not occur.
Interactions with mood-stabilizing drugs
Mood stabilizers can cause drug interactions as well. The simultaneous administration of valproic acid and tricyclic antidepressants raises the seizure threshold (19, 20). The combination of valproic acid with clozapine can alter the plasma levels of both drugs (19, 20). Lamotrigine and valproic acid can elevate each other’s plasma levels, creating a risk of toxic epidermolysis (19, 20).
Interactions with neuroleptic drugs
Neuroleptic drugs can interact with drugs of other types. The combination of clozapine and valproic acid can cause neutropenia (19, 20). Clozapine has a strong anticholinergic effect (19, 20). Risperidone can accentuate the effect of alpha-1 inhibitors such as tamsulosin; if combined with a tricyclic antidepressant or a beta-blocker, it can induce extrapyramidal motor manifestations (19, 20).
Avoidance of drug interactions and polypharmacy
When elderly patients are treated with psychoactive drugs, the physician should choose a drug or drugs that have no anticholinergic side effects, are no more than mildly sedating, carry a low risk of inducing extrapyramidal motor manifestations, do not prolong the QTc interval, have little effect on orthostatic blood pressure, have a broad therapeutic spectrum, are well tolerated by patients with multiple diseases, have little general metabolic activity, and affect electrolyte homeostasis as little as possible.
Tricyclic antidepressants (TCA) should be avoided because of their anticholinergic and cardiotoxic side effects. If a TCA is nonetheless necessary, nortriptyline is to be preferred because of its better side-effect profile (with respect to the QTc interval, orthostasis, sedation, and anticholinergic effects) (e20, e21). Because of their inhibitory effect on CYP, paroxetine, fluoxamine, and fluoxetine should not be used, and ciprofloxacin, erythromycin, and clarithromycin should be critically reassessed. Carbamazepine, ginkgo biloba, and St. John’s wort potently induce multiple isoenzymes and should therefore be avoided. Benzodiazepines are sedating, induce dependence, and have a depressiogenic effect in the elderly; they should be used for carefully chosen indications and only for a short time, if at all.
The indication for any drug given to an elderly patient (e.g., a proton-pump inhibitor or a statin) must first be assessed. If the drug is truly indicated, it should be given at first in the lowest possible initial dose and then gradually titrated upward (“start low, go slow”). Drugs with short half-lives and high bio-availability are to be preferred. They should not be strong CYP inhibitors.
Drugs with a narrow therapeutic spectrum should be avoided. Drugs that can be taken easily are to be preferred, e.g., drugs that are easy to swallow and can be taken once per day. In old age, patients are subject to increasing pharmacokinetic and pharmacodynamic variability. The former can be checked by serial measurement of blood levels of the drug (Figure).
Checklists and instruments
A number of checklists and instruments are available for the avoidance of drug interactions and polypharmacy. The PRISCUS list aids in the choice of drug (8); its main limitation is that the drug assessments and recommended alternatives and monitoring strategies that it comprises are based on expert opinion. The same holds for the FORTA concept (“fit for the aged”) (e22, e23) and the Beers list (39). It has been shown, for example, that low-potency neuroleptic drugs are, in fact, disadvantageous when used by elderly patients because they are sedating, exert anticholinergic effects, and cause orthostatic hypotension (Table 4, eTable 2, eTable 3).
Alongside these checklists, compendia (19) and internet-based tables (“drug interactions Flockhart table”; ) have come into increasing use. They describe the catabolic pathways and CYP-inhibitory and -inductive effects of the psychoactive drugs in current use. The potential side effects and the necessary monitoring are summarized. For patients with renal insufficiency, the internet site dosing.de (e24) is helpful; for those with a prolonged QTc interval, see CredibleMeds (e25).
Interactive platforms, such as www.psiac.de (40) and www.mediq.ch, are also of use (e26). Though not free of charge, they are independent of the pharmaceutical industry. They enable the physician to type in the patient’s drug list and see the potential drug interactions and adverse drug effects that may be associated with it. This enables the minimization of risks associated with polypharmacy, the reassessment of drug indications, and the prevention of prescription of an excessive number of drugs. Interactive platforms are also available for smartphones, such as the independent app called “Arznei-Check,” a product of the Ifap GmbH company (e27). The consistent use of these instruments and aids would help prevent the twin problems of drug interactions and polypharmacy.
Elderly patients are particularly exposed to the risk of polypharmacy. This is generally because of the multimorbidity associated with old age, often combined with physicians’ uncritical, simultaneous application of all of the existing guidelines for each and every one of the patient’s underlying illnesses. The more drugs a patient takes, the greater the risk of drug interactions and undesired side effects. The altered pharmacokinetics and pharmacodynamics of old age elevate this risk as well.
When treating the elderly patient with drugs, it is particularly important for the physician to know the pathway by which each drug is catabolized and any inducing or inhibiting effect it may have on CYP. This holds especially for drugs that are rapidly metabolized and have a low bioavailability, which have a high risk of interacting with other drugs. Numerous aids and instruments are available for clinical practice (eTable 4) that enable practical and reasonable drug monitoring (e.g., by measurement of serum drug levels) and the early detection of risks for possible interactions and undesired side effects, so that these can be effectively avoided. Knowledge of these matters as they relate specifically to elderly patients is necessary, easily acquired, and much simpler to apply in routine clinical practice than one might have expected.
The authors would like to thank Professor Walter Hewer (Christophsbad, Goeppingen) for his helpful comments on the manuscript.
Conflict of interest statement
Prof. Kratz has received payment from the following companies for preparing continuing medical education events; Janssen-Cilag, Lilly, and Novo Nordisk. Prof. Diefenbacher states that he has no conflict of interest.
Manuscript submitted on 18 March 2019, revised version accepted on
19 June 2019.
Translated from the original German by Ethan Taub, M.D.
Prof. Dr. med. Torsten Kratz
Abteilung für Psychiatrie, Psychotherapie und Psychosomatik
Funktionsbereich Gerontopsychiatrie und -psychotherapie
D-10365 Berlin, Germany
Cite this as:
Kratz T, Diefenbacher A: Psychopharmacological treatment in older people—avoiding drug interactions and polypharmacy. Dtsch Arztebl Int 2019; 116: 508–18. DOI: 10.3238/arztebl.2019.0508
|1.||Statistisches Bundesamt: Bevölkerung Deutschlands bis 2060. 2. koordinierte Bevölkerung, Familien, Lebensformen. www.destatis.de/DE/Publikationen/StatistischesJahrbuch/StatistischesJahrbuch.html (last accessed on 06 June 2019).|
|2.||Van der Akker M, Buntinx F, Knottnerus A: Comorbidity or multimorbidity: what’s in a name? A review of the literature. Eur J Gen Pract 1996; 2: 65–70 CrossRef|
|3.||Van der Hooft CS, Dieleman JP, Siemes C, et al.: Adverse drug reaction-related hospitalisations: a population-based cohort study. Pharmacoepidemiol Drug Saf 2008; 17: 365–71 CrossRef MEDLINE|
|4.||Pirmohamed M, James S, Meakin S, et al.: Adverse drug reactions as cause of admission to hospital: prospective analysis of 18 820 patients. BMJ 2004; 329: 15–9 CrossRef CrossRef MEDLINE PubMed Central|
|5.||Leendertse AJ, Egberts AC, Stoker LJ, van den Bemt PM: Frequency of and risk factors for preventable medication-related hospital admis sions in the Netherlands. Arch Intern Med 2008; 168: 1890–6.|
|6.||Stang AS, Wingert AS, Hartling L, Plint AC: Adverse events related to emergency department care: a systematic review. PLoS One 2013; 8: e74214 CrossRef MEDLINE PubMed Central|
|7.||Onder G, Liperoti R, Fialova D, et al.: Polypharmacy in nursing home in Europe: results from the SHELTER study. Gerontol A Biol Sci Med Sci 2012; 67: 698–704 CrossRef MEDLINE|
|8.||Holt S, Schmiedl S, Thürmann PA: Potentially inappropriate medications in the elderly – The PRISCUS List. Dtsch Arztebl Int 2010; 107: 543–51 CrossRef MEDLINE PubMed Central|
|9.||Berdot S, Bertrand M, Dartigues JF, et al.: Inappropriate medication use and risk of falls—a prospective study in a large community-dwelling elderly cohort. BMC Geriatrics 2009; 9: 30 CrossRef MEDLINE PubMed Central|
|10.||Dumbreck S, Flynn A, Nairn M, et al.: Drug-disease and drug-drug interactions: systematic examination of recommendations in 12 UK national clinical guidelines. BMJ 2015; 350: h949 CrossRef MEDLINE PubMed Central|
|11.||Moßhammer D, Haumann H, Mörike K, Joos S: Polypharmacy—an upward trend with unpredictable effects. Dtsch Arztebl Int 2016; 113: 627–33 CrossRef MEDLINE PubMed Central|
|12.||Bertsche T, Pfaff J, Schiller P, et al.: Prevention of adverse drug reactions in intensive care patients by personal intervention based on an electronic clinical decision support system. Intensive Care Med 2010; 36: 665–72 CrossRef MEDLINE|
|13.||Mutschler E, Geisslinger G, Kroemer HK, Menzel S, Ruth P: Arzneimittelwirkungen: Pharmakologie – Klinische Pharmakologie – Toxikologie. 10. Auflage. Stuttgart: Wissenschaftliche Verlagsgesellschaft 2012.|
|14.||Bauer JM, Wirth R, Volker D, Sieber C: Malnutrition, Sarkopenie und Kachexie im Alter – Von der Pathophysiologie zur Therapie. Dtsch Med Wschr 2008; 133: 305–10 CrossRef MEDLINE|
|15.||Müller WE: Sedativa als Beispiel für die Besonderheiten der Psychopharmakotherapie im Alter. In: Förstl H (ed.): Lehrbuch Gerontopsychiatrie. Stuttgart: Thieme Verlag 2002; 220–6.|
|16.||Berthold H, Steinhagen-Thiessen E: Arzneimitteltherapie im Alter – Wo liegen die Probleme? Was soll man tun, was muss man lassen? Internist 2009; 50: 1415–24 CrossRef MEDLINE|
|17.||Jelliffe RW: Creatinine clearance: bedside estimate. Ann Intern Med 1973; 79: 604–5 CrossRef MEDLINE|
|18.||Briciu C, Neag M, Muntean D, et al.: A pharmacokinetic drug interaction study between nebivolol and paroxetine in healthy volunteers. J Clin Pharm Ther 2014; 39: 535–40 CrossRef MEDLINE|
|19.||Benkert O, Hippius H: Kompendium der Psychiatrischen Pharmakotherapie. 12. Auflage. Berlin, Heidelberg: Springer Verlag 2018.|
|20.||Benkert O: Pocket Guide Psychopharmaka von A bis Z. 4th edition. Berlin, Heidelberg: Springer Verlag 2017 CrossRef|
|21.||Poulsen L, Arendt-Nielsen L, Brøsen K, Brøsen K, Sindrup SH: The hypoalgesic effect of tramadol in relation to CYP2D6. Clin Pharmacol Ther 1996; 60: 636–44 CrossRef|
|22.||Petri H: CYP450-Wechselwirkungen: Interaktionen der SSRI-Antidepressiva. Dtsch Arztebl (Suppl. Perspektiven in der Neurologie) 2015; 112: 33–4.|
|23.||Hewer W, Eckermann G: Bedenkliche Arzneimittelkombinationen bei geriatrischen Patienten. Psychopharmakotherapie 2011; 18: 10–17.|
|24.||Flockhart DA, Drici MD, Kerbusch T, et al.: Studies on the mechanism of a fatal clarithromycin-pimozide interaction in a patient with tourette syndrome. J Clin Psychopharmacol 2000; 20: 317–24 CrossRef MEDLINE|
|25.||Etheridge AS, Black SR, Pantel PR, So J, Mathews JM: An in vitro evaluation of cytochrome P450 inhibition and P-glycoprotein interaction with goldseal, ginkgo biloba, grape seed, milk thistle, and ginseng extracts and their constituents. Planta Med 2007; 73: 731–41 CrossRef MEDLINE|
|26.||Petri H: Arzneimitteltherapiesicherheit: Das Interaktionspotenzial konventioneller Zytostatika. Dtsch Arztebl 2017; 114 (Suppl. Perspektiven in der Onkologie): 19–21 VOLLTEXT|
|27.||Ekhart C, Rodenhuis S, Beijnen JH, Huitema AD: Carbamazepine induces bioactivation of cyclophosphamide and thiotepa. Cancer Chemother Pharmacol 2009; 63: 543–7 CrossRefMEDLINE|
|28.||Hu Z, Yang X, Ho PC, Chan SY, et al.: Herb-drug interactions: a literature review. Drugs 2005; 65: 1239–82 CrossRef MEDLINE|
|29.||Wang Z, Gorski JC, Hamman MA, Huang SM, Lesko LJ, Hall SD: The effects of St John´s wort (Hypericum perforatum) on human cytochrome P450 activity. Clin Pharmacol Ther 2001; 70: 317–26 CrossRef|
|30.||Hellum BH, Nilsen OG: In vitro inhibition of CYP3A4 metabolism and P-glycoprotein-mediated transport by trade herbal products. Basic Clin Pharmacol Toxicol 2008; 102: 466–75 CrossRef MEDLINE|
|31.||Lin JH: CYP induction-mediated drug interactions: in vitro assessment and clinical implications. Pharm Res 2006; 23: 1089–116 CrossRef MEDLINE|
|32.||Flockhart DA: Drug interactions: cytochrome P450 drug interaction table. Indiana University School of Medicine 2007. https://drug-interactions.medicine.iu.edu/main-table.aspx (last accessed on 6 June 2019).|
|33.||Unger M: Pharmacokinetic drug interactions involving ginkgo biloba. Drug Metab Rev 2013; 45: 353–85 CrossRef MEDLINE|
|34.||Hakooz N, Hamdan I: Effects of dietary broccoli on human in vivo caffeine metabolism: a pilot study on a group of Jordanian volunteers. Curr Drug Metab 2007; 8: 9–15 CrossRef|
|35.||Lertxundi U, Domingo-Echaburu S, Hernandez R, Peral J, Medrano J: Expertbased drug lists to measure anticholinergic burden: similar names, different results. Psychogeriatrics 2013; 13: 17–24 CrossRef MEDLINE|
|36.||Kratz T: The diagnosis and treatment of behavioral disorders in dementia. Dtsch Arztebl Int 2017; 114: 447–54 CrossRef MEDLINE PubMed Central|
|37.||Kratz T, Heinrich M, Schlauß E, Diefenbacher A: Preventing postoperative delirium – a prospective intervention with psychogeriatric liaison on surgical wards in a general hospital. Dtsch Arztebl Int 2015; 112: 289–96 VOLLTEXT|
|38.||Grandjean EM, Aubry JM: Lithium: updated human knowledge using an evidencebased approach. Part II: clinical pharmacology and therapeutic monitoring. CNS Drugs 2009; 23: 331–49 CrossRef MEDLINE|
|39.||Fick DM, Cooper JW, Wade WE, Waller JL, Maclean JR, Beers MH: Updating the Beers criteria for potentially inappropriate medication use in older adults: results of a US consensus panel of experts. Arch Intern Med 2003; 163: 2716–24 CrossRef MEDLINE|
|40.||Interaktionsplattform PSIAC.de: www.psiac.de (last accessed on 6 June 2019).|
|e1.||Budnitz D, Lovegrove M, Shehab N, Richards CL: Emergency hospitalizations for adverse drug events in older Americans. N Engl J Med 2011; 365: 2002–12 CrossRef MEDLINE|
|e2.||Dubrall D, Schmid M, Alešik E, Paeschke N, Stingl J, Sachs B: Frequent adverse drug reactions, and medication groups under suspicion – a descriptive analysis based on spontaneous reports to the German Federal Institute for Drugs and Medical Devices from 1978–2016. Dtsch Arztebl Int 2018; 115: 393–400 VOLLTEXT|
|e3.||Schurig AM, Böhme M, Just KS, Scholl C, Dormann H, Plank-Kiegele B, et al.: Adverse drug reactions (ADR) and emergencies – the prevalence of suspected ADR in four emergency departments in Germany. Dtsch Arztebl Int 2018; 115: 251–8 VOLLTEXT|
|e4.||Fradet G, Legac X, Charlois T, Ponge T, Cottin S: Iatrogenic drug-induced diseases, requiring hospitalisation, in patients over 65 years of age. 1-year retrospective study in an internal medicine department. Revue de medecine interne 1996; 17: 456–60 CrossRef|
|e5.||Mühlberg W, Sieber C: Häufige unerwünschte Arzneimittelwirkungen (UAW) und Vergiftungen im Alter. Notfall & Hausarztmedizin (Hausarztmedizin) 2005; 31: 276–81 CrossRef CrossRef|
|e6.||Cascorbi I: Drug interactions—principles, examples and clinical consequences. Dtsch Arztebl Int 2012; 109: 546–56 VOLLTEXT|
|e7.||Haen E: Arzneimittelinteraktionen. Interaktionen zwischen körperfremden Substanzen. Nervenarzt 2014; 85: 417–26 CrossRef MEDLINE|
|e8.||König F, Kaschka W: Interaktionen und Wirkmechanismen ausgewählter Psychopharmaka. 2nd revised edition. Stuttgart: Thieme Verlag 2003 CrossRef|
|e9.||Hansen W: Medizin des Alterns und des alten Menschen. Darmstadt: Schattauer Verlag 2007; 96–7.|
|e10.||Kelly CM, Juurlink DN, Gomes T, Duong-Hua M, Pritchard KI, Austin PC, et al.: Selective serotonin reuptake inhibitors and breast cancer mortality in women receiving tamoxifen: a population based cohort study. BMJ 2010; 340: c693 CrossRef MEDLINE PubMed Central|
|e11.||He N, Edeki T: The inhibitory effect of herbal components on CYP2C9 and CYP3A4 catalytic activities in human liver microsomes. Am J Ther 2004; 11: 206–12 CrossRef|
|e12.||Boyer EW, Shannon M: Current concepts: the serotonin syndrome. New Engl J Med 2005; 352: 1112–20 CrossRef MEDLINE|
|e13.||Wehling M, Burkhardt H: Arzneimitteltherapie für Ältere. Heidelberg, Berlin: Springer Verlag 2016; 242–7 CrossRef|
|e14.||Sterke CS, Ziere G, van Beeck EF, Looman CWN, van der Cammen TJM: Dose-response relationship between selective serotonin re-uptake inhibitors and injurious falls: a study in nursing home residents with dementia. Br J Clin Pharmacol 2012; 73: 812–20 CrossRef MEDLINE PubMed Central|
|e15.||Wenzel-Seifert K, Wittmann M, Haen E: QTc prolongation by psychotropic drugs and the risk of torsade de pointes. Dtsch Arztebl Int 2011; 108: 687–93 VOLLTEXT|
|e16.||Voigt N, Ort K, Sossalla S: Arzneimittelinteraktionen, die man kennen muss. Dtsch Med Wochenschr 2019; 144: 264–75 CrossRef MEDLINE|
|e17.||Walraven van C, Mamdam MM, Wells PS, et al.: Inhibition of serotonin reuptake by antidepressants and upper gastrointestinal bleeding in elderly patients: retrospective cohort study. Brit J Med 2001; 323: 655–8 CrossRef MEDLINE PubMed Central|
|e18.||Izzo A, Ernst E: Interactions between herbal medicines and prescribed drugs: a systematic review. Drugs 2001; 61: 2163–75 CrossRef MEDLINE|
|e19.||Müller-Oerlinghausen B: Unerwünschte Wechselwirkungen von Lithiumsalzen mit anderen Arzneimitteln. In: Müller-Oerlinghausen B, Greil W, Berghöfer A (eds): Die Lithiumtherapie. Berlin: Springer Berlin 1997; 446–55 CrossRef|
|e20.||Roose SP, Glassman AH, Giardina EG, Walsh BT, Woodring S, Bigger JT: Tricyclic antidepressants in depressed patients with cardiac conduction disease. Arch Gen Psychiatry 1987; 44: 273–5 CrossRef|
|e21.||Roose SP, Glassman AH, Giardina EG, Johnson LL, Walsh BT, Woodring S, et al.: Nortriptyline in depressed patients with left ventricular impairment. JAMA 1986; 256: 3253–7 CrossRef CrossRef MEDLINE|
|e22.||Wehling M, Burkhardt H, Kuhn-Thiel A, et al.: VALFORTA: a randomised trial to validate the FORTA (Fit fOR The Aged) classification. Age and Ageing 2016; 45: 262–7 CrossRef MEDLINE|
|e23.||Universität Heidelberg Forta-Projekt: www.umm.uni-heidelberg.de/klinische-pharmakologie/forschung/forta-projekt-deutsch/ (last accessed on 6 June 2019).|
|e24.||Universitätsklinikum Heidelberg: DOSING. Informationen zur Arzneimittel-Anwendung & -Sicherheit. Interaktionsplattform: https://dosing.de/ (last accessed on 6 June 2019).|
|e25.||CREDIBLEMEDS® – Interaktionsplattform: https://crediblemeds.org/new-drug-list/ (last accessed on 6 June 2019).|
|e26.||Interaktionsplattform MEDIQ.ch: www.mediq.ch/welcome_public (last accessed on 6 June 2019).|
|e27.||Arzneimittelinteraktionen Android-APP: www.ifap.de/mobile-loesungen/arznei-aktuell-fuer-android/ (last accessed on 6 June 2019).|
|e28.||Schwab M, Marx C, Zanger UM, Eichelbaum M, Fischer-Bosch M: Pharmakogenetik der Zytochrom-P-450-Enzyme. Bedeutung für Wirkungen und Nebenwirkungen von Medikamenten. Dtsch Arztebl 2002; 99: A497–504 VOLLTEXT|
|e29.||Sandson NB: Drug interactions casebook: the cytochrome P450 system and beyond. 1st edition. Washington DC: American Psychiatric Publishing 2003.|
|e30.||Greiner C: Cytochrom-P450-Isoenzyme – Teil 2: Substrate, Induktoren und Inhibitoren. Neurotransmitter 2010; 1: 38–40.|
|e31.||Roe CM, Anderson MJ, Spivack B: Use of anticholinergic medications by older adults with dementia. J Am Geriatr Soc 2002; 50: 836–42 CrossRef MEDLINE|
|e32.||Reinbold H: Psychogenicum. Biochemie der Psychopharmaka, differenzierter Umgang mit Neuroleptika. Dortmund: PsychologenVerlag PGV 2001.|
|e33.||Möller HJ: Aktuelle Bewertung neuer/atypischer Neuroleptika. Nervenarzt 2000; 71: 329–44 CrossRef|
|e34.||Garfinkel D, Mangin D: Feasibility study of a systematic approach for discontinuation of multiple medications in older adults: addressing polypharmacy. Arch Intern Med 2010; 170: 1648–54 CrossRef MEDLINE|
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