Polypharmacy

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Polypharmacy is the use of multiple medications by a patient, especially when too many forms of medication are used by a patient, when more drugs are prescribed than is clinically warranted,[1] or even when all prescribed medications are clinically indicated but there are too many pills to take (pill burden). Furthermore, a portion of the treatments may not be evidence-based. The most common results of polypharmacy are increased adverse drug reactions, drug-drug interactions and higher costs.[2] Polypharmacy is most common in the elderly but is also widespread in the general population.[3]

Pill burden

Pill burden is a term that refers to the number of tablets, capsules or other dosage forms that a patient takes on a regular basis.

High pill burden decreases compliance with drug therapy, resulting from the need to take a large quantity of pills or other forms of medication on a regular basis. It also increases the possibility of adverse medication reactions (side effects) and drug-drug interactions. High pill burden has also been associated with an increased risk of hospitalization, medication errors, and increased costs for both the pharmaceuticals themselves and for the treatment of adverse events. Finally, pill burden it is a source of dissatisfaction for many patients.

High pill burden is commonly associated with antiretroviral drug regimens to control HIV, but can be seen in other patient populations. For instance, adults with multiple chronic conditions such as diabetes, hypertension, lymphedema, hypercholesterolemia, osteoporosis, constipation and clinical depression can often be prescribed more than a dozen different medications daily. The adverse reactions of these combinations of drugs are not reliably predictable. Obesity is implicated in many of the aforementioned conditions, and it is not uncommon for a clinically obese patient to receive pharmacologic treatment for all of these. Because chronic conditions tend to accumulate in the elderly, pill burden is a particular issue in geriatrics.

Reducing pill burden is recognized as a way to improve medication compliance. Common approaches for reducing pill burden include selecting fixed dose combination drug products, products with long-acting active ingredients, and sustained release/extended release formulations when appropriate.

Some combinations of drugs may be available in certain strengths as a single pill, called a fixed dose combination. One notable example of a fixed dose combination drug product is the antiretroviral drug product Atripla, which combines 3 drugs (efavirenz + emtricitabine + tenofovir) into one pill.

The selection of long-acting active ingredients over short-acting ones may also reduce pill burden. For instance, ACE inhibitors are used in the management of hypertension. Both captopril and lisinopril are examples of ACE inhibitors. However, lisinopril is dosed once a day, whereas captopril may be dosed 2-3 times a day. Assuming that there are no contraindications or potential for drug interactions, using lisinopril instead of captopril may be an appropriate way to limit pill burden.

Similarly, sustained release/extended release drug formulations reduce pill burden by reducing the dosing frequency. The same active ingredient is present in both the immediate-release form and the sustained release form.

At risk demographic groups

Patients at greatest risk of polypharmacy consequences include the elderly, psychiatric patients, patients taking five or more drugs concurrently, those with multiple physicians and pharmacies, recently hospitalized patients, individuals with concurrent comorbidities,[4] low educational level,[5] and those with impaired vision or dexterity.

Adverse reactions and interactions

Every medication has potential adverse side-effects. With every drug added, there is an additive risk of side-effects.

Many medications have potential interactions with other substances. As a new drug is prescribed, the risk of interactions increases exponentially. Doctors and pharmacists aim to avoid prescribing medications that interact; often, adjustments in the dose of medications need to be made to avoid interactions, such as with warfarin, as it may lose its effect.

Thoughtful versus thoughtless polypharmacy

A patient with a complex or even an ostensibly straightforward illness whose personal pharmacopoeia reads like a drug store pharmacy is not necessarily receiving poor treatment. A carefully followed patient with whom a physician is using additive drug choice and dosage range on a trial and error basis may lead to a treatment program that, for a real example, includes two antidepressants, three antihypertensives, a beta blocker, a calcium channel blocker, a bone saving bisphosphonate, an antiepileptic, a stomach saving H2 blocker, aspirin, prostaglandin blocker, lactoferrin, a calcium-magnesium supplement and herbal preparations.[citation needed]

Two generally true circumstances underlie the theory of thoughtful, therapeutic polypharmacy: (1) Drugs given for a single somatic locale act on biochemical mechanisms present throughout the body such that their nonlinear interactions can produce an (unknown except empirically) global physiological state of health; [6](2) The more independent variables, "handles", to manipulate, the greater the likelihood of finding and stabilizing a small available parametric space of healthy function while minimizing unwanted effects.[7]

The use of multiple pharmaceuticals to treat a single illness is often the result of a healthcare practitioner attempting, usually through trial and error, to obtain the highest efficacy through the concept of drug synergy. Often certain medications can interact with others in a positive way specifically intended when prescribed together to achieve a greater effect that any of the single agents alone. This is particularly prominent in the field of anesthesia and pain management, where atypical agents such as antiepileptics, antidepressants, muscle relaxants, NMDA antagonists, and other medications are combined with more typical analgesics such as opioids, prostaglandin inhibitors, NSAIDS and others. This practice of pain management drug synergy is known as an analgesia sparring effect. In anesthesia, particularly IV anesthesia and General anesthesia, multiple agents are almost always required, including hypnotics or analgesic inducing/maintenance agents such as Versed or Diprivan, usually an opioid analgesic such as morphine or Demerol, a paralytic such as vecuronium, and in inhaled general anesthesia generally a halogenated ether anesthetic such as sevoflurane or desflurane.

Abuse and misuse

It is not uncommon for those dependent or addicted to substances to enter or remain in a state of polypharmacy misuse or abuse. One of the best examples includes those who chronically or acutely binge on amphetamines or other psychostimulants (particularly those with long half lives such as the amphetamines and methylphenidate). Because these agents have the effect of reducing or eliminating sleep for long periods of time, when sleep is finally desired or in an effort to reduce the "crash," hypnotics such as benzodiazepines, sometimes opiates, and less frequently barbiturates are used to induce sleep and/or hypnosis. Another classic example of concurrent polypharmacy abuse is the "speedball," a solution of typically cocaine and heroin in the same syringe which is injected together. Other combinations like amphetamines, methylphenidate and morphine, oxycodone, hydrocodone etc are also used and sometimes taken orally. The classic combination of cocaine and heroin injection has resulted in numerous high profile deaths as the stimulant effect of cocaine (which has a notably short half life) last much shorter than the depressant effects of opiates, which can then induce respiratory depression, respiratory arrest, and death.

Solutions

Zarowitz et al.[8] studied clinical pharmacists performing drug therapy reviews and the teaching of physicians and their patients about drug safety and polypharmacy, as well as collaborating with physicians and patients to correct polypharmacy problems. This led to a marked improvement in interactions and cost. Similar programs are likely to reduce the potentially deleterious consequences of polypharmacy. Such programs hinge upon patients and doctors informing pharmacists of other medications being prescribed, as well as herbal, over-the-counter substances and supplements that occasionally interfere with prescription-only medication.

See also

References

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External links

de:Polypragmasie is:Lyfjaofgjöf it:Politerapia nl:Polyfarmacie

pl:Polipragmazja
  1. Fulton MM, Allen ER. Polypharmacy in the elderly: a literature review. J Am Acad Nurse Pract 2005;17:123-32. PMID 15819637.
  2. Haider SI, Johnell K, Weitoft GR, Thorslund M, Fastbom J (2009). "The influence of educational level on polypharmacy and inappropriate drug use: a register-based study of more than 600,000 older people". Journal of the American Geriatrics Society. 57 (1): 62–69. doi:10.1111/j.1532-5415.2008.02040.x. PMID 19054196. 
  3. Haider SI, Johnell K, Thorslund M, Fastbom J (2007). "Trends in polypharmacy and potential drug-drug interactions across educational groups in elderly patients in Sweden for the period 1992 - 2002". International Journal of Clinical Pharmacology and Therapeutics. 45 (12): 643–653. PMID 18184532. 
  4. Boyd CM, Darer J, Boult C, Fried LP, Boult L, Wu AW (2005). "Clinical practice guidelines and quality of care for older patients with multiple comorbid diseases: implications for pay for performance". JAMA. 294 (6): 716–24. doi:10.1001/jama.294.6.716. PMID 16091574. 
  5. Haider SI, Johnell K, Thorslund M, Fastbom J (2007). "Analysis of the association between polypharmacy and socioeconomic position among elderly aged >/=77 years in Sweden". Clin Ther. 32 (2): 419–27. doi:10.1016/j.clinthera.2008.02.010. PMID 18343279. 
  6. Mandell, A.J. and Selz, K.A. 1992 Dynamical systems in psychiatry: Now what? Biological Psychiatry 32: 299-301.
  7. Callahan, J. and Sashin, J. I. 1987 Models of affect-response and anorexia nervosa. Ann. N.Y. Acad. Sci. 504:241-259.
  8. Zarowitz BJ, Stebelsky LA, Muma BK, Romain TM, Peterson EL. Reduction of high-risk polypharmacy drug combinations in patients in a managed care setting. Pharmacotherapy 2005;25:1636-45. PMID 16232025.