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350
K. A. Swanson et al.
The START (Screening Tool to Alert Doctors to Right Treatment) (see Table3), is a tool to help identify potentially benecial medications that may have been omit­ted from a LTCF resident’s treatment regimen. The START tool is similar to the STOPP criteria in that both have been validated in the elderly, derived from evidence- based prescribing practice, and arranged by physiological systems; but
Table 3 START: Screening Tool to Alert doctors to Right Treatments
These medications should be considered for people ≥65years of age based on other clinical conditions and no contraindication to the recommendation
Cardiovascular conditions
• Initiate anticoagulation to reduce stroke/thrombosis risk in chronic atrial brillation— direct acting anticoagulant (ex. apixaban, others), warfarin, aspirin (when DOAC or warfarin is contraindicated)
• Aspirin or clopidogrel in documented history of atherosclerotic coronary, cerebral, or peripheral vascular disease in patients with sinus rhythm
• Antihypertensive therapy when systolic blood pressure is consistently >160 mmHg
• Lipid lowering therapy (statin) with documented history of coronary, cerebral, or peripheral vascular disease, where the patient’s functional status remains independent for ADLs and life expectancy is greater than 5years
• Initiate or optimize treatment for chronic heart failure according to current guidelines when not contraindicated by current clinical conditions or status [which may include: ACEi indicates angiotensin-converting enzyme inhibitor(ACEi), angiotensin receptor blocker (ARB), angiotensin receptor-neprilysin inhibitor (ARNi), hydralazine, isosorbide dinitrate, mineralocorticoid receptor antagonist (MRA), sodium-glucose cotransporter 2 inhibitor (SGLT2i), or diuretics]
• Initiate or optimize treatment according to current guidelines for acute myocardial infarction (e.g., ACEi) or chronic stable angina (e.g., beta-blocker)
Respiratory system
• Initiate or optimize treatment for moderate to severe symptoms of COPD and/or frequent emergency room visits or hospitalization (which may include: inhaled beta2 agonist, anticholinergics, inhaled corticosteroids, others)
• Initiate or optimize treatment for moderate to severe symptoms of asthma (which may include: inhaled corticosteroids, inhaled beta2 agonist, others)
• Initiate or optimize oxygen therapy for documented chronic respiratory failure
Central nervous system
• Initiate or optimize treatment for Parkinson’s disease with functional impairment and disability (which may include: -DOPA, COMT inhibitors, MAO-B inhibitors, dopamine receptor agonists, others)
• Initiate or optimize treatment for moderate to severe depressive symptoms with or without anxiety [which may include: selective serotonin reuptake inhibitors (SSRIs), serotonin and norepinephrine reuptake inhibitors (SNRIs), norepinephrine and dopamine reuptake inhibitors (NDRIs), mixed serotonin effect agents, serotonin and α2-adrenergic antagonists, others]
• Initiate or optimize treatment for cognitive impairment/dementia in individuals where the patient’s functional status remains independent for ADLs and life expectancy is greater than 5years and treatment is appropriate according to the individual’s goals of care [which may include: acetylcholinesterase inhibitor (AChI) or n-methyl--aspartate antagonists (NMDA)]
Medication Management inLong-Term Care
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Table 3
(continued)
Gastrointestinal system
• Initiate or optimize treatment for moderate to severe gastroesophageal reux disease (GERD) especially with history of erosive esophagitis and/or strictures [which may include: daily doses of proton pump inhibitor (PPI) or high dose histamine-2 receptor antagonist (H2RA)]
• Initiate or optimize treatment for prevention of peptic ulcers due to nonsteroidal anti­inammatory drugs (NSAIDs) when use is absolutely necessary strictures [which may include: daily doses of proton pump inhibitor (PPI) or high dose histamine-2 receptor antagonist (H2RA)]
• Initiate or optimize ber supplementation for chronic, symptomatic diverticular disease with constipation
Musculoskeletal system
• Initiate or optimize treatment for active moderate to severe rheumatoid arthritis strictures [which may include: disease-modifying anti-rheumatic drugs (DMARDs), immune modulating agents such as monoclonal antibodies against TNF-α, leukocyte adhesion and migration inhibitors, interleukin inhibitors, JAK inhibitors, others]
• Initiate or optimize treatment for osteoporosis or individuals requiring maintenance corticosteroids (therapy may include: bisphosphonates, calcium, and vitamin D, others)
Endocrine system
• Initiate or optimize treatment for diabetes and or metabolic syndrome (therapy may include: metformin, others)
• Initiate or optimize therapy to reduce risk of nephropathy associated with diabetes (therapy may include ACEI or ARB)
• Initiate or optimize therapy to reduce major cardiovascular risk in individuals with diabetes [therapy may include: antiplatelet agents, lipid-lowering agents (e.g., statins), others]
(Adapted from Ref. [16])
351
unlike STOPP, START identies possible prescribing omissions in older adults as opposed to medication overuse by STOPP.These tools can enable practitioners to better evaluate an older person’s “prescription” drug regimen in the context of cur­rent clinical diagnoses [16].
Issues inMedication Management
Anticholinergic Burden
Medications that block cholinergic neurons are considered potentially harmful in older individual due to adverse effects that include dry mouth, constipation, uri­nary retention, precipitation of glaucoma, and altered mental status or cognition. Highly anticholinergic medications have also been associated with increased risk of hospitalization and mortality, dementia, and pneumonia. Several tools have been developed to determine the cumulative risk for anticholinergic effects, such as the Anticholinergic Cognitive Burden List (ACB), the Anticholinergic Drug Scale
352
K. A. Swanson et al.
(ADS), and the Anticholinergic Risk Scale (ARS). These tools categorize medica­tions as Highly Anticholinergic (Score = 3), Moderately Anticholinergic (Score=2), and Mildly Anticholinergic (Score=1). The use of multiple drugs with anticholinergic activity will result in a cumulative anticholinergic burden that in turn increase the risk of delirium, worsening dementia, hospitalization, and mortal­ity [21–23].
“Deprescribing” andGradual Dose Reduction (GDR)
Known as deprescribing, many initiatives have been undertaken to identify the risks and benets to reducing medication burden via systematic evaluation and dis­continuation of potentially unnecessary medication. Prescribers are often hesitant to deprescribe due to concerns that this may cause patient decompensation in clinical and functional status. Cautious and gradual discontinuation of medication through a process termed by CMS as Gradual Dose Reduction (GDR), often causes little if any detrimental effects in older and/or frail adults [24]. In 2021, AMDA-The Society for Post-Acute Care and Long-Term Care Medicine launched an initiative titled “Drive to Deprescribe” (D2D). This program addresses the issue of polypharmacy and inappropriate medication use in post-acute and long-term care (PALTC) with the goal to reduce (unnecessary) medication use by 25% [24]. Federal nursing facil­ity regulation require that gradual dose reductions (GDR) be attempted at least quar­terly for all sedative/hypnotics and psychotropics that are prescribed on a scheduled basis and continued beyond the manufacturer’s recommended duration of use. Current practice extends GDR to all medication. Any medication should be deter­mined as whether necessary in order to lessen the risk of a potentially harmful outcome.
However, a consultant pharmacist’s recommendation for a GDR can be declined on clinical grounds if
1. Continued use of the medication is in accordance with the current standard of practice and a GDR would likely impair the patient’s function or cause psychiat­ric or instability by either exacerbating an underlying medical condition or psy­chiatric disorder.
or
2. Patient’s target symptoms for which the medication had been prescribed either returned or worsened after the most recent GDR, and further GDR attempts would likely impair the patient’s function or psychiatric stability.
Practitioners should note that current State Operations Manual (SOM) guidelines to surveyors state that medication should be prescribed only when necessary and in the lowest effective dose and that each resident’s drug regimen be free from
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353
unnecessary drugs (F-Tag 757). Once symptoms have resolved or stabilized, these guidelines recommend that attempts be made to either discontinue the medication or reduce the dose through GDR.Previous efforts to reduce unnecessary medication focused solely on antipsychotics, benzodiazepines, and centrally acting drugs. The current guidelines encourage GDR be attempted for all medications unless the patient’s current condition would be adversely affected. Refer to Appendix A for more detailed information on what denes an unnecessary medication and the intent of the federal regulation.
Transitions inCare andMedication Errors
Transitions in care portend signicant risk for patients with changes inlocation, level of care, and/or providers. Such transitions can result in unrecognized medica- tion errors and adverse patient outcomes. Medication-related adverse events are common after discharge from the hospital [25]. For this reason, one of the National Patient Safety goals of the Joint Commission on Accreditation of Hospital Organizations (JCAHO) continues to be medication reconciliation and the trans­mission of accurate up-to-date medication information between care settings.
Risk factors for medication-related adverse events during a care transition include:
• Polypharmacy (>4 medications)
• Inadequate monitoring of high-risk medications such as insulin, warfarin
• Chronic complex illness: stroke, cancer, diabetes, COPD, heart disease
• Hurried transfers during nonstandard times of day/night/weekend
• Inadequate patient support post-discharge from one care setting to another
Hand-off communication must include comprehensive and up-to-date records to accompany the patient through any care transition and ensure a timely evaluation of the patient upon admission to their new residence. This can help alleviate medica­tion errors, diagnose new problems, and prevent the occurrence of deteriorating conditions. Use of a universally accessible electronic health care records (EHR) across all care settings is essential to meet this goal [26].
Use ofPsychoactive Medication
Older adults are especially vulnerable to adverse effects from psychoactive medica­tion especially the atypical antipsychotics that can cause delirium, extrapyramidal symptoms, postural hypotension, falls (with/without fractures), and cardiac
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K. A. Swanson et al.
arrhythmias. Although these medications have been used off-label to manage behav­ioral and psychological symptoms of dementia (BPSD), safety concerns have been raised and well documented [17, 27]. Other adverse outcomes include hospitaliza­tion [28] and acute kidney injury [18].
In 2014, the American Geriatrics Society (AGS) recommended Choosing
Wisely® guidelines that staff and physicians should initiate non-pharmacologic
strategies as rst-line treatment for aggression and disruptive behaviors associated with dementia. Identifying and addressing the underlying cause of the behavior (the antecedent) may preclude the use of psychoactive medication. If these approaches fail and the clinician decides that there is a need to prescribe an anti­psychotic medication, patients and their families should be informed on the drug’s potential adverse effects. Many facilities now require the family to sign informed consent prior to their use. Proactive monitoring of blood pressure, as well as serum lipid, glucose, and creatinine levels should be part of the treatment plan for any patient prescribed an antipsychotic medication. Additionally, recent meta-analysis studies have shown (though of low quality) that antipsychotics may be successfully discontinued in older adults with dementia and other neuropsychiatric symptoms who have been on antipsychotics for 3months. The discontinuation of these medi­cations had little or no rebound effect on behavioral and psychological symp­toms [29].
Overprescribing ofAntibiotics
The over-prescribing of antibiotics continues to be a concern in the older aged population, specically those who reside in a nursing home setting. Antibiotic stewardship is an integral component of quality assurance and performance improvement in LTCFs. Antibiotic overuse has been linked to multiple risks includ­ing antibiotic drug–drug interactions, colonization with multiresistant organisms, and creation of “super-bugs” in which no antibiotic will be effective. Preventive use of antibiotics is an ongoing concern in long-term care facilities [30]. Research questions the evidence for prescribing antibiotics to prevent recurrent urinary tract infections, to treating acute bronchitis (often viral) to prevent bacterial pneumonia, to treat acute sinusitis to prevent bacterial superinfection, to ongoing antibiotic treatment in persons with COPD to prevent exacerbations or hospitalizations, to prevent soft tissue skin infections in a patient with frequent cellulitis (often over­diagnosed), and for treatment at the time of dental procedures to prevent endocar­ditis in patients with heart disease or to prevent joint infection in those patients with articial joints.
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Overprescribing ofProton Pump Inhibitors
Proton pump inhibitors (PPIs) are gastric acid suppressive medications that are used to treat gastrointestinal disorders such as Gastroesophageal Reux Disease (GERD) and Peptic Ulcer Disease (PUD). Since their approval for use in the United States over 30years ago, they have expanded to worldwide use, are deemed low risk medi­cations in most countries, and often obtained without a prescription. However more recent studies regarding PPIs have reported adverse effects when prescribed long term. PPIs have been linked to an increased risk of Clostridium difcile infection, increased infection risk in cirrhotic patients, acute interstitial nephritis, prevention of clopidegrol conversion to its active metabolite, increased risk of hip fracture, increased risk of chronic kidney disease, increased risk of community acquired pneumonia, decreased iron, B12, and magnesium absorption leading to decien­cies, and rebound gastric acid hypersecretion after discontinuation of use.
Given these multiple risk factors, cautious prescribing and regular monitoring of PPI use is essential in older adults who may be at higher risk of those adverse reac­tions mentioned above. Deprescribing should be considered and entails decreasing dosage, switching to as needed use, or stopping altogether and starting a different medication for symptom management. Histamine 2 receptor blockers are an appro­priate alternative, and have been associated with less C difcile, and fracture risk [31, 32]. Patients should be educated on non-pharmacologic lifestyle modications to reduce the need for acid suppressive therapy. These include weight loss, elevated head of bed, limiting bedtime meals, and avoiding high-fat greasy meals.
Selection ofDiabetic Medication
Several studies have suggested that older adults with diabetes and high comorbidity have diminished cardiovascular benet from intensive blood glucose control (Hgb A1C less than 6.5–7%), and an increased risk for hypoglycemia. These patients would benet more from improved control of other risk factors including serum lipids, dietary consumption of sodium, and blood pressure [33, 34]. Current treat­ment options for diabetes have increased with multiple medications now available. Each has its own mode of action and risk. Renal status should always be considered when prescribing. Some of these medications have been shown to have cardiovas­cular benets as well. Table4 provides a summary of these medications as to route of administration, risk of hypoglycemia, weight loss or gain, cardiovascular effect, renal effect, and side effect risk and contraindications [35]. For more detailed infor­mation on the management of diabetes in PALTC refer to the chapter on “Common Clinical Conditions in Long-Term Care.”
356
• Potential for B12 deciency
• Lactic acidosis
• Fluid retention/edema-CHF
• Benet in NASH
• Risk of bone fracture
• Bladder cancer (Pioglitazone)
• ↑ LDL (Rosiglitazone)
Not recommender in renal
impairment—can cause uid
retention
population
(Liraglutide, Exenatide,
• Glipizide preferred in older
impaired
Caution if GFR <30 • Risk of thyroid C cell tumors
Dulaglutide, Albiglutide)
emptying → n/v, diarrhea)—care
in elderly/frail/malnourished
• GI side effects (delayed gastric
• Injection site reactions
• ↑ Risk of pancreatitis
• Risk of amputation
• (Canagiozin)
Cangiozin (Cl in GFR <45)
Dapigaozin [caution in GFR
K. A. Swanson et al.
2 DM)
hypotension
• DKA risk (all agents, rare in type
• GU infection (bacterial/fungal)
• Risk of volume depletion/
• ↑ LDL
<60, Cl GFR <30
Empagiozin (Cl GFR <30)]
(Black cox warning:
Rosiglitazone and
Pioglitazone)
Common diabetic medications in older patients
Class/drug Route Hypoglycemia Weight CV effect Renal effect Contraindications/side effects
Table 4 Commonly used diabetic medication in older adults
Metformin Oral NO Loss Potential benet Contraindicated if GFP <30 • GI side common
Thiazolidinediones Oral NO Gain Increased risk of CHF
Sulfonylurea Oral YES Gain Neutral Avoid glyburide in renal
semaglutide)
GLP 1 analogs Subq NO Loss Benet (Liraglutide and
Empagiozin)
SGLT-2 inhibitors Oral NO Loss Benet (Canagiozin,
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• Risk of pancreatitis
• Joint pain
• Well tolerated in elderly
• Injection site reactions
• Hypoglycemia
Dose adjustment required if
renal impaired
impaired
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Alogliptin)
Common diabetic medications in older patients
Class/drug Route Hypoglycemia Weight CV effect Renal effect Contraindications/side effects
DPP-4 inhibitors Oral NO Neutral CHF risk (Saxogliptin,
Insulin Subq YES Gain Neutral Lower doses for renal
Adapted from: https://professional.diabetes.org/sites/professional.diabetes.org/les/media/mendez_how_to_use_the_type_2_diabetes_treatment_algo-
rithm.pdf
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K. A. Swanson et al.
Choice andUse ofAnalgesics
Guidelines published by the American Geriatric Society (AGS ) caution against the use of nonselective NSAIDs (especially those with a long half-life such as naproxen and piroxicam) and COX-2 selective inhibitors due to their potential cardiac (uid and sodium retention), gastrointestinal (inammation, bleeding), CNS (altered mental sta­tus, psychosis), and renal effects (altered blood ow) [36]. Both these classes of medica­tion have signicant drug interactions with ACE inhibitors (potential for hyperkalemia), diuretics (diminished diuresis due to changes in renal blood ow), methotrexate (decreased clearance), anticoagulants (potentiated effects), and lithium (decreased renal clearance and increase risk of lithium toxicity). Additionally, there is concern that con­comitant use of a NSAID (especially ibuprofen) or a COX-2 inhibitor with a once daily cardio-preventive dose of aspirin will negate aspirin’s cardio-preventive effect [37].
An FDA Advisory Panel has recommended sweeping safety restrictions on the use of acetaminophen alone and in combination with opioids such as hydrocodone/ acetaminophen and oxycodone/acetaminophen due to reports of increased cases of liver damage and acute liver failure associated with acetaminophen overuse. This risk increases with current and chronic use of alcohol. The panel advised that com­bination opioid/acetaminophen analgesics increase the possibility of accidental overdose and acute liver failure, especially when taken with over-the-counter for­mulations of acetaminophen. The panel also recommended that the maximal amount per unit dose of acetaminophen be a lowered to 325 mg tablet in lieu of the current 500 and 650mg tablets currently available over the counter. And that the maximum daily dosage for osteoarthritis be less than 4 g per day [38], i.e., 2–3 g per day. Useful medication guidelines for many drugs can be downloaded from the FDA website. These guidelines provide specic information for patients and caregivers and may help prevent ADEs [39]. Current national initiatives focus on reducing the overuse of opioid analgesics due to the risk of accidental overdose and death. The diversion of controlled substances continues to be major concern. This can also occur in LTC facilities! Every patient visit should include a review of current anal­gesic utilization (both scheduled and as needed) with a goal to discontinue any unused, unnecessary, or ineffective drugs.
Medication Treatment Goals forHypertension
The elderly are at high risk for cardiovascular events, thus blood pressure should be monitored and hypertension treated. Recommendations from the Joint National Commission 8 (JNC-8) published in 2014 set BP goals for persons over the age of 60years at <150/90. This goal has been controversial as many clinicians advocate a lower blood pressure goal of 140/90in persons under the age of 80 and a higher goal of 150/90 for those over the age of 80. There also has been a change in the recom­mended BP goals for patients with chronic kidney disease (CKD) and diabetes from <130/80 to <140/90. The Joint National Commission also recommended that clini­cians investigate for secondary causes/contributors to hypertension (see Table 5),
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Table 5 Secondary causes of hypertension
Cause How to identify
Medication Medication reconciliation: check for nonsteroidal anti-inammatory (NSAIDS),
steroids, venlafaxine, estrogen-containing preparations (found in herbals,
over-the-counter meds) Alcohol abuse AUDIT-C Obstructive SAEpworth sleepiness scale, sleep study, snoring history
Lifestyle High sodium diet, increased body mass index (BMI), lack of exercise Primary renal Basic metabolic prole (BMP), urine sediment, urine for microalbumin/
creatinine Renovascular Clinical atherosclerosis: PVD, CAD, CVD
Acute onset/exacerbation of hypertension; +abdominal bruit, deterioration of
renal function after angiotensin-converting enzyme inhibitor (ACEI) or
angiotensin receptor blocker (ARB) Aldosteronism Electrolytes (low potassium)
Adapted from reference [40]
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assess for end organ damage, and better monitor for side effects of antihypertensive medication (including postural hypotension) [40].
Newer recommendations from ACC/AHA in 2017 call for stricter control of blood pressure [41]. These recommendations dene elderly as individuals >65years of age and recommend starting pharmacotherapy with BPs >130/80. It is important to note that the American College of Physicians (ACP) and the American Academy of Family Physicians (AAFP) did not support the ACC/AHA recommendations and continue to recommend the original JNC-8 guidelines with BP goals for individuals over 60years of age at <150/90. Additionally, in 2018 the European Society of Cardiology (ECS) and European Society of Hypertension (ESH) stratied patients further to a “very old” category, dening those 80 years of age. In these patients, they recommended starting pharmacotherapy at BPs >160/90. A lower BP target of 130–139/70–79 could be considered in those over 65years old, but not the very old (>85).
Although the ACC/AHA and the ECS/ESH guidelines differ in denitions and thresholds, both agree that treatment of high blood pressure in the elderly is pivotal to reduce atherosclerotic cardiovascular risk, and recommend caution and close monitoring.
If clinically appropriate, it is particularly important in geriatric patients to opti­mize antihypertensive therapy with lifestyle modications, including the implemen­tation of the Dietary Approaches to Stop Hypertension (DASH) diet with a sodium restriction of 1500 mg/day (4 g or two-thirds of a teaspoon of table salt) [42].
Restrictive diets are not recommended in the frail elderly because of the potential to cause weight loss. If, however, dietary intervention is insufcient to control blood
pressure, a low-dose thiazide diuretic and long-acting calcium channel blocker can be prescribed unless comorbidities merit the choice of other drugs. See chapter: “Common Clinical Conditions in Long-Term Care” for further discussion on the treatment of hypertension.