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CMS Manual System - Louisiana Department of Health and Hospitals

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with recommendations from relevant clinical practice guidelines, current<br />

st<strong>and</strong>ards <strong>of</strong> practice, <strong>and</strong>/or manufacturer‘s specifications.<br />

Defining the methods for communicating, analyzing, <strong>and</strong> acting upon<br />

relevant information. The monitoring process needs to identify who is to<br />

communicate with the prescriber, what information is to be conveyed, <strong>and</strong> when<br />

to ask the prescriber to evaluate <strong>and</strong> consider modifying the medication regimen.<br />

It is important to consider whether a resident‘s medications are promoting or<br />

maintaining a resident‘s highest practicable level <strong>of</strong> function. If the therapeutic<br />

goals are not being met or the resident is experiencing adverse consequences, it is<br />

essential for the prescriber in collaboration with facility staff <strong>and</strong> pharmacist to<br />

consider whether current medications <strong>and</strong> doses continue to be appropriate or<br />

should be reduced, changed, or discontinued.<br />

Re-evaluating <strong>and</strong> updating monitoring approaches. Modification <strong>of</strong><br />

monitoring may be necessary when the resident experiences changes, such as:<br />

o Acute onset <strong>of</strong> signs or symptoms or worsening <strong>of</strong> chronic disease;<br />

o Decline in function or cognition;<br />

o Addition or discontinuation <strong>of</strong> medications <strong>and</strong>/or non-pharmacological<br />

interventions;<br />

o Addition or discontinuation <strong>of</strong> care <strong>and</strong> services such as enteral feedings;<br />

<strong>and</strong><br />

o Significant changes in diet that may affect medication absorption or<br />

effectiveness or increase adverse consequences.<br />

Additional examples <strong>of</strong> circumstances that may indicate a need to modify the<br />

monitoring include: changes in manufacturer‘s specifications, FDA warnings,<br />

pertinent clinical practice guidelines, or other literature about how <strong>and</strong> what to<br />

monitor.<br />

III. Dose (Including Duplicate Therapy)<br />

A prescriber orders medication(s) based on a variety <strong>of</strong> factors including the resident‘s<br />

diagnoses, signs <strong>and</strong> symptoms, current condition, age, coexisting medication regimen,<br />

review <strong>of</strong> lab <strong>and</strong> other test results, input from the interdisciplinary team about the<br />

resident, the type <strong>of</strong> medication(s), <strong>and</strong> therapeutic goals being considered or used.<br />

Factors influencing the appropriateness <strong>of</strong> any dose include the resident‘s clinical<br />

response, possible adverse consequences, <strong>and</strong> other resident <strong>and</strong> medication-related<br />

variables. Often, lab test results such as serum medication concentrations are only a<br />

rough guide to dosing. Significant adverse consequences can occur even when the<br />

concentration is within the therapeutic range. Serum concentrations alone may not

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