WEBVTT

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For our last case, Teresa is going home with a

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changed treatment plan. Teresa is home after a hospitalization for

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worsening heart failure. Her discharge list includes medication changes.

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A cardiology visit is planned, but she does not know

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who will review her next blood test.

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Clinical context. Confirmed heart failure with preserved ejection fraction; left

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ventricular ejection fraction 55 percent; chronic kidney disease and type

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2 diabetes. At the stable follow-up.

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E G F R 42 milliliters per minute per one

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point seven three square meters; potassium 4.7 milliequivalents per liter.

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Current task. Reconcile therapy and assess eligibility and safety before

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adding a mineralocorticoid receptor antagonist.

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Coordination gap. Laboratory date and responsible result reviewer are not

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documented. Reconstruct what is happening at home.

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Ask Teresa to bring the medicines she is actually taking,

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or review them by a reliable remote method.

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Compare the hospital list, the outpatient record, pharmacy information when

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available and her account. Resolve duplicate therapies, stopped medicines that

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remain in the record and prescriptions that were never filled.

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Ask about supplements, salt substitutes and nonprescription agents as part

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of the safety review. Do not interpret a missed dose

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as lack of interest without asking why.

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Cost, transportation, language, vision, manual dexterity and unclear instructions may

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all affect the plan. If the medicine is unaffordable, record

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the barrier and the action needed to address it.

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A plan that depends on a nonexistent supply is not

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an implemented treatment. Review symptoms, volume status, blood pressure and

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the trajectory of kidney function.

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The decision to add treatment must consider stability and the

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existing regimen. This fictional stable follow-up is an opportunity to

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close the monitoring gap; it is not permission to initiate

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therapy in a patient with acute deterioration without reassessment.

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Use the heart-failure label, not a remembered kidney schedule.

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Finerenone’s current US labeling includes adults with heart failure and

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left ventricular ejection fraction of at least 40 percent.

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Baseline potassium and E G F R are required.

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Do not initiate when potassium is above 5.0 milliequivalents per

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liter; initiation below E G F R 25 milliliters per

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minute per one point seven three square meters is not

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recommended. Strong C Y P 3 A 4 inhibitors and

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adrenal insufficiency are contraindications. Review interactions and the entire regimen.

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For the heart failure indication, starting and target doses depend

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on baseline E G F R, with subsequent decisions guided

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by potassium and kidney function.

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At Teresa’s stated baseline E G F R of 42,

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the label’s starting dose is 10 milligrams daily and target

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is 20 milligrams daily, subject to subsequent laboratory results and

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tolerability. Do not replace the heart failure dosing table with

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the chronic kidney disease-with-diabetes table.

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The heart failure label calls for potassium and E G

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F R four weeks after initiation and four weeks after

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dose adjustment, then periodically. Clinical changes may require earlier assessment.

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Use the current label for exact hold, restart and adjustment

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rules. The course does not replace those tables or a

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clinician’s judgment. Here is the decision.

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Teresa’s potassium is 4.7 and E G F R 42.

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After other eligibility and interaction checks, what completes a finerenone

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initiation plan? Pause here if you would like a moment

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to think it through. The best next step in this

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case is: Use the heart failure dosing instructions, arrange four-week

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potassium/E G F R testing, and name the reviewer and

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patient-contact process. The dose, tests, owner and communication process belong

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together. A laboratory order needs an owner.

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'Repeat labs' is not a complete plan.

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Specify the tests, date, location and responsible reviewer.

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The reviewer needs a process for acting on abnormal values

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and contacting Teresa. The team also needs a way to

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detect a test that was not completed; a missing result

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is not a normal result.

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For this case, the plan could read: 'Basic metabolic panel

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at four weeks after initiation, with potassium and E G

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F R review by the prescribing clinician; earlier clinical assessment

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if symptoms or intercurrent illness warrant.

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Nurse care coordinator checks completion and contacts the prescriber for

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missing or abnormal results. Results and instructions communicated to Teresa

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and documented.' The local team must assign real names and

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workable escalation thresholds. Confirm that the testing site is reachable

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and the order can be used there.

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Give Teresa a short written summary of when to go

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and whom to call. With her permission, include a support

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person. If a dose changes, the laboratory date must change

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with it; otherwise the chart can appear complete while the

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relevant monitoring is missed. Record that the result was reviewed

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and the patient informed. Sending a message into a portal

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that Teresa does not use may not complete the loop.

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Ask which contact method works for her and follow the

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organization’s privacy and communication policies.

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Explain benefit and risk in the same conversation.

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Teresa asks, 'Will this medicine keep me out of the

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hospital?' A useful answer respects both evidence and uncertainty: 'In

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a large trial, this treatment reduced the combined rate of

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worsening heart-failure events and cardiovascular death.

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It cannot promise that you will never need hospital care.

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We also need to watch potassium and kidney function.' Use

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the relevant population and endpoint when explaining a result.

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FINEARTS H F included mildly reduced and preserved ejection fraction;

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it counted recurrent worsening-heart failure events as well as cardiovascular

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death. A rate ratio for total events is not an

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individual patient’s chance of avoiding every event.

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The trial’s lack of a significant cardiovascular-death result alone should

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not be hidden. Ask Teresa to explain why the blood

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test matters. If she says it is only to see

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whether the drug is working, clarify the safety purpose.

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Hyperkalemia may not announce itself with a clear symptom.

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Monitoring is part of the treatment, even when she feels

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well. Do not let the routine pathway absorb an emergency.

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Now change the vignette. Teresa calls with new breathlessness at

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rest and chest pressure. This is a different decision from

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arranging the next routine blood test.

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Arrange emergency assessment; in the United States, severe or potentially

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life-threatening symptoms warrant calling 911.

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Do not ask her to wait for the scheduled visit

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or simply repeat an outpatient laboratory test.

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For nonemergency worsening symptoms, the care plan should explain how

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to reach the clinical team and when same-day advice is

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needed. Any individualized weight or symptom action plan should be

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provided by the treating team.

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Do not invent a universal diuretic self-adjustment rule from this

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case. Use teach-back while she is stable: 'If you develop

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chest pressure and cannot catch your breath at rest, what

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will you do?' Then ask whom she contacts for a

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nonemergency concern and when her next test and visit occur.

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Correct the plan in plain language rather than testing whether

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she can repeat clinical terminology.

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Turn a handoff into a completed action.

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A referral, order or discharge document is the start of

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a handoff. A completed handoff identifies the receiving clinician, the

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question to resolve, the current medicines and doses, recent results,

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pending tasks and the next contact.

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If no appointment is available, someone needs to address that

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gap rather than leaving an open-ended instruction to follow up.

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Evidence from STRONG H F supports the value of structured,

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closely monitored care after acute heart failure, but the trial

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was not restricted to heart failure with preserved ejection fraction.

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Its exact titration approach should not be transplanted wholesale to

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every woman with preserved ejection fraction.

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The transferable lesson here is to design follow-up that actively

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checks treatment and safety. For Teresa, the final note should

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make four things easy to find: what changed, what must

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be monitored, who will act and when she will hear

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from the team. At the next contact, confirm the test

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happened, the result was reviewed and the instruction reached her.

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The clinical outcome is not an order in the system;

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it is a patient who knows and can complete the

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next step. Here is the decision.

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The four-week result is missing.

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Which response best closes the care gap?

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Pause here if you would like a moment to think

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it through. The best next step in this case is:

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Check whether testing occurred, resolve access barriers, arrange needed testing

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and ensure clinician review. The team needs to track completion

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as well as interpret results.

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The takeaway: Monitoring and coordination are treatment tasks.

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Pair every medication change with a test date, a responsible

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reviewer, a communication plan and clear symptom escalation.

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Before we move on, let’s apply that reasoning in more

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detail. A safety call that cannot wait for the next

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blood test. Consider a separate development in Teresa’s story: after

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starting an S G L T 2 inhibitor she develops

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vomiting, poor intake, abdominal discomfort and breathlessness.

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Her home glucose is 146 milligrams per deciliter.

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This value does not rule out ketoacidosis associated with S

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G L T 2 treatment.

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Temporarily stop the medicine and arrange urgent clinical assessment for

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ketoacidosis, dehydration and other acute illness.

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Do not use a routine follow-up appointment or reassurance about

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the glucose value as the response.

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For a stable finerenone heart failure candidate with E G

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F R 42 and potassium 4.7, the current label begins

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at 10 milligrams daily, after the remaining eligibility and interaction

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checks. The heart failure target associated with that baseline renal

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category is 20 milligrams daily, if the follow-up potassium, kidney

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function and full dose-adjustment instructions support titration.

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A target is not an instruction to start at the

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target. For baseline E G F R at least 60,

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the heart failure starting and target doses differ again.

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Do not initiate finerenone with potassium above 5.0 milliequivalents per

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liter; initiation below E G F R 25 is not

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recommended. Check contraindications, including strong C Y P 3 A

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4 inhibitors and adrenal insufficiency.

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Use the heart failure-specific table when laboratory values change.

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A newly prescribed interacting medicine, dehydration, falling blood pressure or

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an acute illness can make a previously appropriate plan unsafe

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and may require assessment before the scheduled four-week review.

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Close the visit by asking Teresa to show how she

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will follow the plan: which medicine she is taking, when

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and where testing will occur, who will contact her, and

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which symptoms need immediate help.

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If a laboratory appointment or medication cannot be obtained, make

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the barrier visible to the responsible team.

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The plan is incomplete until it is feasible.

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Before you go, bring the three cases back to one

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question: what will you do differently at the next visit?

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Explain the symptom, use the endpoint the study actually measured,

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and give every monitoring plan an owner.

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You’ll find the source references, transcript and clinical resources beside

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this episode. To record your answers and complete the learning

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activity, return to the activity page for the questions and

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brief evaluation. This has been HEART RESERVE Clinical Conversations.

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I’m Lisa Zahakos. Thank you for listening.
