WEBVTT

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A pregnancy complication can disappear from the chart long before it stops

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being relevant to prevention. What changes when we ask about it?

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Welcome to HEART RESERVE Clinical Conversations.

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I’m Lisa Zahakos, a physician assistant and founder of HEART RESERVE.

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In this episode, we’ll follow Nina after delivery, Maria at a preventive

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visit, and Elena after a heart attack.

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These are fictional teaching cases for clinicians.

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You can listen straight through, or use the chapters to return to

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a case. I’ll ask you to consider a few decisions and then

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walk through the reasoning. The activity page has the objectives, references and

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online questions. Let’s start with Nina.

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A postpartum handoff that needs an owner.

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Nina is 34 and eight weeks postpartum.

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Her pregnancy was complicated by preeclampsia and gestational diabetes.

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She delivered at 34 weeks and is spending much of her time

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at the neonatal intensive care unit.

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An early blood-pressure check occurred, but the obstetric and primary care records

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do not show who owns her long-term follow-up.

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She is breastfeeding, has no acute symptoms, and has not completed postpartum

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glucose testing. Ask before adding another task.

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Nina says, “I thought the blood pressure problem ended when I delivered.”

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Ask what she was told, what testing has already happened, and what

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makes the next appointment difficult. Obtain the discharge summary, recorded blood pressures,

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pregnancy diagnoses, medicines and available laboratory results.

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Record the year and gestational age of the affected pregnancy and distinguish

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a confirmed diagnosis from the patient’s recollection.

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A history of an adverse pregnancy outcome is a reason to assess

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present risk and maintain preventive care.

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It does not establish that Nina has coronary disease.

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Blood pressure, glycemia, lipid assessment, kidney status when indicated, tobacco exposure, physical

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activity, food access and sleep each contribute information.

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The 2026 American College of Cardiology postpartum pathway emphasizes coordinated follow-up for

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patients with or at risk for cardiovascular complications.

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Here is the decision. Which plan best addresses the immediate care gap?

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Pause here if you would like a moment to think it through.

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The best next step in this case is: Arrange the postpartum glucose

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test, a feasible appointment and a named clinician to review and act

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on the result. The recommended plan completes both the clinical task and

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the handoff. The alternative leaves the scheduling and responsibility gaps unresolved.

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The alternative delays an indicated postpartum glucose assessment.

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Ask what makes the visit difficult before finalizing the appointment.

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Separate the urgent problem from the prevention visit.

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Start with symptoms and the current blood pressure, not the list of

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incomplete screening tasks. Nina has no acute symptoms in the opening vignette.

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A later telephone call is a new clinical situation and requires a

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new urgency decision. Do not carry the reassurance from the first visit

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into the second encounter. A useful history asks what happened, when it

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happened, how severe it was, and what remains unresolved.

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“Preeclampsia; delivery at 34 weeks; discharge summary requested” gives another clinician more

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information than “pregnancy problem.” Record patient-reported information as such while obtaining records.

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Avoid making the patient repeat her story to every service.

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Time the right test. American Diabetes Association recommends a fasting 75 gram

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oral glucose tolerance test at 4 to 12 weeks after gestational diabetes,

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interpreted with nonpregnancy criteria. In this early period, an A one C

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does not replace the recommended oral glucose tolerance test.

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Even a normal result does not end follow-up: ongoing screening for prediabetes

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or type 2 diabetes is recommended every 1 to 3 years.

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Put the plan into the record.

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The practice can arrange testing next week.

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Nina prefers a phone call after 3 PM.

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The primary care physician assistant accepts responsibility for reviewing the result and

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contacting her. In this worked example, the team checks for a result

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within two working days of the planned test and calls if the

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test was missed. These operational deadlines are examples, not guideline intervals.

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Here is the decision. Before the test, Nina calls with new chest

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pain and difficulty breathing. What should the team do?

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Pause here if you would like a moment to think it through.

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The best next step in this case is: Arrange emergency assessment now

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and communicate her recent pregnancy and complications.

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New postpartum chest pain and breathing difficulty warrant emergency assessment.

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An office appointment or home measurements must not delay that evaluation.

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Do not diagnose anxiety from this telephone description.

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Teach the earlier postpartum window. American College of Obstetricians and Gynecologists recommends

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blood-pressure evaluation no later than 7 to 10 days postpartum after a

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hypertensive disorder of pregnancy. The 2026 American College of Cardiology pathway specifies

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evaluation within 72 hours after discharge for patients with severe hypertension during

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the delivery hospitalization. Current severe blood pressure or concerning symptoms require urgent

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assessment, not a wait for that appointment.

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Nina’s eight-week visit continues the earlier surveillance.

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A note another clinician can use.

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“Preeclampsia and gestational diabetes in 2026, delivery at 34 weeks.

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Current symptoms reviewed. Early blood pressure follow-up verified.

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Postpartum oral glucose tolerance test arranged for the agreed date.

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the named clinician or team will review the result and contact the

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patient by the agreed date; if missed, the designated team member will

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call using the agreed contact method.

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Cardiovascular and metabolic follow-up booked for the agreed date.” Add the actual

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blood pressure, medication reconciliation, renal findings when relevant and the patient’s next

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pregnancy plans. Confirm receipt of a referral rather than treating a sent

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referral as a completed visit. Make a missed step visible.

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An order, a completed test and an acted-on result are different events.

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In this illustrative workflow, the team records each separately.

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If the test is missed, ask what made it difficult and agree

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on a feasible next step. If the result is abnormal, the responsible

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clinician interprets it and arranges appropriate care; a reminder alone does not

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complete that task. Use teach-back to check your explanation: “I want to

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be sure I explained this clearly.

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What is the next step, and who will contact you?” Ask how

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the patient wants to be reached.

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Coordinate appointments around infant care when possible.

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These workflow choices are practice examples, not prescribed guideline intervals.

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Patient explanation. “What happened in pregnancy is useful information for your health

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now. It gives us a reason to keep checking blood pressure and

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blood sugar and to review other heart risks.

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We can make a plan that works around the neonatal intensive care

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unit. I will tell you who is checking each result.” The takeaway

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from this case: Start with current symptoms and urgency.

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Complete indicated postpartum testing. Name who reviews the result and who contacts

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the patient. Now let’s move forward to Maria’s preventive visit.

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A pregnancy history missing from midlife prevention.

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Maria is 46 and attends a preventive visit.

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She has no known atherosclerotic cardiovascular disease or diabetes and no current

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symptoms. L D L cholesterol is 158 milligrams per deciliter, H D

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L cholesterol 49 milligrams per deciliter and triglycerides 145 milligrams per deciliter.

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She reports treated hypertension and a father who had a myocardial infarction

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at 49. She does not smoke.

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When asked directly, she describes severe preeclampsia with a delivery at 31

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weeks. Her chart does not contain this history.

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She is not pregnant or breastfeeding and has no current pregnancy plans.

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Here is the decision. How should the clinician use the newly elicited

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pregnancy history? Pause here if you would like a moment to think

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

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history, complete the current assessment and discuss the full set of risk

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information. Pregnancy history informs the assessment alongside current risk factors.

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The alternative omits relevant clinical context; The alternative invents an unvalidated adjustment.

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Obtain the missing inputs before using PREVENT atherosclerotic cardiovascular disease and do

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not assign a score from this abbreviated case.

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What is missing before the risk calculation.

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Maria belongs in a primary-prevention assessment because no atherosclerotic cardiovascular disease event

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is reported. The abbreviated vignette does not supply a complete current blood

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pressure, total cholesterol, body mass index or kidney assessment, and her medication

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record needs confirmation. Obtain the inputs required by the current validated calculator

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rather than substituting estimates. The PREVENT result is one part of a

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discussion that also considers reproductive risk markers and family history.

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Keep the tasks distinct: record the pregnancy history, measure current risks, interpret

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the calculated estimate, then discuss treatment.

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Do not add an arbitrary percentage for preeclampsia or substitute the lipoprotein

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a concentration for a risk score.

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A low short-term estimate is also not permission to erase an important

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history from the record. Use additional tests for a decision.

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The 2026 dyslipidemia guideline recommends lipoprotein a measurement at least once in

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adulthood and selective apolipoprotein B assessment.

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lipoprotein a can reveal inherited risk not evident from a standard lipid

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panel. apolipoprotein B may help when cholesterol concentrations and atherogenic particle burden

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are discordant, including selected patients with metabolic disease or high triglycerides.

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A test is useful when its result changes the risk discussion or

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management. Maria’s lipoprotein a returns at 165 nanomoles per liter.

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Record the laboratory units exactly. Avoid a fixed conversion between nanomoles per

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liter and milligrams per deciliter. Explain that the result supports closer attention

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to modifiable risks and family history; it is not a measurement of

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an arterial blockage. Do not promise that diet will normalize an inherited

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lipoprotein a level. Build a feasible prevention plan.

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Discuss blood-pressure control, a heart-healthy dietary pattern, activity appropriate to function, smoking

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avoidance and medication options when indicated.

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Ask what Maria can sustain. A registered dietitian can help translate dietary

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advice into meals, budget and cultural preferences.

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Document the next measurement and review date rather than ending with “lifestyle

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counseling provided.” Reproductive plans can change the prescription.

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Consider a separate 34-year-old patient with hyperlipidemia who takes a statin for

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primary prevention and now wants to become pregnant.

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Her case requires a different discussion from Maria’s.

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Confirm the medication, dose, indication, current pregnancy status, plans, contraceptive method and

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breastfeeding status. Avoid assuming that age alone establishes whether pregnancy is possible.

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Here is the decision. Which counseling statement is most appropriate?

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Pause here if you would like a moment to think it through.

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The best next step in this case is: “Let’s review the exact

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medicine and indication with your prescriber before conception and agree on continuing

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cardiovascular care.” Plan the treatment transition before conception with the prescriber.

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The alternative postpones the discussion; The alternative interrupts follow-up.

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Most pregnant patients discontinue statins, while very high-risk exceptions need individual specialist

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assessment. FDA advises against breastfeeding when ongoing statin treatment is required.

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Questions that prevent an incomplete transition.

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Why was this medicine prescribed, and how high is the patient’s current

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risk? What does the current product information say for conception, pregnancy and

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lactation? Who will agree on the timing, provide an alternative when needed

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and monitor the patient? How will the plan be revisited after delivery

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or when breastfeeding ends? The 2026 guideline generally defers most lipid-lowering therapies

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during conception, pregnancy and lactation. For established atherosclerotic cardiovascular disease or severe

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familial hypercholesterolemia, coordinate preventive cardiology or lipid expertise with obstetric care.

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Do not apply one washout rule to every drug, substitute an investigational

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therapy, or leave a high-risk patient without follow-up.

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“Before you start trying to conceive, let’s review the medication with the

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clinician who prescribed it. We will agree on when to change it

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and how to look after your cholesterol and other risks during that

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time.” Work through the treatment transition.

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In the separate pregnancy-planning case, medication reconciliation starts with the actual drug

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and indication. The vignette does not name a product or dose, so

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do not invent either in the referral.

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Ask the prescriber to agree on a plan before conception, document who

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will explain it, and specify how it will be revisited.

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The pregnancy plan belongs in the prescribing record as well as the

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obstetric record. The FDA removed the blanket pregnancy contraindication for statins while

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continuing to advise discontinuation in most pregnant patients.

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A small group with very high cardiovascular risk may require individual assessment.

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This change does not establish safety for every lipid drug or support

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routine statin use in pregnancy. When ongoing statin treatment is required after

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delivery, FDA advises against breastfeeding. Discuss feeding and cardiovascular treatment together.

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Return to Maria. Record Maria’s preferences, agreed prevention plan and the clinician

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who will reassess her response. Pregnancy history can improve the conversation without

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becoming a reason to overtest or to promise an unproven therapy.

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The takeaway from this case: Record the pregnancy history without labeling it

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an atherosclerotic cardiovascular disease event. Complete current risk information before choosing treatment.

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Include reproductive plans in medication decisions.

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For the third case, the clinical setting changes to secondary prevention.

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Residual risk after a myocardial infarction.

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Elena is 58, has type 2 diabetes, and had a myocardial infarction

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two years ago. She is postmenopausal.

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L D L cholesterol is 92 milligrams per deciliter while prescribed a

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high-intensity statin. She also reports preeclampsia many years earlier.

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The current decision is secondary prevention for established atherosclerotic cardiovascular disease.

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Her pregnancy history remains part of her record, but it does not

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replace the evidence-based treatment pathway for her myocardial infarction and diabetes.

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Here is the decision. What is the best next step?

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Pause here if you would like a moment to think it through.

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The best next step in this case is: Confirm actual treatment use

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and response, address barriers, and choose additional evidence-based LDL lowering when indicated.

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Establish what Elena actually takes and tolerates, then act on the appropriate

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L D L cholesterol goal. The alternative can miss access, adherence or

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adverse-effect problems. The alternative can prolong avoidable residual risk.

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The guideline restores L D L cholesterol and non H D L

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cholesterol goals, including L D L cholesterol below 55 milligrams per deciliter

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for very-high-risk atherosclerotic cardiovascular disease. Confirm that Elena meets the full criteria

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before assigning this category; a prior myocardial infarction and diabetes alone do

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not establish multiple high-risk conditions. Apply the appropriate secondary-prevention pathway.

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Select additional treatment using the reduction needed, outcome evidence, safety, patient preference

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and access. Maximally tolerated statin. Reason to discuss it: Foundational therapy in

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appropriate atherosclerotic cardiovascular disease care. Question before selecting: Actual use, symptoms, interactions

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and response?. Ezetimibe. Reason to discuss it: An oral nonstatin option for

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additional LDL lowering. Question before selecting: Enough reduction for the patient’s goal?.

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P C S K 9 monoclonal antibody.

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Reason to discuss it: Potent LDL lowering with cardiovascular outcomes evidence.

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Question before selecting: Access, administration and treatment burden?.

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Bempedoic acid. Reason to discuss it: Oral option with outcomes evidence in

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studied statin-intolerant patients. Question before selecting: Indication, adverse effects, interactions and current

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label?. Inclisiran. Reason to discuss it: LDL lowering through a different dosing

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approach. Question before selecting: Do not equate lipid efficacy with completed event-outcome

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evidence; check current data. This comparison supports a treatment discussion; it does

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not establish a preferred product for every patient.

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Review current prescribing information before use.

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Turn the L D L cholesterol result into a decision.

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“Prescribed a high-intensity statin” is not the same as taking and tolerating

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it. Ask Elena to describe the medicine, dose and schedule she actually

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uses. Explore symptoms without dismissing them, and distinguish a clinical adverse effect

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from an affordability or refill problem.

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Review other causes of an inadequate lipid response and agree on a

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feasible regimen. If actual use is confirmed and L D L cholesterol

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remains above the appropriate goal, discuss additional LDL-lowering therapy using the size

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of reduction needed, the evidence for her clinical setting and the practical

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burden of treatment. An oral agent and an injected agent may present

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different adherence and access issues. A lower laboratory value is useful only

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when the plan can be implemented and reviewed.

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Benefits and harms belong in the same discussion.

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CLEAR Outcomes reported more gout and cholelithiasis with bempedoic acid than placebo.

00:16:56.885 --> 00:17:01.280
The current FDA label warns about hyperuricemia and tendon injury and includes

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drug-interaction precautions. Ask about relevant history and review the exact current label

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before choosing treatment. These considerations accompany the cardiovascular result rather than disappearing

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because a trial met its endpoint.

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Check the endpoint before recommending a medicine.

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What the trials establish. CLEAR Outcomes randomized 13,970 statin-intolerant patients with or

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at high cardiovascular risk. The primary composite occurred in 11.7 percent with

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bempedoic acid and 13.3 percent with placebo; hazard ratio 0.87, 95 percent

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confidence interval 0.79 to 0.96. These findings support an option for the

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studied population. They do not demonstrate safety in pregnancy or a benefit

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specifically after preeclampsia. VESALIUS-cardiovascular studied evolocumab in patients with atherosclerosis or diabetes

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who had no previous myocardial infarction or stroke and found fewer first

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cardiovascular events than placebo. “No previous myocardial infarction or stroke” does not

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mean a healthy, low-risk population. Elena already has a prior myocardial infarction,

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so this trial should not be presented as a direct match to

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her history. In September 2026, Novartis reported that pelacarsen lowered lipoprotein a

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in lipoprotein a HORIZON but did not meet the primary cardiovascular endpoint.

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This is a sponsor topline announcement; detailed methods and results require appraisal

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when available. Pelacarsen remains investigational in this report.

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Lowering a biomarker does not by itself establish clinical benefit, and one

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trial does not establish a class-wide conclusion.

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Here is the decision. Elena asks whether a large fall in lipoprotein

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a means an investigational medicine will prevent her next myocardial infarction.

00:18:46.455 --> 00:18:49.143
Which answer is best? Pause here if you would like a moment

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

00:18:52.195 --> 00:18:56.888
“We need cardiovascular outcome results for the particular treatment and population while

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treating the risks we can address now.” The alternative substitutes a biomarker

00:19:01.226 --> 00:19:05.876
response for a clinical outcome. The alternative overgeneralizes one trial to a

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whole class. Check the population, comparator, endpoint, absolute effect, uncertainty and harms.

00:19:12.801 --> 00:19:15.550
Consider absolute effects as well as the headline.

00:19:15.825 --> 00:19:21.116
In CLEAR Outcomes, subtracting 11.7 percent from 13.3 percent gives an absolute

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difference of 1.6 percentage points in the primary composite over the trial

00:19:25.382 --> 00:19:30.988
follow-up. The hazard ratio of 0.87 is a relative time-to-event comparison; it

00:19:31.030 --> 00:19:33.804
is not a 13-percentage-point absolute reduction.

00:19:34.102 --> 00:19:36.757
Neither number predicts Elena’s individual benefit.

00:19:37.066 --> 00:19:41.418
The studied population, background care and follow-up must remain attached to the

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estimate. A composite endpoint combines several outcomes.

00:19:45.287 --> 00:19:49.554
Check which components changed, how harms were collected and whether follow-up was

00:19:49.596 --> 00:19:53.091
sufficient for the question. Do not infer a proven benefit for women

00:19:53.261 --> 00:19:57.827
with prior preeclampsia from an overall result unless an applicable analysis supports

00:19:57.912 --> 00:20:02.162
that claim. This activity uses trials to practice appraisal, not to create

00:20:02.290 --> 00:20:05.975
a pregnancy-specific treatment indication. Elena’s next visit.

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Agree on the treatment decision and review interval with Elena, document access

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arrangements, and name the clinician responsible for reassessing adherence, tolerance and laboratory

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response. Ask her to explain the plan in her own words.

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A prescription without access or follow-up is an incomplete plan.

00:20:23.256 --> 00:20:27.125
The takeaway from this case: Distinguish prescribed treatment from actual use.

00:20:27.453 --> 00:20:30.461
Apply evidence from the appropriate patient population.

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Agree on an accessible treatment and follow-up plan.

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Before you go, bring the three cases back to one question: what

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will you do differently at the next visit?

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Ask what happened in pregnancy. Assess the risk that exists today.

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And make the next step someone’s responsibility.

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

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To record your answers and complete the learning activity, return to the

00:20:54.309 --> 00:20:56.944
activity page for the questions and brief evaluation.

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This has been HEART RESERVE Clinical Conversations.

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I’m Lisa Zahakos. Thank you for listening.
