01 — Clinic Overview

Table of Contents

1.0 Mission Statement

The Sandusky Dyslipidemia Model is a specialized outpatient clinic dedicated to the evidence-based management of dyslipidemia and associated cardiovascular risk. The clinic serves as a regional referral center for patients requiring focused evaluation and treatment of lipid disorders.

Our mission is to reduce atherosclerotic cardiovascular disease (ASCVD) events through rigorous application of the 2026 ACC/AHA/Multisociety Guidelines on the Management of Dyslipidemia [1], enhanced by advanced diagnostic tools and a “lower is better” treatment philosophy.

1.1 Treatment Philosophy

The clinic adheres to a “lower is better” philosophy for atherogenic lipoproteins, supported by the totality of evidence from randomized controlled trials and Mendelian randomization studies demonstrating that the relationship between LDL-C exposure and ASCVD risk is log-linear and that lower achieved levels of atherogenic lipoproteins translate to lower cardiovascular event rates [2, 3].

1.1.1 Guideline Adherence

All clinical decisions are grounded in the 2026 ACC/AHA/Multisociety Guideline on the Management of Dyslipidemia [1]. Guideline-recommended LDL-C thresholds are maintained as the minimum treatment targets.

1.1.2 Beyond-Guideline Intensification

Where advanced tools — including apolipoprotein B (ApoB), lipoprotein(a) [Lp(a)], coronary artery calcium (CAC) scoring, and advanced lipid fractionation — reveal residual or under-recognized risk, more aggressive lipid-lowering is pursued even in patients who have achieved standard guideline targets.

2.0 Scope of Practice

2.1 Services Provided

  • Comprehensive lipid evaluation and risk assessment
  • ASCVD risk stratification using the AHA PREVENT equations [4]
  • Advanced lipid testing (ApoB, NMR LipoProfile, Lp(a))
  • In-house coronary artery calcium (CAC) scoring
  • Carotid duplex ultrasonography (standard indications)
  • Coronary computed tomography angiography (CCTA) for selected patients (see Section 2.1.1)
  • Pharmacotherapy initiation, optimization, and escalation
  • Familial hypercholesterolemia (FH) evaluation, genetic testing, and cascade screening
  • Statin intolerance evaluation and management
  • Secondary dyslipidemia screening
  • Prior authorization support for advanced therapies (PCSK9 inhibitors, inclisiran)

2.1.1 CCTA Eligibility

CCTA is available for patients meeting all of the following criteria:

  • Symptomatic with low-to-intermediate pre-test probability of coronary artery disease
  • Not in atrial fibrillation
  • BMI ≤ 40 kg/m²
  • No prior coronary stents

2.2 Services Not Provided

The following services are outside the scope of this clinic:

Service Notes
Management of diabetes, CKD, or other comorbidities These conditions are documented as risk modifiers but managed by the referring provider
Dietary counseling services Diet and exercise are discussed as adjuncts; formal counseling is referred out
Telemedicine visits Not currently offered; may be added in future versions to expand access
EHR-integrated decision support Not currently available
Pediatric lipid management Adults ≥ 18 years only; pediatric patients are referred to appropriate specialists

3.0 Staffing Model

The clinic is staffed by:

Role Count Responsibilities
Physician (MD/DO) 1 Clinical oversight, complex cases, FH evaluation, advanced imaging interpretation
Nurse Practitioner (NP) 1 Follow-up visits, medication titration, prior authorizations, patient education
Nursing Staff (RN/MA) As needed Patient intake, vital signs, scheduling, lab coordination

4.0 Visit Structure

4.1 New Patient Visit — 40 Minutes

Phase Duration Activities
Nursing intake 10 min Vital signs, medication reconciliation, chief complaint
Provider encounter 25 min History, physical exam, review of records/labs, risk assessment, treatment plan discussion
Wrap-up 5 min Orders placed, follow-up scheduled, patient education materials provided

4.2 Follow-Up Visit — 20 Minutes

Phase Duration Activities
Nursing intake 5 min Vital signs, medication reconciliation, interval history
Provider encounter 12 min Lab review, medication tolerance/efficacy, treatment adjustment
Wrap-up 3 min Orders placed, follow-up scheduled

4.3 Lab Timing

Laboratories are ordered at the conclusion of each visit to be completed prior to the next scheduled visit. This ensures that results are available for review at the time of the encounter. The specific laboratory panel is at the provider’s discretion (see 03 — Initial Assessment, Section 3.0).

5.0 Follow-Up Cadence

Patient Status Follow-Up Interval
New medication start or dose change 4–8 weeks
Titrating to goal, not yet stable Every 3–6 months
At goal, stable on therapy Annually

6.0 Excluded Therapies

The following therapies are not included in this clinic’s therapeutic plan:

6.1 Bile Acid Sequestrants

Bile acid sequestrants (cholestyramine, colestipol, colesevelam) are not used due to gastrointestinal tolerability concerns, drug interaction burden, and the availability of better-tolerated alternatives with stronger outcomes data.

6.2 Nutraceuticals

Nutraceuticals such as plant sterols/stanols, red yeast rice, bergamot, berberine, and omega-3 supplements are not included in this clinic’s therapeutic plan. These agents lack sufficient randomized controlled trial evidence for ASCVD event reduction and may provide false reassurance, delay initiation of proven therapies, or introduce unmonitored drug interactions.

6.3 Emerging Investigational Agents

Lp(a)-targeted therapies (muvalaplin, lepodisiran, olpasiran) and CETP inhibitors (obicetrapib) are not currently included. These may be incorporated in future versions as trial data mature and regulatory approvals are obtained.

7.0 Referral Process

Patients are referred through the standard referral processes of the referring provider’s clinic or health system. No custom referral form is required. The clinic accepts referrals from:

  • Primary care providers
  • Cardiologists
  • Neurologists
  • Endocrinologists
  • Other specialists as appropriate

Upon receipt of a referral, the clinic applies eligibility criteria (see 02 — Patient Eligibility) and schedules the patient for a new patient visit.

8.0 Version History

Version Date Description
1.0.0 2026-03-30 Initial release

References

  1. 2026 ACC/AHA/Multisociety Guideline on the Management of Dyslipidemia. J Am Coll Cardiol. 2026.
  2. Ference BA, Ginsberg HN, Graham I, et al. Low-density lipoproteins cause atherosclerotic cardiovascular disease. 1. Evidence from genetic, epidemiologic, and clinical studies. A consensus statement from the European Atherosclerosis Society Consensus Panel. Eur Heart J. 2017;38(32):2459–2472.
  3. Cholesterol Treatment Trialists’ (CTT) Collaboration. Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170,000 participants in 26 randomised trials. Lancet. 2010;376(9753):1670–1681.
  4. Khan SS, Matsushita K, Sang Y, et al. Development and validation of the American Heart Association’s PREVENT equations. Circulation. 2024;149(6):e430–e449.

© 2026 The Sandusky Dyslipidemia Model. For clinical decision support only. Not a substitute for clinical judgment.