1
Intake
2
Risk Profile
3
Recommendation
4
Formulary
5
Guidelines
Patient Demographics
Core clinical identifiers and menopausal staging
Age & Menopausal Timing
Menopausal Classification
Perimenopausal
Postmenopausal
Surgical/oophorectomy
POI (<40)
Early meno (40–45)
Unsure
Intact uterus
Total hysterectomy
Subtotal/supracervical
Still menstruating (regular)
Menstruating (irregular / skipping cycles)
Spotting only
Amenorrhea <12 months
Amenorrhea ≥12 months
Post-hysterectomy / no uterus
Normal for stage
Heavy/prolonged (HMB)
Intermenstrual bleeding
Postcoital bleeding
Post-menopausal bleeding
⚠️ Heavy, intermenstrual, or postmenopausal bleeding requires TVUS ± endometrial biopsy before initiating HRT
Indications & Symptoms
Select all active clinical indications for HRT consideration
Hormonal Indications
Symptom Severity
None
Mild
Moderate
Severe / debilitating
0–2/day
3–6/day
7–12/day
≥13/day
No
Yes
Unsure
Never used
Currently on HRT
Prior HRT (stopped)
Laboratory Values (optional)
Not required for a recommendation — add if available. Abnormal values will flag clinical guidance.
▸ Show labs & bone health imaging
Hormonal Markers
Metabolic Panel
Hematologic / Renal
Bone Health Imaging
Normal
Osteopenia
Osteoporosis
Current (normal)
Current (abnormal/pending)
Not current
Contraindication Screening
Absolute contraindications preclude systemic HRT; relative require route modification
Absolute Contraindications
Relative Contraindications
Breast Cancer Risk Profile
WHI, ESTHER, CGHFBC data · FDA 2026: boxed warning removed for breast cancer
Personal History
No
Yes
A: Fatty
B: Scattered
C: Heterogeneous
D: Extremely dense
Hereditary & Family Risk
No
Yes
<15% (average)
15–20% (intermediate)
>20% (high)
Not calculated
Cardiovascular & VTE Risk
ACC/AHA ASCVD 2023 · ESTHER trial · WHI re-analysis 2025
ASCVD Risk Factors
ASCVD Risk Score & VTE
Unknown
<5% (low)
5–7.5% (borderline)
7.5–20% (intermediate)
>20% (high)
VTE Risk Factors
Additional Clinical Context
Bone, cognitive, metabolic, and psychosocial factors
Cognitive & Neurological
Never
Former
Current
Metabolic & Other
Good candidate
Candidate with modification
Marginal candidacy
Non-candidate
Complete Patient Intake (Step 1) and Risk Assessment (Step 2), then click Generate Full Recommendation to view the clinical decision summary.
HRT Formulary Reference
Approved formulations, routes, VTE/breast cancer risk signal, and efficacy — FDA 2026
Clinical Guideline Summary
Contraindications, evidence by outcome domain, and guideline statements