Women's Health/Hormonal Visit Note (Naturopathic)
A concise, problem-oriented note template for naturopathic women's health visits addressing menstrual, perimenopausal/menopausal, and hormonal concerns. Features a staged intervention framework (Foundations → Targeted Th…
Document Type
clinical note / Progress Note
Specialties
Template Preview
Date/Time: [Date and time of encounter]
Visit Type: [new / established]; [problem-focused / follow-up]
Setting: [in-person / telehealth: video / telehealth: phone] (If telehealth, note patient location and that identity verification and consent were obtained.)
Clinician: [Name, credentials]
Reason for Visit: [Primary concern(s)]
Subjective
Chief Concern & HPI: [Chief concern in patient's words when helpful] [Narrative HPI covering onset, trajectory, severity, functional impact, prior treatments and responses, patient goals/preferences]
- [Symptom inventory — menstrual/cycle] (Include only if relevant: cycle-related pain, bleeding changes, PMS/PMDD features, ovulatory signs, intermenstrual bleeding.)
- [Symptom inventory — vasomotor/sleep/mood] (Include only if relevant: hot flashes/night sweats, sleep quality, mood/anxiety/cognitive changes.)
- [Symptom inventory — genitourinary] (Include only if relevant: vaginal dryness, dyspareunia, urinary symptoms.)
- [Symptom inventory — hyperandrogen] (Include only if relevant: hirsutism, acne, alopecia.)
Red-flag symptoms: [postmenopausal bleeding / syncope / severe pelvic pain / rapidly progressive symptoms / none reported] (Document only items explicitly asked or volunteered.)
Reproductive & Relevant Medical History
LMP: [Date / unknown]
Cycle pattern: [Length, regularity, flow]
Obstetric history: [G/P; relevant complications]
Contraception/pregnancy intention: [Current method; intentions]
Menopause status: [Premenopausal / Perimenopausal / Postmenopausal] (Note how determined if applicable.)
Relevant PMH: [VTE, migraine with aura, hypertension, liver disease, cancer history, thyroid disease] (List only relevant items.)
Current medications: [Name, dose, frequency, indication]
Supplements/botanicals: [Name, dose, frequency, purpose for each]
Allergies: [Drug/food allergies and reactions]
Hormone exposure history: [Prior/current hormonal therapies, adverse events, reasons stopped]
Lifestyle factors: [Sleep; nutrition pattern; exercise; stress load; caffeine/alcohol/nicotine use]
Objective
Vitals: [BP, HR, weight/BMI as relevant]
Exam: [General, thyroid, abdomen, skin/hair as indicated] (If breast or pelvic exam performed, document indication, chaperone status, and findings. If deferred, note reason.)
Data reviewed: [Prior labs with dates, imaging, outside records] (Note what was reviewed and how it influenced decisions.)
Assessment
-
[Problem 1]: [Working diagnosis or symptom-based problem] — [new / stable / worsening]
- [Key supporting data: 2–4 items]
- [Differential diagnosis] (Include only if uncertain; acknowledge level of uncertainty.)
- [Safety considerations: pregnancy possibility, contraindications, red flags]
-
[Problem 2]: [Working diagnosis or symptom-based problem] — [new / stable / worsening]
- [Key supporting data]
- [Differential diagnosis] (If applicable.)
- [Safety considerations]
(Add additional problems as needed, in order of clinical priority.)
Plan
[Problem 1]: [Diagnosis or symptom focus]
Phase 0 (Safety/Rule-outs): [Pregnancy exclusion if relevant] [Red-flag evaluation/referral] [Contraindication screening before hormones or high-risk therapy]
Phase 1 (Foundations): [Sleep, nutrition, movement, stress regulation, trigger tracking recommendations with timeline of 2–6 weeks]
Phase 2 (Targeted Therapeutics):
- [Supplement/botanical: name, dose, frequency, duration, purpose, monitoring plan]
- [Prescription therapy if any: name, dose, frequency, monitoring plan]
- (For therapies with limited evidence, document that uncertainty was discussed.)
Hormone therapy (if initiated): [Indication] [Contraindication screening documented] [Product: name, route, dose, frequency] [Counseling: benefits, side effects, warning signs] [Follow-up plan] (If compounded, document rationale and counseling vs FDA-approved options.)
Phase 3 (Escalation/Referral): [Criteria for escalation, specialty referral, or advanced workup]
Testing ordered: [Test name] — [Clinical question] — [How results will change management]
Preventive screening: [Cervical, breast, bone density, depression, IPV as addressed] (Note briefly if discussed or ordered.)
Return precautions: [Specific red flags warranting earlier contact]
Follow-up: [Timeline] [What will be reassessed]
(Repeat plan sections for additional problems as needed. Document missing clinically important information as "unknown" rather than omitting. Do not document findings for exams not performed.)
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