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Icsm Testosterone Monitoring Schedule

ASecurity

This skill outlines the monitoring schedule for testosterone therapy, detailing baseline, 3‑month, 6‑month, and yearly assessments of symptoms, adverse events, total testosterone, hematocrit, PSA, and DRE. Use it when a patient is receiving testosterone and the clinician asks what labs and checks are needed today or when the next monitoring visit should occur.

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  • Added September 9, 2026
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Works with

  • cli

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A100/100

Scanned September 9, 2026

npx -y skills add dromlakhani/MD2SKILL --skill icsm-testosterone-monitoring-schedule --agent claude-code

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SKILL.md
---
name: icsm-testosterone-monitoring-schedule
description: This skill outlines the monitoring schedule for testosterone therapy, detailing baseline, 3‑month, 6‑month, and yearly assessments of symptoms, adverse events, total testosterone, hematocrit, PSA, and DRE. Use it when a patient is receiving testosterone and the clinician asks what labs and checks are needed today or when the next monitoring visit should occur.
---

# Follow testosterone therapy monitoring schedule

## STEP 1 — Gather Information
Confirm the patient is on testosterone therapy, note the date of initiation, and record the date of the last monitoring visit; collect any new symptoms or adverse events reported since the last check.

## STEP 2 — Rule In / Rule Out
If the time since the last visit matches a scheduled interval (baseline, 3 months, 6 months, or >12 months), proceed to classify the required assessments; otherwise, inform the patient that no monitoring is due today and schedule the next visit based on the interval.

## STEP 3 — Classify or Stratify
Determine which assessments are due for this visit: symptoms evaluation and adverse events are always checked; total testosterone and hematocrit are due at baseline, 3 months, 6 months, and yearly; PSA is due at baseline, 3 months, 6 months, and yearly; DRE is due at baseline and 6 months (per Table 4).

## STEP 4 — Decide
Order the indicated laboratory tests (total testosterone, hematocrit, PSA), perform symptom and adverse event review, and conduct DRE if the visit aligns with the 6‑month or baseline point; document results and adjust testosterone dose if hematocrit exceeds 54% or if symptomatic adverse events arise.

## Clinical Guardrails / Mimics / Pitfalls
Do not omit hematocrit monitoring due to the risk of testosterone‑induced polycythemia; avoid delaying PSA or DRE when indicated, as prostate assessment is required before and during therapy; never rely solely on symptom changes without corroborating labs; ensure testosterone is drawn fasting between 07:00–11:00 h for accurate interpretation.

## Concrete Clinical Example
A 52‑year‑old man started testosterone enanthate 100 mg weekly 4 months ago. He reports no new symptoms. According to the schedule, a 3‑month visit is overdue; you order total testosterone, hematocrit, PSA, review symptoms and adverse events, and note that DRE is not required until the 6‑month mark. His hematocrit is 52 %, testosterone is 520 ng/dL, PSA 1.1 ng/mL; you continue the current dose and schedule the next visit in 3 months (for the 6‑month assessment).

**Source:** Male hypogonadism: recommendations from the Fifth International Consultation on Sexual Medicine (ICSM 2024), International Society for Sexual Medicine, 2025, https://doi.org/10.1093/sxmrev/qeaf036

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