跳到正文
cccskills
免费在 GitHub 公开

es-follow-pubertal-suppression-monitoring

Provides a monitoring schedule for patients receiving GnRH agonist therapy for pubertal suppression. Trigger phrases include 'patient undergoing GnRH agonist therapy' or 'initiating pubertal suppression'.

中文简介正在准备中。当前显示原文说明。

实测评分 未实测

查看安装方法

包含的文件(1)

  • SKILL.md2.4 KB

SKILL.md(原文)

安装前可以查看交给 AI 代理的指令内容。

Follow monitoring protocol during pubertal suppression

STEP 1 — Gather Information

Collect baseline and follow-up data: every 3–6 months measure height, weight, sitting height, blood pressure, and Tanner stages; every 6–12 months obtain LH, FSH, estradiol/testosterone, and 25OH vitamin D; every 1–2 years perform DXA bone density and left-hand X-ray for bone age if clinically indicated.

STEP 2 — Rule In / Rule Out

Assess Tanner stage progression and laboratory markers (LH, FSH, estradiol/testosterone). If no Tanner advancement and LH/FSH are at prepubertal levels with sex steroids suppressed → Rule In (adequate suppression). Otherwise → Rule Out (inadequate suppression).

STEP 3 — Classify or Stratify

For adequate suppression, classify as stable and continue routine monitoring; for inadequate suppression, classify as non‑suppressed and trigger adherence evaluation and dose reassessment.

STEP 4 — Decide

If stable: maintain current GnRH agonist dose and follow‑up schedule. If non‑suppressed: verify adherence, consider dose increase, investigate causes (e.g., drug interactions, metabolism), and repeat assessment in 1–3 months.

Clinical Guardrails / Mimics / Pitfalls

Do not rely on Tanner stages alone without corroborating LH/FSH and sex steroid levels; do not omit vitamin D assessment in patients with limited sun exposure or malabsorption; avoid delaying bone density monitoring beyond 2‑year intervals in those with risk factors for osteoporosis; do not overlook psychosocial stressors that may affect medication adherence; never adjust GnRH agonist dose based solely on symptomatic changes without laboratory confirmation.

Concrete Clinical Example

A 13‑year‑old transgender female starts leuprolide 3.75 mg SC monthly. At 4‑month visit, Tanner breast stage remains G2, LH is 0.2 IU/L, estradiol is 5 pg/mL. Assessment rules in adequate suppression; she continues the same dose with repeat labs and Tanner staging in 3 months.

Source: Endocrine Treatment of Gender-Dysphoric/Gender-Incongruent Persons: An Endocrine Society Clinical Practice Guideline, Endocrine Society, 2017, https://doi.org/10.1210/jc.2017-01658

评价

还没有评价。欢迎分享你的使用感受。

评论

无需登录即可发表。欢迎分享使用感受、提问,或说明在哪些环境下无法运行。

还没有评论。来写第一条吧。

提交后会立即公开。请勿填写邮箱、电话等个人信息。URL 最多 2 个。

0 / 1000 字

此表单受 reCAPTCHA 保护,适用 Google 的隐私权政策和服务条款。

同一仓库的技能

Guide pump setting adjustments for the MiniMed 780G system based on CareLink data, using Medtronic's 3-step follow-up workflow. Use when a clinician has CareLink data for a 780G patient and wants to know what to change — which setting, by how much, and how to program it. Triggers include: "what do I adjust", "how to fix high TIR", "how to reduce hypos", "adjust ICR/ISF/basal", "SmartGuard settings", "780G pump settings review", or any question about optimising 780G therapy after reviewing a download.

中文简介正在准备中。当前显示原文说明。

dromlakhani/MD2SKILL142026年10月20日 更新

Performs corticotropin stimulation test to diagnose adrenal insufficiency when morning cortisol is indeterminate (3-15 µg/dL). Triggers include morning cortisol 3-15 µg/dL requiring further AI testing.

中文简介正在准备中。当前显示原文说明。

dromlakhani/MD2SKILL142026年10月20日 更新

Administers immediate parenteral injection of 50–100 mg hydrocortisone for suspected adrenal crisis secondary to adrenal insufficiency. Triggers include hypotension, hypoglycemia, or acute illness in a patient with known adrenal insufficiency.

中文简介正在准备中。当前显示原文说明。

dromlakhani/MD2SKILL142026年10月20日 更新

Clinicians educate adrenal insufficiency patients taking nondexamethasone glucocorticoids who initiate enzyme-inducing antiepileptic drugs about early signs of adrenal insufficiency. Trigger when an AI patient on nondexamethasone GC starts an enzyme-inducing AED such as phenytoin, carbamazepine, or oxcarbazepine.

中文简介正在准备中。当前显示原文说明。

dromlakhani/MD2SKILL142026年10月20日 更新

In central hypothyroidism patients receiving levothyroxine who initiate enzyme‑inducing antiepileptic drugs, the guideline recommends checking free T4 at least 6 weeks after AED start and increasing the levothyroxine dose if free T4 falls below the target range. Triggers include: central hypothyroidism patient on levothyroxine starting antiepileptic drug such as phenytoin, carbamazepine, or oxcarbazepine.

中文简介正在准备中。当前显示原文说明。

dromlakhani/MD2SKILL142026年10月20日 更新

Applies serum cortisol cutoffs (<3 μg/dL indicates central adrenal insufficiency; >15 μg/dL likely excludes it) when evaluating morning cortisol for suspected adrenal insufficiency. Triggers include morning cortisol measurement in suspected AI and use when interpreting morning cortisol levels for adrenal insufficiency workup.

中文简介正在准备中。当前显示原文说明。

dromlakhani/MD2SKILL142026年10月20日 更新

查看 dromlakhani 的全部技能

报告此技能的问题