Delayed puberty medical therapy: Difference between revisions
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****Alternative regimen (1): [[Progestogens]]/[[Progestins]] 5-10 mg of [[Medroxyprogesterone acetate|medroxyprogesterone acetate (MPA)]] PO per day during the last 7 days of menstrual cycle | ****Alternative regimen (1): [[Progestogens]]/[[Progestins]] 5-10 mg of [[Medroxyprogesterone acetate|medroxyprogesterone acetate (MPA)]] PO per day during the last 7 days of menstrual cycle | ||
****Alternative regimen (2): Micronized [[progesterone]] 100-200 μg PO per day | ****Alternative regimen (2): Micronized [[progesterone]] 100-200 μg PO per day | ||
{| class="wikitable" | |||
! | |||
!Group | |||
!Medicine | |||
!Route | |||
!Constitutional Delay of Growth and Puberty | |||
(CDGP) | |||
!Hypogonadism | |||
!Side effects | |||
!Notes | |||
|- | |||
| rowspan="6" |'''Girls''' | |||
| rowspan="4" |[[Estrogen]] | |||
|[[Ethinyl estradiol|Ethinyl estradiol (EE)]] | |||
|PO | |||
| | |||
* Initial dose 2 μg daily. | |||
* Increase after 6-12 months to 5 μg daily | |||
| | |||
* Initial dose 2 μg daily. | |||
* Increase every 6 to 12 months to 5 μg, 10 μg, and 20 μg daily (adult dose). | |||
| | |||
* [[Hepatotoxicity]] | |||
* Increasing plasma binding proteins | |||
* Higher risks of thromboembolism and arterial hypertension than natural [[estrogens]]. | |||
| | |||
* Component of [[Oral contraceptive|oral contraceptive pills]]. | |||
* Lower dose [[Ethinylestradiol|EE]] oral pills are available in Europe. | |||
|- | |||
| rowspan="2" |17β-[[estradiol]] | |||
|PO | |||
| | |||
* Initial dose 5 μg/kg daily | |||
* Increase after 6-12 months to 10 μg/kg daily | |||
| | |||
* Initial dose 5 μg/kg daily | |||
* Increase every 6-12 months to 10 μg/kg daily, then to 15 μg/kg, and to 20μg/kg daily. | |||
* Adult dose 1-2 mg daily. | |||
| | |||
* [[Transdermal]] is better than oral administration. | |||
| | |||
* Natural [[estrogen]] is preferable to synthetic [[estrogens]]. | |||
|- | |||
|[[Estradiol patch|Transdermal patch]] or gel | |||
| | |||
* Initial dose 3.1-6.2 μg/24h (1/8-1/4 of 25 μg/24h patch) | |||
* Increase by 3.1-6.2 μg/24h every 6 months | |||
| | |||
* Initial dose 3.1-6.2 μg/24h (1/8-1/4 of 25 μg/24h patch) | |||
* Increase by 3.1-6.2 μg/24h every 6 months. | |||
* Adult dose 50-100 μg/24h | |||
| - | |||
| | |||
* Patches applied overnight | |||
* Topical gel applied during the day | |||
* No dosage equivalent data between patches and gel available in younger patients | |||
|- | |||
|[[Conjugated estrogens|Conjugated equine estrogens (CEE)]] | |||
|PO | |||
| | |||
* Initial dose 0.1625 mg daily for 6-12 months, and then titrating to 0.325 mg daily | |||
* Dosing depends on formulation | |||
| | |||
* Initial dose 0.1625 mg for 6-12 months, increase every 6-12 months to 0.325, 0.45, and 0.625 mg daily | |||
* Common adult dose 0.625 mg | |||
| | |||
* Use cautiously because of reported increased cardiovascular risks in postmenopausal women | |||
| | |||
* [[Conjugated estrogens|CEE]] are not [[estradiol]] precursors. | |||
|- | |||
|[[Progestogens]] | |||
|[[Progestogens]]/[[Progestins]] | |||
|PO | |||
| | |||
* Only if treatment continues longer than 12 months | |||
| | |||
* 5-10 mg of [[Medroxyprogesterone acetate|medroxyprogesterone acetate (MPA)]] daily during the last 7 days of [[menstrual cycle]]. | |||
* Alternative: micronized [[progesterone]], dose 100-200 μg daily. | |||
|<nowiki>-</nowiki> | |||
|Progesterone added to induce endometrial cycling after 12-18 months of estrogen therapy: | |||
* Later if estrogen dose increased slowly | |||
* Sooner if break-through bleeding | |||
|- | |||
|Pulsatile [[GnRH]] | |||
| | |||
* [[Subcutaneous]] pump | |||
|SC | |||
| | |||
* Not recommended routinely | |||
|Used for fertility | |||
| - | |||
| | |||
* Very expert route of treatment | |||
* Most [[physiological]] form therapy | |||
|- | |||
| rowspan="7" |'''Boys''' | |||
| rowspan="3" |[[Testosterone]] | |||
| | |||
* [[Testosterone enanthate]] (most potent) | |||
* [[Testosterone cypionate]] | |||
* [[Testosterone propionate]] | |||
|IM | |||
| | |||
* Not recommend for less than 14 years old. | |||
* Initial dose 50-100 mg every 4 weeks for 3 to 6 months | |||
* Repeated treatment with 25-50 mg increment in dose (not exceeding 100 mg) | |||
| | |||
* Can administered after 12 years old. | |||
* Initial dose 50 mg every 4 weeks. | |||
* Increase with 50 mg increments every 6 to 12 months. | |||
* After reaching 100-150 mg monthly, decrease interval to every 2 weeks. | |||
* Adult dose 200 mg every 2 weeks. | |||
| rowspan="2" | | |||
* Local side effects ([[pain]], [[erythema]], [[inflammatory]] reaction, and sterile [[abscess]]). | |||
* [[Priapism]] can occur in patients with [[sickle cell disease]]. | |||
| rowspan="3" | | |||
* General side effects: | |||
** [[Erythrocytosis]] | |||
** [[Weight gain]] | |||
** [[Benign prostatic hyperplasia|Prostate hyperplasia]] | |||
* High doses can cause premature [[epiphyseal]] closure | |||
* Not for use in boys with [[bone age]] < 10 years | |||
|- | |||
| | |||
* [[Testosterone]] undecanoate | |||
|IM | |||
| | |||
* No data available | |||
| | |||
* Adult dose is 1000 mg every 10-14 weeks | |||
|- | |||
| | |||
* [[Testosterone]] gel | |||
|[[Transdermal]] | |||
| | |||
* No data available | |||
| | |||
* Initiated when approximately 50% adult dose achieved with IM [[testosterone]] | |||
* Adult dose 50-80 mg daily | |||
| | |||
* Local [[irritation]] | |||
* Avoid close skin contact after applying | |||
|- | |||
| rowspan="2" |[[Aromatase inhibitors]] | |||
| | |||
* [[Letrozole]] | |||
|PO | |||
| | |||
* 2.5 mg daily | |||
| | |||
* No data available | |||
| | |||
* Decreased level of [[High-density lipoprotein|high-density lipoprotein (HDL)]] [[cholesterol]] | |||
* [[Erythrocytosis]] | |||
* [[Vertebral anomalies|Vertebral deformities]]<ref name="pmid20200972">{{cite journal |vauthors=Hero M, Toiviainen-Salo S, Wickman S, Mäkitie O, Dunkel L |title=Vertebral morphology in aromatase inhibitor-treated males with idiopathic short stature or constitutional delay of puberty |journal=J. Bone Miner. Res. |volume=25 |issue=7 |pages=1536–43 |year=2010 |pmid=20200972 |doi=10.1002/jbmr.56 |url=}}</ref> | |||
| rowspan="2" | | |||
* Not yet approved for this indication. | |||
* After onset of [[puberty]], may increase [[gonadotropin]] secretion and circulating [[testosterone]] levels.<ref name="pmid11600558">{{cite journal |vauthors=Wickman S, Dunkel L |title=Inhibition of P450 aromatase enhances gonadotropin secretion in early and midpubertal boys: evidence for a pituitary site of action of endogenous E |journal=J. Clin. Endocrinol. Metab. |volume=86 |issue=10 |pages=4887–94 |year=2001 |pmid=11600558 |doi=10.1210/jcem.86.10.7927 |url=}}</ref> | |||
|- | |||
| | |||
* [[Anastozole]] | |||
|PO | |||
| | |||
* 1.0 mg daily | |||
| | |||
* No data available | |||
| - | |||
|- | |||
|Pulsatile [[GnRH]] | |||
| | |||
* [[Subcutaneous]] pump | |||
|SC | |||
| | |||
* Not recommended routinely | |||
| | |||
* Initial dose 5-25 ng/kg/pulse every 90-120 min | |||
* Maintenance dose increase to 25-600 ng/kg/pulse | |||
| - | |||
| | |||
* Very expert route of treatment | |||
* Most [[physiological]] form therapy | |||
|- | |||
|Combination therapy | |||
| | |||
* [[hCG]] plus [[recombinant]] [[FSH]] | |||
| | |||
* [[subcutaneous]] or [[intramuscular]] [[hCG]] | |||
* [[subcutaneous]] [[FSH|rhFSH]] | |||
| | |||
* Not recommended routinely | |||
| | |||
* '''''[[hCG]]''''' | |||
** 500 to 3000IU twice weekly | |||
** Increased to every 2 days | |||
** Dose adjusted based on serum [[testosterone]] levels | |||
* [[FSH|'''''rhFSH''''']] | |||
** 75 to 225 IU 2-3 times weekly. | |||
| | |||
* [[hCG]] | |||
** [[Testicular]] local [[inflammation]] | |||
** Maybe [[germ cell]] [[apoptosis]] | |||
| | |||
* In [[hypogonadotropic hypogonadism]] with prepubertal onset, in order to [[testicular]] development and also [[spermatogenesis]], [[FSH]] is needed. | |||
* No data on effects on future [[fertility]]. | |||
|} | |||
==Reference== | ==Reference== | ||
{{reflist|2}} | {{reflist|2}} |
Revision as of 16:34, 13 September 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Medical Therapy
General approach to pharmacological medical therapy for delayed puberty[1]
Delayed Puberty | |||||||||||||||||||||||||||||||||||
Initial assessment | |||||||||||||||||||||||||||||||||||
• Clinical history • Physical examinations • Pubertal phenotype • Left wrist radiograph for bone age | |||||||||||||||||||||||||||||||||||
Unremarkable | Abnormal | Chronic disease | |||||||||||||||||||||||||||||||||
• Delayed puberty • Lack of growth spurt • Bone age delayed upon chronological age | • Possibility of chromosomal disorder • Bone age may delayed | • Chronic disease • Decreased growth rate or short stature • Bone age delayed upon chronological age | |||||||||||||||||||||||||||||||||
Diagnosis: • Constitutional delay of growth and puberty (CDGP) • Gonadotropin deficiency • Primary gonadal failure • Extreme athletic exercise | Diagnosis: Girls: • Turner syndrome Boys: • Klinefelter syndrome | Diagnosis: • Hypopituitarism • Chronic systemic diseases • Anorexia nervosa • Malnutrition • Kallman syndrome • Iatrogenic | |||||||||||||||||||||||||||||||||
Actions: • Evaluation hypothalamus-pituitary-gonadal axis • Consider an MRI to exclude the CNS lesions | Actions: • Chromosome analysis (Karyotyping) | Actions: • Upon the underlying disease | |||||||||||||||||||||||||||||||||
Treatment: 1. Psychologic support 2. Observation 3. Sex hormone replacement therapy | Treatment: 1. Psychologic support 2. Sex hormone replacement 3. Excision of ovaries in Turner syndrome because of risk of malignancy | ||||||||||||||||||||||||||||||||||
- Generally, the main pharmacological medical therapy for delayed puberty is sex hormone replacement therapy.
- The aim of treatment is to initiate the puberty progress and to merge the secondary sexual characteristics in patients.
- Regarding that the delayed puberty involve only adolescents, all of the therapy options are for them.
Delayed puberty[2]
- 1 Stage 1 - Constitutional delay of growth and puberty
- 1.1 Boys
- Preferred regimen (1): Testosterone, not indicated before 14 years of age
- Initial dose: 50-100 mg IM every 4 weeks for 3-6 months
- Repeated treatment: To add 25-50 mg in dose (maximum, 100 mg per dose)
- Preferred regimen (2): Letrozole 2.5 mg PO per day
- Preferred regimen (3): Anastozole 1mg PO per day
- Preferred regimen (1): Testosterone, not indicated before 14 years of age
- 1.2 Girls
- Preferred regimen (1): Ethinyl estradiol (EE)
- Initial dose: 2 μg PO per day for 6-12 months
- Repeated treatment: Increase to 5 μg PO per day after 6-12 months
- Preferred regimen (2): 17β-estradiol (pill)
- Initial dose: 5 μg/kg PO per day for 6-12 months
- Repeated treatment: Increase to 10 μg/kg PO per day after 6-12 months
- Preferred regimen (3): 17β-estradiol (transdermal patch)
- Initial dose: 3.1-6.2 μg (1/8-1/4 of 25 μg patch) per day for 6 months
- Repeated treatment: Increase 3.1-6.2 μg (1/8-1/4 of 25 μg patch) per day every 6 months
- Preferred regimen (4): Conjugated equine estrogens (CEE)
- Initial dose: 0.1625 mg PO per day for 6-12 months
- Repeated treatment: Titrating to 0.325 mg PO per day after 6-12 months
- Alternative regimen (1): Progestogens/Progestins in various formulations, only if treatment last more than 12 months
- Preferred regimen (1): Ethinyl estradiol (EE)
- 1.1 Boys
- 2 Stage 2 - Hypogonadism
- 2.1 Pediatric
- 2.1.1 Boys
- Preferred regimen (1): Testosterone, can be started after 12 years of age
- Initial dose of 50 mg IM per month
- Increase with 50 mg in dose IM every 6-12 months
- After reaching 100-150 mg IM monthly, decrease interval to every 2 weeks
- Preferred regimen (2): Pulsatile GnRH
- Initial dose: 5-25 ng/kg/pulse SC every 90-120 min
- Continued treatment: Increase to 25-600 ng/kg/pulse SC every 90-120 min
- Alternative regimen (1): Testosterone undecanoate 1000 mg IM every 10-14 weeks
- Alternative regimen (2): Testosterone gel, apply at bed time
- Started when approximately 50% adult dose has been achieved with intramuscular testosterone
- Alternative regimen (3): hCG plus recombinant FSH
- hCG: 500 to 3000 IU SC or IM twice weekly, increased to every 2 days
- rhFSH: 75 to 225 IU SC 2-3 times weekly
- Preferred regimen (1): Testosterone, can be started after 12 years of age
- 2.1.2 Girls
- Preferred regimen (1): Ethinyl estradiol (EE)
- Initial dose: 2 μg PO per day for 6-12 months
- Repeated treatment: Increase every 6-12 months to 5 μg, 10 μg, and 20 μg PO per day
- Preferred regimen (2): 17β-estradiol (pill)
- Initial dose: 5 μg/kg PO per day for 6-12 months
- Repeated treatment: Increase to 10 μg/kg PO per day after 6-12 months, then to 15 μg/kg, and to 20μg/kg per day
- Preferred regimen (3): 17β-estradiol (transdermal patch)
- Initial dose: 3.1-6.2 μg (1/8-1/4 of 25 μg patch) per day for 6 months
- Repeated treatment: Increase 3.1-6.2 μg (1/8-1/4 of 25 μg patch) per day every 6 months
- Preferred regimen (4): Conjugated equine estrogens (CEE)
- Initial dose: 0.1625 mg PO per day for 6-12 months
- Repeated treatment: Increase every 6-12 months to 0.325, 0.45, and 0.625 mg PO per day
- Alternative regimen (1): Progestogens/Progestins in various formulations, only if treatment last more than 12 months
- Preferred regimen (1): Ethinyl estradiol (EE)
- 2.1.1 Boys
- 2.1 Adults
- 2.1.1 Male
- Preferred regimen (1): Testosterone 200 mg IM every 2 weeks
- Preferred regimen (2): Testosterone undecanoate 1000 mg IM every 10-14 weeks
- Preferred regimen (3): Testosterone gel 50-80 mg transdermal per day
- Alternative regimen (1): Pulsatile GnRH
- Initial dose: 5-25 ng/kg/pulse SC every 90-120 min
- Continued treatment: Increase to 25-600 ng/kg/pulse SC every 90-120 min
- Alternative regimen (2): hCG plus recombinant FSH
- hCG: 500 to 3000 IU SC or IM twice weekly, increased to every 2 days
- rhFSH: 75 to 225 IU SC 2-3 times weekly
- 2.1.2 Female
- Preferred regimen (1): Ethinyl estradiol (EE) 20 μg PO per day
- Preferred regimen (2): 17β-estradiol (pill) 1-2 mg PO per day
- Preferred regimen (3): 17β-estradiol (transdermal patch) 50-100 μg transdermal per day
- Preferred regimen (4): Conjugated equine estrogens (CEE) 0.625 mg PO per day
- Alternative regimen (1): Progestogens/Progestins 5-10 mg of medroxyprogesterone acetate (MPA) PO per day during the last 7 days of menstrual cycle
- Alternative regimen (2): Micronized progesterone 100-200 μg PO per day
- 2.1.1 Male
- 2.1 Pediatric
Group | Medicine | Route | Constitutional Delay of Growth and Puberty
(CDGP) |
Hypogonadism | Side effects | Notes | |
---|---|---|---|---|---|---|---|
Girls | Estrogen | Ethinyl estradiol (EE) | PO |
|
|
|
|
17β-estradiol | PO |
|
|
|
|||
Transdermal patch or gel |
|
|
- |
| |||
Conjugated equine estrogens (CEE) | PO |
|
|
|
|||
Progestogens | Progestogens/Progestins | PO |
|
|
- | Progesterone added to induce endometrial cycling after 12-18 months of estrogen therapy:
| |
Pulsatile GnRH |
|
SC |
|
Used for fertility | - |
| |
Boys | Testosterone | IM |
|
|
|
| |
|
IM |
|
| ||||
|
Transdermal |
|
|
| |||
Aromatase inhibitors | PO |
|
|
|
| ||
PO |
|
|
- | ||||
Pulsatile GnRH |
|
SC |
|
|
- |
| |
Combination therapy |
|
|
|
|
|
Reference
- ↑ Blondell RD, Foster MB, Dave KC (1999). "Disorders of puberty". Am Fam Physician. 60 (1): 209–18, 223–4. PMID 10414639.
- ↑ Palmert, Mark R.; Dunkel, Leo (2012). "Delayed Puberty". New England Journal of Medicine. 366 (5): 443–453. doi:10.1056/NEJMcp1109290. ISSN 0028-4793.
- ↑ Hero M, Toiviainen-Salo S, Wickman S, Mäkitie O, Dunkel L (2010). "Vertebral morphology in aromatase inhibitor-treated males with idiopathic short stature or constitutional delay of puberty". J. Bone Miner. Res. 25 (7): 1536–43. doi:10.1002/jbmr.56. PMID 20200972.
- ↑ Wickman S, Dunkel L (2001). "Inhibition of P450 aromatase enhances gonadotropin secretion in early and midpubertal boys: evidence for a pituitary site of action of endogenous E". J. Clin. Endocrinol. Metab. 86 (10): 4887–94. doi:10.1210/jcem.86.10.7927. PMID 11600558.