Hydrocortisone: Difference between revisions

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''By slow intravenous injection
''By slow intravenous injection
Up to 1 year: 25 mg
*Up to 1 year: 25 mg
1-5 years: 50 mg
*1-5 years: 50 mg
6-12 years: 100 mg
*6-12 years: 100 mg
 
 
==Side Effects==
 
Short-term use include nausea and feeling tired. More severe side effects include psychiatric problems including euphoria, nightmares, insomnia, irritability, confusion, suicidal thoughts and behavioral disturbances.  This may occur in about 5% of people.
Long-term steroid use can lead to:
 
{| class = "wikitable"
!style="text-align: left"| Adrenal suppression
|
|-
!|Steroid-induced diabetes
|
|-
!|Osteoporosis, muscle wasting and weakness
|which is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae
|-
!style="text-align: left"| Susceptibility to infection
|
|-
!style="text-align: left"| Cushing’s syndrome
|moon face, striae, and acne
|-
!style="text-align: left"| Endocrine side effects
|menstrual irregularities and amenorrhea, hirsutism, weight gain, hyperlipidemia
|-
!Neuropsychiatric side effects
|aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, mood changes
|-
!Dermatological effects
|easy bruising, impaired wound healing, and thinning of skin
|-
!Ophthalmic effects
|glaucoma, corneal or scleral thinning and exacerbation of ophthalmic viral or fungal disease
 
|}
Side-effects can be minimized by using lowest effective dose for minimum period possible.
 
 
==Pharmacokinetics==
 
Hydrocortisone is readily absorbed from the gastrointestinal tract. Peak blood concentrations occur in about an hour. The plasma half-life is about 100 minutes.
 
It is more than 90% bound to plasma proteins.
 
Following intramuscular injection, the absorption of the water-soluble sodium phosphate and sodium succinate esters is rapid. Absorption of hydrocortisone acetate after intra-articular or soft-tissue injection is slower. Hydrocortisone is absorbed through the skin.
 
Hydrocortisone is metabolized in the liver and is excreted in the urine.
 
Hydrocortisone crosses the placenta and may distributed in small amounts into breast milk.

Revision as of 01:49, 5 October 2020


Pronunciation

Hydrocortisone 20mg


Introduction

Hydrocortisone is a steroid with anti-inflammatory and immunosuppressant effects. Indications include:

  • Hypersensitivity reactions e.g. anaphylaxis and angioedema
  • Asthma
  • Inflammatory bowel disease
  • Eczema, psoriasis and other inflammatory skin conditions
  • Rheumatoid arthritis
  • Treatment of choice for adrenocortical insufficiency

Hydrocortisone can be given by mouth, topically, or by injection.

Equivalent anti-inflammatory doses of steroids

Prednisolone 5 mg is equivalent to Betamethasone 750 micrograms
dexamethasone 750 micrograms
hydrocortisone 20 mg
methylprednisolone 4 mg
triamcinolone 4 mg


Mechanism of Action

Immunosuppression agent, Steroid replacement agent, Anti-inflammatory agent

Generic Name

藥名

HA Code 藥物代碼 Classification藥物分類
Hydrocortisone Tablet 20mg HYDR06 P1S1S3


Dosage

Hydrocortisone is used, usually with a more potent mineralocorticoid fludrocortisone, for replacement therapy in adrenocortical insufficiency.

By Oral: as replacement therapy, 20-30 mg daily (usually in 2 doses, the larger in the morning and the smaller in the early evening, to mimic the circadian rhythm of the body). By intramuscular injection or slow intravenous injection: 100-500 mg, 3-4 times in 24 hours or as required. Child dose: as replacement therapy in adrenocortical insufficiency,

By slow intravenous injection

  • Up to 1 year: 25 mg
  • 1-5 years: 50 mg
  • 6-12 years: 100 mg


Side Effects

Short-term use include nausea and feeling tired. More severe side effects include psychiatric problems including euphoria, nightmares, insomnia, irritability, confusion, suicidal thoughts and behavioral disturbances. This may occur in about 5% of people. Long-term steroid use can lead to:

Adrenal suppression
Steroid-induced diabetes
Osteoporosis, muscle wasting and weakness which is a danger, particularly in the elderly, as it can result in osteoporotic fractures for example of the hip or vertebrae
Susceptibility to infection
Cushing’s syndrome moon face, striae, and acne
Endocrine side effects menstrual irregularities and amenorrhea, hirsutism, weight gain, hyperlipidemia
Neuropsychiatric side effects aggravation of schizophrenia, aggravation of epilepsy, insomnia, irritability, mood changes
Dermatological effects easy bruising, impaired wound healing, and thinning of skin
Ophthalmic effects glaucoma, corneal or scleral thinning and exacerbation of ophthalmic viral or fungal disease

Side-effects can be minimized by using lowest effective dose for minimum period possible.


Pharmacokinetics

Hydrocortisone is readily absorbed from the gastrointestinal tract. Peak blood concentrations occur in about an hour. The plasma half-life is about 100 minutes.

It is more than 90% bound to plasma proteins.

Following intramuscular injection, the absorption of the water-soluble sodium phosphate and sodium succinate esters is rapid. Absorption of hydrocortisone acetate after intra-articular or soft-tissue injection is slower. Hydrocortisone is absorbed through the skin.

Hydrocortisone is metabolized in the liver and is excreted in the urine.

Hydrocortisone crosses the placenta and may distributed in small amounts into breast milk.