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Steroid in pregnancy



       제일병원 주산기분과
          전임의 안계형
Steroid의 분류
• Corticosteroid
- glucocorticoid: regulate many aspects of
 metabolism and immune function (cortisol)
- mineralcorticoid: maintain blood volume and
  control
 renal excretion of electrolytes (aldosterone)
 Most medical “steroid” drugs are cortocosteroid

• Anabolic steroid: interact with androgen receptors
  to increase muscle and bone synthesis

• Sex hormone: produce sex difference or support
  reproduction (androgens,
  estrogens,progesterones)
Steroid in pregnancy
• Systemic corticosteroids:
  autoimmune and inflammatory
conditions
• Inhaled steroids:
  first-line treatment for asthma
• Topical corticosteroids:
  allergic and inflammatory dermatologic
  diseases(atopic dermatitis and
psoriasis)
Steroid in pregnancy
    Molecular weight

•   Prednisolone: 360g/mol C21H28O5
•   Prednisone: 358g/mol C21H26O5
•   Cortisone: 376g/mol C21H28O5
•   Dexamethasone: 392g/mol C22H9FO5

=>Cross human placenta
Half life of corticosteroid
www.motherisk.org
Motherisk update 2004
          Systemic corticosteroid
• Prednisone, cortisone, prednisolone,
  dexamethasone
• Association with oral clefts
• one case-control and several prospective
  cohort studies:
 failed to show such an association.
• A metaanalysis conducted by the Motherisk
  program of 123175 women who received oral
  corticosteroids during the first trimester :
  showed a slightly increased risk of oral clefts.
Motherisk update 2004
          Systemic corticosteroid

• Odd ratios (ORs) in case control studies:
  threefold increase in oral clefts among off
  spring of women who received oral
  corticosteroids during pregnancy.
• six cohort studies : no significant increase in
  oral clefts.
Motherisk update 2004
         Systemic corticosteroid

• Increase incidence of low birth weight and
  stillbirths(often associated with the
  condotion for which the mothers were given
  the drugs)
Motherisk update 2004
          Inhaled corticosteroids
• asthma or other respiratory symptoms
• beclomethasone,budesonide,flunisolide,flutic
  asone,mometasone, and triamcinoloneIt
• up to 4% of all pregnancies : complicated by
  maternal asthma.
• Poor control of chronic asthma and
  exacerbation of acute asthma during
  pregnancy -> hypoxia, low birth weight, and
 intrauterine growth restriction
Motherisk update 2004
          Inhaled corticosteroids


A randomized controlled study
• long-term use of low-dose budesonide
  decreases the risk of severe exacerbations
• improves asthma control in patients with
  mild, persistent asthma of recent onset.
• reduce risk of hospitalization due to asthma.
Motherisk update 2004
          Topical corticosteroids

• The systemic effects of topical corticosteroids
 -> generally limited
 -> only about 3% of the medication in topical
  preparations is absorbed systemically
  following 8 hours of contact
Motherisk update 2004
         Topical corticosteroids
• When corticosteroids are used long term
   or on large areas of skin
  -> systemic effects
• Epidemiologic fetal safety data on topical
   corticosteroids -> sparse.
• Two population-based studies
 : treatment with topical corticosteroids
   during pregnancy did not increase risk of
   congenital abnormalities in humans.
Motherisk update
                 discussion
• oral clefts : occur at about one per thousand
  births
• minimal absolute effect on the overall
  malformation rate of 3%.
• palate formation : completed by 12 weeks’
  gestation
 -> no risk of oral clefts exists thereafter.
Motherisk update
                  discussion
• When exposure has already occurred
  -> a level II ultrasound scan
   (to detect clefting)
• More studies are needed to determine which
  cleft phenotype is associated with
  corticosteroids and whether it is cleft lip
  (with or without palate) or cleft palate alone,
  or both
Corticosteroids During Pregnancy and Oral
         Clefts: A Case-Control Study

• Case subjects: 1,184 liveborn infants with
   nonsyndromic oral clefts.
• results (logistic regression analysis):
  show a relationship between exposure to
  corticosteroids during the first trimester of
  pregnancy and an increased risk of cleft
  lip (with or without cleft palate) in the
  newborn infants
 (OR: 6.55; CI: 1.44–29.76; P: 0.015)
Corticosteroids During Pregnancy and Oral
       Clefts: A Case-Control Study
Corticosteroids During Pregnancy and Oral
        Clefts: A Case-Control Study

• Use of corticosteroids during the first
  trimester of pregnancy, should be
  restricted to the following situations:
life-threatening situations
diseases without any other safe
  therapeutic alternative
cases with replacement therapy.
Birth Defects After Maternal Exposure to
  Corticosteroids: Prospective Cohort Study
and Meta-Analysis of Epidemiological Studies


• 184 women exposed to prednisone in
  pregnancy
• 188 pregnant women who were counseled
  by Motherisk for nonteratogenic
  exposure.
• primary outcome:
  rate of major birth defects.
• A meta-analysis of all epidemiological
  studies was conducted.
Birth Defects After Maternal Exposure to
  Corticosteroids: Prospective Cohort Study
and Meta-Analysis of Epidemiological Studies

• Results: no statistical difference in the rate of
  major anomalies between the corticosteroid-
  exposed and control groups.
• In the meta-analysis
 odds ratio for major malformations with all cohort
 studies:1.45 and 3.03

• odds ratio for case-control studies examining oral
  clefts was significant (3.35 [95% CI 1.97, 5.69]).
Birth Defects After Maternal Exposure to
  Corticosteroids: Prospective Cohort Study
and Meta-Analysis of Epidemiological Studies


• Conclusions: Although prednisone does
  not represent a major teratogenic risk
  in humans at therapeutic doses, it does
  increase by an order of 3.4-fold the
  risk of oral cleft, which is consistent
  with the existing animal
  studies.
Birth Defects After Maternal Exposure to
  Corticosteroids: Prospective Cohort Study
and Meta-Analysis of Epidemiological Studies
Birth Defects After Maternal Exposure to
  Corticosteroids: Prospective Cohort Study
and Meta-Analysis of Epidemiological Studies
Birth Defects After Maternal Exposure to
  Corticosteroids: Prospective Cohort Study
and Meta-Analysis of Epidemiological Studies
Guideline on Steroids in Pregnancy

  Major possible adverse effects
• orofacial clefts when used preconception and in the
  first trimester of pregnancy, and foetal growth
  restriction and preterm delivery
• especially potent/very potent topical corticosteroids

  (evidence from a Cochrane Review an d data
   mining of the World Health Organisation
   International Database of Adverse Drug Reactions)
Guideline on Steroids in Pregnancy

A large population-based cohort studies
 (84,133 pregnant women from the UK
  General Practice Research Database)
• significant association of foetal growth
  restriction with maternal exposure to
  potent/very potent topical corticosteroids
• but not with mild/moderate topical
  steroids
Guideline on Steroids in Pregnancy
• No associations of any potency with orofacial
  cleft, preterm delivery, and foetal death
• antibiotic-containing topical corticosteroid:
  associated with an increased risk for foetal
  growth restriction and foetal death
• current evidence is sufficient for doctors and
  pregnant women to a well-informed decision as
  to whether to use topical corticosteroids in
  pregnancy.
Guideline on Steroids in Pregnancy

• The evidence suggests that mild/moderate
  topical corticosteroids are preferred to
  potent/very potent ones in pregnancy,
  because of the risk of foetal growth
  restriction.
Guideline on Steroids in Pregnancy
Guideline on Steroids in Pregnancy
Guideline on Steroids in Pregnancy
Guideline on Steroids in Pregnancy
Guideline on Steroids in Pregnancy
Guideline on Steroids in Pregnancy
Recommendations

1. Mild/moderate topical corticosteroids should be
   used in preference to more potent corticosteroids in
   pregnancy (Grade of recommendation: B).

2.Potent/very potent topical corticosteroids should be
 used as second-line therapy for as short a time as
 possible, and appropriate obstetric care should be
 provided as they increase the risk of foetal growth
 restriction (Grade of recommendation: B).
Recommendations

3.systemic corticosteroids have a greater
  bioavailability than that of topical
  corticosteroids, and have a higher potential for
  foetotoxicity than topical corticosteroids
 (systemic corticosteroids are associated with a
  reduction in fetal birth weight and an increase in
  preterm delivery and should not be used in
  preference (Grade of recommendation: B).
Recommendations

4.the danger of adverse events is increased
  when areas with high absorption (e.g.genitals,
  eyelids, flexures) are treated
 (Grade of recommendation: B)

5.The data are not available to determine if newer
 more lipophilic topical corticosteroids (mometasone,
 fluticasone and methylprednisolone aceponate,) with
 a good therapeutic index are associated with less
 foetal growth restriction despite theoretical grounds
 to suggest this and the practical advantage of
 once daily application (Grade of recommendation:C).
Recommendations

6. Antibiotic-containing topical corticosteroid
 preparations should be avoided in pregnancy
 (until more robust evidence is available)
 because of concern for increased risk for
 foetal growth restriction and foetal death.
 (Grade of recommendation: C).
Advice to women about using topical
     corticosteroids in pregnancy

1. Women can be reassured
• no significantly increased risk for orofacial cleft,
  preterm delivery and foetal death when using
  topical corticosteroids in pregnancy.
• no increased risk for foetal growth restriction
  when using mild/moderate topical
  corticosteroids in pregnancy.
Advice to women about using topical
     corticosteroids in pregnancy
2. Women should be informed
• small risk for foetal growth restriction when using
   potent/very potent topical corticosteroids
• but this risk is less than that of systemic
   corticosteroids
• additional risk for preterm delivery has been
   found in women using systemic corticosteroids.

3. Depending on the severity of their skin
  conditions, women should use topical
  corticosteroids of the least potency required and
  limit the amount of use
Williams OBSTETRICS 24th

• systemic corticosteroids are category
  D if used in the first trimester,
  however, they are not considered to
  represent a major teratogenic risk.
?
“should be used during pregnancy
only if the potential benefit justifies
the potential risk to the foetus”
감사합니다.
마더리스크라운드 - Steroid in pregnancy
마더리스크라운드 - Steroid in pregnancy
마더리스크라운드 - Steroid in pregnancy
마더리스크라운드 - Steroid in pregnancy

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마더리스크라운드 - Steroid in pregnancy

  • 1. Steroid in pregnancy 제일병원 주산기분과 전임의 안계형
  • 2. Steroid의 분류 • Corticosteroid - glucocorticoid: regulate many aspects of metabolism and immune function (cortisol) - mineralcorticoid: maintain blood volume and control renal excretion of electrolytes (aldosterone) Most medical “steroid” drugs are cortocosteroid • Anabolic steroid: interact with androgen receptors to increase muscle and bone synthesis • Sex hormone: produce sex difference or support reproduction (androgens, estrogens,progesterones)
  • 3. Steroid in pregnancy • Systemic corticosteroids: autoimmune and inflammatory conditions • Inhaled steroids: first-line treatment for asthma • Topical corticosteroids: allergic and inflammatory dermatologic diseases(atopic dermatitis and psoriasis)
  • 4. Steroid in pregnancy Molecular weight • Prednisolone: 360g/mol C21H28O5 • Prednisone: 358g/mol C21H26O5 • Cortisone: 376g/mol C21H28O5 • Dexamethasone: 392g/mol C22H9FO5 =>Cross human placenta
  • 5. Half life of corticosteroid
  • 7. Motherisk update 2004 Systemic corticosteroid • Prednisone, cortisone, prednisolone, dexamethasone • Association with oral clefts • one case-control and several prospective cohort studies: failed to show such an association. • A metaanalysis conducted by the Motherisk program of 123175 women who received oral corticosteroids during the first trimester : showed a slightly increased risk of oral clefts.
  • 8. Motherisk update 2004 Systemic corticosteroid • Odd ratios (ORs) in case control studies: threefold increase in oral clefts among off spring of women who received oral corticosteroids during pregnancy. • six cohort studies : no significant increase in oral clefts.
  • 9. Motherisk update 2004 Systemic corticosteroid • Increase incidence of low birth weight and stillbirths(often associated with the condotion for which the mothers were given the drugs)
  • 10. Motherisk update 2004 Inhaled corticosteroids • asthma or other respiratory symptoms • beclomethasone,budesonide,flunisolide,flutic asone,mometasone, and triamcinoloneIt • up to 4% of all pregnancies : complicated by maternal asthma. • Poor control of chronic asthma and exacerbation of acute asthma during pregnancy -> hypoxia, low birth weight, and intrauterine growth restriction
  • 11. Motherisk update 2004 Inhaled corticosteroids A randomized controlled study • long-term use of low-dose budesonide decreases the risk of severe exacerbations • improves asthma control in patients with mild, persistent asthma of recent onset. • reduce risk of hospitalization due to asthma.
  • 12. Motherisk update 2004 Topical corticosteroids • The systemic effects of topical corticosteroids -> generally limited -> only about 3% of the medication in topical preparations is absorbed systemically following 8 hours of contact
  • 13. Motherisk update 2004 Topical corticosteroids • When corticosteroids are used long term or on large areas of skin -> systemic effects • Epidemiologic fetal safety data on topical corticosteroids -> sparse. • Two population-based studies : treatment with topical corticosteroids during pregnancy did not increase risk of congenital abnormalities in humans.
  • 14. Motherisk update discussion • oral clefts : occur at about one per thousand births • minimal absolute effect on the overall malformation rate of 3%. • palate formation : completed by 12 weeks’ gestation -> no risk of oral clefts exists thereafter.
  • 15. Motherisk update discussion • When exposure has already occurred -> a level II ultrasound scan (to detect clefting) • More studies are needed to determine which cleft phenotype is associated with corticosteroids and whether it is cleft lip (with or without palate) or cleft palate alone, or both
  • 16.
  • 17. Corticosteroids During Pregnancy and Oral Clefts: A Case-Control Study • Case subjects: 1,184 liveborn infants with nonsyndromic oral clefts. • results (logistic regression analysis): show a relationship between exposure to corticosteroids during the first trimester of pregnancy and an increased risk of cleft lip (with or without cleft palate) in the newborn infants (OR: 6.55; CI: 1.44–29.76; P: 0.015)
  • 18. Corticosteroids During Pregnancy and Oral Clefts: A Case-Control Study
  • 19. Corticosteroids During Pregnancy and Oral Clefts: A Case-Control Study • Use of corticosteroids during the first trimester of pregnancy, should be restricted to the following situations: life-threatening situations diseases without any other safe therapeutic alternative cases with replacement therapy.
  • 20.
  • 21. Birth Defects After Maternal Exposure to Corticosteroids: Prospective Cohort Study and Meta-Analysis of Epidemiological Studies • 184 women exposed to prednisone in pregnancy • 188 pregnant women who were counseled by Motherisk for nonteratogenic exposure. • primary outcome: rate of major birth defects. • A meta-analysis of all epidemiological studies was conducted.
  • 22. Birth Defects After Maternal Exposure to Corticosteroids: Prospective Cohort Study and Meta-Analysis of Epidemiological Studies • Results: no statistical difference in the rate of major anomalies between the corticosteroid- exposed and control groups. • In the meta-analysis odds ratio for major malformations with all cohort studies:1.45 and 3.03 • odds ratio for case-control studies examining oral clefts was significant (3.35 [95% CI 1.97, 5.69]).
  • 23. Birth Defects After Maternal Exposure to Corticosteroids: Prospective Cohort Study and Meta-Analysis of Epidemiological Studies • Conclusions: Although prednisone does not represent a major teratogenic risk in humans at therapeutic doses, it does increase by an order of 3.4-fold the risk of oral cleft, which is consistent with the existing animal studies.
  • 24. Birth Defects After Maternal Exposure to Corticosteroids: Prospective Cohort Study and Meta-Analysis of Epidemiological Studies
  • 25. Birth Defects After Maternal Exposure to Corticosteroids: Prospective Cohort Study and Meta-Analysis of Epidemiological Studies
  • 26. Birth Defects After Maternal Exposure to Corticosteroids: Prospective Cohort Study and Meta-Analysis of Epidemiological Studies
  • 27.
  • 28.
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  • 35. Guideline on Steroids in Pregnancy Major possible adverse effects • orofacial clefts when used preconception and in the first trimester of pregnancy, and foetal growth restriction and preterm delivery • especially potent/very potent topical corticosteroids (evidence from a Cochrane Review an d data mining of the World Health Organisation International Database of Adverse Drug Reactions)
  • 36. Guideline on Steroids in Pregnancy A large population-based cohort studies (84,133 pregnant women from the UK General Practice Research Database) • significant association of foetal growth restriction with maternal exposure to potent/very potent topical corticosteroids • but not with mild/moderate topical steroids
  • 37. Guideline on Steroids in Pregnancy • No associations of any potency with orofacial cleft, preterm delivery, and foetal death • antibiotic-containing topical corticosteroid: associated with an increased risk for foetal growth restriction and foetal death • current evidence is sufficient for doctors and pregnant women to a well-informed decision as to whether to use topical corticosteroids in pregnancy.
  • 38. Guideline on Steroids in Pregnancy • The evidence suggests that mild/moderate topical corticosteroids are preferred to potent/very potent ones in pregnancy, because of the risk of foetal growth restriction.
  • 39. Guideline on Steroids in Pregnancy
  • 40. Guideline on Steroids in Pregnancy
  • 41. Guideline on Steroids in Pregnancy
  • 42. Guideline on Steroids in Pregnancy
  • 43. Guideline on Steroids in Pregnancy
  • 44. Guideline on Steroids in Pregnancy
  • 45. Recommendations 1. Mild/moderate topical corticosteroids should be used in preference to more potent corticosteroids in pregnancy (Grade of recommendation: B). 2.Potent/very potent topical corticosteroids should be used as second-line therapy for as short a time as possible, and appropriate obstetric care should be provided as they increase the risk of foetal growth restriction (Grade of recommendation: B).
  • 46. Recommendations 3.systemic corticosteroids have a greater bioavailability than that of topical corticosteroids, and have a higher potential for foetotoxicity than topical corticosteroids (systemic corticosteroids are associated with a reduction in fetal birth weight and an increase in preterm delivery and should not be used in preference (Grade of recommendation: B).
  • 47. Recommendations 4.the danger of adverse events is increased when areas with high absorption (e.g.genitals, eyelids, flexures) are treated (Grade of recommendation: B) 5.The data are not available to determine if newer more lipophilic topical corticosteroids (mometasone, fluticasone and methylprednisolone aceponate,) with a good therapeutic index are associated with less foetal growth restriction despite theoretical grounds to suggest this and the practical advantage of once daily application (Grade of recommendation:C).
  • 48. Recommendations 6. Antibiotic-containing topical corticosteroid preparations should be avoided in pregnancy (until more robust evidence is available) because of concern for increased risk for foetal growth restriction and foetal death. (Grade of recommendation: C).
  • 49. Advice to women about using topical corticosteroids in pregnancy 1. Women can be reassured • no significantly increased risk for orofacial cleft, preterm delivery and foetal death when using topical corticosteroids in pregnancy. • no increased risk for foetal growth restriction when using mild/moderate topical corticosteroids in pregnancy.
  • 50. Advice to women about using topical corticosteroids in pregnancy 2. Women should be informed • small risk for foetal growth restriction when using potent/very potent topical corticosteroids • but this risk is less than that of systemic corticosteroids • additional risk for preterm delivery has been found in women using systemic corticosteroids. 3. Depending on the severity of their skin conditions, women should use topical corticosteroids of the least potency required and limit the amount of use
  • 51. Williams OBSTETRICS 24th • systemic corticosteroids are category D if used in the first trimester, however, they are not considered to represent a major teratogenic risk.
  • 52. ? “should be used during pregnancy only if the potential benefit justifies the potential risk to the foetus”