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ORAL CONTRACEPTION :
1.WHO ELLIGIBILITY CRITERIA
2. PRACTICAL ISSUES
DR NAZIMAH IDRIS
O& G
HOSPITAL ALOR SETAR
WHO Medical Eligibility Criteria
for Starting Contraceptive
Methods
CATEGORIES
• WHO 1 : Use the method. No
restrictions.
• WHO 2 : Can use the method. Benefits
outweighs risk.
• WHO 3 : Should not use the method.
Risk
outweighs advantages.
• WHO 4 : Do not use the method.
Unacceptable health risk.
Simplified 2-category system
(with Limited Clinical Judgment)
• WHO 1 & 2 : USE the method
• WHO 3 & 4 : DO NOT USE the
method
CRITERIA
Personal Characteristics &
Reproductive History
• Age : <40 yrs, >40 yrs
• Parity
• Breastfeeding : <6weeks postpartum, 6weeks
to 6 mths, >6mths postpartum
• Postpartum : <21days, >21days
• Smoking : age <35yrs, age >35yrs <15
cig/day, age >35yrs >15cig/day
• Obesity : BMI >30 kg/m2
Cardiovascular disease
• Multiple risk factors for CAD (older age,
smoking, diabetes, HPT)
• Hypertension : BP control, vascular disease
• Hypertension during pregnancy, now normal
• DVT/Pulmonary Embolism : Current or past,
surgery with/without prolonged
immobilization, Family history
Cardiovascular disease
• Superficial venous thrombosis
• Ischemic Heart Disease : Current or
past
• Stroke : Current or past
• Hyperlipidemia
• Valvular Heart Disease :
complicated/uncomplicated
Neurologic conditions
• Epilepsy
• Headaches :
–
–
–
–

Non-migraine (mild or severe)
Migraine <35, no focal neuro symptoms
Migraine >35, no focal neuro symptoms
Migraine with focal neuro symptoms, any
age
Reproductive Tract Infections
& Disorders
•
•
•
•
•
•

Irregular menses
Unexplained vaginal bleeding
Ovarian tumours (benign/malignant)
Endometrial cancer
Uterine fibroids
Gestational Trophoblastic Disease
(benign/malignant)
Reproductive Tract Infections
& Disorders
•
•
•
•

Cervical cancer/CIN
Breast disease : benign/undiagnosed
Breast cancer : current/past
Pelvic inflammatory disease :
current/past
• Sexually transmitted infections :
current/past
Endocrine conditions
• History of Gestational diabetes
• Insulin/Non-insulin dependant diabetes
: non-vascular disease
• Diabetis with
nephropathy/retinopathy/neuropathy
• Other microangiopathy, diabetes
>20yrs
• Thyroid disorders
Gastrointestinal conditions
• Gall bladder disease : with or no symptoms,
medical or surgical treatment
• History of pregnancy-related cholestasis
• Past COC-related cholestasis
• Viral hepatitis : active/carrier
• Cirrhosis
• Liver tumour : benign/malignant
In summary…
CATEGORY 4
•
•
•
•

Breastfeeding <6weeks postpartum
Smoking at age >35yrs >15 cig/day
Multiple risk factors for CAD
Poorly controlled hypertension, vascular
disease
• DVT/PE, major surgery with prolonged
immobilization
• Ischemic Heart Disease
CATEGORY 4 (cont.)
• Cerebrovascular accident
• Complicated valvular heart disease
• Migraine with focal neurological
symptoms
• Current breast cancer
• Diabetes with angiopathy
• Active viral hepatitis, liver tumour
CATEGORY 3
•
•
•
•
•

Postpartum <21days
Lactation 6 weeks to 6 mths
Undiagnosed vaginal/uterine bleed
Age >35yrs smoke >15cig/day
History of breast cancer, no recurrence past
5 yrs
• Interacting drugs
• Gallbladder disease
CATEGORY 2
• Headache after OCP, not migraine
• Diabetes, no complications
• Major surgery, no prolonged
immobilization
• Mild hypertension
• Undiagnosed breast mass
• Cervical cancer/CIN
OCP – PRACTICAL ISSUES
ISSUES
• Patterns of use & Efficacy rates
• Drawbacks & Fears of OCP use
• Formulations of OCP – which type to
choose?
• Instructions on use
• Drug Interactions
• Emergency contraception
Patterns of use & Efficacy rates
• Typical user vs perfect user
• Perfect user – never misses taking a
pill, takes at the same time everyday,
never vomits or has diarrhoea.
Pregnancy rate: 1 in 1000/year.
• Typical user – Pregnancy rate: 50 in
1000/year
Drawback & Fears
• No protection against infection
• Systemic side effects – nausea,
vomiting, headache, breast tenderness,
acne, ?weight gain
• More serious events - myocardial
infarct, ischemic stroke, hemorrhagic
stroke
• Fears of side effects – premature
discontinuation
Formulations
• Estrogen : dosage : 150ug -> 50ug ->
35ug
->25ug ->20ug
• Progestogen : 1st/2nd/3rd generation
Factors to consider in
starting/switching OCP

OBJECTIVE

ACTION

Lower VTE risk

Lower E dose

Reduce nausea,
breast tenderness,
headache

Lower E dose

Minimise abnormal
bleed

Higher E, more
potent P

Minimise
androgenic effects

3rd generation P

Avoid dyslipidemia

3rd generation P
Instructions on use – missed pill
• <24H : take immediately, cont. others
• 24H : take the missed and scheduled
pill together
• >24H (2 or more missed pills) : take last
missed pill, discard other missed pill,
take next pill on time, use additional
contraception for remainder of cycle
Instructions on use – additional
contraceptive method
• 1st 7 days after start of use
• Use for 7 days if >12H late in taking
OCP
• Use while taking interacting drug + 7
days thereafter

•

Adapted from Hatcher et al. Contraceptive Technology. 17 th rev.ed. New York: Ardent
Media, 1998: 451-3.
Drug Interactions
• Drug decreases effectiveness of OCP:
– Anti-epileptic : Carbamazepine, Dilantin,
Phenobarbitone – 40%. Others: Valproate,
Gabapentin – no effect.
– Antibiotics : Rifampicin. Others: Amoxycillin
Metronidazole – weak association
Emergency contraception
• Pre-treatment with oral anti-emetic 1
hour before each OCP dose
• First dose of OCP within 72 hours of
unprotected intercourse, repeat after 12
hours
• Dosage: 500ug of levonorgestrel +
100ug of ethinyl estradiol
• Reduces pregnancy rate by 75%
Thank You

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ORAL CONTRACEPTION GUIDELINES FOR ELIGIBILITY AND PRACTICAL USE

  • 1. ORAL CONTRACEPTION : 1.WHO ELLIGIBILITY CRITERIA 2. PRACTICAL ISSUES DR NAZIMAH IDRIS O& G HOSPITAL ALOR SETAR
  • 2. WHO Medical Eligibility Criteria for Starting Contraceptive Methods
  • 3. CATEGORIES • WHO 1 : Use the method. No restrictions. • WHO 2 : Can use the method. Benefits outweighs risk. • WHO 3 : Should not use the method. Risk outweighs advantages. • WHO 4 : Do not use the method. Unacceptable health risk.
  • 4. Simplified 2-category system (with Limited Clinical Judgment) • WHO 1 & 2 : USE the method • WHO 3 & 4 : DO NOT USE the method
  • 6. Personal Characteristics & Reproductive History • Age : <40 yrs, >40 yrs • Parity • Breastfeeding : <6weeks postpartum, 6weeks to 6 mths, >6mths postpartum • Postpartum : <21days, >21days • Smoking : age <35yrs, age >35yrs <15 cig/day, age >35yrs >15cig/day • Obesity : BMI >30 kg/m2
  • 7. Cardiovascular disease • Multiple risk factors for CAD (older age, smoking, diabetes, HPT) • Hypertension : BP control, vascular disease • Hypertension during pregnancy, now normal • DVT/Pulmonary Embolism : Current or past, surgery with/without prolonged immobilization, Family history
  • 8. Cardiovascular disease • Superficial venous thrombosis • Ischemic Heart Disease : Current or past • Stroke : Current or past • Hyperlipidemia • Valvular Heart Disease : complicated/uncomplicated
  • 9. Neurologic conditions • Epilepsy • Headaches : – – – – Non-migraine (mild or severe) Migraine <35, no focal neuro symptoms Migraine >35, no focal neuro symptoms Migraine with focal neuro symptoms, any age
  • 10. Reproductive Tract Infections & Disorders • • • • • • Irregular menses Unexplained vaginal bleeding Ovarian tumours (benign/malignant) Endometrial cancer Uterine fibroids Gestational Trophoblastic Disease (benign/malignant)
  • 11. Reproductive Tract Infections & Disorders • • • • Cervical cancer/CIN Breast disease : benign/undiagnosed Breast cancer : current/past Pelvic inflammatory disease : current/past • Sexually transmitted infections : current/past
  • 12. Endocrine conditions • History of Gestational diabetes • Insulin/Non-insulin dependant diabetes : non-vascular disease • Diabetis with nephropathy/retinopathy/neuropathy • Other microangiopathy, diabetes >20yrs • Thyroid disorders
  • 13. Gastrointestinal conditions • Gall bladder disease : with or no symptoms, medical or surgical treatment • History of pregnancy-related cholestasis • Past COC-related cholestasis • Viral hepatitis : active/carrier • Cirrhosis • Liver tumour : benign/malignant
  • 15. CATEGORY 4 • • • • Breastfeeding <6weeks postpartum Smoking at age >35yrs >15 cig/day Multiple risk factors for CAD Poorly controlled hypertension, vascular disease • DVT/PE, major surgery with prolonged immobilization • Ischemic Heart Disease
  • 16. CATEGORY 4 (cont.) • Cerebrovascular accident • Complicated valvular heart disease • Migraine with focal neurological symptoms • Current breast cancer • Diabetes with angiopathy • Active viral hepatitis, liver tumour
  • 17. CATEGORY 3 • • • • • Postpartum <21days Lactation 6 weeks to 6 mths Undiagnosed vaginal/uterine bleed Age >35yrs smoke >15cig/day History of breast cancer, no recurrence past 5 yrs • Interacting drugs • Gallbladder disease
  • 18. CATEGORY 2 • Headache after OCP, not migraine • Diabetes, no complications • Major surgery, no prolonged immobilization • Mild hypertension • Undiagnosed breast mass • Cervical cancer/CIN
  • 20. ISSUES • Patterns of use & Efficacy rates • Drawbacks & Fears of OCP use • Formulations of OCP – which type to choose? • Instructions on use • Drug Interactions • Emergency contraception
  • 21. Patterns of use & Efficacy rates • Typical user vs perfect user • Perfect user – never misses taking a pill, takes at the same time everyday, never vomits or has diarrhoea. Pregnancy rate: 1 in 1000/year. • Typical user – Pregnancy rate: 50 in 1000/year
  • 22. Drawback & Fears • No protection against infection • Systemic side effects – nausea, vomiting, headache, breast tenderness, acne, ?weight gain • More serious events - myocardial infarct, ischemic stroke, hemorrhagic stroke • Fears of side effects – premature discontinuation
  • 23. Formulations • Estrogen : dosage : 150ug -> 50ug -> 35ug ->25ug ->20ug • Progestogen : 1st/2nd/3rd generation
  • 24. Factors to consider in starting/switching OCP OBJECTIVE ACTION Lower VTE risk Lower E dose Reduce nausea, breast tenderness, headache Lower E dose Minimise abnormal bleed Higher E, more potent P Minimise androgenic effects 3rd generation P Avoid dyslipidemia 3rd generation P
  • 25. Instructions on use – missed pill • <24H : take immediately, cont. others • 24H : take the missed and scheduled pill together • >24H (2 or more missed pills) : take last missed pill, discard other missed pill, take next pill on time, use additional contraception for remainder of cycle
  • 26. Instructions on use – additional contraceptive method • 1st 7 days after start of use • Use for 7 days if >12H late in taking OCP • Use while taking interacting drug + 7 days thereafter • Adapted from Hatcher et al. Contraceptive Technology. 17 th rev.ed. New York: Ardent Media, 1998: 451-3.
  • 27. Drug Interactions • Drug decreases effectiveness of OCP: – Anti-epileptic : Carbamazepine, Dilantin, Phenobarbitone – 40%. Others: Valproate, Gabapentin – no effect. – Antibiotics : Rifampicin. Others: Amoxycillin Metronidazole – weak association
  • 28. Emergency contraception • Pre-treatment with oral anti-emetic 1 hour before each OCP dose • First dose of OCP within 72 hours of unprotected intercourse, repeat after 12 hours • Dosage: 500ug of levonorgestrel + 100ug of ethinyl estradiol • Reduces pregnancy rate by 75%