Contraception and medical disorders in pregnancy prof ken
1.
2. The ideal reversible
contraception
100% effective after a single simple procedure
100% safe with no danger or unwanted side
effects
Independent of the medical professions
100% reversible by simple procedure
Independent of coitus
Not relying on user motivation
Cheap and easy to distribute
Pre fertilisation in action
Used by or visible to the woman
Additional beneficial effects
3. The balance of advantage
The efficacy of the method
The patient’s wishes
The advantages and disadvantages of the
method
Medical problems
4. Failure rates during the first year of contraceptive use
(USA 1995- National survey)
Method
Female sterilisation
IUD-LNG
Male sterilisation
Implant
IUD-Copper T380A
IUD- progesterone
POP
Injectable
COC
Diaphragm and spermicides
Male condom
Cervical cap-Nulliparous
Sponge- nulliparous
Periodic abstinence
Female condom
Withdrawal
Spermicides
Cervical cap-parous
Sponge- parous
No method
Ideal use(per cent)
Typical use(per cent)
0.05
0.1
0.1
0.05
0.6
1.5
0.5
0.3
0.1
6.0
3.0
9.0
9.0
0.05
0.1
0.15
0.2
0.8
2.0
3.0
3.1
7.6
12.1
13.9
20.0
20.0
20.5
21.0
23.6
25.7
40.0
40.0
85
5.0
7.0
6.0
20.0
20.0
85
5. Relative popularity with
different methods(U.K.)
COCP ------------------------ 36%
Barrier methods--------------21%
Vasectomy -------------------16%
Female sterilisation --------- 10%
IUCD ------------------------- 7%
O.C. with barrier ------------ 3%
NFP --------------------------- 2%
CI ------------------------------ 1%
No method ------------------- 4%
6. Medical conditions which contraindicate the
use of a contraceptive method
(WHO classification 1994)
A condition in which there is no restriction for
the use of the contraceptive method
A condition where the advantage of the method
generally outweighs the theoretical or proven
risks
A condition where the theoretical or proven risks
usually outweigh the advantages. But if the
patient accepts the risks and rejects or should not
use relevant alternatives, the method can be used
with caution/ additional care
A condition which represents unacceptable health
risks.
7. Mechanism of action and
biologic activity of COC
Inhibition of ovulation through combined action
of progestogen and oestrogen
Dominant component is progestogen:
Suppresses LH release
Creates thick cervical mucous
Inhibits capacitation
Oestrogen- suppresses FSH and LH release
-Accelerates ovum transport
-Alters secretion affecting
implantation
8. Oestrogen induced alterations
in the blood
Encourages venous thrombo-embolism
Reduced anti-thrombin3
Elevated fibrinogen
Elevated Vit.K dependent coagulation factors
Increased fibrinolytic activity
In the presence of significant arterial wall
disease, oestrogen may also promote
superimposed arterial thrombosis
Elevated blood lipids with reduced HDLcholesterol
9. Effect of COCP on the Liver
The liver is affected in more ways than any other
extra-genital organ
Active transport of biliary constituents is
impaired by both Oestrogen and Progestogen
The mechanism is unclear, but cholestatic
jaundice and pruritus are associated with the
COCP
The COCP can cause an increase in cholesterol
saturation of the G.B. bile with an increased
incidence of gall stones
Benign hepatic adenomas are associated with the
COCP
A few cases of hepato-cellular cancer have been
reported
10. Absolute contraindications to the COC
(WHO System 1994)
Cardiovascular
Venous thrombosis- h/o thromboembolic
disorders or close family history
Arterial thrombosis- angina, MI
Cerebral thrombosis or haemorrhage
Severe hypertension
Elective major surgery
Leg immobilisation
Hyperlipidemia (Cholesterol > 8mmol/l)
Congenital or acquired heart disease
11. Absolute contraindication to COC
(WHO System 1994)
Cardiovascular
Focal migrane or status migranous
Transient ischaemic attacks
Coagulation tendency
- thrombophylias
•
•
•
•
- Fac. V Leiden mutation
- Phospholipid syndrome
- activated protein C resistance
- blood dyscrasias
- some autoimmune/ rheumatoid disorders
- Post-splenectomy (platelets > 500 x 109)
Severe inflammatory bowel disease- Chron’s, Ulcerative colitis
Opthalmic vascular disease
Exposure to high altitude
Combination of risk factors
12. Absolute contraindications to
COC
Hepatic
Acute liver disease (whenever LFTs abnormal)
Chronic liver disease
Cholestatic jaundice of pregnancy or OC
associated
Chronic idiopathic jaundice
History of liver adenoma, carcinoma
Focal nodular hyperplasia
Galstones causing symptoms
The acute porphyrias
13. Absolute contraindications to COC
Other
Known or suspected oestrogen dependent neoplasia
Serious condition affected by sex steroids
- pemphigoid gestationis
- Haemolytic uraemic syndromes
- Pancreatitis
- Hypertrigliceridaemia
- Chorea
- Erythema multiforme
- Thrombocytopenic purpura
Undiagnosed abnormal vaginal bleeding
Pregnancy
Throphoblastic disease
Continuing anxiety unrelieved by counselling
14. Relative contraindication to
COC
Women over 35, who smoke
Essential hypertension, but controlled on
treatment
Latent or established diabetes mellitus
Cholelithiasis, but can be used after
cholecystectomy
Young, first degree relative with breast cancer
Obesity, if associated with other risk factors
Non- focal migraine when ergotamine not
required
Sickle cell disease
Chron’s Disease
15. Reduced OC efficacy due to
interactions
Gastroenteritis
impaired absorption of
OC
Drugs causing induction
of hepatic enzymes
↑ metabolite activity
& ↑ elimination in bile of
both oestrogen and
progesterone
Some anti-epileptics:
- phenobarbitone
- carbamazepine
- phenytoin
- primidone
use alternative method
IUD or IUS or 50µg
containing OC
16. Reduced OC efficacy due to
interactions
Anti- TB:
- Rifampicin
very potent enzyme inducer
use DMPA with 8 week
injection interval or alternate
method
wait 8 weeks after end of
course before recommencing
COC
Antibiotics causing
change in bowel flora:
- Penicillin
- Tetracyclines
- Cephalosporins
OC are conjugated in the
liver, excreted in the bile and
partly reabsorbed. If gut
bacteria are inhibited by
antibiotics, reabsorption may
not occur
17. Other drugs that may reduce
efficacy of COC
Cholesterol lowering
agents
↓ cholesterol and
triglycerides
↓ OC efficacy
Sedatives and hypnotics
Enzyme inducer
Antacids
retroviral
↓ intestinal absorption:
take 2 hours apart
Do not use COCs
18. Drugs that may increase COC
level
Paracetamol
Completes in bowel wall
for conjugation to
sulphate
⇒possible more O2
available for absorption:
take 2 hours apart
erythromycin
* Potent inhibitor of
oestradiol metabolism
19. Modification of other drug
action by OC
Alcohol
Anticoagulants
Aminocaproic acid
Caffeine
Corticosteroids
Cyclosporine
Phenothyzines
Sedatives/ hypnotics
Tricyclic
antidepressants
Vitamine B12
Beta blockers
antipyretics
20. Medical disorders for which
COCP prescribed
Spasmodic dysmenorrhoea
Menstrual irregularities
Premenstrual tension
Menorrhagia (even with fibroid) and anaemia
Endometriosis
Functional ovarian cysts
Ovulation pain
Oestrogen deficiency
PCOS
Acne
Prophylaxis against ovarian carcinoma
21. Other non contraceptive benefits
of the COCP
Prevents ectopic pregnancies
Reduces incidence of benign breast disease
? Reduces fibroid size and menorrhagia
Protects against ovarian and endometrial
carcinoma
22. Mechanism of action of POPs
Inhibition of ovulation in at least 60% and
more often in older women
Alteration in cervical mucous
Inhibits capacitation
23. Indications for POP
During lactation
Contraindications to or side effects with COCP
Hormonal method preferred
Women > 35 years old who smoke
Chronic systemic disease which oestrogen might
exacerbate (SLE,Chron’s disease,Ulcerative
Colitis)
Diabetes
Hypertension
Migraine
Preference
24. Contraindications to POP
Severe arterial wall disease
or at risk of :– Liver adenoma or carcinoma
– Severe cholestatic jaundice
– Recent trophoblastic disease
– Acute porphyria
25. Indications for IUCD
Effective
Safe
Indepent of coitus
No effort required
Motivation necessary only at time of insertion
Relatively cheap and easy to distribute
Does not influence milk volume/composition
Under woman’s control
Continuation rates high
Nearly always reversible
26. Contraindications to IUCD
Pregnancy
Serious related pregnancy related infection
within previous year
Acute pelvic inflammatory disease
Significant uterine abnormality
Severe dysmenorrhoea
Undiagnosed uterine bleeding
Carcinoma of cervix or endometrium
Previous ectopic pregnancy
Risk from bacteraemia
e.g. valvular heart disease
renal dialysis
immunosuppressive drugs
29. Subdermal implants
Jadelle (2 rods) or Implanon are now available
(Norplant is no more!)
Work by ovulation inhibition, supplemented by
the usual mucus and endometrial effects
Last 3 years
But tissue levels are lower in heavier women especially by 3rd year
⇒re- implant sooner
30. Advantages of subdermal implant
Efficacy and convenience
Long action
Absence of initial peak dose given orally
Blood level steady
HDL/LDL ratio and clotting factors unchanged
No concern regarding past history of venous
thrombosis
Excellent choice for Diabetics
No effect on blood pressure
Can be used with past ectopic history
Rapidly reversible
31. Disadvantages of Implants
Altered bleeding pattern- 18%
Frequent bleeding and spotting
(Treat with cyclical COCP therapy)
Minor side effects- acne, headache, breast pain,↓
libido
Weight ↑- 35% put on 3 kg
Possible hypo-oestrogenaemia- because
ovulation suppressed and no oestrogen supplied
Local adverse effects
32. Advantages of injectables
High effectiveness - > than COCP
Freedom from fear of forgetting
Highly convenient- not coitus-related
Fully reversible (though some delay)
33. Disadvantages of injectables
Irreversible for at least 2-3 months
⇒have to tolerate early side effects for a long time
Can cause menstrual disturbance
? Risk of hypo-oestrogenism
Delay in return of fertility
Weight gain (↑appetite +? Anabolic effect)
↑ prolactin and galactorrhoea
Acne (surprisingly uncommon, mildly androgenic effects)
Enuresis
Subjective effects(loss of libido, depression,
bloatedness, headache, leg cramps)
34. Implant and Injectables
Menstrual bleeding patterns are highly
variable among users of implant
contraception.Some will experience
increased flow/bleeding days
Depo-Provera can be used to treat
menorrhagia if regularity of the cycle is
not a concern.
35. Barrier Methods
Condom useful – no adverse effects on
pre-existing disease (limited by poor
compliance and high failure rate)
Protective against STDs
The diaphragm,Femidom and spermicides
are alternatives (high failure rate)
Less protective against STDs
38. Valvular/congenital Heart
Disease
Valvular/Congenital Heart Disease is the leading medical cause
of maternal mortality in Malaysia
It complicates 1 to 4% of all Obstetric admissions
Contraception is all important in management:- from the general health point of view
-family should be small and completed early
-space between pregnancies will allow for
definitive treatment.
-There are conditions where pregnancy may
be contraindicated.
39. IUCD and Valvular/Congenital
Heart disease
In patients with valvular and congenital heart
disease IUCD use is limited by the risk of
bacterial endocarditis
The IUCD may be used when other options are
restricted
-- insertion under antibiotic cover
Absolute contraindications in those with prosthetic
valve and those with a past history of endocarditis
Injectables and Implants are safe methods
COCP contraindicated in valvular/congenital heart
disease
40. For completed family or
pregnancy contraindicated
Surgical method is ideal
Vasectomy rather than tubal ligation
Interval Ligation is preferred to
immediately post-partum
Minilaparotomy is ideal but laporoscopy in
selected cases
41. COC Pill and Venous
Thrombosis
Oestrogen increases the production of
clotting factors
Progestogens have no significant impact
on clotting factors
All low dose COCPs have an increased
risk of venous thromboembolism
Smoking has no effect on the risk of
venous thrombosis
42. Factor V Leiden mutation
Produces changes in structure of factor V
Normally protein C inhibits clotting at level of factor V
In Factor V Leiden mutation, this does not happen
The entire clotting cascade is then resistant to the Protein C system
--------------------------------------------------------------- The most common inherited form of venous thrombosis
Heterozygotes for Factor V Leiden mutation- x8 ↑ risk of thrombosis
Homozygotes for Factor V Leiden mutation- x80↑ risk of thrombosis
Highest prevalence of Factor V Leiden mutation is in Europeans(34%)
Very rare in Africans/Asians (0.4%)
44. 3rd.generation progestogens and D.V.T.s
Less androgenic than the older progestogens with a
lesser adverse effect onserum lipids
Women on 3rd. Generation progesterones have a
higher circulating conc. of HDL and lower conc. of
LDL
Considered therefore that risk of MI and Stroke
would be lower – but not possible to prove
BUT – 3 studies(95/96) suggested a x2-3 increased
risk of venous TE with pills containing gestodene
or desogestrol compared with levonogestrel or
norethisterone
CSM advised – all women at increased risk of
thrombosis(BMI>30),VVs,FH of DVT,PIH,should
change to a 2nd.generation pill
45. Relative risk and actual
incidence of VTE
Population
Relative risk
Incidence
Young femalegeneral population
Pregnant
High dose OC
Low dose OC
Leiden mutation
carrier
Leiden carrier +
OC
Leiden mutation
homogenous
1
4.5/100,000
12
6-10
3-4
6-8
48-60
24-50
12-20
24-40
30
120-150
80
320-400
46. COCP Contraception and
Surgery
X4to6 fold increased risk of thromboembolic
complications in users of COCP
COCP should be discontinued at least 4 weeks
before major surgery or prolonged immobilisation
Can be recommenced on the first day of the next
period but at least 14 days after the operation
No need to discontinue for minor
surgery/laparoscopy
No need to discontinue if taking POP/other
progesterone preparation
47.
48. Ischaemic Heart Disease and
COCP
Oestrogen increases the production of clotting
factors
Progestogens have no significant impact on
clotting factors
Past users of OC do not have an increase
incidence of CV disease
POP pill has a negligible impact on lipoprotein
profile - no increase risk of venous or arterial
thrombosis
Avoid if hypercholesterolaemia
49. Arterial thrombosis and the
COCP
Smoking and oestrogen have an addictive effect on the
risk for arterial thrombosis
Hypertension is a very important additive risk factor for
stroke in the COCP patient
Almost all M.I. and strokes in OC users occur with high
dose products or users with cardiovascular risk factors
and more than 35 years old.
Arterial thrombosis has a dose- response relationship with
oestrogen but insufficient data to determine whether there
is a risk difference with 20, 30 or 35µg ethinyl oestradiol
50. Incidence of M.I. In
reproductive age women
< 35 years old
Overall increased
Non- smokers
Non- smokers +
OC
Smokers
Non- smokers +
OC
5/100000/year
4
4
8
43
> 35 years old
Non- smokers
Non- smokers +
OC
Smokers
Smokers + OC
16
40
88
485
51. Contraception and Ischaemic
Heart Disease
– COCP best avoided
– Patients on anticoagulants should not be on
COCP
– IUCD is an excellent form of contraception
– (LNG-IUS ---- very useful)
52. In Ischaemic Heart Disease
Use alternative contraception to the
COCP:
- IUCD/IUS
- Barrier method
- Implant – may be used in heavy
smokers
- those older than 35yrs.
- hypertensives
- hypercholesterolaemia
53. Injectables and Implants are safe method
fir those with heart disease
Antibiotic cover for the implants may be
necessary
Failure rates are low(PI 0-1.0) and these
methods provide long periods of
contraception
54. Incidence of stroke in
reproductive age women
Incidence of ischaemic
stroke
Haemorrhagic stroke
Excess cases/year
~OCs including
Smokers & HPT
5/100,000/year
1-3 under 35
10 over 35
6/100,000/ year
2/100,000/year in low dose
OC users
1/100,000/year in low dose
OC users <35
8/100,000/year in high dose
users
55. Migraine Sufferers
Increased risk of ischaemic stroke in
COCP users
Especially - with other arterial risk factors
- focal neurological symptoms
(asymetrical)
56. Risk of Thrombotic stroke in
Migraine
Background risk for women aged 20 – 2/100,000
Migraine>once a month + COCP - 10/100,000
------------------------Background risk for women aged 40 –
20/100,000
Migraine >once a month - 56/100,000
Migraine > once a month + COCP - 100/100,000
57. COCP contra-indicated in the
following groups of patients
Migraine with aura during which there are
focal neurological symptoms
Status Migrainosis>72 hours
All migraines treated with ergot
deriveratives
Moderately severe migraine without auras
but with other additional arterial risk
factors
58. Stop the COCP
Consider --- the POP
--- Implant/Injection
--- IUCD/LNG-IUS
59. Opthalmic Disorders and the
COCP
Occasional eye discomfort with contact
lenses
---------------------------------- Loss of vision: Retinal artery/vein thrombosis
Transient cerebral ischaemia
Benign intracranial hypertension
60. Elevated BP and COC
↑ BP reported in some on COCP- occasionally
within a few months of use
Age is strongly correlated with ↑ BP in COCP
users
Women with previous HPT in pregnancy may be
more likely to develop ↑ BP on COCP
↑ BP that developes on COCP usually returns to
normal after stopping
Women < 35, otherwise healthy and with BP
well controlled can be prescribed the lowest
oestrogen dose medication under close
supervision
In any patient BP rises markedly stop
61. Diabetes Mellitus
– Arterial Disease is a major hazard for diabetics
– Avoid Oestrogen with its thrombotic risks
– POP can be a method of choice
– Alternatively – Implant
–
–
–
–
- Injection
- IUCD/IUS
- Barrier method
- Sterilisation
62. Possible Use of COCP in
Diabetes Mellitus
Young <25 : recent DM
Free of any complications – arteries, nerves,
kidneys, retina.
Non smoker, normotensive, BMI<30
Perceived to need maximum protection against
pregnancy
No satisfactory alternative
------------------------------------------ Can use an ultra-low COCP using only a lipid
friendly progestogen –mercilon with only 20ug.
Oestrogen
But COCP for the shortest possible time
Encourage family as soon as circs. Permit
63. Epilepsy and Contraception
Effectiveness of hormonal contraception is reduced
in women on anticonvulsants which are liver
enzyme-inducers
(phenobarbitone, phenotoin,
carbamezapine, primidone)
Sodium valproate,
lamotrigine,vigabatrine,benzodiazepine, do not
have this effect.
Liver enzyme inducing drugs also increase the
metabolism of progestogens and double the usual
dose may be required
64. Epilepsy and contraception
If hormonal contraception: COCP ----------- 50ugEO should be used with a
reduced pill free interval
POP ----------- Only to be used if no other
acceptable method
Depot Provera – Reduce dosing interval
From 12 to 10 weeks
------------------------------- Alternative non hormonal methods are better
used
65. Depression
Patients with a history of emotional disturbance
may be prone to depression on the OC
If severe – change to alternative form of
contraception
Women with PMS may have a varying response
to OC – ranging from symptomatic improvement
to a worsening of the condition
66. Smoking
Smoking produces a shift to
hypercoaguability
A former smoker must have stopped for at
least one year to be regarded as a non
smoker
Women who have nicotine obtained from
patches or gum in their blood stream
should be regarded as smokers
67. Abdominal pain and COC use
Thrombosis of major intra-abdominal
vessels
Gallstones
Pancreatitis
Liver adenoma
Chron’s disease
Acute porphyria
70. Gestational Trophoblastic
Disease and Contraception
No evidence of Increased risk in GTD by previous
COCP use
Close monitoring is required after hydatidiform mole
by serial hCG levels
Must avoid pregnancy until after 6 months of normal
levels
(may mask a rise in hCG due to malignancy)
Must not take COCP until after hCG levels have
returned to normal
(prolongs high hCG status
increases risk of requiring chemotherapy after HM)
71. COCP and menorrhagia
Low dose pills are as effective as high in
reducing menstrual flow
COCP can be used to treat menorrhagia
a/w DUB among teenage and
perimenopausal groups
COCP used to treat menorrhagia reduces
menstrual blood flow by 50%
72. IUCD and menorrhagia
Inert and copper IUCD a/w increase in
menstrual blood loss (55% ↑ with copper
IUCD)
But menstrual blood loss ↓ if device
impregnated with progestogen
LNG-IUS- 20% amenorrhoeic after 1 year
Menorrhagia a/w inert/ copper IUCD can
be treated with NSAIDs
73. Endometriosis
The use of COCP is a/w a lower incidence of
endometriosis
The protective effect is probably limited to
current or recent use
Consistent with the belief that hormonal
treatment of endometriosis should be viewed as
suppressive not curative
Use progestogen dominant COCP on a‘tricyclic’
regime
74. Uterine fibroids
Uterine fibroids are not a contraindication for low dose
COCP
There is evidence that the risk of fibroids is decreased by 1/3
in women who used higher dose of COCP for 10 years
Case controlled studies with lower dose have found neither a
decrease nor an increase in risk although Nurses Health
Study reported a slightly increased risk when COCP was
used in early teenage
The administration of low dose COCP to women with fibroid
does not stimulate fibroid growth
COCP is a/w reduction in menstrual bleeding
75. COCP and Pelvic infection
Pelvic Inflammatory Disease usually a consequence
of STD
The risk of hospitalisation for PID is reduced by about
50-60% in COCP users - but at least 12 months of use
are necessary & protection is limited to current users
If the patient does get pelvic infection, the severity of
salphingitis found at laparoscopy is reduced
(gonococcus)
76. COCP and Pelvic infection
The mechanism of protection is unknown:
? Thickening of cervical mucous to prevent movement of
pathogens and bacteria laden sperm in uterus and tube
↓menstrual bleeding ↓ movement of pathogens into tubes
↓ in culture medium
But suggested that chlamydial infection may be
enhanced- 15 of 17 studies showed an association
of COCP and chlamydial cervicitis (? Due to
ectropion)
But COCP users are protected against
symptomatic PID and there is no evidence for ↑
tubal infertility
77. Examination and follow- up
Thorough history and
examination
BP
Breasts
Liver
Extremities
Pelvic organs
Cervical smear
Follow- up visits
First 3 months after
OC
Thereafter yearly if no
risk factors
If risk factorssee 36 monthly by trained
personnel
78.
79. Blood tests
Glucose, lipid and
lipoproteins
Young women at least
once
Women > 35 years old
Strong family history of
heart disease, HPT, DM
History of gestational
DM
Zanthomatosis
Obese women
Diabetic women
Coagulation screen
Personal/family history in
young first degree
relative of idiopathic
thrombophilia
Check for:
Antithrombin III
deficiency
Protein C deficiency
Protein S deficiency
Factor V Leiden mutation
Prothrombin gene
mutation
Antiphospholipid
syndrome
80. Consider whether the medical
condition would : Increase the risk of venous thromboembolism
Predispose to arterial wall disease
Adversely affect liver function
Be influenced by sex hormones
Require treatment with an enzyme
inducing drug
Risk of exacerbating pelvic sepsis