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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
The balance of advantage
 The efficacy of the method
 The patient’s wishes
 The advantages and disadvantages of the
method
 Medical problems
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
Relative popularity with
different methods(U.K.)
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COCP ------------------------ 36%
Barrier methods--------------21%
Vasectomy -------------------16%
Female sterilisation --------- 10%
IUCD ------------------------- 7%
O.C. with barrier ------------ 3%
NFP --------------------------- 2%
CI ------------------------------ 1%
No method ------------------- 4%
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.
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
Oestrogen induced alterations
in the blood

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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
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
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
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
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
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
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
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
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
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
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
Modification of other drug
action by OC
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Alcohol
Anticoagulants
Aminocaproic acid
Caffeine
Corticosteroids
Cyclosporine
Phenothyzines
Sedatives/ hypnotics

 Tricyclic
antidepressants
 Vitamine B12
 Beta blockers
 antipyretics
Medical disorders for which
COCP prescribed
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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
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
Mechanism of action of POPs
 Inhibition of ovulation in at least 60% and
more often in older women
 Alteration in cervical mucous
 Inhibits capacitation
Indications for POP
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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
Contraindications to POP
 Severe arterial wall disease
or at risk of :– Liver adenoma or carcinoma
– Severe cholestatic jaundice
– Recent trophoblastic disease
– Acute porphyria
Indications for IUCD
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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
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
Relative contraindications to
IUCD
 Past history of STDs
 Multiple sexual partners
 Menorrhagia
 Copper allergy
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
Advantages of subdermal implant
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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
Disadvantages of Implants
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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
Advantages of injectables
 High effectiveness - > than COCP
 Freedom from fear of forgetting
 Highly convenient- not coitus-related
 Fully reversible (though some delay)
Disadvantages of injectables
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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)
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.
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
General Medical Disorders
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Congenital/Valvular Heart Disease
Venous Thrombo-embolism
Arterial Heart Disease
Stroke
Migraine
Opthalmic Disorder
Hypertension
Diebetes mellitus
Epilepsy
Depression
Smoking
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.
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
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
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
Factor V Leiden mutation
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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%)
Clotting mechanism
Fibrinolysins
Protein C
Protein S
Antithrombins
Plasmin

Prothrombin

Antithrombins

Protein C & S

Thrombin

Factor V +
other clotting
factors

Plasminogen
Fibrinogen

Fibrin ← Plasmin
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
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
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
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
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
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
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)
In Ischaemic Heart Disease
 Use alternative contraception to the
COCP:
- IUCD/IUS
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- Barrier method
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- Implant – may be used in heavy
smokers
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- those older than 35yrs.
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- hypertensives

- hypercholesterolaemia
 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
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
Migraine Sufferers
 Increased risk of ischaemic stroke in
COCP users
 Especially - with other arterial risk factors

- focal neurological symptoms
(asymetrical)
Risk of Thrombotic stroke in
Migraine
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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
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
 Stop the COCP
 Consider --- the POP
--- Implant/Injection
--- IUCD/LNG-IUS
Opthalmic Disorders and the
COCP
 Occasional eye discomfort with contact
lenses
---------------------------------- Loss of vision: Retinal artery/vein thrombosis
 Transient cerebral ischaemia
 Benign intracranial hypertension
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
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
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
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
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
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
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
Abdominal pain and COC use
 Thrombosis of major intra-abdominal
vessels
 Gallstones
 Pancreatitis
 Liver adenoma
 Chron’s disease
 Acute porphyria
Gynaecological Problems
 Gestational Trophoblastic Disease
 Ectopic Pregnancy
 Menorrhagia
 Endometriosis
 Fibroids
 Pelvic Infection
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)
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%
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
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
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
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)
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
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 factorssee 36 monthly by trained
personnel
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
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
Remember


DIMS



BNF
Contraception and medical disorders in pregnancy prof ken
Contraception and medical disorders in pregnancy prof ken

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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
  • 27. Relative contraindications to IUCD  Past history of STDs  Multiple sexual partners  Menorrhagia  Copper allergy
  • 28.
  • 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
  • 36.
  • 37. General Medical Disorders            Congenital/Valvular Heart Disease Venous Thrombo-embolism Arterial Heart Disease Stroke Migraine Opthalmic Disorder Hypertension Diebetes mellitus Epilepsy Depression Smoking
  • 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%)
  • 43. Clotting mechanism Fibrinolysins Protein C Protein S Antithrombins Plasmin Prothrombin Antithrombins Protein C & S Thrombin Factor V + other clotting factors Plasminogen Fibrinogen Fibrin ← Plasmin
  • 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
  • 68.
  • 69. Gynaecological Problems  Gestational Trophoblastic Disease  Ectopic Pregnancy  Menorrhagia  Endometriosis  Fibroids  Pelvic Infection
  • 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 factorssee 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

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