i and/or non-gynaecologic referrals
2.Chronic pain management and
multidisciplinary support
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Figure 8. Society of Obstetricians and Gynaecologists of Canada (SOGC) guidelines for treatment of
endometriosis
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GY13 Gynaecology Toronto Notes 2023
Treatment
• surgical confirmation of disease is NOT required prior to starting medical management.
Asymptomatic endometriosis does not require treatment.Management depends on certainty of the
diagnosis,severity ofsymptoms,extent of disease, desire for future fertility, and impact to Gl/GU
systems(e.g.intestinal obstruction)
• medical
NSAlDs (e.g. naproxen sodium -Anaprox*).Avoid selective COX-2 inhibitors(celecoxib,
rofecoxib, valdecoxib) in those who are attempting conception assome studies indicate these
drugs can prevent or delay ovulation
• 1st line
cyclic/continuous estrogen-progestin (OCP)
progestin (1M medroxyprogesterone (Depo-Provera*) or oral dienogest (Visanne’))
. Mirena'lUS
• 2nd line
GnRH agonist (e.g.leuprolide (Lupron*)):suppresses pituitary glands
- side effects:hot flashes, vaginal dryness,reduced libido
- use >6 mo:include add-back progestin or estrogen to prevent decreased BMD,
reduce vasomotor side effects
danazol (Danocrine*): weak androgen
- side effects: weight gain, fluid retention, acne, hirsutism, voice change (not
commonly used due to side effects)
• surgical
conservative laparoscopy using laser, electrocautery ± laparotomy
ablation/resection of implants,lysis of adhesions,ovarian cystectomy of endometriomas
definitive:hysterectomy ± bilateral salpingo-oophorectomy
best time to become pregnant is immediately after conservative surgery
if patient is not planning to become pregnant postoperatively,suppress ovulation medically to
prevent recurrence (not proven)
• above treatments are for the pain, not for the infertility associated with endometriosis, which usually
involvessurgery + assisted reproductive technologies.Also, management for endometriomas is
surgical for symptomatic and expanding masses, but this can decrease ovarian reserve,so if it is
asymptomatic and small (<5 cm), then no surgery is necessary
Adenomyosis E®
•synonym: “endometriosis interna” (uterine wall may be diffusely involved)
Epidemiology
•15% of females >35 y/o;found in 20-40% of hysterectomy specimens
•mean age at presentation: 40-50 y/o (older age group than seen in endometriosis)
•adenomyosis is a common histologic finding in asymptomatic patients
Clinical Features
•often asymptomatic
•heavy menstrual bleeding,secondary dysmenorrhea, pelvic discomfort
•dyspareunia, dyschezia
•uterus symmetrically bulky, usually <14 cm
•Halban’
ssign:tender, softened uterus on premenstrual bimanual exam
Investigations
•clinical diagnosis
•U/S or MR1 can be helpful
•endometrial sampling to rule out other pathology
Treatment
•medical
• iron supplements for anemia
• analgesics, NSAlDs
. Mirena'1US
• CHC,medroxyprogesterone (Depo-Provera*) -limited evidence for efficacy
• GnRH agonists (e.g. leuprolide (Lupron * ))
danazol 100-200 mg PO once daily (trial x 4 mo)
•surgical
definitive: hysterectomy -treatment of choice in women who have completed childbearing
Adenomyosis
Extension of areas of endometrial glands
and stroma into the myometrium
Final diagnosis of adenomyosisis based
on pathologic findings, but predictably
identified on MRI
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GYM Gynaecology Toronto Notes 2023
Fibroids
Leiomyomata/Fibroids
Benign smooth muscle tumour ol the
uterus (most common gynaecological
tumour)
Epidemiology
• diagnosed in approximately 40-50% of premenopausal women >35 yr
• more common in Black women, where they are also larger and occur at earlier age
• common indication for majorsurgery in females
• minimal malignant potential (1 in 1000)
• typically regress after menopause
Pathogenesis
• estrogen stimulates monoclonalsmooth muscle proliferation
• progesterone stimulates production of proteins that inhibit apoptosis
• degenerative changes (occur when tumour outgrows blood supply)
fibroids can painfully degenerate, become calcified,develop sarcomatous component,or obtain
parasitic blood supply
Classification
• intramural: most common, grow within the muscular wall of the uterus
• submucosal:grow within myometrium, can grow into endometrial cavity
• subscrosal: grow from the serosa
• fibroids can also grow in the cervix and vagina
Submucosal leiomyomata are most
symptomatic (bleeding,infertility)
Large fibroids can cause distressing bulk
symptoms
The effect of pregnancy on fibroid siie
is variable
'Pedunculated iubserosal Clinical Features
• majority asymptomatic (60%), often discovered as incidental finding on pelvic exam or U/S (occur in
50% of ALL women)
• abnormal uterine bleeding (30%):dysmenorrhea, heavy menstrual bleeding
• pressure/bulk symptoms(20-50%)
pelvic pressure/heaviness
• increased abdominal girth
urinary'frequency and urgency
constipation, bloating (rare)
acute urinary retention (extremely rare, butsurgical emergency!)
• acute pelvic pain
fibroid degeneration
fibroid torsion (if pedunculated subserosal)
• infertility,recurrent pregnancy loss
• pregnancy complications (potential enlargement and Increased pain, obstructed labour,
malprcsentation, difficult cesarean delivery)
Investigations
• bimanual exam: uterus asymmetrically enlarged, usually mobile
• CBC:anemia (only found if associated with AUB/heavy menstrual bleeding)
• pelvic and/or transvaginal U/S: to confirm diagnosis and assesslocation of fibroids
• sonohvsterogram: useful for differentiating endometrial polyps from submucosal fibroids,for
assessing intracavitary growth or for assessing potential risks with fertility associated with the fibroid
(submucosal only)
• endometrial biopsy to rule out uterine cancer for abnormal uterine bleeding (especially if age >40 yr)
• occasionally MRI is used for preoperative planning (e.g.before myomectomy)
Treatment
• only ifsymptomatic (heavy menstrual bleeding, bulk symptoms), rapidly enlarging or intracavitary
• treat anemia if present
• conservative approach (watch and wait) if:
• symptoms absent or minimal
fibroids <6-8cm or stable In size
not submucosal (submucosal fibroids are more likely to be symptomatic)
currently pregnant due to increased risk of bleeding (follow-up U/S if symptoms progress)
• medical approach to treat AUB-L
antiprostaglandins (ibuprofen, other NSAIDs)
tranexamic acid (Cyklokapron*)
• CHC,1US,or Depo-Provera*
GnKH agonist:leuprolide (Lupron*)
often used for 3 mo preoperatively to increase Hb and reduce fibroid size
reduces bleeding,shrinks fibroids, and corrects anemia
can be used long-term to bridge to menopause in combination with add-back progestin or
estrogen
• interventional radiology approach: UAE occludes both uterine arteries,shrinks fibroids by 50% at 6
mo; improves heavy bleeding in 90% of patients within 1-2 mo; not an option in women considering
childbearing
higher risk ofsurgical re-intervention than with surgical approaches
bubskir usdl
Intramura
'
Cervical
Pedunculated
submucosal
g) Camilla Matuk ^
Figure 9. Possible anatomic
locations of uterine leiomyomata
Uterine Artery Embolization let Symptomatic
Uterine Fibroids
C ochrane OBSyst See 2014:12
^
0005073
Purpose:locompare outcomes of UAE to otter
medical orsurgical therapiesfor symptomatic uterine
fibroids.Primary outcomes were pabeotsatisfactirm
and live birth rate
Results:Seven RCTs with 793women were included.
There was noevidence ola difference in the primary
outcomes or risk of major com plications between the
interventions.UAE was associated with a higher risk
of minor complications and the need for adddional
surgical intervention within 2 yr
Conclusions: No significant differences m patent
satisfaction or major complications m UAE complied
losu rgrcal intervention.UAC is associated wrtk an
increased riskof surgical ri
-mterrenboa
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GY15 Gynaecology Toronto Notes 2023
• surgical approach
myomectomy (hysteroscopic, transabdominal, or laparoscopic)
hysteroscopic resection of fibroid and endometrial ablation for AUB-Lsm
• hysterectomy (see Hysterectomy, G
'
1
'
6)
• note: avoid operating on fibroids during pregnancy (due to vascularity and potential pregnancy
loss); expectant management is usually best
Contraception
• see Family Medicine, TM23
Table 7. Classification of Contraceptive Methods
Type Effectiveness (Perfect Use, Typical Use')
Physiological
Withdrawalicoitus interruptus
Rhythm
Method calendar/mucuslsymptothermal
Lactational amenorrhea
Counselling the Adolescent about
Contraception
More than 90% of adolescent
pregnancies are unintended,and "
50%
of all pregnancies occur within the
first 6 mo of initiating sexual activity:
in addition.85% of sexually active
women become pregnant within1yr
if no contraception is used and even
some of the least effective contraceptive
methods markedly decrease the risk of
pregnancy
96%.77%
76%
93% (first 6mo postpartum)
15%
Abstinence of all sexual activity 100%
Barrier Methods
Condom alone
Spermicide alone
Sponge
Parous
Multiparous
Diaphragm with spermicide
Female condom
Cenhcal cap
Parous
Nulliparous
98%.82%
82%.72%
80%.76%
91%.88%
94%.88%
95%.79%
If-..68%
91%.84%
Hormonal
Combined (Estrogen and Progesterone)
0CP 99.7%.92%
99.7%.92%
99.7%.92%
MuvaRing:
Iransdermal(Ortho Evra*
)
Progesterone-Only
Progestin-only injection (Depo-Provera-)
MiTena:
IUS
99.7%.97%
99.9%
Etonogestrel implant (NEXPLAN0NT ) 99%
Copper IUD 99.3%
Surgical
Tubal ligation
Vasectomy
99.65%
99.9%
Emergency Postcoital Contraception (EPC)
Ywpe:method
"Plan 8'
levonorgestrel only
Postcoital IUD
98%(within 24 h). decreases by 30% at 72 h
98% (within 24h).decreases by 70% at 72 h
99.9% (within 7 d)
Ella 99.9%(within7 d)
’EPediveress:percentage ot womenreporting no pregrancy after 1yr of use
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Hormonal Methods
Combined Oral Contraceptive Pills
• daily pill with a 4-7 d placebo or pill free break to allow for menstruation
• estrogen:suppresses 1SH and follicular development
• progestin:prevents LH surge,suppresses ovulation, thickens cervical mucus,decreases tubal motility,
decidualizes endometrium
• most contain low dose ethinyl estradiol (20-35 pg) plus progestin (norethindrone, norgestrel,
levonorgestrei,desogestrel, norgestimate, drospirenone)
• failure rate (0.3-8.0%) depending on compliance
• monophasic formulations have the same amount of progestin throughout cycle while triphasic
formulations have a varying amount of progestin throughout cycle
Transdermal (Ortho Evra 1)
• patch that is changed every week for 3 consecutive weeks then left off for a week to allow for
menstruation
• continuous release of 6 mg norelgestromin and 0.60 mg ethinyl estradiol into bloodstream
• applied to lower abdomen, back, upper arm, buttocks, NOT breasts
• as effective as OCP in preventing pregnancy (>99% with perfect use)
• may be less effective in women >90 kg
Contraceptive Ring (Nuva Ring;
)
• thin flexible plastic ring that is inserted into the vagina by the patient and left there for 3 wk then
removed for a week to allow for menstruation; releases etonogestrel 120 pg/d and estradiol 15 pg/d
• as effective as(KIP in preventing pregnancy (98%)
• side effects:vaginal infections/irritation, vaginal discharge
• associated with less breakthrough bleeding than other methods
Starting Hormonal Contraceptives
• thorough history and BP measurement (post-pandemic SOGC guidelines do not require BP reading
anymore to allow for virtual appointments)
• pelvic exam not required as ST1 screening can be done by urine, and pap smear screening does not
start until >25 yr
• can start at any time during cycle but ideally within 5 d of LMP
• follow-up visit 3 mo after hormonal contraceptives prescribed
• generally recommended to use back-up contraception for 7days, particularly if initiated >5 days front
LMP
Table 8. Combined Estrogen and Progestin Contraceptive Methods
Advantages Side Effects Contraindications
Highly effective
Reversible
Cycle regulation
Decreased dysmenorrhea andheavy menslrual Fluid retention,1
bloating/edema
Weight gain (rare)
Decreasedbenign breast disease and ovarian Migraine,headaches
cyst development
Decreased risk of ovarian and endometrial
cancer
Increased cervical mucuswhich may lower
risk ofSTIs
Decreased PMS symptoms
Less acne
Osteoporosis protection (possibly)
Patient controlled
Estrogen-related
Nausea
Breast changes (tenderness,enlargement)
Absolute
4 wk postpartum(breastfeeding) or <21 d
postpartum (not breastfeeding)
Major surgery with prolonged immobilication
ttnown/suspectedpregnancy
Undiagnosed abnormal vaginalbleeding
Prior thromboembolic events,thromboembolic
disorders (FactorIf Leiden mutation;protein
bleeding|1ess anemia)
Thromboembolic events
Liver adenoma (rare)
Breakthrough bleeding (low estradiol levels) Cor S.or anbthrombin III deficiency),active
thrombophlebitis
Cerebrovascular or coronary artery disease
Estrogen-dependent tumours (breast,uterus)
Impaired liver function associatedwith acute
liver disease
Progestin-related
Amenorrhea!breakthrough bleeding
Headaches
Breast tenderness
Increased appetite
Decreased libido
Mood changes
Congenital hypertriglyceridemia
Smoker age>35 yr
Migraines with focal neurological symptoms
(eidudingaura)
Uncontrolled HTN
H1N
Acnefoilyskin*
Hirsutism*
Relative
'Androgenic side effects may beminimiced Migraines (non-local with aura <1h)
by prescribing formulations containing DM complicated by vascular disease
desogestrel,norgestimate.drospvenone.or SIE
cyprolerone acetate Controlled HI
Hyperlipidemia
*
Sickle cellanemia
Gallbladder disease r m
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Drug Interactions
' Risks
Rifampin,phenobarbital.phenytoin.griseofulvin.
primidone,andSt.John's wort can decrease
efficacy of CHC requiring use of back-up method
Ko evidence of fetal abnormalities if conceived
onOCP
No evidence that OCP is harmful to nursing infant
but may decrease milk production
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Table 9. Selected Examples of OCPs
Type Active Compounds
(estradiol and progestin
derivative)
Advantages Disadvantages
Missed Combined OCPs
Miss1pill in <24 h
• Take1 pil ASAP, and the next pill at
the usual time
Miss >1pill in a row in 1st wk
• Take1ptH ASAP, and continue taking
1 pttl daily until the end of the pack
• Use back up contraception for 7 d:
EPC may be necessary
Miss <3 pills in 2nd or 3rd wk of cycle
• Take 1 pi0 ASAP, and continue taking
1pdf daily until the end of the pack
• Do not take placebo (28-d packs) or
do not take a hormone free interval
(21-d packs)
• Start the next pack immediately after
finishing the previous one
• No need for back up contraception
Mss >3 pills during the 2nd or 3rd wk
• Take1pil ASAP, and continue taking
1pill daily until the end of the pack
• Do not take placebo (28-d packs) or
do not take a hormone free interval
(21-d packs)
• Start the next pack immediately after
finishing the previous one
• Use back up contraception for 7 d;
EPC may be necessary
S0KCaunOtt Opnon on Messed Hor monj!
Cnctuuptnv »r» hKorarwiidibwis.
jMcnosjottso
-tott.
Alesse 20|ig ethinyl estradiol and 0.5 mg Low dose (20 pg) OCP
Less estrogen side effects
Low-dose pills can often result in
breakthrough bleeding
If this persistsfor longer than 3
mo. patientshould be switched
to an OCP with higher estrogen
content
Unlike monophasic OCP. triphasic
OCPs can not be used for
continuous menstrual suppression
levonorgestrel
Tri-cytlen'
35 pg ethinyl estradiol and
0.180(0.215/0.250 mg
norgestimate
Triphasic oral contraceptive
(graduated levels of progesterone)
Low androgenic activity can help
with acne
Yasmin: and Yaz Yasmin-:30 pg ethinyl estradiol Decreased perception of cyclic
n 3mg drospirenone (a new weight gaivtiloating
progestin) Fewer PUSsymptoms
Yaz5: 20 pg ethinyl estradiol-3 Improved acne
mg drospirenone - 24/4-d pill (4 d
pill free interval)
Drospirenone has
antimineralocorticoid activity and
antiandrogenic effects
Hyperkalemia (rare,
contraindicated in renal and
adrenal insufficiency)
Check potassium if patient also
on ACEI. ARB. K-*-sparing diuretic,
heparin
PROGESTIN-ONLY METHOD
Progestin-Only Pill
• progestcrone-onlv pill taken daily with no pill free interval
• advantages: patient controlled, does not impact breast milk supply
• disadvantages: must take at exactly the same time every day so compliance can be challenging
Progesterone Intrauterine System (IUS)
• small device left inside uterus for a maximum of 5 yr
• Mirena IL'
S:52 pg lev onorgestrel - better for women with very heavy"
or painful periods, 20%
amenorrhea rate
• Kyleena IUS:19.5 pg levonorgestrel - best for people who want a light period every mo and are mainly
looking for birth control
• advantages:convenient,low hormone dose, minimalside effects, no effect on breast milk, quick
return to fertility once removed
• disadvantages:uncomfortable to put in, must be inserted and removed by a doctor, rarely can have
uterine perforation or IUS expulsion
• very- effective reversible contraception; more likely to be an ectopic pregnancy if conception occurs.
Lower absolute risk of ectopic pregnancy compared to other contraceptive methods
Irregular breakthrough bleeding often
occurs ui the first few mo after starting
OCP:usually resolves after three cycles
Progestin-only contraceptives must be
taken at the same time every day
Coatiaioas«Extended Cycle vs. Cyclic Use
of Coabiaed Hormonal Contraceptives lor
Contraception
Cochrane 03Systker 2014:)
Purpose Systematicmen of RCIs assessing (lie
eScecyeedsdeeSectsof cyclic administration
vs.titeded ose (oc-ger periods of acbve pills
and orshorter penods placebo) or continuous
use (a uterrupted active pdladministration) of
coaptation oral contraceptives (C0C).
Base its The r ta: -eve*
published in 2012
berried12 KCTs that.bmately showed no
ddfeterce tehreen groups with regards to efficacy
pregzaecy rated,safety,and compiiaice rates.
Contoneusor eiterded COCs were shown to reduce
menstrual symptoms (headaches, tiredness, bloating,
and nenstizai pan),baddition.11 of 12 studies
-ercmecls mrbar or rmproved bleeding patternswith
cottmsous or eiten ded cycles.
CoKhsiots: Itsrecently published updated
systesatc renew dettfieda further 4 RCIs,
hawever.resultsrtid not change.
Depo-Provera
• injectable depot medroxyprogesterone acetate 150 mg 1M every 12 wk (convenient dosing)
• advantages:suppresses ovulation, complete amenorrhea in 70% of women after 1 -2 yr of use, does not
affect breast milk,effective for dysmenorrhea
• disadvantages:breakthrough bleeding, iveight gain, decreased bone density (may be reversible),
restoration of fertility may take up to 1-2 yr
Nexplanotv
• 4 cm long 60 mg etonogestrel implant that is placed in the inner arm and lastsfor a maximum of 3 yr
• advantages:does not affect breast milk, do not have to putsomething in uterus, good bleeding and
pain control, no change in bone density, quick return to fertility once removed
• disadvantages:breakthrough bleeding,weight gain
Table 10. Progestin-Only Contraceptive Methods
Indications Mechanism of Action Side Effects Contraindications
Does not affect breast milk supply Progestin prevents IH surge
Women with contraindications
to combined OCP (e.g.
thromboembolic or myocardial
disease)
Women intolerant ot estrogenic
side effects of combined OCPs
Irregular menstrual bleeding
Weight gam
Headache
Breast tenderness
Mood changes
Functional ovarian cysts
Acne/oityskin
Hirsutism
Absolute
Current breast cancer
Known/suspected pregnancy
Undiagnosed vaginal bleeding
Benign or malignant liver tumours,
severe cirrhosis,or acute liver
disease
Thickening ol cervical mucus
Decreases tubal motility
Endometrial decidualization
Ovulation suppression - oral
progestins do notconsistently
suppress ovulation
compared to combined OCPs
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Intrauterine Device
Table 11. IUS Contraceptive Methods
Mechanism of Action Benefits of all IUS Risks of all IUS Side Effects Contraindications
Copper-Containing IUS
(Nova-T ):mild foreign body removal is very fast
reactionIn endometrium,toxic No estrogen (doesn't alfed
lo sperm and alters sperm motility breastfeeding,can use il
Return to baseline fertility after Insertion is uncomfortable
Must be inserted and removed by
a doctor
Infection (especially ilmultiple
smoker,hypertension,previous partners and withinlirsl10 d ol
insertion)
Uterine wall perforation on Insertion
(1/10000)
Expulsion (5% in the 1st yr,greatest
in the 1st mo)
Chance ol pregnancy very low, but if
piegnant,higher relative risk ol an
ectopic pregnancy or miscarriage
IUS do not protect agamstSlls’
Copper IUS:increased blood
loss and duration of menses,
dysmenorrhea,increased vaginal
discharge
Absolute
Both Copper andProgesterone IUS
Known or suspectedpregnancy
Undiagnosed genital Had bleeding
Acute or chronic PIP
lifestyle risk foi Slls
Known distorted uterinccavity
Immediately post-septic abortion
Progesterone IUS:spotting,
bloating,headache,acne,breast
tenderness,nausea.headaches,
ovarian cyst formation, vaginal
discharge,and/or mood changes.
Usually very mild.
Progcstcrone-Reteasing VII)
IUS (Mircna'
,Kylccna ): lasts Syr but can be removed
decidualiialion of endometrium before that it desired
and thickening ol cervical mucus: Can insert immediately alter
minimal effect on ovulation placental delivery and post
abortion
CopperIUS
Known allergy lo copper or Wilson's disease
Relative:
Both Copper andProgesterone IUS
Valvular heart disease
PMHx of PIP or edopic pregnancy
Presence of prosthesis
Abnormalities of uterine cavity
Intracavitary fibroids
Cervical stenosis
Immunosuppressed individuals (e.g.HIV)
Abnormalities of uterinecavity (excluding
distorted uterine cavity)
Copper IUS-Severe dysmenorrhea or heavy
menstrual bleeding
'Cervical swabs lor gonorrhea and chlamydia should be done prior loinsertion
Emergency Postcoital Contraception
Table 12. Emergency Postcoital Contraceptive (EPC) Methods
Method Mechanism of Action Side Effects Contraindications
HORMONAL
Yuzpe Method
Ovral5
2 tablets then repeat in12 h(100 pg ethinyl
estradiol 500 pglevonorgestrel)
Can substitute vnth any OCP as long as it contains100
pg ethinyl estradiol
2% overall risk of pregnancy
Used within 72 h olunprotected intercourse,limited
evidence of benefit up to 5 d
Efficacy decreased with lime
(e.g. less effective at 72 h than 24 h)
“PlanB '
"
Use within 72 ft of unprotected intercourse,can use
up to 5 d alter
750 pg levonorgestrel q12 h for 2 doses (can also take
2 doses together)
Creater efficacy (75-95%ilused within 24 h) and
better side effect profile than Yurpe method
No estrogen thus wry few conlraindications/side
effects (less nausea)
less eflectivc if >75 kg.not recommendedil>80 kg
Ulipristal (Ella )
30 mg P0 within 5 d ol unprotected intercourse
Unknown:theories include:
Suppresses ovulation or causes deficient luteal Irregular spotting
phase
Alters endometrium to prevent implantation
Affects spetm/ova transport
Nausea (due to estrogen:treat with Gravol '
) Pre-existing pregnancy (although not
teratogenic)
Caution in women with contraindications
to OCP (although no absolute
contraindications)
Samcasabovc Same as above Same as above but no caution in women
with contraindications lo OCP
Selective Progesterone Receptor Modulator
(SPRM) with primarily antiprogestin activity:
may delay ovulation by up to 5 d
Headache,hot Hashes, constipation.vertigo,
endometrial thickening
Same as above but no caution in women
with contraindications lo OCP
N0N-H0HM0NAI
Postcoital IUD(Copper)
Insert up to 7 dpostcoitus
Prevents implantation
1% failure rate
Can use (or short duration in higherrisk individuals
See fable 11 See table11 See labfe 11
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