Fertility Control Flashcards

1
Q

Anovulatory level of ENG

A

90pmol/l
max at day 4

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2
Q

UKMEC for TB

A

Non-pelvic= 1
Pelvic=
I= 4
C=3

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3
Q

UKMEC for hepatitis

A

acute viral=
I=3
C=2
Chronic=1

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4
Q

UKMEC for cirrhosis

A

If severe:
POC=3
CHC=4

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5
Q

UKMEC for transplantation

A

Uncomplicated= 2
Complicated
COC= 3
IUD I=3 C=2

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6
Q

UKMEC for chlamydia

A

symptomatic I=4 C=2
asymptomatic I=3 C=2

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7
Q

UKMEC Bariatric Surgery

A

1

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8
Q

Breast Cancer UKMEC

A

Current= 4
Past =3
FHx=1
BRCA=2 (CHC=3)

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9
Q

Implant <4 years and IUD fit?

A

Can fit with normal E/P

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10
Q

DMPA and cholesterol levels

A

initial reduction in HDL leads to increased LDL to HDL ratio
normalise over 24/12 of use

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11
Q

What is Z score?

A

comparison of BMD ith those same age/sex as you
-2.0 or less = low

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12
Q

EHC and Breast Ca

A

Probably safe if E receptor -ve but no evidence
unlikely to have a significant impact

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13
Q

HC and Breast Ca

A

LNGIUD best avoided but can always remove if recurrence

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14
Q

Estretol (E1)

A

Drovelis
Estretol 14.2mg / DRSP 3mg
ERa > ERb
less potent that EE/E2
not significantly metabolised by CYP450

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15
Q

Qlaira

A

estradiol valerate/ dienogest
contains lactose
quadraphasic COCP
28 tablets, 9/7 EP if QS or not Day 1

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16
Q

What are the licenses for different coils?

A

52mg:
all contraception 8 years
all HMB 5 years
only mirena for endometrial protection

minimum length- benilexa/levosert is 5.5cm

insertion tube- 4.8mm benilexa/levosert. 4.4mm mirena. others 3.8mm.
frame size- 32 x 32
Jaydess/Kyleena 28 x 30

Maximum length- copper only, 9cm
T safe 32x 36 (4.75mm tube)
NovaT 31.9 x 35.9 (3.6mm tube)

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17
Q

What is the release rate of the LNG-IUDs?

A

Start:
Mirena 20mcg/24hr (benilexa/levosert 20.1)
Kyleena 17.5, Jaydess 14

End:
Mirena 7mcg/24h, benilexa/levosert 6.5
Kyleena 7.4, jaydess 5

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18
Q

What weight reduces effectiveness of CTP?

A

90kg

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19
Q

Contents of first line COCP

A

less than/equal to 30mcg EE and NET (500mcg/1mg) / LNG (150mcg)

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20
Q

VTE in COCP-progestogens

A

reduced risk with:
LNG
NET
Norgestimate

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21
Q

Co-cyprindiol

A

35mcg EE+ cyproterone acetate (anti-androgenic)
treatment for acne/hirsutism (do not need contraception on top but should not be used for contraception)
Clairette/Dianette

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22
Q

Contents of CHP

A

33.9mcg EE + 203mcg norelgestromin over 24hrs

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23
Q

Contents of ring

A

15mcg EE + 120mcg etonogestrel over 24 hrs

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24
Q

Norethisterone VTE risk

A

converted to EE if >5mg/OD
NET 10-20mg OD equivalent to 20-30mcg EE

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25
Mechanism of CHC
D1-7 inhibits ovulation D8-14 maintains anovulation -may have escape ovulation in HFI as reduced suppression
26
Regimes of CHC
1) Standard (only licensed) 2) Shorten HFI (4/7) 3) tricycle with 4-7/7 break 4) continuous -nil evidence of increased effectivenesss -return to fertility within 3 months
27
Quickstarting limitations
<20/7 cycle- day 1 only 9/7 E/P if estradiol valerate/dienogest
28
LSUP- HSUP-
1000 20 (clear blue from 10)
29
traditional POP to COCP
7/7 EP as primary mechanism not inhibition of ovulation -same as LNGIUD
30
Enzyme Inducer
stop during treatment and 28/7 after (or use condoms) OR use a 20mcg and 30mcg COCP with 4/7 PFIs if >70mcg will need specialist advice as unknown VTE risk - not rifampicin/rifabutin Recommended to switch if >2/12 of use
31
Lamotrigine and COCP
CHC can reduce lamotrigine levels- ?increased seizures potential toxicity on stopping/HFI CHC effectiveness may also be reduced
32
Lamotrigine and EC
33
D+V with oral methods
vomit <3 hours diarrhoea >24hrs
34
prolonged HFI
>9 days since active pill (Monday to following wednesday, 2 days late to restart=ok) -EC if UPSI in HFI -7/7 EP UPT 3/52
35
Missed pills CHC -1 pill
NAD
36
CHC missed 2-7 pills week 1
EC if UPSI in HFI/week 1 take pill ASAP E/P 7/7 and UPT 3/52
37
CHC missed 2-7 pills week 3
take ASAP omit HFI nil EC 7/7 EP
38
CHC missed 2-7 pills week 2
take ASAP nil EC 7/7 EP
39
>7 days missed CHC
EC and treat as new starter
40
Missed ring rules
>8 days since removed -EC if HFI/week 1 -7/7 EP -UPT 3/52
41
Ring fallen out <48hrs
NFA, put back in
42
Ring fallen out >48hrs
week 1- EC if UPSI HFI/week1, EP 7/7 and UPT week 2- EC not required, take pill ASAP, 7/7 EP week 3- EC not required, take pill ASAP, omit HFI, 7/7 EP
43
Prolonged ring use
<28/7- NAD <35/7- omit HFI, 7/7 EP, nil EC >35/7, EC if UPSI during week 5, treat as new starter
44
CHC and Endometrial Cancer
reduced risk, further reduced with longer use, persists many years 34% reduction if >10 years use
45
CHC and Ovarian Cancer
reduced risk 30-50% reduction if >5 years compared to never user/<1 year use even if BRCA carrier
46
CHC and Colorectal Cancer
19% reduction in risk
47
CHC and overall cancer risk
overall reduction in cancer and all cause mortality
48
CHC and <20yo
UKMEC2
49
CHC and VTE rates
Risk per 10,000 women per year Background- 2 LNG, NET, Norgestimate- 5-7 Etonogestrel, Norelgestromin- 6-12 DRSP, DSG, Gestodene- 9-12 some evidence that reduced dose EE reduces risk conflicting evidence re route
50
Antithrombin/protein C/S and CHC
risk of VTE 4 in 100 8-70 fold increased risk
51
CHC and Migraine
double risk of ischaemic stroke OR 2.7-6.1 not much increase if migraines without aura
51
CHC and ATE
increased risk MI/stroke increased by EE dose does not vary by progestogen type
52
CHC and Breast Ca risk
Not significant after 10 years stopped increased risk with longer use slight but not significant increase
52
CHC and Cervical Ca
Small increased risk if used over 5 years Not significant after 10 years stopped
53
CHC and Headache
Some may reduce, worsen or remain the same may reduce after a few cycles/remove HFI no better regime
54
CHC and unscheduled bleeding
10-18% per cycle (similar to baseline population) reduce over time but not if persists at 4 months ?CVR better bleed control Rx: Increase EE if 20mcg 3rd >2nd>1st gen progestogen
55
Progesterone generations
1) NET 2) LNG 3) DSG/Gestodene/Norgestimate 4) DRSP/Dienogest/norgesterol acetate | O**NE>NE**T
56
CHC and Mood
mood change is common and often due to external factors nil good evidence recommend change progesterone
57
Length of dispensing
Increased rates of continuation if more packs given Nuvaring needs to be in fridge >4/12- Syreni ok for 12/12 to be given
58
CHC and travel
minimise immobility >4500m or 14500 ft for >7/7- switch method Increase erythropoiesis at altitude= increased thrombosis risk
59
CHC and surgery
planned immobility- stop 28/7 before restart at first menses and after 2/52 full mobilising OR clexane
60
IUC failure rates
0.6-0.8% Cu-IUD 0.1-0.2% LNG-IUD 0.3% Jaydess/Kyleena
61
Risks with IUC
Infection <1% Perforation 1-2 in 1000, 6x increased in BF acne/breast tenderness/headache/mood
62
MoA of IUC
Mainly pre-fertilisation effects CuIUD- reduce fertilisation LNGIUD- mucus, endo, implantation -mucus may stil be penetrable 5/7 after insertion ->75% still ovulate (more for non 52mg devices)
63
IUC and GTD
-ve HcG= 1 declining=3 persistent=4
64
LNGIUD and Breast Ca
current-4 past-3
65
BMI >30 and other RF LNGIUD score
UKMEC 2 for LNGIUD
66
IUC and Cavity distortion
UKMEC3 abnormal but not distorted=UKMEC2 fibroid alone=UKMEC1
67
Endometrial ablation- IUC
At ablation: increased risk complication potential reduced satisfaction due to increased risk of intervention After: By ultrasound/hysteroscopy by specialist Can try to remove in clinic
68
PID and IUC
past=1 C=2 I=4
69
Chlamydia
symptoms: I=4 C=2 no symptoms: I=3 C=2
70
IUC and purulent cervicitis/GC
I=4 C=2
71
Other STI (Non GC/C4) and IUC
UKMEC2 insert once treated and asymptomatic BV/TV/Candida- insert and treat GBS- nil GAS- treat and delay
72
Other considerations for IUC and immunity
Immunosuppressed/EDS: D/w team Adrenal insufficiency: early AM, double dose before and for 24hrs following PLWH:
73
IUC and Cardiac Disease
Small risk vasovagal (2% background) antibiotics not routinely recommended do not withold beta blocker hospital fit: arrhythmia Eisenmenger Fontan/Single ventricle Long QT Impaired VF
74
Anticoagulation and IUC
multitooth tenaculum pressure/silver nitrate avoid NSAIDs Ensure INR <3.5 -within 72hours if recent change/unstable Trough of LMWH
75
IUC and allergy
CuIUD is contraindicated in allergy, avoid in Wilson's -no difference in serum levels may contain nickel/gold/silver Kyleena and Jaydess have a silver ring
76
IUC and cysts
Not a contraindication to LNGIUD, may increase but not clinically significant
77
LNGIUD and amenorrhoea
At end of licence: 52mg 40% 19.5mg 23% 13.5mg 11-12% 52mg 1 in 5 by 12/12
78
Fitting IUC-technique
tissue forceps should usually be used uterine sound should be used
79
IUC and pain
Appear to help: -paracervical/intracervical block -10% lidocaine spray (wait 3 minutes) -lidocaine/prilocaine cream No good studies on oral analgesia. NSAIDs can help post fit pain
80
IUC and MRI
Limited data suggest safe steel ring not safe
81
IUC and menstrual products
nil evidence tampons/pads ?association of cups and expulsion
82
IUC and ectopic (hx)
UKMEC 1
83
IUC and infection
<1% risk but increased for first 3 weeks wait 48-72hrs before removal to assess response
84
IUC and BV/Candida
?biofilm and recurrent IUC (protects yeasts from azoles) mixed evidence, may choose to switch BV potentially associated with CuIUD but not LNGIUD
85
Malposition
>2cm from fundus too limited evidence to know about effectiveness incidence 7-19% no evidence for increased pain/pvb >2 expulsions: do USS to assess cavity before fit Postpartum/D1-8 of cycle may have higher risk
86
NVT
18% 30% after NVD, 50% after LSCS
87
SDI and ovulation
0.05% in first year too limited evidence that this is maintained beyond year 3 maximum conc at 2 weeks 111-202 by year 3 may be over 90 for up to 5 years -no correlation with BMI ovulatory activity not 100% suppressed, may have some follicular development with fluctuant estradiol levels
88
SDI removal- fertility
undetectable levels 7/7 ovulate at 6/52 (reports of pregnancy at 14/7)
89
POC UKMEC 3
unexplained pvb Hx Breast Ca severe liver cirrhosis, hepatocellular adenoma or carcinoma Continuation with stroke/IHD (initiation is a 2)
90
POC UKMEC 4
CURRENT breast Ca
91
SDI and Endometriosis
may lead to reduced pain, evidence limited to first year of use
92
Breast Ca risk and POC
possible association small increase in risk but absolute risk is low
93
SDI and ectopic
0.2 per 100,000 4.7% of pregnancies with the implant (1% of all pregnancies)
94
SDI and Bleeding
median reduction when compared to: no method, CHC but less predictable if bad 3/12, 50% chance will get better -3/12 CHC or 5/7 MFA Stats: 1 in 3 once a month 1 in 3 less than once a month 1 in 4 amenorrheic <1 in 5 prolonged -10-20% will remove device due to bleeding pattern
95
Analgesia for SDI
lidocaine 1% 2-3ml insertion/ 0.5-1ml removal ethylchloride spray- 60 second duration
96
SDI and bleeding
anticoagulants- NAD Plt <50= discuss
97
SDi complications
1% deep -can leave indefinitely broken: -increased surface area so increased hormone levels -likely still effective but can offer replacement
98
SDI cost
12/12 cost effective
99
DMPA effectiveness
0.2% typical 6%
100
Norethisterat
200mg in 1ml IM Stat (oily, warm in water before use) slow gluteal injection licensed for short term use whilst a/w semen analysis post vasectomy duration 8 weeks must have rubella vaccine
101
DMPA benefits
-may reduce pain of endometriosis -may protect from ovarian/endometrial cancer -may reduce severity of sickle cell pain
102
BMD and DMPA
small loss, recovered on discontinuation <40= UKMEC1 >40= UKMEC2
103
Breast Ca and DMPA
small increased risk, absolute risk is small
104
Cervical Ca and DMPA
weak association if used for more than 5 years reduces after discontinuation
105
Weight gain and DMPA
higher risk if BMI>30 and <18 if gain >5% in first 6 months may continue to gain limited data of effectiveness if BMI >40
106
Injection site reactions and DMPA
Higher risk if SC (1-20% all site reactions, common) If concerned re BMi go for deltoid
107
Timing of injections
13/52 supported- can give up to 14/52 (IM DMPA SPC 12, SC DMPA SPC 13) early- 10/52 DMPA -6/52 NET (late at 10 weeks)
108
DRSP Quick-starting
D1 of cycle/post TOP/d21 childbirth
109
DRSP Missed pill rules
24hr window omit HFI if any of last 7 missed EC if missed D1-7 and SI during HFI/week 1
110
Vomiting with POP
DRSP/DSG- 3-4 hours LNG/NET- 2 hours
111
Extra considerations with DRSP and MHx
c/i- severe renal disease avoid- K+ supplements, hyperkalemia, diuretics untreated hypoaldosteronism/Addison's/adrenal insufficiency caution and monitor- mild renal disease/treated hypoaldosteronism check U+E/BP before- Risk factors for CKD (HTN/CVD/DM) especially if >50yo | Addison's/Adrenal insufficiency= Avoid
112
POP and Cancer
potential increased risk of Breast Ca nil risk ovarian/cervical unclear evidence on ovarian cysts nil risk of positive impact of endometrial cancer
113
Bleeding and traditional POP
<1 in 10 amenorrhoeic 1 in 10 infrequent 8 in 10 normal 1 in 10 frequent <1 in 10 prolonger
114
Bleeding and DRSP/DSG POP
2-3 in 10 amenorrhoeic 3 in 10 infrequent 4 in 10 normal <1 in 10 frequent <1 in 10 prolonged DSG may reduce HMB Both may reduce dysmenorrhea
115
How to use diaphragm/cap
reapply gel if in place over 3 hours or further SI retain 6 hours after sex diaphragm- max 30 hours cap- max 48 hours 65 to 80mm, 24hrs (caya)
116
Effectiveness of barrier methods
External condoms: 2% and 18% Internal condoms: 5% and 21% Diaphragm: 6% and 12%
117
Latex condoms- lubricants
Water/silicone oil= no
118
Concerns with diaphragms/caps
UKMEC 3: Hx toxic shock high risk HIV transmission
119
Nonoxynol-9
spermicidal gel, immobilises/kills sperm -denatures lipids in acrosome->lysis of membranes->immobilisation and death Can also change vaginal flora-> genital irritation and higher risk HIV acquisition
120
Caya gel
acts as a physical barrier to sperm, stabilises high vaginal pH
121
Advice post vasectomy
NSAIDs rest, avoid strenuous activity abstain 2-7/7 wear supportive underwear for 48 hours
122
Consenting for sterilisation
Written consent recommended counsel at least 2 weeks prior to CS additional care if <30 yo or nulliparous
123
Vasectomy- procedure details
occlusion of vas deferens under LA (GA may worsen pain and has similar recovery) warm LA to 37 before giving-subcuticular tissue and vas minimum exposure-reduces complications many methods (cautery and division best), removal of 1-3cm section must be accompanied by another method bury one end in spermatic fascia to prevent recanalisation histology not required
124
PVSA-criteria
12 weeks (may be up to 16) -by this time 80% have no spermatazoa need 11-20 ejaculations before sample may get special clearance at <100,000 sperm/ml
125
PVSA- failure
motile sperm at 6-7/12 >100,000 but not motile may get given special clearance
126
Vasectomy- anatomical variation
absent vas is associated with ipsilateral renal agenesis - do one side and await PVSA if bilateral absence: -urology referral Double vas: -USS to confirm ectopic ureter
127
Complications of vasectomy
haematoma/infection: 1-2% Failure 1 in 2000 (1 in 100 if not waited for PVSA) chronic pain >1%- NSAIDs/neuropathic drugs
128
Vasectomy reversal
Dependent on length of time <3 years 97% but pregnancy rate 70% 9-14 years 79% but pregnancy 40-45% >20 years 40% but <10%
129
Tubal occlusion- method
Filshie should be laparoscopic method of choice
130
Tubal occlusion- pregnancy risk
2-3 in 1000 luteal phase pregnancies can continue contraception 7/7 after but SDI can be removed at time of Lifetime failure- 1 in 200 Filshie at 10 years- 2-3 in 1000
131
Survival times for FAM
ovum ~24 hours sperm ~7 days (average 1-2) fertile window 8-9/7
132
days conception most likely
day of ovulation and 24hrs before
133
FAM effectiveness
24% 0.3-0.4% Need to record for 3 months before use
134
Indicators for FAM
progesterone increases basal body temp -3/7 of temp >0.2 degrees higher than previous 6 days = post ovulatory infertile window may be less sensitive than mucus/LH indicator sticks Need to take T after 3 hours of rest 6.6% failure if single indicator used
135
Cervical secretions for FAM
1) menses 2) dryness 3) sticky secretions and cervix high (2 days before and final day of this= most fertile time) 4)thick/absent secretions safe= 4/7 after peak 3% and 14% failure rates
136
Calendar method
Record for 1 year before starting 21% accuracy Do not use if cycles <26 or >32 days 12% failure
137
Highest risk days
6 days before + day of ovulation -30% risk pregnancy if SI at this time If any SI- 25% chance during fertile time
138
Delayed Menses after EC
>7/7 <10% LNG EC 20% UPA-EC (some IMB (10%), some earlier, some later (4%))
139
Failure of withdrawal
22%
140
Lactational Amenorrhoea
Exclusively BF (4 hrs day 6 hrs night) high prolactin= low GnRH= reduced LH/SH and suppressed ovulation 2% risk (may increase if expressing/dummies) not if teratogens
141
When can use dates after HC
>3 cycles minimum
142
When does implantation occur?
Day 6 post ovulation 80% day 8-10
143
EC licenses
LNG 72 hrs (can use to 96) UPA 120 hrs - offer any day of cycle
144
Double dose LNG
BMI >26 or weight >70kg - unknown if this or UPA is more effective enzyme inducer -UPA-EC not recommended
145
How does oral EC work
delays ovulation by at least 5 days so sperm no longer viable UPA up to start of LH surge- LNG before only
146
EC Effectiveness
CuIUD <0.1% failure UPA 1-2% (really 60-80%)
147
C/i to PO EC
both contain lactose can take in severe liver disease as pregnancy much greater risk
148
EC and vomiting
<3 hours= another dose
149
EC and ectopic
same as baseline risk
150
UPA and menses
take UPT if delayed >7 days 75% normal/within 7 days
151
UPA and POC
7 days before and 5 days after
152
PO EC side effects
headache, nausea, dysmenorrhea
153
Why do we flex the elbow for implant fit?
to move ulnar nerve out the way
154
Which structures lie in the sulcus?
median nerve basilic vein brachial artery ulnar runs below (over triceps)
155
Ulnar nerve injury
sensory= 1.5 lateral fingers fingers pulled back (4th and 5th) C8-T1 intrinsic muscles of hand Froment sign- thumb change
156
Median nerve injury
fingers pulled in C6-T1 thenar + lateral 2 lumbricals sensory= 3/5 digits of hand (median= lateral) Bottle sign- unable to grip glass tightly
157
Pharmacokinetics of EE/P
both conjugated in liver and intestinal mucosa excreted in feces some EE conjugates are cleared by colonic flora- EE reabsorbed
158
Pharmacokinetic interactions
n+v CYP450 gastric pH increasing glucuronidation of lamotrigine (CHC)
159
Pharmacodynamic interactions
POC and UPA DRSP/potassium
160
Topiramate
teratogen- need pregnancy prevention programme IUC/DMPA + condoms consider as enzyme inducer (regardless of dose)
161
Valproate
teratogen- need pregnancy prevention programme IUC/SDI, or others + condoms inhibits glucuronidation, if taking CHC and lamotrigine may help maintain lamotrigine levels not an enzyme inducer
162
Sugammadex
used to reverse neuromuscular blockade T 1/2 2 hours, excreted in 24 hours treat as 1 missed pill and use E/P - less worried if DMPA/IUC
163
Thyroxine
oral HRT can increase requirement by increasing TBG - no evidence but consider the same for CHC -transdermal has less effect as not 1st pass metabolism check TFT 6/52 after starting CHC (may need to increase thryoxine dose)
164
Lamotrigine
CHC increases glucuronidation, may need to increase dose and have toxicity on discontinuation/HFI DSG may increase levels POC- check for signs of toxicity and measure levels when stopping HC- condoms on top, DMPA/IUC preferred
165
Signs of lamotrigine toxicity
diplopia ataxia dizziness
166
Griseofulvin
not an inducer, potentially teratogenic increased risk of bleeding changes/pregnancy with PO (condoms) DMPA/IUC
167
Gastric pH
PPIs may reduce exposure to UPA, but not other HC LNG/IUD EC
168
ARTs that induce CYP450
efavirenz ritonavir boosted PIs
169
CYP450 inhibitors ART
PIs (-avirs)
170
Ritonavir
inhibits CYP but induces glucuronidation - increases P, reduces EE
171
cobicistat
increases P and EE ## Footnote cobIcIstat= Increase and Increase
172
elvetigravir/cobicistat
reduces EE
173
BMD and ART
reduced by TDF and DMPA - may consider TAF or another contraception
174
NRTIs
no issue
175
NNRTIs
refavirenz/etravine/nevirapine= reduce dorarivine and ripivirine= ok
176
INSTIs
end in -gravir no changes except i fbooster EVG/c, may change CHC
177
Fostemsavir
may change CHC
178
Paternal valproate use
use contraception during and for 3/12 after (1 complete sperm cycle) increase risk of neurodevelopmental disorders eg autism F 30-40% M 5% IUC/DMPA or others and condoms
179
Maternal lamotrigine/Keppra
3 in 100 Neurodevelopmental
180
Orlistat/laxatives
may reduce effectiveness of POP/COC/Oral EC
181
Mounjaro
Tirzepatide slows gastric emptying reduces levels of oral methods wait 1/12 to concieve condoms 1/12 after each dose change
182
Semaglutide
Ozempic/Wegovy does not change levels of oral HC 2/12 before ttc
183
St John's Wort
CYP450 inducer DMPA/IUC
184
Breast Ca treatment
many remain sexually active and fertile treatment is teraogenic pregnancy may delay treatment and worsen outcomes avoid HC regardless of receptor status Chemo can raise FSH IUD/sterilisation CHC and Ca can increase VTE risk
185
Current Breast Ca and CHC risk
stop immediately increases risk, persists 5-10 years after stopping could negate aromatase inhibitors
186
Current Breast Ca and POC
can continue short term until decisions re treatment are made no evidence risk id does related, theoretically LNGIUD preferred but no evidence DMPA may increase VTE risk
187
Where to look up teratogenicity of drugs
UKTIS -teratology information service
188
CHC after delivery-factors affecting
not for 6/52 if: immobility PPH LSCS PET BMI >30 smoking
189
Contraception when breastfeeding
<6 weeks UKMEC 2 DMPA UKMEC 4 CHC <6/12 UKMEC 2 CHC all others 1
190
Contraception not breastfeeding
<3 weeks DMPA 2 CHC 4 if RF, 3 if nil RF <6 weeks DMPA 2 if RF, 1 if nil CHC 3 if RF, 2 if nil >6 weeks all 1 all other 1
191
IUC after delivery
1 <48 hours and >4 weeks 3 between above 4 if sepsis
192
IUC after abortion
2 if second trimester 4 if sepsis decreases likelihood of another abortion within 2 years
193
DMPA and abortion
increased risk of failure if given at time of mifepristone
194
Contraception and miscarriage
better outcomes if conceive within 6 months than after 6 months
195
Recurrent early miscarriage and CHC
consider ?APL and avoid until excluded
196
Contraception and GTD
previous GTD increases risk of future GTD complete- avoid pregnancy 6/12 partial- avoid until 2 negative hCGs chemo-avoid until 12/12 after rx IUC when levels normal static- 4 decreasing-3 EC- go for oral, can consider CuIUD if d/w specialist start HC whenever
197
CHC and weight
patch less effective >90kg UKMEC 2 BMI >30 UKMEC 3 BMI >35
198
UPA and weight
may be less effective at BMI >30 or weight >85kg
199
PO method and RF for CVD
UKMEC 2
200
DMPA and VTE
limited data to exclude causal link HDL levels decrease, changes LDL:HDL level at 6 months, normalises at 24 months
201
CHC and bariatric surgery
If BMI >30 =2 >35= 3
202
IUC and DMPA for <18yo
UKMEC2
203
Advanced EC and pregnancy rate
not shown to reduce
204
<16yo SI
1 in 3 have YP make up 65% chlamydia, 55% AGW and 50% GC
205
Pregnancy risk >40yo
<45 10-20% >45 15% higher risk of poor outcomes 30x increased than those age 20-24
206
>40 and change to bleeding pattern
investigate
207
UKMEC >40yo
CHC = 2 DMPA = 2 >45
208
Stopping contraception (age)
40-50 = 2 years amenorrhea >50 = 1 year amenorrhoea CHC- switch POI- consider switching POC- FSH >30 - stop 1 year -FSH<30- repeat on 1 year as above
209
DMPA and oestrogen
hypo-oestrogenic, lowers BMD
210
Cardiac disorders that raise stroke risk
R to L shunt (cyanotic heart disease) pulmonary AV malformation ASD Patent FO -avoid CHC
211
Cardiac disorders that raise vasovagal risk
single ventricle/ fontan Eisenmenger's arrhythmia (tachy or brady) - IUC in hospital
212
Cardiac disorders that raise infective endocarditis risk
valvular disease valve replacement structural changes (defects/PDA) previous endocarditis -liaise with cardiology
213
Progestogens and INR
unclear impact/evidence
214
Macrolides and cardiac disease
-mycins can change long QT so can oestrogen only HRT
215
Impaired conduction and contraception
caution with LA, especially LA with adrenaline
216
LVEF <25%
avoid pregnancy and CHC
217
Organ transplant
avoid pregnancy 12 months uncomplicated: all methods 2 complicated: eg rejection CHC 3 IUC I is 3 all others 2
218
Low risk cardiac patients
not on any meds (including aspirin) discharged or follow up every 2 years normal sats
219
PPCM
last 1 month of pregnancy or 6 months
220
bosentan
reduces effects of P and E | BOsentan= reduction of BOth
221
IBD and fertility
reduced by flares reduced by reconstructive surgery active disease increases poor fetal outcomes 1 parent- 2% risk both- 30% risk normal dose folate unless malabsorption/sulfasalazine
222
Methotrexate
wait 3/12
223
Mycophenolate- wait to conceive
6/52 F 3/12 M
224
Sulfasalazine
5 mg folate reversible reduction of sperm count and motility may be seen in MTX/infliximab | SulfaSalazine- Sperm
225
TNF alpha inhibitors + pregnancy
6/12 | -mabs
226
IBD safe drugs for pregnancy
aminosalicylates- + 5mg folate Thiopurines (mercaptopurine is maybe teratogenic) no data on tacrolimus
227
Apixaban and contraception
avoid SDI/IUC in first two weeks (higher dose)
228
INR >3.5
IUC in hospital SDI in community
229
Prolactinoma
not a c/i to any method but may wish to d/w endo
230
Problematic bleeding basics
do not change for 3/12 may choose to increase EE to 35mcg or change progesterone 20% COC have changes to pattern first 3/12 SDI broadly predictive
231
Bleeding patterns at 12/12
CHC- CVR>COCP DMPA- 50% amenorrhoeic SDI- 2 in 10 prolonged LNGIUD- 90% have a reduction
232
Management of problematic bleeding >3/12
Ensure: STI/UPT/Smear pain- bimanual and refer no pain- speculum, if normal reassure CHC: increase EE to 35mcg switch P try CVR POP: Change P SDI/POI/LNGIUD: COC 3/12 DMPA: ?give at 10/52 (no evidence) MFA/TXA
233
Sterilisation and previous bowel resection
c/i
234
Nerve most commonly impacted SDI
ulnar
235
enzyme inducers and osteoporosis
increase risk
236
Amenorrhoea with SDI
1 in 4
237
Highest risk time for VTE with CHC
In the months immediately after initiation or when restarting after a break of >1 month reduces over first year then stable ie stopping/starting is discouraged
238
IBD UKMEC
1 2 for oral methods
239
GB and CHC
UKMEC 3 if: medically treated/current previous COC related all POC is UKMEC 2 for all kinds as is CHC but had cholecystectomy
240
Obstetric Cholestasis- UKMEC
1 POC 2 CHC