TABLE. K1. Summary of classifications for hormonal contraceptive methods and intrauterine devices.
Condition | Cu-IUD |
LNG-IUD |
Implant |
DMPA |
POP |
CHC |
||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Personal Characteristics and Reproductive
History
| ||||||||||||
Pregnancy
|
4* |
4* |
NA* |
NA* |
NA* |
NA* |
||||||
Age
|
Menarche to
<20 years: 2 |
Menarche to
<20 years: 2 |
Menarche to
<18 years: 1 |
Menarche to
<18 years: 2 |
Menarche to
<18 years: 1 |
Menarche to
<40 years: 1 |
||||||
≥20 years: 1 |
≥20 years: 1 |
18–45 years:
1 |
18–45 years:
1 |
18–45 years:
1 |
≥40 years: 2 |
|||||||
>45
years: 1 |
>45 years:
2 |
>45 years:
1 |
||||||||||
Parity
| ||||||||||||
a.
Nulliparous |
2 |
2 |
1 |
1 |
1 |
1 |
||||||
b. Parous |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
Breastfeeding
| ||||||||||||
a. <21 days
postpartum |
— |
— |
2* |
2* |
2* |
4* |
||||||
b. 21 to
<30 days postpartum | ||||||||||||
i.
With other risk factors for VTE (e.g., age ≥35 years,
previous VTE, thrombophilia, immobility, transfusion at
delivery, peripartum cardiomyopathy, BMI ≥30
kg/m2, postpartum hemorrhage, postcesarean
delivery, preeclampsia, or smoking) |
— |
— |
2* |
2* |
2* |
3* |
||||||
ii.
Without other risk factors for VTE |
— |
— |
2* |
2* |
2* |
3* |
||||||
c.
30–42 days postpartum | ||||||||||||
i.
With other risk factors for VTE (e.g., age ≥35 years,
previous VTE, thrombophilia, immobility, transfusion at
delivery, peripartum cardiomyopathy, BMI ≥30
kg/m2, postpartum hemorrhage, postcesarean
delivery, preeclampsia, or smoking) |
— |
— |
1* |
2* |
1* |
3* |
||||||
ii.
Without other risk factors for VTE |
— |
— |
1* |
1* |
1* |
2* |
||||||
d. >42 days
postpartum |
— |
— |
1* |
1* |
1* |
2* |
||||||
Postpartum (nonbreastfeeding) | ||||||||||||
a. <21 days
postpartum |
— |
— |
1 |
2 |
1 |
4 |
||||||
b.
21–42 days postpartum | ||||||||||||
i.
With other risk factors for VTE (e.g., age ≥35 years,
previous VTE, thrombophilia, immobility, transfusion at
delivery, peripartum cardiomyopathy, BMI ≥30
kg/m2, postpartum hemorrhage, postcesarean
delivery, preeclampsia, or smoking) |
— |
— |
1 |
2 |
1 |
3* |
||||||
ii.
Without other risk factors for VTE |
— |
— |
1 |
1 |
1 |
2 |
||||||
c. >42 days
postpartum |
— |
— |
1 |
1 |
1 |
1 |
||||||
Postpartum (including cesarean delivery,
breastfeeding,
or nonbreastfeeding) | ||||||||||||
a. <10 minutes
after delivery of the placenta |
2* |
2* |
— |
— |
— |
— |
||||||
b. 10 minutes after
delivery of the placenta to <4 weeks |
2* |
2* |
— |
— |
— |
— |
||||||
c. ≥4
weeks |
1* |
1* |
— |
— |
— |
— |
||||||
d. Postpartum
sepsis |
4 |
4 |
— |
— |
— |
— |
||||||
Postabortion (spontaneous or
induced) | ||||||||||||
a. First
trimester abortion | ||||||||||||
i.
Procedural (surgical) |
1* |
1* |
1* |
1* |
1* |
1* |
||||||
ii.
Medication |
1* |
1* |
1* |
1/2* |
1* |
1* |
||||||
iii.
Spontaneous abortion with no intervention |
1* |
1* |
1* |
1* |
1* |
1* |
||||||
b. Second
trimester abortion | ||||||||||||
i.
Procedural (surgical) |
2* |
2* |
1* |
1* |
1* |
1* |
||||||
ii.
Medication |
2* |
2* |
1* |
1* |
1* |
1* |
||||||
iii.
Spontaneous abortion with no intervention |
2* |
2* |
1* |
1* |
1* |
1* |
||||||
c. Immediate
postseptic abortion |
4 |
4 |
1* |
1* |
1* |
1* |
||||||
Past ectopic
pregnancy
|
1 |
1 |
1 |
1 |
2 |
1 |
||||||
History of
pelvic surgery (see recommendations for
Postpartum [including cesarean delivery]) |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
Smoking
| ||||||||||||
a. Age <35
years |
1 |
1 |
1 |
1 |
1 |
2 |
||||||
b. Age
≥35 years | ||||||||||||
i.
<15 cigarettes per day |
1 |
1 |
1 |
1 |
1 |
3 |
||||||
ii.
≥15 cigarettes per day |
1 |
1 |
1 |
1 |
1 |
4 |
||||||
Obesity
| ||||||||||||
a. BMI ≥30
kg/m2 |
1 |
1 |
1 |
1 |
1 |
2* |
||||||
b. Menarche to <18
years and BMI ≥30 kg/m2 |
1 |
1 |
1 |
2 |
1 |
2* |
||||||
History of bariatric surgery This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). | ||||||||||||
a. Restrictive
procedures: decrease storage capacity of the stomach
(vertical banded gastroplasty, laparoscopic adjustable
gastric band, or laparoscopic sleeve gastrectomy) |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
b. Malabsorptive
procedures: decrease absorption of nutrients and calories by
shortening the functional length of the small intestine
(Roux-en-Y gastric bypass or biliopancreatic
diversion) |
1 |
1 |
1 |
1 |
3 |
COCs: 3 Patch and ring: 1 |
||||||
Surgery
| ||||||||||||
a. Minor surgery
without immobilization |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
b. Major
surgery | ||||||||||||
i.
Without prolonged immobilization |
1 |
1 |
1 |
1 |
1 |
2 |
||||||
ii.
With prolonged immobilization |
1 |
1 |
1 |
2 |
1 |
4 |
||||||
Cardiovascular Disease
| ||||||||||||
Multiple risk
factors for atherosclerotic cardiovascular
disease (e.g., older age, smoking, diabetes,
hypertension, low HDL, high LDL, or high triglyceride
levels) |
1 |
2 |
2* |
3* |
2* |
3/4* |
||||||
Hypertension Systolic blood pressure ≥160 mm Hg or diastolic blood pressure ≥100 mm Hg are associated with increased risk for adverse health events as a result of pregnancy (Box 3). | ||||||||||||
a. Adequately
controlled hypertension |
1* |
1* |
1* |
2* |
1* |
3* |
||||||
b.
Elevated blood pressure levels (properly
taken
measurements) | ||||||||||||
i.
Systolic 140–159 mm Hg or diastolic 90–99 mm
Hg |
1* |
1* |
1* |
2* |
1* |
3* |
||||||
ii.
Systolic ≥160 mm Hg or diastolic ≥100 mm
Hg |
1* |
2* |
2* |
3* |
2* |
4* |
||||||
c. Vascular
disease |
1* |
2* |
2* |
3* |
2* |
4* |
||||||
History of high
blood pressure during pregnancy (when current
blood pressure is measurable and normal) |
1 |
1 |
1 |
1 |
1 |
2 |
||||||
Deep venous thrombosis/Pulmonary
embolism This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). | ||||||||||||
a. Current or history
of DVT/PE, receiving anticoagulant therapy (therapeutic
dose) (e.g., acute DVT/PE or long-term therapeutic
dose) |
2* |
2* |
2* |
2* |
2* |
3* |
||||||
b.
History of DVT/PE, receiving anticoagulant
therapy
(prophylactic dose) | ||||||||||||
i.
Higher risk for recurrent DVT/PE (one or more risk
factors) |
2* |
2* |
2* |
3* |
2* |
4* |
||||||
•
Thrombophilia (e.g., factor V Leiden mutation; prothrombin
gene mutation; protein S, protein C, and antithrombin
deficiencies; or antiphospholipid
syndrome) • Active cancer (metastatic, receiving therapy, or within 6 months after clinical remission), excluding nonmelanoma skin cancer • History of recurrent DVT/PE | ||||||||||||
ii.
Lower risk for recurrent DVT/PE (no risk factors) |
2* |
2* |
2* |
2* |
2* |
3* |
||||||
c.
History of DVT/PE, not receiving anticoagulant
therapy | ||||||||||||
i.
Higher risk for recurrent DVT/PE (one or more risk
factors |
1 |
2 |
2 |
3 |
2 |
4 |
||||||
• History of
estrogen-associated
DVT/PE • Pregnancy-associated DVT/PE • Idiopathic DVT/PE • Thrombophilia (e.g., factor V Leiden mutation; prothrombin gene mutation; protein S, protein C, and antithrombin deficiencies; or antiphospholipid syndrome) • Active cancer (metastatic, receiving therapy, or within 6 months after clinical remission), excluding nonmelanoma skin cancer • History of recurrent DVT/PE | ||||||||||||
ii.
Lower risk for recurrent DVT/PE (no risk factors) |
1 |
2 |
2 |
2 |
2 |
3 |
||||||
d. Family history
(first-degree relatives) |
1 |
1 |
1 |
1 |
1 |
2 |
||||||
Thrombophilia (e.g., factor V Leiden
mutation; prothrombin gene mutation; protein S, protein C,
and antithrombin deficiencies; or antiphospholipid
syndrome) This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). |
1* |
2* |
2* |
3* |
2* |
4* |
||||||
Superficial venous disorders
| ||||||||||||
a. Varicose
veins |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
b. Superficial venous
thrombosis (acute or history) |
1 |
1 |
1 |
2 |
1 |
3* |
||||||
Current and history of ischemic heart
disease This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). |
1 |
Initiation |
Continuation |
Initiation |
Continuation |
3 |
Initiation |
Continuation |
4 |
|||
2 |
3 |
2 |
3 |
2 |
3 |
|||||||
Stroke (history of cerebrovascular
accident)
This condition is associated with increased
risk for adverse health events as a result of pregnancy
(Box
3). |
1 |
2 |
Initiation |
Continuation |
3 |
Initiation |
Continuation |
4 |
||||
2 |
3 |
2 |
3 |
|||||||||
Valvular heart disease Complicated valvular heart disease is associated with increased risk for adverse health events as a result of pregnancy (Box 3). | ||||||||||||
a.
Uncomplicated |
1 |
1 |
1 |
1 |
1 |
2 |
||||||
b. Complicated
(pulmonary hypertension, risk for atrial fibrillation, or
history of subacute bacterial endocarditis) |
1 |
1 |
1 |
2 |
1 |
4 |
||||||
Peripartum cardiomyopathy This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). | ||||||||||||
a. Normal
or mildly impaired cardiac function (New
York Heart
Association Functional Class I or II: no
limitation
of activities or slight, mild limitation
of activity)
(3) | ||||||||||||
i.
<6 months |
2 |
2 |
1 |
2 |
1 |
4 |
||||||
ii.
≥6 months |
2 |
2 |
1 |
2 |
1 |
3 |
||||||
b. Moderately or
severely impaired cardiac function (New York Heart
Association Functional Class III or IV: marked limitation of
activity or should be at complete rest) (3) |
2 |
2 |
2 |
3 |
2 |
4 |
||||||
Renal Disease
| ||||||||||||
Chronic kidney
disease This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). |
Initiation |
Continuation |
Initiation |
Continuation |
— |
|||||||
a. Current nephrotic
syndrome |
1 |
1 |
2 |
2 |
2 |
3 |
2* DRSP POP with known hyperkalemia: 4* |
4 |
||||
b.
Hemodialysis |
1 |
1 |
2 |
2 |
2 |
3 |
2* DRSP POP with known hyperkalemia: 4* |
4 |
||||
c. Peritoneal
dialysis |
2 |
1 |
2 |
2 |
2 |
3 |
2* DRSP POP with known hyperkalemia: 4* |
4 |
||||
Rheumatic Diseases
| ||||||||||||
Systemic lupus
erythematosus This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). |
Initiation |
Continuation |
— |
Initiation |
Continuation |
— |
||||||
a. Positive (or
unknown) antiphospholipid antibodies |
1* |
1* |
2* |
2* |
3* |
3* |
2* |
4* |
||||
b. Severe
thrombocytopenia |
3* |
2* |
2* |
2* |
3* |
2* |
2* |
2* |
||||
c. Immunosuppressive
therapy |
2* |
1* |
2* |
2* |
2* |
2* |
2* |
2* |
||||
d. None of the
above |
1* |
1* |
2* |
2* |
2* |
2* |
2* |
2* |
||||
Rheumatoid
arthritis
|
Initiation |
Continuation |
Initiation |
Continuation |
— |
|||||||
a. Not receiving
immunosuppressive therapy |
1 |
1 |
1 |
1 |
1 |
2 |
1 |
2 |
||||
b. Receiving
immunosuppressive therapy |
2 |
1 |
2 |
1 |
1 |
2/3* |
1 |
2 |
||||
Neurologic Conditions
| ||||||||||||
Headaches
| ||||||||||||
a. Nonmigraine (mild
or severe) |
1 |
1 |
1 |
1 |
1 |
1* |
||||||
b.
Migraine | ||||||||||||
i.
Without aura (includes menstrual migraine) |
1 |
1 |
1 |
1 |
1 |
2* |
||||||
ii.
With aura |
1 |
1 |
1 |
1 |
1 |
4* |
||||||
Epilepsy This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). |
1 |
1 |
1* |
1* |
1* |
1* |
||||||
Multiple sclerosis
| ||||||||||||
a. Without prolonged
immobility |
1 |
1 |
1 |
2 |
1 |
1 |
||||||
b. With prolonged
immobility |
1 |
1 |
1 |
2 |
1 |
3 |
||||||
Depressive Disorders
| ||||||||||||
Depressive
disorders
|
1* |
1* |
1* |
1* |
1* |
1* |
||||||
Reproductive Tract Infections and
Disorders
| ||||||||||||
Vaginal bleeding patterns
|
Initiation |
Continuation |
— |
|||||||||
a. Irregular pattern
without heavy bleeding |
1 |
1 |
1 |
2 |
2 |
2 |
1 |
|||||
b. Heavy or prolonged
bleeding (includes regular and irregular patterns) |
2* |
1* |
2* |
2* |
2* |
2* |
1* |
|||||
Unexplained vaginal
bleeding (suspicious for serious condition) before evaluation |
Initiation |
Continuation |
Initiation |
Continuation |
— |
|||||||
4* |
2* |
4* |
2* |
3* |
3* |
2* |
2* |
|||||
Endometriosis
|
2 |
1 |
1 |
1 |
1 |
1 |
||||||
Benign ovarian
tumors (including cysts) |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
Severe
dysmenorrhea
|
2 |
1 |
1 |
1 |
1 |
1 |
||||||
Gestational trophoblastic
disease This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). | ||||||||||||
a.
Suspected gestational trophoblastic
disease
(immediate postevacuation) | ||||||||||||
i.
Uterine size first trimester |
1* |
1* |
1* |
1* |
1* |
1* |
||||||
ii.
Uterine size second trimester |
2* |
2* |
1* |
1* |
1* |
1* |
||||||
b. Confirmed
gestational trophoblastic disease (after initial evacuation
and during monitoring) |
Initiation |
Continuation |
Initiation |
Continuation |
— |
|||||||
i.
Undetectable or nonpregnant β-hCG levels |
1* |
1* |
1* |
1* |
1* |
1* |
1* |
1* |
||||
ii.
Decreasing β-hCG levels |
2* |
1* |
2* |
1* |
1* |
1* |
1* |
1* |
||||
iii.
Persistently elevated β-hCG levels or malignant
disease, with no evidence or suspicion of intrauterine
disease |
2* |
1* |
2* |
1* |
1* |
1* |
1* |
1* |
||||
iv.
Persistently elevated β-hCG levels or malignant
disease, with evidence or suspicion of intrauterine
disease |
4* |
2* |
4* |
2* |
1* |
1* |
1* |
1* |
||||
Cervical
ectropion
|
1 |
1 |
1 |
1 |
1 |
1 |
||||||
Cervical
intraepithelial neoplasia
|
1 |
2 |
2 |
2 |
1 |
2 |
||||||
Cervical cancer (awaiting
treatment) |
Initiation |
Continuation |
Initiation |
Continuation |
— |
|||||||
4 |
2 |
4 |
2 |
2 |
2 |
1 |
2 |
|||||
Breast disease Breast cancer is associated with increased risk for adverse health events as a result of pregnancy (Box 3). | ||||||||||||
a. Undiagnosed
mass |
1 |
2* |
2* |
2* |
2* |
2* |
||||||
b. Benign breast
disease |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
c. Family history of
cancer |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
d. Breast
cancer | ||||||||||||
i.
Current |
1 |
4 |
4 |
4 |
4 |
4 |
||||||
ii.
Past and no evidence of current disease for 5
years |
1 |
3 |
3 |
3 |
3 |
3 |
||||||
Endometrial
hyperplasia
|
1 |
1 |
1 |
1 |
1 |
1 |
||||||
Endometrial cancer This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). |
Initiation |
Continuation |
Initiation |
Continuation |
— |
|||||||
4 |
2 |
4 |
2 |
1 |
1 |
1 |
1 |
|||||
Ovarian
cancer This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
Uterine
fibroids
|
2 |
2 |
1 |
1 |
1 |
1 |
||||||
Anatomical abnormalities
| ||||||||||||
a. Distorted uterine
cavity (any congenital or acquired uterine abnormality
distorting the uterine cavity in a manner that is
incompatible with IUD placement) |
4 |
4 |
— |
|||||||||
b. Other abnormalities
(including cervical stenosis or cervical lacerations) not
distorting the uterine cavity or interfering with IUD
placement |
2 |
2 |
||||||||||
Pelvic
inflammatory disease
|
Initiation |
Continuation |
Initiation |
Continuation |
— |
|||||||
a. Current
PID |
4 |
2* |
4 |
2* |
1 |
1 |
1 |
1 |
||||
b. Past
PID | ||||||||||||
i.
With subsequent pregnancy |
1 |
1 |
1 |
1 |
1 |
1 |
1 |
1 |
||||
ii.
Without subsequent pregnancy |
2 |
2 |
2 |
2 |
1 |
1 |
1 |
1 |
||||
Sexually
transmitted infections
|
Initiation |
Continuation |
Initiation |
Continuation |
— |
|||||||
a. Current purulent
cervicitis or chlamydial infection or gonococcal
infection |
4 |
2* |
4 |
2* |
1 |
1 |
1 |
1 |
||||
b. Vaginitis
(including Trichomonas vaginalis and
bacterial vaginosis) |
2 |
2 |
2 |
2 |
1 |
1 |
1 |
1 |
||||
c. Other factors
related to STIs |
2* |
2 |
2* |
2 |
1 |
1 |
1 |
1 |
||||
HIV
| ||||||||||||
High
risk for HIV infection
|
Initiation |
Continuation |
Initiation |
Continuation |
— |
|||||||
1* |
1* |
1* |
1* |
1 |
1 |
1 |
1 |
|||||
HIV
infection For persons with HIV infection who are not clinically well or not receiving ARV therapy, this condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). |
— |
— |
— |
— |
1* |
1* |
1* |
1* |
||||
a. Clinically well
receiving ARV therapy |
1 |
1 |
1 |
1 |
— |
— |
— |
— |
||||
b. Not clinically well
or not receiving ARV therapy |
2 |
1 |
2 |
1 |
— |
— |
— |
— |
||||
Other Infections
| ||||||||||||
Schistosomiasis Schistosomiasis with fibrosis of the liver is associated with increased risk for adverse health events as a result of pregnancy (Box 3). | ||||||||||||
a.
Uncomplicated |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
b. Fibrosis of the
liver (if severe, see recommendations for
Cirrhosis) |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
Tuberculosis This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). |
Initiation |
Continuation |
Initiation |
Continuation |
— |
|||||||
a. Nonpelvic |
1 |
1 |
1 |
1 |
1* |
1* |
1* |
1* |
||||
b. Pelvic |
4 |
3 |
4 |
3 |
1* |
1* |
1* |
1* |
||||
Malaria
|
1 |
1 |
1 |
1 |
1 |
1 |
||||||
Endocrine Conditions
| ||||||||||||
Diabetes Insulin-dependent diabetes; diabetes with nephropathy, retinopathy, or neuropathy; diabetes with other vascular disease; or diabetes of >20 years’ duration are associated with increased risk for adverse health events as a result of pregnancy (Box 3). | ||||||||||||
a. History of
gestational disease |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
b.
Nonvascular disease | ||||||||||||
i.
Non-insulin dependent |
1 |
2 |
2 |
2 |
2 |
2 |
||||||
ii.
Insulin dependent |
1 |
2 |
2 |
2 |
2 |
2 |
||||||
c. Nephropathy,
retinopathy, or neuropathy |
1 |
2 |
2 |
3 |
2 |
3/4* |
||||||
d. Other vascular
disease or diabetes of >20 years’
duration |
1 |
2 |
2 |
3 |
2 |
3/4* |
||||||
Thyroid disorders
| ||||||||||||
a. Simple
goiter |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
b.
Hyperthyroid |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
c.
Hypothyroid |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
Gastrointestinal Conditions
| ||||||||||||
Inflammatory
bowel disease (ulcerative colitis or
Crohn’s disease) |
1 |
1 |
1 |
2 |
2 |
2/3* |
||||||
Gallbladder disease
| ||||||||||||
a.
Asymptomatic |
1 |
2 |
2 |
2 |
2 |
2 |
||||||
b.
Symptomatic | ||||||||||||
i.
Current |
1 |
2 |
2 |
2 |
2 |
3 |
||||||
ii.
Treated by cholecystectomy |
1 |
2 |
2 |
2 |
2 |
2 |
||||||
iii.
Medically treated |
1 |
2 |
2 |
2 |
2 |
3 |
||||||
History of cholestasis
| ||||||||||||
a. Pregnancy
related |
1 |
1 |
1 |
1 |
1 |
2 |
||||||
b. Past COC
related |
1 |
2 |
2 |
2 |
2 |
3 |
||||||
Viral hepatitis
|
Initiation |
Continuation |
||||||||||
a. Acute or
flare |
1 |
1 |
1 |
1 |
1 |
3/4* |
2 |
|||||
b. Chronic |
1 |
1 |
1 |
1 |
1 |
1 |
1 |
|||||
Cirrhosis Decompensated cirrhosis is associated with increased risk for adverse health events as a result of pregnancy (Box 3). | ||||||||||||
a. Compensated (normal
liver function) |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
b. Decompensated
(impaired liver function) |
1 |
2 |
2 |
3 |
2 |
4 |
||||||
Liver tumors Hepatocellular adenoma and malignant liver tumors are associated with increased risk for adverse health events as a result of pregnancy (Box 3). | ||||||||||||
a.
Benign | ||||||||||||
i.
Focal nodular hyperplasia |
1 |
2 |
2 |
2 |
2 |
2 |
||||||
ii.
Hepatocellular adenoma |
1 |
2 |
2 |
3 |
2 |
4 |
||||||
b. Malignant
(hepatocellular carcinoma) |
1 |
3 |
3 |
3 |
3 |
4 |
||||||
Respiratory Conditions
| ||||||||||||
Cystic
fibrosis This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). |
1* |
1* |
1* |
2* |
1* |
1* |
||||||
Hematologic Conditions
| ||||||||||||
Thalassemia
|
2 |
1 |
1 |
1 |
1 |
1 |
||||||
Sickle cell
disease This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). |
2 |
1 |
1 |
2/3* |
1 |
4 |
||||||
Iron-deficiency
anemia
|
2 |
1 |
1 |
1 |
1 |
1 |
||||||
Solid Organ Transplantation
| ||||||||||||
Solid organ
transplantation This condition is associated with increased risk for adverse health events as a result of pregnancy (Box 3). |
Initiation |
Continuation |
Initiation |
Continuation |
— |
|||||||
a. No graft
failure |
1 |
1 |
1 |
1 |
2 |
2/3* |
2 |
2* |
||||
b. Graft
failure |
2 |
1 |
2 |
1 |
2 |
2/3* |
2 |
4 |
||||
Drug Interactions
| ||||||||||||
Antiretrovirals used for prevention
(PrEP)
or treatment of HIV
infection
| ||||||||||||
See the
following guidelines for the most up-to-date recommendations
on drug-drug interactions between hormonal contraception and
antiretrovirals: 1) Recommendations for the Use of
Antiretroviral Drugs During Pregnancy and Interventions to
Reduce Perinatal HIV Transmission in the United (https://clinicalinfo.hiv.gov/en/guidelines/perinatal/prepregnancy-counseling-childbearing-age-overview?view=full#table-3)
(4) and 2) Guidelines for the
Use of Antiretroviral Agents in Adults and Adolescents with
HIV (https://clinicalinfo.hiv.gov/en/guidelines/hiv-clinical-guidelines-adult-and-adolescent-arv/drug-interactions-overview?view=full)
(5). | ||||||||||||
a. Nucleoside reverse
transcriptase inhibitors (NRTIs) |
Initiation |
Continuation |
Initiation |
Continuation |
— |
|||||||
i.
Abacavir (ABC) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
ii.
Tenofovir (TDF) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
iii.
Zidovudine (AZT) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
iv.
Lamivudine (3TC) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
v.
Didanosine (DDI) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
vi.
Emtricitabine (FTC) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
vii.
Stavudine (D4T) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
b.
Nonnucleoside reverse transcriptase inhibitors
(NNRTIs) | ||||||||||||
i.
Efavirenz (EFV) |
1/2* |
1* |
1/2* |
1* |
2* |
1* |
2* |
2* |
||||
ii.
Etravirine (ETR) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
iii.
Nevirapine (NVP) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
iv.
Rilpivirine (RPV) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
c.
Ritonavir-boosted protease inhibitors | ||||||||||||
i.
Ritonavir-boosted atazanavir (ATV/r) |
1/2* |
1* |
1/2* |
1* |
2* |
1* |
2* |
2* |
||||
ii.
Ritonavir-boosted darunavir (DRV/r) |
1/2* |
1* |
1/2* |
1* |
2* |
1* |
2* |
2* |
||||
iii.
Ritonavir-boosted fosamprenavir (FPV/r) |
1/2* |
1* |
1/2* |
1* |
2* |
1* |
2* |
2* |
||||
iv.
Ritonavir-boosted lopinavir (LPV/r) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
v.
Ritonavir-boosted saquinavir (SQV/r) |
1/2* |
1* |
1/2* |
1* |
2* |
1* |
2* |
2* |
||||
vi.
Ritonavir-boosted tipranavir (TPV/r) |
1/2* |
1* |
1/2* |
1* |
2* |
1* |
2* |
2* |
||||
d.
Protease inhibitors without ritonavir | ||||||||||||
i.
Atazanavir (ATV) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
2* |
||||
ii.
Fosamprenavir (FPV) |
1/2* |
1* |
1/2* |
1* |
2* |
2* |
2* |
3* |
||||
iii.
Indinavir (IDV) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
iv.
Nelfinavir (NFV) |
1/2* |
1* |
1/2* |
1* |
2* |
1* |
2* |
2* |
||||
e. CCR5
co-receptor antagonists | ||||||||||||
i.
Maraviroc (MVC) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
f. HIV
integrase strand transfer inhibitors | ||||||||||||
i.
Raltegravir (RAL) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
ii.
Dolutegravir (DTG) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
iii.
Elvitegravir (EVG) |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
g. Fusion
inhibitors | ||||||||||||
i.
Enfuvirtide |
1/2* |
1* |
1/2* |
1* |
1 |
1 |
1 |
1 |
||||
Anticonvulsant therapy
| ||||||||||||
a. Certain
anticonvulsants (phenytoin, carbamazepine, barbiturates,
primidone, topiramate, and oxcarbazepine) |
1 |
1 |
2* |
1* |
3* |
3* |
||||||
b.
Lamotrigine |
1 |
1 |
1 |
1 |
1 |
3* |
||||||
Antimicrobial therapy
| ||||||||||||
a. Broad-spectrum
antibiotics |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
b.
Antifungals |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
c.
Antiparasitics |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
d. Rifampin or
rifabutin therapy |
1 |
1 |
2* |
1* |
3* |
3* |
||||||
Psychotropic medications
| ||||||||||||
a. Selective serotonin
reuptake inhibitors (SSRIs) |
1 |
1 |
1 |
1 |
1 |
1 |
||||||
St. John’s wort | 1 |
1 |
2 |
1 |
2 |
2 |
Abbreviations: ARV = antiretroviral; BMI = body mass index; CHC = combined hormonal contraceptive; COC = combined oral contraceptive; Cu-IUD = copper intrauterine device; DMPA = depot medroxyprogesterone acetate; DRSP = drospirenone; DVT = deep venous thrombosis; hCG = human chorionic gonadotropin; HDL = high-density lipoprotein; IUD = intrauterine device; LDL = low-density lipoprotein; LNG-IUD = levonorgestrel intrauterine device; NA = not applicable; PE = pulmonary embolism; PID = pelvic inflammatory disease; POP = progestin-only pill; PrEP = pre-exposure prophylaxis; STI = sexually transmitted infection; VTE = venous thromboembolism.
* Consult the appendix for this contraceptive method for a clarification to this classification.