Appendices for U.S. Selected Practice Recommendations for Contraceptive Use, 2016

Appendix A

Summary Chart of U.S. Medical Eligibility Criteria for Contraceptive Use, 2016

Health-care providers can use the summary table as a quick reference guide to the classifications for hormonal contraceptive methods and intrauterine contraception to compare classifications across these methods ( Box A1) ( Table A1). For complete guidance, see the 2016 U.S. Medical Eligibility Criteria for Contraceptive Use (U.S. MEC) (Curtis KM, Tepper NK, Jatlaoui TC, et al. U.S. medical eligibility criteria for contraceptive use, 2016. MMWR Recomm Rep 2016;65[No. RR-3]) for clarifications to the numeric categories, as well as for summaries of the evidence and additional comments. Hormonal contraceptives and intrauterine devices do not protect against sexually transmitted diseases (STDs), including human immunodeficiency virus (HIV), and women using these methods should be counseled that consistent and correct use of the male latex condom reduces the risk for transmission of HIV and other STDs. Use of female condoms can provide protection from transmission of STDs, although data are limited.

TABLE A1. Summary of classifications for hormonal contraceptive methods and intrauterine devices

Condition	Cu-IUD		LNG-IUD		Implants		DMPA		POP		CHCs
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*		1*		1*		3*
ii. Without other risk factors for VTE	—		—		1*		1*		1*		2*
d. >42 days postpartum	—		—		1*		1*		1*		2*
Postpartum (nonbreastfeeding women)
a. <21 days postpartum	—		—		1		1		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		1		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)
a. <10 minutes after delivery of the placenta
i. Breastfeeding	1*		2*		—		—		—		—
ii. Nonbreastfeeding	1*		1*		—		—		—		—
b. 10 minutes after delivery of the placenta to <4 weeks (breastfeeding or nonbreastfeeding)	2*		2*		—		—		—		—
c. =4 weeks (breastfeeding or nonbreastfeeding)	1*		1*		—		—		—		—
d. Postpartum sepsis	4		4		—		—		—		—
Postabortion
a. First trimester	1*		1*		1*		1*		1*		1*
b. Second trimester	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 Postpartum [Including Cesarean Delivery] section)	1		1		1		1		1		1
Smoking
a. Age <35 years	1		1		1		1		1		2
b. Age =35 years
i. <15 cigarettes/day	1		1		1		1		1		3
ii. =15 cigarettes/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.
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
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.
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
a. History of DVT/PE, not receiving anticoagulant therapy
i. Higher risk for recurrent DVT/PE (one or more risk factors)	1		2		2		2		2		4
• History of estrogen-associated DVT/PE • Pregnancy-associated DVT/PE • Idiopathic DVT/PE • Known thrombophilia, including 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
b. Acute DVT/PE	2		2		2		2		2		4
c. DVT/PE and established receiving anticoagulant therapy for at least 3 months
i. Higher risk for recurrent DVT/PE (one or more risk factors)	2		2		2		2		2		4*
• Known thrombophilia, including 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*
d. Family history (first-degree relatives)	1		1		1		1		1		2
e. Major surgery
i. With prolonged immobilization	1		2		2		2		2		4
ii. Without prolonged immobilization	1		1		1		1		1		2
f. Minor surgery without immobilization	1		1		1		1		1		1
Known thrombogenic mutations (e.g., factor V Leiden; prothrombin mutation; and protein S, protein C, and antithrombin deficiencies) This condition is associated with increased risk for adverse health events as a result of pregnancy.	1*		2*		2*		2*		2*		4*
Superficial venous disorders
a. Varicose veins	1		1		1		1		1		1
b. Superficial venous thrombosis (acute or history)	1		1		1		1		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.			Initiation	Continuation	Initiation	Continuation			Initiation	Continuation
	1		2	3	2	3	3		2	3	4
Stroke (history of cerebrovascular accident) This condition is associated with increased risk for adverse health events as a result of pregnancy.					Initiation	Continuation			Initiation	Continuation
	1		2		2	3	3		2	3	4
Valvular heart disease Complicated valvular heart disease is associated with increased risk for adverse health events as a result of pregnancy.
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		1		1		4
Peripartum cardiomyopathy This condition is associated with increased risk for adverse health events as a result of pregnancy.
a. Normal or mildly impaired cardiac function (New York Heart Association Functional Class I or II: patients with no limitation of activities or patients with slight, mild limitation of activity) (2)
i. <6 months	2		2		1		1		1		4
ii. =6 months	2		2		1		1		1		3
b. Moderately or severely impaired cardiac function (New York Heart Association Functional Class III or IV: patients with marked limitation of activity or patients who should be at complete rest) (2).	2		2		2		2		2		4
Rheumatic Diseases
Systemic lupus erythematosus This condition is associated with increased risk for adverse health events as a result of pregnancy.	Initiation	Continuation					Initiation	Continuation
a. Positive (or unknown) antiphospholipid antibodies	1*	1*	3*		3*		3*	3*	3*		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. Receiving immunosuppressive therapy	2	1	2	1	1		2/3*		1		2
b. Not receiving immunosuppressive therapy	1		1		1		2		1		2
Neurologic Conditions
Headaches
a. Nonmigraine (mild or severe)	1		1		1		1		1		1*
b. Migraine
i. Without aura (This category of migraine 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.	1		1		1*		1*		1*		1*
Multiple sclerosis
a. With prolonged immobility	1		1		1		2		1		3
b. Without prolonged immobility	1		1		1		2		1		1
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.
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/nonpregnant ß-hCG levels	1*	1*	1*	1*	1*		1*		1*		1*
ii. Decreasing ß-hCG levels	2*	1*	2*	1*	1*		1*		1*		1*
iii. Persistently elevated ß-hCG levels or malignant disease, with no evidence or suspicion of intrauterine disease	2*	1*	2*	1*	1*		1*		1*		1*
iv. Persistently elevated ß-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 of adverse health events as a result of pregnancy.
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.	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.	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 insertion)	4		4		—		—		—		—
b. Other abnormalities (including cervical stenosis or cervical lacerations) not distorting the uterine cavity or interfering with IUD insertion	2		2		—		—		—		—
Pelvic inflammatory disease
a. Past PID (assuming no current risk factors for STDs)	Initiation	Continuation	Initiation	Continuation
i. With subsequent pregnancy	1	1	1	1	1		1		1		1
ii. Without subsequent pregnancy	2	2	2	2	1		1		1		1
b. Current PID	4	2*	4	2*	1		1		1		1
Sexually transmitted diseases	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 STDs	2*	2	2*	2	1		1		1		1
HIV
	Initiation	Continuation	Initiation	Continuation
High risk for HIV	2	2	2	2	1		1*		1		1
HIV infection For women 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.	—	—	—	—	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.
a. Uncomplicated	1		1		1		1		1		1
b. Fibrosis of the liver (if severe, see Cirrhosis)	1		1		1		1		1		1
Tuberculosis This condition is associated with increased risk for adverse health events as a result of pregnancy.	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, neuropathy, or diabetes with other vascular disease; or diabetes of >20 years’ duration are associated with increased risk of adverse health events as a result of pregnancy.
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. Symptomatic
i. Treated by cholecystectomy	1		2		2		2		2		2
ii. Medically treated	1		2		2		2		2		3
iii. Current	1		2		2		2		2		3
b. Asymptomatic	1		2		2		2		2		2
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. Carrier	1		1		1		1		1		1	1
c. Chronic	1		1		1		1		1		1	1
Cirrhosis Severe cirrhosis is associated with increased risk for adverse health events as a result of pregnancy.
a. Mild (compensated)	1		1		1		1		1		1
b. Severe (decompensated)	1		3		3		3		3		4
Liver tumors Hepatocellular adenoma and malignant liver tumors are associated with increased risk for adverse health events as a result of pregnancy.
a. Benign
i. Focal nodular hyperplasia	1		2		2		2		2		2
ii. Hepatocellular adenoma	1		3		3		3		3		4
b. Malignant (hepatoma)	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.	1*		1*		1*		2*		1*		1*
Anemias
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.	2		1		1		1		1		2
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.	Initiation	Continuation	Initiation	Continuation
a. Complicated: graft failure (acute or chronic), rejection, or cardiac allograft vasculopathy	3	2	3	2	2		2		2		4
b. Uncomplicated	2		2		2		2		2		2*
Drug Interactions
Antiretroviral therapy	Initiation	Continuation	Initiation	Continuation
a. Nucleoside reverse transcriptase inhibitors (NRTIs)
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 fosemprenavir (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. SSRIs	1		1		1		1		1		1
St. John’s wort	1		1		2		1		2		2

Abbreviations: BMI = body mass index; COC = combined oral contraceptive; Cu-IUD = copper-containing IUD; DMPA = depot medroxyprogesterone acetate; DVT = deep venous thrombosis; hCG = human chorionic gonadotropin; HDL = high-density lipoprotein; HIV = human immunodeficiency virus.; IUD = intrauterine device; LDL = low-density lipoprotein; LNG-IUD = levonorgestrel-releasing IUD; NA = not applicable; PE = pulmonary embolism; PID = pelvic inflammatory disease; POP = progestin-only pill; SSRI = selective serotonin reuptake inhibitor; STD = sexually transmitted disease.

*Consult the respective appendix for each contraceptive method in the 2016 U.S. Medical Eligibility Criteria for Contraceptive Use (1) for clarifications to the numeric categories.

References

1. Curtis KM, Tepper NK, Jatlaoui TC, et al. U.S. medical eligibility criteria for contraceptive use, 2016. MMWR Recomm Rep 2016;65(No. RR-3).
2. The Criteria Committee of the New York Heart Association. Nomenclature and criteria for diagnosis of diseases of the heart and great vessels. 9th ed. Boston, MA: Little, Brown & Co; 1994.

Abbreviations: BMI = body mass index; HIV = human immunodeficiency virus; IUD = intrauterine device; STD = sexually transmitted disease; U.S. MEC = U.S. Medical Eligibility Criteria for Contraceptive Use.

* Weight (BMI) measurement is not needed to determine medical eligibility for any methods of contraception because all methods can be used (U.S. MEC 1) or generally can be used (U.S. MEC 2) among obese women (Box 1). However, measuring weight and calculating BMI (weight [kg] / height [m]²) at baseline might be helpful for monitoring any changes and counseling women who might be concerned about weight change perceived to be associated with their contraceptive method.

^† Most women do not require additional STD screening at the time of IUD insertion. If a woman with risk factors for STDs has not been screened for gonorrhea and chlamydia according to CDC’s STD Treatment Guidelines (http://www.cdc.gov/std/treatment), screening can be performed at the time of IUD insertion, and insertion should not be delayed. Women with current purulent cervicitis or chlamydial infection or gonococcal infection should not undergo IUD insertion (U.S. MEC 4).

Appendix C

Examinations and Tests Needed Before Initiation of Contraceptive Methods

The examinations or tests noted apply to women who are presumed to be healthy ( Table C1). Those with known medical problems or other special conditions might need additional examinations or tests before being determined to be appropriate candidates for a particular method of contraception. The 2016 U.S. Medical Eligibility Criteria for Contraceptive Use (U.S. MEC) might be useful in such circumstances (1). The following classification was considered useful in differentiating the applicability of the various examinations or tests:

• Class A: essential and mandatory in all circumstances for safe and effective use of the contraceptive method.
• Class B: contributes substantially to safe and effective use, but implementation may be considered within the public health and/or service context; risk of not performing an examination or test should be balanced against the benefits of making the contraceptive method available.
• Class C: does not contribute substantially to safe and effective use of the contraceptive method.

These classifications focus on the relationship of the examinations or tests to safe initiation of a contraceptive method. They are not intended to address the appropriateness of these examinations or tests in other circumstances. For example, some of the examinations or tests that are not deemed necessary for safe and effective contraceptive use might be appropriate for good preventive health care or for diagnosing or assessing suspected medical conditions. Any additional screening needed for preventive health care can be performed at the time of contraception initiation and initiation should not be delayed for test results.

No examinations or tests are needed before initiating condoms or spermicides. A bimanual examination is necessary for diaphragm fitting. A bimanual examination and cervical inspection are needed for cervical cap fitting.

References

1. Curtis KM, Tepper NK, Jatlaoui TC, et al. U.S. medical eligibility criteria for contraceptive use, 2016. MMWR Recomm Rep 2016;65(No. RR-3).

TABLE C1. Examinations and tests needed before initiation of contraceptive methods

Examination or test	Contraceptive method and class
	Cu-IUD and LNG-IUD	Implant	Injectable	CHC	POP	Condom	Diaphragm or cervical cap	Spermicide
Examination
Blood pressure	C	C	C	A*	C	C	C	C
Weight (BMI) (weight [kg] / height [m]2)	—†	—†	—†	—†	—†	C	C	C
Clinical breast examination	C	C	C	C	C	C	C	C
Bimanual examination and cervical inspection	A	C	C	C	C	C	A§	C
Laboratory test
Glucose	C	C	C	C	C	C	C	C
Lipids	C	C	C	C	C	C	C	C
Liver enzymes	C	C	C	C	C	C	C	C
Hemoglobin	C	C	C	C	C	C	C	C
Thrombogenic mutations	C	C	C	C	C	C	C	C
Cervical cytology (Papanicolaou test)	C	C	C	C	C	C	C	C
STD screening with laboratory tests	—¶	C	C	C	C	C	C	C
HIV screening with laboratory tests	C	C	C	C	C	C	C	C

Abbreviations: BMI = body mass index; CHC = combined hormonal contraceptive; Cu-IUD = copper-containing intrauterine device; HIV = human immunodeficiency virus; LNG-IUD = levonorgestrel-releasing intrauterine device; POP = progestin-only pill; STD = sexually transmitted disease; U.S. MEC = U.S. Medical Eligibility Criteria for Contraceptive Use.

* In instances in which blood pressure cannot be measured by a provider, blood pressure measured in other settings can be reported by the woman to her provider.

^† Weight (BMI) measurement is not needed to determine medical eligibility for any methods of contraception because all methods can be used (U.S. MEC 1) or generally can be used (U.S. MEC 2) among obese women (Box 1). However, measuring weight and calculating BMI at baseline might be helpful for monitoring any changes and counseling women who might be concerned about weight change perceived to be associated with their contraceptive method.

^§A bimanual examination (not cervical inspection) is needed for diaphragm fitting.

^¶ Most women do not require additional STD screening at the time of IUD insertion. If a woman with risk factors for STDs has not been screened for gonorrhea and chlamydia according to CDC’s STD Treatment Guidelines (http://www.cdc.gov/std/treatment), screening can be performed at the time of IUD insertion, and insertion should not be delayed. Women with current purulent cervicitis or chlamydial infection or gonococcal infection should not undergo IUD insertion (U.S. MEC 4).

Appendix D

Routine Follow-Up After Contraceptive Initiation

These recommendations address when routine follow-up is recommended for safe and effective continued use of contraception for healthy women ( Table D1). The recommendations refer to general situations and might vary for different users and different situations. Specific populations who might benefit from frequent follow-up visits include adolescents, those with certain medical conditions or characteristics, and those with multiple medical conditions.

Abbreviations: CHC = combined hormonal contraceptives; Cu-IUD = copper-containing intrauterine device; HIV = human immunodeficiency virus; IUD = intrauterine device; LNG-IUD = levonorgestrel-releasing intrauterine device; POP = progestin-only pills; U.S. MEC = U.S. Medical Eligibility Criteria for Contraceptive Use.

Appendix E

Management of Women with Bleeding Irregularities While Using Contraception*

Management of women with bleeding irregularities while using contraception

Abbreviations: CHC = combined hormonal contraceptive; COC = combined oral contraceptive; Cu-IUD = copper-containing intrauterine device; DMPA = depot medroxyprogesterone acetate; LNG-IUD = levonorgestrel-releasing intrauterine device; NSAIDs = nonsteroidal antiinflammatory drugs.

* If clinically warranted, evaluate for underlying condition. Treat the condition or refer for care. Heavy or prolonged bleeding, either unscheduled or menstrual, is uncommon among LNG-IUD users and implant users.

Appendix F

Management of Intrauterine Devices When Users are Found To Have Pelvic Inflammatory Disease

Management of intrauterine devices when users of copper-containing intrauterine devices or levonorgestrel-releasing intrauterine devices are found to have pelvic inflammatory disease

Abbreviations: IUD = intrauterine device; PID = pelvic inflammatory disease.

* Treat according to the CDC Sexually Transmitted Diseases Treatment Guidelines (http://www.cdc.gov/std/treatment).

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