Copper Intrauterine Device (IUD)
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Contraception: Choosing the Right Method for You
Contraception: Choosing the Right Method for You Megan Sax, MD and James L. Whiteside, MD What’s available? Choosing a method of contraception can be overwhelming. The most commonly used methods of reversible contraception in the United States are: hormonal methods the intrauterine device (IUD) the implant barrier methods (e.g. male condom)1 Friends, family, and the Internet are full of stories of failed contraception or bad reactions and these stories can have a big influence that doesn’t always line up with the facts.2 However, knowing these facts is critical to figuring out what type will work best for you. Highly Effective Contraception The best place to start in choosing your contraception is to determine when, if ever, you are planning on starting a family. If you do not wish to become pregnant in the next year, a Long-Acting Reversible Contraceptive (LARC) device may be a good option. LARCs include an implant placed under the skin of the upper, inner arm (brand name Nexplanon) and the IUD. IUDs are placed inside the uterus (see Figure 1). They use copper (brand name ParaGard) or hormones (brand names: Mirena, Lilleta, Skyla, Kyleena) to stop a pregnancy from happening. LARCs are the most effective reversible form of contraception. Less than 1% of users experience unintended pregnancy during the first year of use.3 Currently, the implant Nexplanon is effective for 3 years. The hormonal IUD may be used for 3 to 5 years, depending on the brand. The copper IUD works for 10 years. These devices are inserted and removed by a medical care provider. -
Contraception Pearls for Practice
Contraception Pearls for Practice Academic Detailing Service Planning committee Content Experts Clinical reviewer Gillian Graves MD FRCS(C), Professor, Department of Obstetrics and Gynecology, Faculty of Medicine, Dalhousie University Drug evaluation pharmacist Pam McLean-Veysey BScPharm, Drug Evaluation Unit, Nova Scotia Health Family Physician Advisory Panel Bernie Buffett MD, Neils Harbour, Nova Scotia Ken Cameron BSc MD CCFP, Dartmouth, Nova Scotia Norah Mogan MD CCFP, Liverpool, Nova Scotia Dalhousie CPD Bronwen Jones MD CCFP – Family Physician, Director Evidence-based Programs in CPD, Associate Professor, Faculty of Medicine, Dalhousie University Michael Allen MD MSc – Family Physician, Professor, Post-retirement Appointment, Consultant Michael Fleming MD CCFP FCFP – Family Physician, Director Family Physician Programs in CPD Academic Detailers Isobel Fleming BScPharm ACPR, Director of Academic Detailing Service Lillian Berry BScPharm Julia Green-Clements BScPharm Kelley LeBlanc BScPharm Gabrielle Richard-McGibney BScPharm, BCPS, PharmD Cathy Ross RN BScNursing Thanks to Katie McLean, Librarian Educator, NSHA Central Zone for her help with literature searching. Cover artwork generated with Tagxedo.com Disclosure statements The Academic Detailing Service is operated by Dalhousie Continuing Professional Development, Faculty of Medicine and funded by the Nova Scotia Department of Health and Wellness. Dalhousie University Office of Continuing Professional Development has full control over content. Dr Bronwen Jones receives funding for her Academic Detailing work from the Nova Scotia Department of Health and Wellness. Dr Michael Allen has received funding from the Nova Scotia Department of Health and Wellness for research projects and to develop CME programs. Dr Gillian Graves has received funding for presentations from Actavis (Fibristal®) and is on the board of AbbVie (for Lupron®). -
Copper Intrauterine Device (IUD)
Copper Intrauterine Device (IUD) What is it? An IUD is a small, flexible device which is inserted into the uterus by a health professional to prevent pregnancy. The copper IUD is a plastic frame with copper bands and/or wire. It has fine threads which extend through the cervix into the vagina. Once inserted, IUDs are not usually noticeable to you or your partner/s. How does it work? The copper IUD prevents pregnancy by: Quick Facts • affecting sperm movement so they cannot move through the uterus • affecting egg movement, and in the rare instance of an egg being A long-acting reversible fertilised, preventing the egg from attaching to the lining of the uterus. contraception (LARC). One of the most effective How effective is it? methods of contraception The copper IUD is more than 99% effective at preventing pregnancy and can last for 5-10 years (depending on the type). Copper IUDs inserted in available in Australia. people over 40 can be left until after menopause. Method Copper IUDs can also be used as a very effective form of emergency Non hormonal contraception, up to five days after unprotected sex or up to day 12 of your menstrual cycle. Contact the Sexual Health Helpline for more Effectiveness information. More than 99% Who can use it? Return to Fertility A health professional will take a detailed medical history and pelvic No delay examination to ensure that an IUD is suitable for you. Availability Copper IUDs are suitable for those who: Simple insertion and • are looking for very effective and reliable long-term contraception removal by a health • cannot tolerate hormones due to side effects or other medical conditions professional. -
Plan C: Copper IUD As Emergency Contraception IMPLEMENTATION TOOLKIT for Administrators and Clinicians
Plan C: Copper IUD as Emergency Contraception IMPLEMENTATION TOOLKIT for Administrators and Clinicians March 2016 Developed by TABLE OF CONTENTS SECTION 1: OVERVIEW ● Introduction Page 1 ● Background Page 2 ● Who It’s For Page 3 ● How to Use It Page 4 ● Additional Considerations Page 5 SECTION 2: ADMINISTRATIVE ● Pre-Implementation Tools Page 6 1.1 Overview: Plan C 1.2 Checklist: Pre-Implementation 1.3 Staff Buy-in 1.4 Checklist: Policies and Procedures 1.5 Sample: Policies and Procedures 1.6 Marketing Plan C 1.7 Sample: Data Collection Tool SECTION 3: CLINICAL ● Implementation Tools Page 21 2.1 The Facts: The Copper-T as Plan C 2.2 Sample: EC Screening Questionnaire 2.3 Triage Scripts 2.4 Contraceptive Counseling 2.5 Eligibility Flowchart: Plan C 2.6 Checklist: Exam Room Preparation 2.7 Checklist: Client-Centered Approach 2.8 Fact Sheet: Copper IUD Aftercare 2.9 Side Effects Management: Steps in the Delivery of Care 2.10 Side Effects Management: Messages, Assessment & Treatment SECTION 4: ADDITIONAL RESOURCES ● Client Education Material: F.A.Q.’s Page 40 ● Client Education Material: EC Chart Page 42 SECTION 5: REFERENCES Page 44 OVERVIEW Introduction The New York State Center of Excellence for Family Planning and Reproductive Health Services (NYS COE) developed this toolkit to support agencies that receive Title X family planning funding through the New York State Department of Health (NYS DOH) Comprehensive Family Planning and Reproductive Health Care Services Program – as well as other sexual and reproductive health service providers – to implement Plan C: Copper IUD as Emergency Contraception (Plan C). -
F.8 Ethinylestradiol-Etonogestrel.Pdf
General Items 1. Summary statement of the proposal for inclusion, change or deletion. Here within, please find the evidence to support the inclusion Ethinylestradiol/Etonogestrel Vaginal Ring in the World Health Organization’s Essential Medicines List (EML). Unintended pregnancy is regarded as a serious public health issue both in developed and developing countries and has received growing research and policy attention during last few decades (1). It is a major global concern due to its association with adverse physical, mental, social and economic outcomes. Developing countries account for approximately 99% of the global maternal deaths in 2015, with sub-Saharan Africa alone accounting for roughly 66% (2). Even though the incidence of unintended pregnancy has declined globally in the past decade, the rate of unintended pregnancy remains high, particularly in developing regions. (3) Regarding the use of contraceptive vaginal rings, updated bibliography (4,5,6) states that contraceptive vaginal rings (CVR) offer an effective contraceptive option, expanding the available choices of hormonal contraception. Ethinylestradiol/Etonogestrel Vaginal Ring is a non-biodegradable, flexible, transparent with an outer diameter of 54 mm and a cross-sectional diameter of 4 mm. It contains 11.7 mg etonogestrel and 2.7 mg ethinyl estradiol. When placed in the vagina, each ring releases on average 0.120 mg/day of etonogestrel and 0.015 mg/day of ethinyl estradiol over a three-week period of use. Ethinylestradiol/Etonogestrel Vaginal Ring is intended for women of fertile age. The safety and efficacy have been established in women aged 18 to 40 years. The main advantages of CVRs are their effectiveness (similar or slightly better than the pill), ease of use without the need of remembering a daily routine, user ability to control initiation and discontinuation, nearly constant release rate allowing for lower doses, greater bioavailability and good cycle control with the combined ring, in comparison with oral contraceptives. -
U.S. Medical Eligibility Criteria for Contraceptive Use, 2010
Morbidity and Mortality Weekly Report www.cdc.gov/mmwr Early Release May 28, 2010 / Vol. 59 U.S. Medical Eligibility Criteria for Contraceptive Use, 2010 Adapted from the World Health Organization Medical Eligibility Criteria for Contraceptive Use, 4th edition department of health and human services Centers for Disease Control and Prevention Early Release CONTENTS The MMWR series of publications is published by the Office of Surveillance, Epidemiology, and Laboratory Services, Centers for Introduction .............................................................................. 1 Disease Control and Prevention (CDC), U.S. Department of Health Methods ................................................................................... 2 and Human Services, Atlanta, GA 30333. How to Use This Document ......................................................... 3 Suggested Citation: Centers for Disease Control and Prevention. [Title]. MMWR Early Release 2010;59[Date]:[inclusive page numbers]. Using the Categories in Practice ............................................... 3 Recommendations for Use of Contraceptive Methods ................. 4 Centers for Disease Control and Prevention Contraceptive Method Choice .................................................. 4 Thomas R. Frieden, MD, MPH Director Contraceptive Method Effectiveness .......................................... 4 Peter A. Briss, MD, MPH Unintended Pregnancy and Increased Health Risk ..................... 4 Acting Associate Director for Science Keeping Guidance Up to Date ................................................... -
FLOW (Finding Lasting Options for Women) Multicentre Randomized Controlled Trial Comparing Tampons with Menstrual Cups
Research | Web exclusive FLOW (finding lasting options for women) Multicentre randomized controlled trial comparing tampons with menstrual cups Courtney Howard MD CCFP(EM) Caren Lee Rose MSc Konia Trouton MD CCFP MPH Holly Stamm MD CCFP Danielle Marentette MD CCFP Nicole Kirkpatrick MD CCFP(EM) Sanja Karalic MD CCFP MSc Renee Fernandez MD CCFP Julie Paget MD CCFP Abstract Objective To determine whether menstrual cups are a viable alternative to tampons. Design Randomized controlled trial. EDITOR’S KEY POINTS Setting Prince George, Victoria, and Vancouver, BC. • Patients are increasingly asking physicians about more environmentally friendly Participants A total of 110 women aged 19 to 40 years who had previously alternatives to disposable menstrual used tampons as their main method of menstrual management. management products, particularly menstrual cups, and about their Intervention Participants were randomized into 2 groups, a tampon group effectiveness compared with tampons. and a menstrual cup group. Using online diaries, participants tracked 1 Although the safety and efficacy of menstrual cycle using their regular method and 3 menstrual cycles using menstrual cups have been studied the method of their allocated group. previously, a randomized controlled trial comparing cups with tampons has never Main outcome measures Overall satisfaction; secondary outcomes been done. included discomfort, urovaginal infection, cost, and waste. • This study compared the experiences of Results Forty-seven women in each group completed the final survey, 5 of women using only tampons with women whom were subsequently excluded from analysis (3 from the tampon group using only menstrual cups over a period and 2 from the menstrual cup group). -
Birth Control
Call 311 for Women’s Healthline Free, confidential information and referrals Birth Control New York City Human Resources Administration Infoline Or visit www.nyc.gov/html/hra/pdf/medicaid-offices.pdf What’s Right for You? Information on public health insurance (including Medicaid) for family planning services Other Resources Planned Parenthood of New York City 212-965-7000 or 1-800-230-PLAN (1-800-230-7526) www.ppnyc.org National Women’s Information Center 1-800-994-WOMAN (1-800-994-9662) www.4woman.gov National Family Planning Reproductive Health Association www.nfprha.org Sexuality Information and Education Council of the United States www.siecus.org TAKE CONTROL The New York City Department of Health and Mental Hygiene Michael R. Bloomberg, Mayor Thomas R. Frieden, M.D., M.P.H., Commissioner nyc.gov/health Contents Why Use Birth Control?................................................. 2 Non-Hormonal Methods Male Condoms............................................................. 4 Female Condoms........................................................... 5 Diaphragms and Cervical Caps............................................. 6 Spermicides................................................................ 7 Copper IUDs (Intrauterine Devices)........................................ 8 Fertility Awareness and Periodic Abstinence............................... 9 Hormonal Methods Birth Control Pills (Oral Contraceptives)...................................10 The Birth Control Patch....................................................12 Vaginal -
Regulations Governing the Classification of Medical Devices (Draft)
Regulations Governing the Classification of Medical Devices (Draft) Article 1 These Regulations are enacted pursuant to Paragraph 2, Article 3 of the Medical Devices Act (hereinafter “this Act”). Article 2 Medical devices are classified into the following categories according to their function, intended use, operating instructions, and working principle, depending on the applicable medical specialty: 1. Clinical chemistry and clinical toxicology devices 2. Hematology and pathology devices 3. Immunology and microbiology devices 4. Anesthesiology devices 5. Cardiovascular devices 6. Dental devices 7. Ear, nose, and throat devices 8. Gastroenterology and urology devices 9. General and plastic surgery devices 10. General hospital and personal use devices 11. Neurological devices 12. Obstetrical and gynecological devices 13. Ophthalmic devices 14. Orthopedic devices 15. Physical medicine devices 16. Radiology devices Article 3 Medical devices are classified into the following classes according to their risk level: 1. Class I: Low risk 2. Class II: Medium risk 3. Class III: High risk 1 Article 4 Product items of the medical device classification are specified in the Annex. In addition to rules stated in the Annex, medical devices whose function, intended use, or working principle are special may have their classification determined according to the following rules: 1. If two or more categories, classes, or product items are applicable to the same medical device, the highest class of risk level is assigned. 2. The accessory to a medical device, intended specifically by the manufacturer for use with a particular medical device, is classified the same as the particular medical device, unless otherwise specified in the Annex. 3. -
Guide to Menstrual Hygiene Materials May 2019
Guide to menstrual hygiene materials May 2019 First edition Supply Division / Water, Sanitation & Education Centre Programme Division / Water, Sanitation & Hygiene 3 United Nations Plaza New York, NY 10017 USA www.unicef.org Commentaries represent the personal views of the authors and do not necessarily reflect the positions of the United Nations Children’s Fund (UNICEF). The designations employed in this publication and the presentation of the material do not imply on the part of UNICEF the expression of any opinion whatsoever concerning the legal status of any country or territory, or of its authorities or the delimitations of its frontiers. Edited by Phil Poirier and designed by Noha Habaieb Cover illustration credits : © Noha Habaieb For more information on this document, please contact: Anne Cabrera-Clerget, Contracts Manager [email protected] Brooke Yamakoshi, WASH Specialist, [email protected] Guide to menstrual hygiene materials Contents Acknowledgements 6 Key terms 7 Overview 8 Introduction 9 Procuring menstrual hygiene materials and supplies 12 Consulting with girls and women 16 Understanding menstrual hygiene materials 20 Menstrual cloth 22 Reusable pad 24 Disposable sanitary pad 26 Tampon 28 Menstrual Cup 30 Summary of materials 32 Monitoring and learning 34 Annex I: Additional resources 36 Guide to menstrual hygiene materials 5 © UNICEF/UNI132359/Nesbitt Guide to menstrual hygiene materials Acknowledgements This guidance was prepared by Sophia Roeckel, menstrual hygiene management intern, Anne Cabrera-Clerget, -
1 Effects Ethinyl Estradiol Ethinyl Estradiol & Its Effects On
1 Effects Ethinyl Estradiol Ethinyl Estradiol & Its Effects on Cardiovascular Health Mary Eilert Lourdes University Spring 2019 BIO 490 Section A Dr. Anjali Gray 2 Effects Ethinyl Estradiol ABSTRACT Combined hormonal birth control regulates the menstrual cycle in women by manipulating the hormonal level. Combined hormonal contraception utilizes progestin and Ethinyl estradiol, which are synthetics of progesterone and estrogen. These synthetic hormones help regulate ovulation in women and in turn menstruation. Venous thromboembolism (VTE), stroke, and myocardial infarction are all risk factors when taking combined hormonal contraception due to the chemical composition of Ethinyl estradiol. Ethinyl estradiol’s binding mechanism to an estrogen receptor causes clots and therefore a risk for cardiovascular disease. The dosage of Ethinyl estradiol is related to an increased risk for VTE, stroke, and myocardial infarction. Due to the increased threat to cardiovascular health, physicians should screen patient health history carefully when prescribing combined hormonal birth control. Analyzing the risk Ethinyl estradiol poses to cardiovascular health in women can be used to determine if combined hormonal birth control is the ideal choice for contraception. 3 Effects Ethinyl Estradiol INTRODUCTION Birth control, a contraceptive, is frequently prescribed to women of varying ages throughout the United States. Birth control can be used for its primary use as a contraceptive or prescribed as a means of lessening symptoms of reproductive diseases, such as endometriosis. Birth control comes in various forms and methods. Intrauterine devices (IUDs) and birth control implants are forms which are implanted into the women and rely on the release of hormones to regulate the menstrual cycle (Planned Parenthood). -
Drospirenone and Ethinyl Estradiol
YASMIN 28 TABLETS (drospirenone and ethinyl estradiol) PHYSICIAN LABELING Rx only PATIENTS SHOULD BE COUNSELED THAT THIS PRODUCT DOES NOT PROTECT AGAINST HIV INFECTION (AIDS) AND OTHER SEXUALLY TRANSMITTED DISEASES. DESCRIPTION YASMIN® provides an oral contraceptive regimen consisting of 21 active film coated tablets each containing 3 mg of drospirenone and 0.03 mg of ethinyl estradiol and 7 inert film coated tablets. The inactive ingredients are lactose monohydrate NF, corn starch NF, modified starch NF, povidone 25000 USP, magnesium stearate NF, hydroxylpropylmethyl cellulose USP, macrogol 6000 NF, talc USP, titanium dioxide USP, ferric oxide pigment, yellow NF. The inert film coated tablets contain lactose monohydrate NF, corn starch NF, povidone 25000 USP, magnesium stearate NF, hydroxylpropylmethyl cellulose USP, talc USP, titanium dioxide USP. Drospirenone (6R,7R,8R,9S,10R,13S,14S,15S,16S,17S)-1,3',4',6,6a,7,8,9,10,11,12,13, 14,15,15a,16-hexadecahydro-10,13-dimethylspiro-[17H-dicyclopropa-6,7:15,16] cyclopenta[ a]phenanthrene-17,2'(5H)-furan]-3,5'(2H)-dione) is a synthetic progestational compound and has a molecular weight of 366.5 and a molecular formula of C24H30O3. Ethinyl estradiol (19-nor 17α-pregna 1,3,5(10)-triene-20-yne-3,17-diol) is a synthetic estrogenic compound and has a molecular weight of 296.4 and a molecular formula of C20H24O2. The structural formulas are as follows: CLINICAL PHARMACOLOGY PHARMACODYNAMICS Combination oral contraceptives (COCs) act by suppression of gonadotropins. Although the primary mechanism of this action is inhibition of ovulation, other alterations include changes in the cervical mucus (which increases the difficulty of sperm entry into the uterus) and the endometrium (which reduces the likelihood of implantation).