1.Management of Abnormal Uterine Bleeding
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Endometriosis and PCOS: Two Major Pathologies Linked to Oxidative Stress in Women Sajal Gupta1, Avi Harlev1 and Ashok Agarwal1
Chapter 5 Chapter 5 Endometriosis and PCOS: Two major pathologies… Endometriosis and PCOS: Two major pathologies linked to oxidative stress in women Sajal Gupta1, Avi Harlev1 and Ashok Agarwal1 Introduction Oxidative stress (OS) ensues when the detrimental activity of reactive oxygen species (ROS) prevails over that of anti-oxidants causing lipid peroxidation, protein carbonylation, and DNA damage and/or cell apoptosis. Moreover, reactive nitrogen species (RNS), such as nitrogen oxide (NO) with an unpaired electron, is also highly reactive and toxic (Agarwal et al. 2012, Doshi et al. 2012). OS has been known to participate in the pathogenesis of PCOS and endometriosis. Several OS biomarkers have been scrutinized by investigators, in the past, including MDA (malondialdehyde), protein carbonyl, TAC (total antioxidant capacity), SOD (superoxide dismutase), GPx (glutathione peroxidase), and GSH (reduced glutathione) to determine the role of OS in PCOS (Azziz et al.) and endometriosis (Jackson et al. 2005, Murri et al. 2013). Free radicals are known to impact several microenvironments in different biological windows, such as in the follicular microenvironment (Gonzalez et al. 2006, Murri et al. 2013). Both PCOS and endometriosis are associated with poor oocyte quality and infertility (Gupta et al. 2008, Goud et al. 2014, Huang et al. 2015). Our current review addresses the role of OS in both these disease conditions and the role of antioxidants and lifestyle modifications in preempting the impact of free radicals in PCOS and endometriosis. Polycystic ovary syndrome (PCOS) is a multicomponent disorder affecting many adolescent girls as well as women of reproductive age, characteristically 1 Affiliation: 1 Center for Reproductive Medicine, 10681 Carnegie Avenue, Glickman Urology & Kidney Institute, Cleveland Clinic, Cleveland, Ohio-44195. -
Polycystic Ovary Syndrome, Oligomenorrhea, and Risk of Ovarian Cancer Histotypes: Evidence from the Ovarian Cancer Association Consortium
Published OnlineFirst November 15, 2017; DOI: 10.1158/1055-9965.EPI-17-0655 Research Article Cancer Epidemiology, Biomarkers Polycystic Ovary Syndrome, Oligomenorrhea, and & Prevention Risk of Ovarian Cancer Histotypes: Evidence from the Ovarian Cancer Association Consortium Holly R. Harris1, Ana Babic2, Penelope M. Webb3,4, Christina M. Nagle3, Susan J. Jordan3,5, on behalf of the Australian Ovarian Cancer Study Group4; Harvey A. Risch6, Mary Anne Rossing1,7, Jennifer A. Doherty8, Marc T.Goodman9,10, Francesmary Modugno11, Roberta B. Ness12, Kirsten B. Moysich13, Susanne K. Kjær14,15, Estrid Høgdall14,16, Allan Jensen14, Joellen M. Schildkraut17, Andrew Berchuck18, Daniel W. Cramer19,20, Elisa V. Bandera21, Nicolas Wentzensen22, Joanne Kotsopoulos23, Steven A. Narod23, † Catherine M. Phelan24, , John R. McLaughlin25, Hoda Anton-Culver26, Argyrios Ziogas26, Celeste L. Pearce27,28, Anna H. Wu28, and Kathryn L. Terry19,20, on behalf of the Ovarian Cancer Association Consortium Abstract Background: Polycystic ovary syndrome (PCOS), and one of its cancer was also observed among women who reported irregular distinguishing characteristics, oligomenorrhea, have both been menstrual cycles compared with women with regular cycles (OR ¼ associated with ovarian cancer risk in some but not all studies. 0.83; 95% CI ¼ 0.76–0.89). No significant association was However, these associations have been rarely examined by observed between self-reported PCOS and invasive ovarian cancer ovarian cancer histotypes, which may explain the lack of clear risk (OR ¼ 0.87; 95% CI ¼ 0.65–1.15). There was a decreased risk associations reported in previous studies. of all individual invasive histotypes for women with menstrual Methods: We analyzed data from 14 case–control studies cycle length >35 days, but no association with serous borderline including 16,594 women with invasive ovarian cancer (n ¼ tumors (Pheterogeneity ¼ 0.006). -
Ultrasonographic Prevalence of Polycystic Ovarian Disease – a Cross-Sectional Study in a Rural Medical College of West Bengal
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS) e-ISSN: 2279-0853, p-ISSN: 2279-0861.Volume 15, Issue 1 Ver. X (Jan. 2016), PP 115-120 www.iosrjournals.org Ultrasonographic Prevalence of Polycystic Ovarian Disease – A Cross-Sectional Study in a Rural Medical College of West Bengal Monojit Chakrabarti1, Md Abdur Rahaman2, Swadha Priyo Basu3 1(Assistant Professor, Dept. of Radiology, Malda Medical College & Hospital, West Bengal, India) 2(R.M.O. cum Clinical Tutor, Dept. of Radiology, Malda Medical College & Hospital, West Bengal, India ) 3(Professor & HOD, Dept. of Radiology, Malda Medical College & Hospital, West Bengal, India ) Abstract : Introduction: Polycystic ovary disease (PCOD) is the most common and complex endocrinal disorder of females in their early child bearing age group. It may complicated to Infertility. Methodology: Trans Abdominal Ultrasonography was carried out over 157 women in a rural medical college of West Bengal and 51 females were diagnosed of PCOD using Rotterdam’s criteria. Results: Maximum prevalence of PCOD was seen between 15 to 24 years age group. Dominantly oligomenorrhea was seen among PCOD (75%) patients. 33.4% obese patients were diagnosed PCOD. Conclusion: It is commonly observed in early child bearing age group, especially those females having oligomenorrhea. Lifestyle management is now considered one of the principal way to deal with PCOS. Keywords: Anovulation, B.M.I. (Body Mass Index), Oligomenorrhea, Polycystic Ovarian Disease (PCOD), Trans Abdominal Ultrasound (TAS). I. Introduction Polycystic ovarian disease (PCOD) is the most common and complex endocrinal disorder affecting females of child bearing age1. It is also known as Hyperandrogenic Anovulation and Stein-Leventhal Syndrome2,3. -
How to Evaluate Vaginal Bleeding and Discharge
How to Evaluate Vaginal Bleeding and Discharge Is the bleeding normal or abnormal? When does vaginal discharge reflect something as innocuous as irritation caused by a new soap? And when does it signal something more serious? The authors’ discussion of eight actual patient presentations will help you through the next differential diagnosis for a woman with vulvovaginal complaints. By Vincent Ball, MD, MAJ, USA, Diane Devita, MD, FACEP, LTC, USA, and Warren Johnson, MD, CPT, USA bnormal vaginal bleeding or discharge is typically due to either inadequate levels of estrogen one of the most common reasons women or a persistent corpus luteum. Structural causes of come to the emergency department.1,2 bleeding include leiomyomas, endometrial polyps, or Because the possible underlying causes malignancy. Infectious etiologies include pelvic in- Aare diverse, the patient’s age, key historical factors, flammatory disease (PID). Additionally, a variety of and a directed physical examination are instrumental bleeding dyscrasias involving platelet or clotting fac- in deciding on diagnosis and treatment. This article tors can complicate the normal menstrual period. Iat- will review some common case presentations of rogenic causes of vaginal bleeding include hormone nonpregnant female patients with abnormal vaginal replacement therapy, steroid hormone contraception, bleeding, inflammation, or discharge. and contraceptive intrauterine devices.3-5 Anovulatory bleeding is common in perimenar- ABNORMAL VAGINAL BLEEDING chal girls as a result of an immature hypothalamic- To ensure appropriate patient management, “Is she pituitary axis and in perimenopausal women due to pregnant?” should be the first question addressed, declining levels of estrogen. During reproductive since some vulvovaginal signs and symptoms will years, dysfunctional uterine differ in significance and urgency depending on the bleeding (DUB) is the most >>FAST TRACK<< answer. -
Changes Before the Change1.06 MB
Changes before the Change Perimenopausal bleeding Although some women may abruptly stop having periods leading up to the menopause, many will notice changes in patterns and irregular bleeding. Whilst this can be a natural phase in your life, it may be important to see your healthcare professional to rule out other health conditions if other worrying symptoms occur. For further information visit www.imsociety.org International Menopause Society, PO Box 751, Cornwall TR2 4WD Tel: +44 01726 884 221 Email: [email protected] Changes before the Change Perimenopausal bleeding What is menopause? Strictly defined, menopause is the last menstrual period. It defines the end of a woman’s reproductive years as her ovaries run out of eggs. Now the cells in the ovary are producing less and less hormones and menstruation eventually stops. What is perimenopause? On average, the perimenopause can last one to four years. It is the period of time preceding and just after the menopause itself. In industrialized countries, the median age of onset of the perimenopause is 47.5 years. However, this is highly variable. It is important to note that menopause itself occurs on average at age 51 and can occur between ages 45 to 55. Actually the time to one’s last menstrual period is defined as the perimenopausal transition. Often the transition can even last longer, five to seven years. What hormonal changes occur during the perimenopause? When a woman cycles, she produces two major hormones, Estrogen and Progesterone. Both of these hormones come from the cells surrounding the eggs. Estrogen is needed for the uterine lining to grow and Progesterone is produced when the egg is released at ovulation. -
Selected Topics in WOMEN’S HEALTH
www.bpac.org.nz keyword: womenshealth Selected topics in WOMEN’S HEALTH Laboratory investigation of amenorrhoea Polycystic ovary syndrome An overview of dysfunctional uterine bleeding Perimenopause and menopause Sexual dysfunction - loss of libido 8 | September 2010 | best tests Amenorrhoea Amenorrhoea is the absence of menstruation flow. It can Causes of primary amenorrhoea2 be classified as either primary or secondary,1 relative to menarche: ■ Hypergonadotropic hypogonadism/primary hypogonadism/gonadal failure: ■ Primary amenorrhoea: absence of menses by age 16 years in a female with appropriate development – Abnormal sex chromosomes e.g. Turner of secondary sexual characteristics; or absence syndrome of menses by age 13 years and no other pubertal – Normal sex chromosomes e.g. premature maturation2 ovarian failure ■ Secondary amenorrhoea: lack of menses in a ■ Hypogonadotropic hypogonadism/secondary previously menstruating, non-pregnant female, for hypogonadism: 2 greater than six months – In many cases this may be due to a familial delay in puberty and growth. Other causes include congenital abnormalities Primary amenorrhoea e.g. isolated GnRH deficiency, acquired Key messages: lesions, endocrine disturbance, tumour, systemic illness or eating disorder. ■ The most common cause of primary amenorrhoea in a female with no secondary sexual characteristics ■ Eugonadism: is a constitutional delay in growth and puberty. – Anatomic e.g. congenital absence of the In the first instance, watchful waiting is the most uterus and vagina, intersex -
PCOD: a Closer Look by : Teresa Kenney, APRN, CFCP
Vol. 3 No. 3 12/29/2011 PCOD: A Closer Look By : Teresa Kenney, APRN, CFCP Polycystic ovarian disease (PCOD) is a disorder of the and the increase in symptoms like hair growth and acne. reproductive system caused by changes in hormones. After time the ovaries begin to form small immature follicles The most common symptom is irregular cycles. PCOD or cysts. This can be seen on an ultrasound and it is affects 5-10% of all women and it is one of the leading sometimes referred to as a “string of pearls”. Elevated insulin causes of infertility. Women who experience other common levels are another effect of PCOD. This is also referred to as symptoms associated with PCOD—increase in hair growth, pre-diabetes. It leads to increased sugar levels in the body acne, insulin resistance, and weight gain—are said to have and, therefore, weight gain. Insulin resistance can be treated polycystic ovarian syndrome (PCOS). with medication and dietary intervention. In order to determine if someone has PCOD, a doctor orders Using NaProTechnology, a doctor can treat both the certain blood tests, a pelvic ultrasound, and a physical symptoms of PCOD and the menstrual cycles. Through exam. PCOD can be a genetic disorder; therefore, if it runs the use of different cooperative medications, we can in your family you may be more likely to have the disorder. regulate the menstrual cycle. It is not necessary or helpful to use the birth control pill to treat PCOD. In fact, the birth Polycystic ovaries develop control pill does not treat diseases of women’s health like when the ovaries begin to PCOS. -
What Is and What Is Not PCOS (Polycystic Ovarian Syndrome)?
What is and What is not PCOS (Polycystic ovarian syndrome)? Chhaya Makhija, MD Assistant Clinical Professor in Medicine, UCSF, Fresno. No disclosures Learning Objectives • Discuss clinical vignettes and formulate differential diagnosis while evaluating a patient for polycystic ovarian syndrome. • Identify an organized approach for diagnosis of polycystic ovarian syndrome and the associated disorders. DISCUSSION Clinical vignettes of differential diagnosis Brief review of Polycystic ovarian syndrome (PCOS) Therapeutic approach for PCOS Clinical vignettes – Case based approach for PCOS Summary CASE - 1 • 25 yo Hispanic F, referred for 5 years of amenorrhea. Diagnosed with PCOS, was on metformin for 2 years. Self discontinuation. Seen by gynecologist • Progesterone withdrawal – positive. OCP’s – intolerance (weight gain, headache). Denies galactorrhea. Has some facial hair (upper lips) – no change since teenage years. No neurological symptoms, weight changes, fatigue, HTN, DM-2. • Currently – plans for conception. • Pertinent P/E – BMI: 24 kg/m², BP= 120/66 mm Hg. Fine vellus hair (upper lips/side burns). CASE - 1 Labs Values Range TSH 2.23 0.3 – 4.12 uIU/ml Prolactin 903 1.9-25 ng/ml CMP/CBC unremarkable Estradiol 33 0-400 pg/ml Progesterone <0.5 LH 3.3 0-77 mIU/ml FSH 2.8 0-153 mIU/ml NEXT BEST STEP? Hyperprolactinemia • Reported Prevalence of Prolactinomas: of clinically apparent prolactinomas ranges from 6 –10 per 100,000 to approximately 50 per 100,000. • Rule out physiological causes/drugs/systemic causes. Mild elevations in prolactin are common in women with PCOS. • MRI pituitary if clinically indicated (to rule out pituitary adenoma). Prl >100 ng/ml Moderate Mild Prl =50-100 ng/ml Prl = 20-50 ng/ml Typically associated with Low normal or subnormal Insufficient progesterone subnormal estradiol estradiol concentrations. -
Spontaneous Ovulation and Pregnancy in Women with Polycystic Ovarian Disease; a Cross Sectional Study
International Journal of Reproduction, Contraception, Obstetrics and Gynecology Sleem MA et al. Int J Reprod Contracept Obstet Gynecol. 2018 Feb;7(2):359-363 www.ijrcog.org pISSN 2320-1770 | eISSN 2320-1789 DOI: http://dx.doi.org/10.18203/2320-1770.ijrcog20180148 Original Research Article Spontaneous ovulation and pregnancy in women with polycystic ovarian disease; a cross sectional study Mostafa A. Sleem, Ibrahim I. Mohamed, Mahmoud S. Zakherah, Ahmed M. Abbas*, Momen A. Kamel Department of Obstetrics and Gynecology, Woman's Health Hospital, Faculty of Medicine, Assiut University, Egypt Received: 19 November 2017 Accepted: 19 December 2017 *Correspondence: Dr. Ahmed M. Abbas, E-mail: [email protected] Copyright: © the author(s), publisher and licensee Medip Academy. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. ABSTRACT Background: Polycystic ovary disease (PCOD) is the most common endocrine disorder in women of reproductive age, with a prevalence of approximately 5-10%. This study aims to assess the rate of spontaneous ovulation and pregnancy in patients. The present study was a cross sectional study conducted at Woman's Health Hospital, Assiut University, Assiut, Egypt. Methods: The current study was a cross sectional study carried out in Assiut Women's Health Hospital between the 1st October 2016 and 31st July 2017. The patients were selected as infertile patients with PCOD. The patient ages range between 20 and 35 years. The BMI is between 18 and 30 Kg/m2. -
Cumulative Pregnancy Rates in Couples with Anovulatory Infertility Compared with Unexplained Infertility in an Ovulation Induction Programme
Human Reproduction vol.12 no.9 pp.1939–1944, 1997 Cumulative pregnancy rates in couples with anovulatory infertility compared with unexplained infertility in an ovulation induction programme N.Tadokoro1, B.Vollenhoven1,3, S.Clark2, G.Baker2, hypogonadism. From 1970 until 1985, the ovulation induction G.Kovacs2, H.Burger2 and D.Healy1 medication was human pituitary gonadotrophin (Healy et al., 1980; Kovacs et al., 1984). From 1985, human menopausal 1Department of Obstetrics and Gynaecology, Monash University, 2Prince Henry’s Institute of Medical Research, Monash Medical gonadotrophin (HMG) or purified urinary gonadotrophin Centre, 246 Clayton Rd, Clayton, Victoria 3168, Australia (follicle stimulating hormone, FSH) was used. From 1991, couples with unexplained infertility were 3To whom correspondence should be addressed treated with up to four cycles of ovarian stimulation prior Using a retrospective analysis, we compared cumulative to either in-vitro fertilization (IVF) or gamete intra-Fallopian pregnancy rates, early pregnancy failure rates and transfer (GIFT). None of the couples in any of the groups multiple pregnancy rates in couples with polycystic had intrauterine insemination (IUI) performed as part of ovarian syndrome (PCOS) (n J 148), hypogonadotrophic their treatment. or eugonadotrophic hypogonadism (n J 91) and unex- By performing a retrospective analysis, we tested whether plained infertility (n J 117), who were treated in an application of the same method of treatment (ovulation ovulation induction clinic between January 1991 and induction) known to be effective in couples with anovulatory December 1995. The women were treated with either infertility would be beneficial to couples with unexplained human menopausal gonadotrophin (HMG) or purified infertility receiving ovarian stimulation. -
Polycystic Ovarian Syndrome; Pattern of Disease in Patients
The Professional Medical Journal www.theprofesional.com ORIGINAL PROF-2317 POLYCYSTIC OVARIAN SYNDROME; PATTERN OF DISEASE IN PATIENTS Dr. Misbah Yasin1, Dr. Fouzia Yasmeen2 1. FCPS, Senior Registrar, Department of Obs. & Gynae, Ghurki Trust Teaching Hospital, Lahore ABSTRACT … Objectives: The objective of this study is to: describe the pattern of disease in 2. FCPS, Assistant Professor, patients with polycystic ovarian syndrome. Data Source: Medline Data Base. Design Of Study: Department of Obs. & Gynae, Ghurki Trust Teaching Hospital, Lahore Descriptive case series study. Settings: Gynaecological Outpatient Department of Ghurki trust teaching hospital Lahore. Duration: 6months period, from 8th October 2012 to 7th April 2013. Materials & Methods: Sixty cases of polycystic ovarian syndrome as diagnosed on ultrasound were selected. These cases were examined for height, weight, body mass index, hirsutism, acne, acnthosis nigricans, breast examination (galactorrhoea). These cases were investigated for blood sugar (random), Fasting Insulin, pelvic ultrasound, LH, FSH and serum prolactin. Results: The mean age of the patients were 24.93±5.67 years. There were 28 (47%) patients of menstrual disturbance, 18 (30%) patients of subfertility, 9 (13%) of obesity. There were 13 (21.7%) patients 2 Correspondence Address: of BMI level of equal to or less than 25 kg/m and 47 (78.3%) patients of BMI level more than 25 Dr. Misbah Yasin kg/m2. There were 25 (41.7%) patients of hirsuitim, 14 (23.3%) patients of acne and 17 (28.3%) 809 A Gulshan Ravi,Lahore [email protected] patients of acanthoris nigricans on physical examination. There were 28 (46.7%) patients of LH level of more than 10 IU/L (raised) and 1 (1.7%) patient of more than 350 mU/L prolactin (raised). -
Amenorrhea—Etiologic Approach to Diagnosis
MODERN TRENDS'IltEl~DS Edward Wallach, M.D. Associate Editor FERTILITY AND STERILITY Vol. 30, No. I, July 1978 Copyright © 1978 The American Fertility Society Printed in U.S.A. AMENORRHEA-ETIOLOGIC APPROACH TO DIAGNOSIS PAUL G. McDONOUGH, M.D. Division of Reproductive Endocrinology, Department of Obstetrics and Gynecology, Medical College of Georgia, Augusta, Georgia 30901 A delay in the initiation of menses at the time nated. All types of normally and ectopically lo of puberty or the interruption of an established cated trophoblastic proliferations should be menstrual pattern constitutes amenorrhea. Ces thought of collectively and suspected in every pa sation of menses normally occurs in the human tient who has a positive test for human chorionic female at the time of menopause. Failure to in gonadotropin. If suspicion of trophoblast persists itiate menses, interruption of a normal cyclic pat in spite of a negative routine pregnancy test, then tern of menses, or premature cessation of menses the more sensitive ,8-subunit human chorionic constitutes unphysiologic amenorrhea. Arbitrar gonadotropin determination should be performed. ily classifying menarchal failure and the inter Excluding the presence of active, viable, pro ruption of a normal cyclic menstrual pattern into liferating trophoblast in all patients with primary and secondary amenorrhea is largely amenorrhea should be the first consideration be semantic, since the same etiologic factors may be fore other etiologies are considered. operative in either instance. Over the past decade the evaluation of amen The average age for first menses is 13.5 years. orrhea has been assisted by advances and refine Menarche at chronologie ages 11 and 15 are 2 ments in diagnostic techniques.