The Relationship Between Female Genital Aesthetic Perceptions and Gynecological Care
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A Study on Cervical Screening by PAP Smear and Correlation with Microbiological and Clinical Finding
International Journal of Health and Clinical Research, 2021;4(5):280-283 e-ISSN: 2590-3241, p-ISSN: 2590-325X ____________________________________________________________________________________________________________________________________________ Original Research Article A study on cervical screening by PAP smear and correlation with microbiological and clinical finding Sona Goyal1, Manish Kumar Singhal2*,Kamlesh Yadav3, Rachna Agrawal4, Neil Sharma 5 1Consultant Pathologist, Department of Pathology, NIA , Jaipur, Rajasthan, India 2Associate Professor, Department of Pathology, Govt Medical college, Bhartapur, Rajasthan, India 3Professor, Department of Pathology, SMS Medical college Jaipur, Rajasthan, India 4Assistant Professor, Department of Anatomy, Govt Medical college , Bhartapur, Rajasthan, India 5Assistant Professor, Department of Pathology, Govt Medical college, Bhartapur, Rajasthan, India Received: 03-01-2021 / Revised: 08-02-2021 / Accepted: 25-02-2021 Abstract Introduction: Cervical cancer is one of the most common cause in India with over 75% of incidence and mortality. The objective of cervical cancer screening, therefore, is the detection of these lesions before developing into invasive cervical cancer.Methods: This prospective study was carried out over 2 year at the Department of Obstetrics and Gynaecology in National Institute of Ayurveda, Jaipur. Pap smears were collected from 400 sexually active women who were more than 21 years of age.Result: Most common findings were Inflammatory lesion (46.5%), followed by NILM(30%). Atrophic smear was seen in 16 cases (4%), rest had abnormal cellular changes in the form of ASCUS (1.25 %), LSIL (2 %) and Carcinoma (1%).Conclusion : Inflammatory smear is most common cytological finding in premenopausal age group . Epithelial cell abnormality is most common finding in premenopausal and postmenopausal age groups. Pap smear examination can be coupled with culture and sensitivity of vaginal swab to provide adequate treatment. -
Developmental Abnormalities Easy to Misdiagnose
8 Gynecology O B .GYN. NEWS • March 15, 2005 Developmental Abnormalities Easy to Misdiagnose BY JANE SALODOF MACNEIL inappropriate surgery, according to Dr. even an entity called obstructed hemi- Abnormalities of the vulva include con- Contributing Writer Zurawin, chief of the section of pediatric vagina.” genital labial fusion, which he said could and adolescent gynecology at Baylor and Clitoral hypertrophy is the only devel- be corrected with a simple flap proce- H OUSTON — Developmental abnor- of the gynecology service at Texas Chil- opmental abnormality of the clitoris, ac- dure. Surgery is rarely used, however, for malities of the vulva and vagina are often dren’s Hospital in Houston. cording to Dr. Zurawin. It used to be acquired labial agglutination. “This is one easy to correct, but also easy to misdiag- “You need to be familiar with the syn- treated by clitoridectomy with “very un- of most common referrals from pediatri- nose, Robert K. Zurawin, M.D., warned at dromes before you treat. Many people satisfactory results,” he said, describing cians, because they don’t know what to do a conference on vulvovaginal diseases are confronted with these conditions, and more conservative procedures in use to- with it and they are afraid,” Dr. Zurawin sponsored by Baylor College of Medicine. they don’t know what they really are,” he day. “This is mainly a cosmetic problem said. Many physicians have not been trained said. “With the obstructions, for example, for patients, and the surgical management He attributed most cases to diaper rash, to recognize these rare disorders and, as a they may just think it is an imperforate hy- is resection of the enlarged clitoris,” he bubble baths, and detergents that can in- result, run the risk of doing excessive or men and are not even aware that there is said. -
Vaginal Screening After Hysterectomy in Australia
CATEGORY: BEST PRACTICE Vaginal screening after hysterectomy in Australia Objectives: To provide advice on vaginal This statement has been developed and screening after hysterectomy. reviewed by the Women’s Health Committee and approved by the RANZCOG Target audience: Health professionals Board and Council. providing gynaecological care. A list of Women’s Health Committee Values: The evidence was reviewed by the Members can be found in Appendix A. Women’s Health Committee (RANZCOG), and applied to local factors relating to Disclosure statements have been received Australia. from all members of this committee. Background: This statement was first developed by Women’s Health Disclaimer This information is intended to Committee in November 2010 and provide general advice to practitioners. This reviewed in March 2020. information should not be relied on as a substitute for proper assessment with respect Funding: This statement was developed by to the particular circumstances of each RANZCOG and there are no relevant case and the needs of any patient. This financial disclosures. document reflects emerging clinical and scientific advances as of the date issued and is subject to change. The document has been prepared having regard to general circumstances. First endorsed by RANZCOG: November 2010 Current: March 2020 Review due: March 2023 1 1. Introduction In December 2017, the National Cervical Screening Program in Australia changed from 2 yearly cervical cytology testing to 5 yearly primary HPV screening with reflex liquid-based cytology for those women in whom oncogenic HPV is detected in women aged 25–74 years. New Zealand has not yet transitioned to primary HPV screening. -
2021 – the Following CPT Codes Are Approved for Billing Through Women’S Way
WHAT’S COVERED – 2021 Women’s Way CPT Code Medicare Part B Rate List Effective January 1, 2021 For questions, call the Women’s Way State Office 800-280-5512 or 701-328-2389 • CPT codes that are specifically not covered are 77061, 77062 and 87623 • Reimbursement for treatment services is not allowed. (See note on page 8). • CPT code 99201 has been removed from What’s Covered List • New CPT codes are in bold font. 2021 – The following CPT codes are approved for billing through Women’s Way. Description of Services CPT $ Rate Office Visits New patient; medically appropriate history/exam; straightforward decision making; 15-29 minutes 99202 72.19 New patient; medically appropriate history/exam; low level decision making; 30-44 minutes 99203 110.77 New patient; medically appropriate history/exam; moderate level decision making; 45-59 minutes 99204 165.36 New patient; medically appropriate history/exam; high level decision making; 60-74 minutes. 99205 218.21 Established patient; evaluation and management, may not require presence of physician; 99211 22.83 presenting problems are minimal Established patient; medically appropriate history/exam, straightforward decision making; 10-19 99212 55.88 minutes Established patient; medically appropriate history/exam, low level decision making; 20-29 minutes 99213 90.48 Established patient; medically appropriate history/exam, moderate level decision making; 30-39 99214 128.42 minutes Established patient; comprehensive history exam, high complex decision making; 40-54 minutes 99215 128.42 Initial comprehensive -
Colposcopy.Pdf
CCololppooscoscoppyy ► Chris DeSimone, M.D. ► Gynecologic Oncology ► Images from Colposcopy Cervical Pathology, 3rd Ed., 1998 HistoHistorryy ► ColColpposcopyoscopy wwasas ppiioneeredoneered inin GGeermrmaanyny bbyy DrDr.. HinselmannHinselmann dduriurinngg tthhee 19201920’s’s ► HeHe sousougghtht ttoo prprooveve ththaatt micmicrroscopicoscopic eexaminxaminaationtion ofof thethe cervixcervix wouwoulldd detectdetect cervicalcervical ccancanceerr eeararlliierer tthhaann 44 ccmm ► HisHis workwork identidentiifiefiedd severalseveral atatyypicalpical appeappeararanancceses whwhicichh araree stistillll usedused ttooddaay:y: . Luekoplakia . Punctation . Felderung (mosaicism) Colposcopy Cervical Pathology 3rd Ed. 1998 HistoHistorryy ► ThrThrooughugh thethe 3030’s’s aanndd 4040’s’s brbreaeaktkthrhrouougghshs wwereere mamaddee regregaarrddinging whwhicichh aapppepeararancanceess wweerere moremore liklikelelyy toto prprogogressress toto invinvaasivesive ccaarcinomrcinomaa;; HHOOWEWEVVERER,, ► TheThessee ffiinndingsdings wweerere didifffficiculultt toto inteinterrpretpret sincesince theythey werweree notnot corcorrrelatedelated wwithith histologhistologyy ► OneOne resreseaearcrchherer wwouldould claclaiimm hhiiss ppatatientsients wwithith XX ffindindiingsngs nevernever hahadd ccaarcinomarcinoma whwhililee aannothotheerr emphemphaatiticcallyally belibelieevedved itit diddid ► WorldWorld wiwidede colposcopycolposcopy waswas uunnderderuutitillizizeedd asas aa diadiaggnosticnostic tooltool sseeconcondadaryry ttoo tthheseese discrepadiscrepannciescies HistoHistorryy -
2021 HEDIS Reference Guidefor Primary Care
2021 HEDIS Reference Guide for Primary Care Cervical Cancer Screening (CCS) Patient Profile MVP members 21–64 years of age who have been screened for cervical cancer. Appropriate screening is defined by one of the following criteria: • Women 21–64 years of age who have a cervical cytology performed within the last three years (the measurement year and up to two years prior) • Women 30–64 years of age who have a cervical high-risk human papillomavirus (hrHPV) testing performed within the last five years (Note: Evidence of hrHPV testing within the last 5 years also captures patients who had cotesting; therefore additional methods to identify cotesting are not necessary.) • Women 30-64 years of age who had cervical cytology cotesting within the last five years Those excluded are women who have had a hysterectomy with no residual cervix (complete, total, or radical abdominal or vaginal hysterectomy), cervical agenesis, or acquired absence of cervix any time during the member's history through December 31 of the measurement year. How to Implement Best Practices and Improve Performance • Documentation in the medical record must include the name of the cervical screening, date of the test, and the result. This may be documented in an office note or a lab report, and can be submitted. • Cervical biopsies are not valid for primary cervical cancer screening and cannot be submitted. • When documenting medical/surgical history, avoid the use of “hysterectomy” alone, as this is not sufficient evidence that the cervix was removed. Be specific: “TAH”, TVH”, etc. • Documentation of “hysterectomy” alone in combination with documentation that the “patient no longer needs cervical cancer screening,” does meet criteria. -
Diagnostic Tests for Vaginosis/Vaginitis
Alberta Heritage Foundation for Medical Research Diagnostic tests for vaginosis/vaginitis Christa Harstall and Paula Corabian October 1998 HTA12 Diagnostic tests for vaginosis/vaginitis Christa Harstall and Paula Corabian October 1998 © Copyight Alberta Heritage Foundation for Medical Research, 1998 This Health Technology Assessment Report has been prepared on the basis of available information of which the Foundation is aware from public literature and expert opinion, and attempts to be current to the date of publication. The report has been externally reviewed. Additional information and comments relative to the Report are welcome, and should be sent to: Director, Health Technology Assessment Alberta Heritage Foundation for Medical Research 3125 Manulife Place, 10180 - 101 Street Edmonton Alberta T5J 3S4 CANADA Tel: 403-423-5727, Fax: 403-429-3509 This study is based, in part, on data provided by Alberta Health. The interpretation of the data in the report is that of the authors and does not necessarily represent the views of the Government of Alberta. ISBN 1-896956-15-7 Alberta's health technology assessment program has been established under the Health Research Collaboration Agreement between the Alberta Heritage Foundation for Medical Research and the Alberta Health Ministry. Acknowledgements The Alberta Heritage Foundation for Medical Research is most grateful to the following persons for their comments on the draft report and for provision of information. The views expressed in the final report are those of the Foundation. Dr. Jane Ballantine, Section of General Practice, Calgary Dr. Deirdre L. Church, Microbiology, Calgary Laboratory Services, Calgary Dr. Nestor N. Demianczuk, Royal Alexandra Hospital, Edmonton Dr. -
Key Points: • a Pap Test and Pelvic Exam Are Important Parts of A
Key Points: • A Pap test and pelvic exam are important parts of a woman’s routine health care because they can detect cancer or abnormalities that may lead to cancer of the cervix (see Question 3). • Women should have a Pap test at least once every three years, beginning about three years after they begin to have sexual intercourse, but no later than age 21 (see Question 6). • If the Pap test shows abnormalities, further tests an/or treatment may be necessary (see Question 11). • Human papillomavirus (HPV) infection is the primary risk factor for cervical cancer (see Question 13). 1. What is a Pap test? The Pap test (sometimes called a Pap smear) is a way to examine cells collected from the cervix (the lower, narrow end of the uterus). The main purpose of the Pap test is to find abnormal cell changes that may arise from cervical cancer or before cancer develops. 2. What is a pelvic exam? In a pelvic exam, the uterus, vagina, ovaries, fallopian tubes, bladder, and rectum are felt to find any abnormality in their shape or size. During a pelvic exam, an instrument called a speculum is used to widen the vagina so that the upper portion of the vagina and the cervix can be seen. 3. Why are a Pap test and pelvic exam important? A Pap test and pelvic exam are important parts of a woman’s routine health care because they can detect abnormalities that may lead to invasive cancer of the cervix. These abnormalities can be treated before cancer develops. -
Cervical Cancer Screening Guidelines Reviewed and Approved by CHAC Clinical Committee on August 8, 2018
Cervical Cancer Screening Guidelines Reviewed and approved by CHAC Clinical Committee on August 8, 2018 Cervical Cancer Screening Description: The percentage of women 21–64 years of age who were screened for cervical cancer using either of the following criteria: • Women age 21–64 who had cervical cytology performed every 3 years. • Women age 30–64 who had cervical cytology/ HPV co-testing every 5 years. Numerator: Documentation of one or more of the following cancer screenings and date(s) Women with one or more screenings for cervical cancer. Appropriate screenings are defined by any one of the following criteria: Cervical cytology performed during the measurement period or the two years prior to the measurement period for women who are at least 21 years old at the time of the test Cervical cytology/human papillomavirus (HPV) co-testing performed during the measurement period or the four years prior to the measurement period for women who are at least 30 years old at the time of the test _____________________________________________________________ Denominator: Ages 23-64 with a visit in the measurement period Denominator Exclusions: Women who had a hysterectomy with no residual cervix Patients who were in hospice care during the measurement year Measure Source: eCQI Resource Center, CMS (Aligns with CY 2018 UDS requirements) https://ecqi.healthit.gov/ecqm/measures/cms124v6 Health care providers play a critical role in raising awareness of cervical cancer and increasing screening among women and HPV vaccination among boys and girls. What is the problem and what is known about it so far? Cancer is the leading cause of death in Vermont. -
FGM – Female Genital Mutilation Kvinnlig Könsstympning
Trollhättan, 17+18/11 2016 Senior FGM – Female Genital Mutilation Kvinnlig Könsstympning Dr. med. Johannes Leidinger, MD., MPH. Senior Consultant in Gynaecology and Obstetrics Överläkare på Kvinnokliniken Södersjukhuset Stockholm & Mälarsjukhuset Eskilstuna Lehrbeauftragter/Dozent der Ludwig-Maximilians-Universität München 16 days of activism 2016 From 25 November, the International Day for the Elimination of Violence against Women, to 10 December, Human Rights Day, the 16 Days of Activism against Gender-Based Violence Campaign is a time to galvanize action to end violence against women and girls around the world. http://www.unwomen.org/en/what-we-do/ending-violence-against-women/ take-action/16-days-of-activism#sthash.zXvSzU8E.dpuf Sexual Violence: ¨ Rape ¨ Indecent Assault ¨ Forced Marriage ¨ Sexual Slavery http://www.eldis.org ¨ FGM (Female Genital Mutilation) ¨ Forced Pregnancy ¨ Forced Abortion ¨ Sexual Harassment WHO: FGM ¨ „FGM comprises all procedures that involve altering or injuring the female genitalia for non medical reasons - , and is recognized internationally as a violation of the human rights of girls and women. It reflects deep-rooted inequality between the sexes, and constitutes an extreme form of discrimination against women and girls.“ Program 18 Nov 2016, 9-12 am ¨ Nomenklatur ¨ Klassifikation ¨ Global Prevalens ¨ Förklaringsmodeller ¨ Medicinska komplikationer ¨ Nationell & internationell Lagstiftning ¨ Vård i Sverige – AMEL-mottagning – Operativa rekonstruktioner – Desert Flower Scandinavia ¨ Global perspektiv – Internationella strategier (WHO och NGOs) – Medicalization of FGM Terminology ¨ The expression ”Female Genital Mutilation" gained growing support from the late 1970s. The word ”mutilation” establishes a clear linguistic distinction from male circumcision, and emphasizes the gravity and harm of the act. ¨ In 1990, this term was adopted at the ”3rd Conference of the Inter-African Committee on Traditional Practices Affecting the Health of Women and Children”, in Addis Ababa, Ethiopia. -
Laboratory Test: Wet Prep Standing Order in N.C
Laboratory Test: Wet Prep Standing Order in N.C. Board of Nursing Format INSTRUCTIONS FOR LOCAL HEALTH DEPARTMENT STAFF ONLY Use the approved language in this standing order to create a customized standing order exclusively for your agency. Print the customized standing order on agency letterhead. Review standing order at least annually and obtain Medical Director’s signature. Standing order must include the effective start date and the expiration date. Assessment Subjective Findings The following subjective criteria meet the requirement for an STD ERRN to collect a Wet Prep by standing order: Vaginal discharge with or without foul odor Dyspareunia Dysuria New or multiple sex partner(s) Lack of condom use Reports contact to: Chlamydia (CT), Gonorrhea Asymptomatic (GC), Non-Gonococcal Urethritis (NGU), Pelvic Anonymous sex Inflammatory Disease (PID), Mucopurulent Cervicitis (MPC), or Trichomonas vaginalis (TV) Objective Findings If one or more of these clinical findings are present, the STD ERRN shall collect a Wet Prep by standing order: 1. vaginal discharge 2. endocervical discharge 3. foul odor 4. cervical inflammation, usually manifest as edema or easily induced cervical bleeding upon cervical swabbing 5. petechiae on cervix 6. vaginal or vulva irritation 7. warts or other abnormal growths in vagina or on cervix 8. vaginal exposure within last 60 days 9. verified contact Gonorrhea, Chlamydia, NGU, MPC or Trichomonas Plan of Care Implementation A registered nurse or STD ERRN employed or contracted by the local health department may order a Wet Prep collected by the STD ERRN or other medical provider. Nursing Actions A. Specimen Collection by STD ERRN: To collect a Wet Prep specimen: 1. -
GM EUR Generic Funding Request Form NOTE
2017-19 Effective Use of Resources Treatment Policies GM EUR Team Contacts Tel Email Version 5.7 Funding applications / Process 0161 212 6250 [email protected] List Last Updated 22 January 2019 Policy development 0161 212 6212 [email protected] Approval Funding Approval Category Notes Funding Request Forms Required Individual Funding Request A decision has been taken not to commission a specific treatment. Funding will only be approved if there is evidence of clinical GM EUR Generic Funding Request Form Yes (Exceptional Case) Approval (IFR) exceptional circumstances. NOTE: GM policies have specific funding request forms, please see the end column on the The Commissioner has specifically requested that funding is sought for a particular treatment. The treatment must not be Yes blue coloured rows below. Individual Prior Approval (IPA) undertaken without funding approval from commissioners. Exceptional circumstances do not always have to be demonstrated. PbR Excluded Lists Monitored Approval (MA) The specific treatment may be undertaken in line with agreed EUR policy criteria/routine commissioning arrangements provided the policy criteria is met, clinicians can refer patients without seeking approval. If the patient does not meet the policy NOTE: Only applies if the patient No PbR Excluded Devices List PbR Excluded Drugs List criteria clinicians should apply for Individual Funding Request (Exceptional Case) Approval. Audits may be undertaken to meets the policy critiera. ensure adherence with agreed commissioning arrangements.