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  6. Copper Intrauterine Device Cu-IUD
  7. Cu-IUD Use in Specific Groups
Important: please update your RDS app to version 4.7.3 Details with newsletter below.

Please update your RDS app to v4.7.3

We asked you in January to update to v4.7.2.  After the deployment planned for 27th February, this new update will be needed to ensure that you are able to download RDS toolkits even when the RDS website is not available. We will wait until as many users as possible have downloaded the new version before switching off the old system for app downloads and moving entirely to the new approach.

To check your current RDS version, click on the three dots bottom right of the RDS app screen. This takes you to a “More” page where you will see the version number. 

To update to the latest release:

 On iPhones – go to the Apple store, click on your profile icon top right, scroll down to see the apps waiting to be updated and update the RDS app.

On Android phones – these can vary, but try going to the Google Play store, click on your profile icon top right, click on “Manage apps and device”, select and update the RDS app.

Right Decision Service newsletter: February 2025

Welcome to the February 2025 update from the RDS team

1.     Next release of RDS

 

A new release of RDS is planned (subject to outcomes of current testing) for week beginning 24th February. This will deliver:

 

  • Fixes to mitigate the recurring glitches with the RDS admin area and the occasional brief user interface outages which have arisen following implementation of the new distributed technology infrastructure in December 2024.

 

  • Capability to embed content from Google calendar, Google Maps, Daily Motion, Twitter feeds, Microsoft Stream into RDS pages.

 

  • Capability to include simple multiplication in RDS calculators.

 

The release will also incorporate a number of small fixes, including:

  • Exporting of form within Medicines Sick Day Guidance in polypharmacy toolkit
  • Links to redundant content appearing in search in some RDS toolkits
  • Inclusion of accordion headers alongside accordion text in search result snippets.
  • Feedback form on mobile app.
  • Internal links on mobile app version of benzo tapering tool

 

We will let you know when the date and time for the new release are confirmed.

 

2.     New RDS developments

There is now the capability to publish toolkits on the web with left hand side navigation rather than tiles on the homepage. To use this feature, turn on the “Toggle navigation panel” option at the top of the Page settings menu at toolkit homepage level – see below. Please note that publication to downloadable mobile app for this type of navigation is still under development.

The Benzodiazepine tapering tool (https://rightdecisions.scot.nhs.uk/benzotapering) is now available as part of the RDS toolkit for the national benzodiazepine prescribing guidance developed by the Scottish Government Effective Prescribing team. The tool uses this national guidance developed with a wide-ranging multidisciplinary group. This should be used in combination with professional judgement and an understanding of the needs of the individual patient.

3.     Archiving and version control and new RDS Search and Browse interface

Due to the intensive work Tactuum has had to undertake on the new technology infrastructure has pushed back the delivery dates again and some new requirements have come out of the recent user acceptance testing. It now looks likely to be an April release for the search and browse interface. The archiving and version control functionality may be released earlier. We’ll keep you posted.

4.     Statistics

At the end of January, Olivia completed the generation of the latest set of usage statistics for all RDS toolkits. If you would like a copy of the stats for your toolkit, please contact Olivia.graham@nhs.scot .

 

5.     Review of content past its review date

We have now generated reports of all RDS toolkit content that has exceeded its review date by 6 months or more. We will be in touch later this month with toolkit owners and editors to agree the plan for updating or withdrawing out of date content.

 

6.     Toolkits in development

Some important toolkits in development by the RDS team include:

  • National CVD prevention pathways – due for release end of March 2025.
  • National respiratory pathways, optimal cancer diagnostic pathways and cancer prehabilitation pathways from the Centre for Sustainable Delivery. We will shortly start work on the national cancer referral pathways, first version due for release via RDS around end of June 2025.
  • HIS Quality of Care Review toolkit – currently in final stages of quality assurance.

 

The RDS team and other information scientists in HIS have also been producing evidence summaries for the Scottish Government Realistic Medicine team, to inform development of national guidance around Procedures of Limited Clinical Value. This guidance will in due course be translated into an RDS toolkit.

 

7. Training sessions for new editors (also serve as refresher sessions for existing editors) will take place on the following dates:

  • Friday 28th February 12-1 pm
  • Tuesday 11th March 4-5 pm

 

To book a place, please contact Olivia.graham@nhs.scot, providing your name, organisation, job role, and level of experience with RDS editing (none, a little, moderate, extensive.)

 

To invite colleagues to sign up to receive this newsletter, please signpost them to the registration form  - also available in End-user and Provider sections of the RDS Learning and Support area.   If you have any questions about the content of this newsletter, please contact his.decisionsupport@nhs.scot  If you would prefer not to receive future newsletters, please email Olivia.graham@nhs.scot and ask to be removed from the circulation list.

With kind regards

 

Right Decision Service team

Healthcare Improvement Scotland

 

 

Cu-IUD Use in Specific Groups

Warning

Cu-IUD Use in Specific Groups

  • Young People, individuals who have never been pregnant and individuals who have
    never been sexually active can use a cu-IUD.
  • Transgender and gender-diverse individuals assigned female at birth (TGD-AFB)

The medical indications and contraindications for Cu-IUD are the same for transgender and gender-diverse individuals assigned female at birth (TGD-AFB) and cis-gender women. The Cu IUD may appeal to TGD-AFB individuals who wish to avoid hormones. The LNG-IUD may help individuals who wish menstrual suppression. Pelvic cramping and bleeding can exacerbate gender dysphoria so clinicians should give adequate pre-procedure counselling about expected side effects and their duration, to improve tolerability. TGD individuals experience varying levels of dysphoria with their anatomy, and genital examination during IUC procedures may cause additional physical or emotional discomfort. Testosterone is teratogenic so TGD-AFB individuals
using testosterone therapy and engaging in sex where there is a risk of pregnancy should use effective contraception. Testosterone treatment is not contraceptive, even if the individual is amenorrhoeic. Testosterone can cause vaginal atrophy and dryness, which may add to the physical discomfort of examination- consider pre-procedure treatment with local vaginal estrogen for 2 weeks prior to IUC insertion

  • After Pregnancy

Immediate postpartum IUC (within 48 hours of childbirth) is safe, effective, convenient and associated with high continuation rates. When inserted within 48 hours of childbirth, the insertion technique is different to that of standard IUC insertion and clinicians need to be appropriately trained in this technique

If >48 hours have passed since childbirth, insertion should be delayed until 28 days after childbirth. The risks of insertion from 48 hours until 28 days after childbirth generally outweigh the benefits (UKMEC3).

IUC insertion after abortion is convenient and acceptable and has been associated with high continuation rates and reduced likelihood of another abortion within the next 2 years.

After medical abortion, or medical or expectant management of miscarriage, IUC can be inserted any time after expulsion of the pregnancy, providing there is no clinical suspicion of sepsis and no new risk of pregnancy. In addition when there has been early medical discharge (products passed at home) ensure there is no ongoing pregnancy prior to insertion with low sensitivity pregnancy testing done no sooner than 3 weeks post abortion.

An IUC can be inserted immediately after surgical abortion or surgical management of miscarriage or ectopic pregnancy, providing there is no clinical suspicion of sepsis.

  • After gestational trophoblastic disease (GTD)

IUC should not be inserted after gestational trophoblastic disease (GTD) until human chorionic gonadotropin (hCG) levels are normal.

  • Peri-menopause

The Cu-IUD may be associated with heavier, more painful or prolonged bleeding and so may not be appropriate for individuals with heavy menstrual bleeding or perimenopausal individuals who experience problematic menstrual bleeding patterns.

Examination and endometrial assessment/investigation should be considered prior IUC insertion for perimenopausal individuals who have heavy and/or erratic bleeding or a recent change in bleeding pattern, taking into account any risk factors for gynaecological disease. Requirement for investigation should follow local guidelines.

  • Breast Cancer

There are no contraindications to use of a Cu-IUD for an individual with current or previous breast cancer (UKMEC1)

  • Individuals with raised BMI

Assessment of uterine position and gaining access to the uterus IUC insertion can be more challenging in individuals with raised BMI. Some practicalities may need to be considered in order to maximise the chances of insertion success (e.g. having a range of speculum sizes and an examination couch with an appropriate weight limit). In addition, availability of a large blood pressure cuff for measuring blood pressure is essential.

  • Individuals at Risk of Infection 

Current pelvic inflammatory disease (PID), postpartum or post-abortion sepsis, known gonorrhoea infection, symptomatic Chlamydia infection, and purulent cervicitis are all contraindications to IUC insertion (UKMEC4). The risks associated with IUC insertion in the presence of known asymptomatic chlamydia infection are generally considered to outweigh benefits (UKMEC3). Individuals who have symptoms of possible bacterial STI and/or PID should ideally delay IUC insertion until test results are available, until PID or confirmed STI have been treated, and until symptoms have resolved. Offer a bridging contraceptive method if required.

If an individual is considered to be at increased risk for sexually transmitted infections (STIs) but has none of the aforementioned specific conditions and is not a recent contact of gonorrhoea or Chlamydia, benefits of IUC insertion are generally considered to outweigh risks.

Routine STI screening of asymptomatic individuals requesting IUC is not necessary; however, a sexual history should be taken prior to IUC insertion and screening offered, to individuals at risk of sexually transmitted infections. Providing the individual is asymptomatic and the individual is not a current or recent contact of gonorrhoea or Chlamydia, screening can be performed at the time of IUC insertion and the IUC can be inserted without awaiting results and without prophylactic antibiotic treatment so long as the user can be contacted and treated promptly, if indicated, when the results are known.

Asymptomatic individuals who are a current or recent contact of gonorrhoea or Chlamydia should delay IUC insertion until infection excluded (based on tests done outwith the window period). 

Following a positive chlamydia or gonorrhoea result, an intrauterine method can be inserted if the individual has completed antibiotic treatment (and, if applicable, completed any test of cure requirements and / or additional recommended follow-up or imaging, for example, in the case of complicated pelvic infection such as a tubo-ovarian abscess) and is asymptomatic.

Any treatment for confirmed or suspected chlamydia, gonorrhoea or PID should be in line with British Association for Sexual Health and HIV (BASHH) guidance.

In the absence of robust evidence to guide practice and until a formal recommendation is made by UKMEC update, it is suggested that IUC insertion should, where possible, be delayed until known Mycoplasma genitalium has been adequately treated and any associated symptoms have resolved.

With specific regard to emergency IUD insertion that cannot be delayed:

  • An individual with known asymptomatic chlamydia infection who requires an emergency Cu-IUD could consider insertion on the same day that chlamydia treatment is commenced. (UKMEC indicates that asymptomatic untreated gonorrhoea infection would contraindicate Cu-IUD insertion).
  • Where results of CT (chlamydia) and GC (gonorrhoea) tests are not yet available, antibiotic prophylaxis for CT and/or GC could be considered for an individual who requires emergency IUD insertion and has no symptoms relevant to CT or GC infection but has a current or recent partner who is known to have CT or GC infection.
  • Where results of CT and GC tests are not yet available, antibiotic prophylaxis for chlamydia and/or gonorrhoea could be considered on a case-by-case basis for individuals who require emergency Cu- IUD insertion but have symptoms for which CT or GC infection cannot be excluded as a cause

Other infections (and bacterial vaginosis)

There is no indication to screen for other lower genital tract organisms in asymptomatic individuals considering IUC. If bacterial vaginosis, Trichomonas vaginalis or candida infection is diagnosed or suspected, these should be treated but the IUC can be inserted without delay.

There is no need to delay IUC insertion or treat asymptomatic individuals who have been identified as having Group B Streptococcus.

Group A streptococcus (GAS) is a rare but serious infection that can cause life-threatening septicaemia, invasive GAS (e.g. necrotising fasciitis) and streptococcal toxic shock syndrome. Therefore, if GAS is incidentally detected it is important that it is treated urgently. IUC insertion should be delayed until treatment is complete.

  • Wilson’s disease

This is a rare genetic disorder of copper metabolism, resulting in accumulation of copper in the individual’s organs and tissues. It is established practice that use of the Cu-IUD is avoided in those with Wilson’s disease because of any potential risk that it could contribute further to the excessive accumulation of copper in the body.

Refer to a senior clinician if

  • Uterine cavity distortion
  • Previous endometrial ablation
  • After large loop excision of the transformation zone (LLETZ) procedure
  • Under follow up for gestational trophoblastic disease
  • Immunosuppression/ taking immunosuppressants including patients with adrenal insufficiency and / or taking corticosteroids
  • History of postural orthostatic tachycardia syndrome (PoTS)
  • Known to have inherited bleeding disorders
  • Anticoagulants
  • Cardiac disease

Contraception choice for individuals with cardiac disease will often require a multidisciplinary approach and discussion with the individual’s cardiologist is recommended. See also FSRH Clinical Guideline: Contraceptive Choices for Women with Cardiac Disease (June 2014)

FSRH Clinical Guideline: Intrauterine contraception (March 2023, Amended July 2023)

 

Editorial Information

Last reviewed: 31/08/2023

Next review date: 30/09/2025

Author(s): West of Scotland Managed Clinical Network in Sexual Health Clinical Guidelines Group .

Version: 10.1

Reviewer name(s): West of Scotland Managed Clinical Network in Sexual Health .