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  6. Quick starting contraception
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

 

 

Quick starting contraception

Warning

What’s new

There are no changes to this Guidance since the previous update.

 

Background

Quick starting (QS) is the immediate initiation of a contraceptive method at the time a woman requests it, rather than waiting for the next natural menstrual period.

This practice may be outside the product licence / device instructions of the chosen method, but may have potential benefits such as reducing the time she is at risk of pregnancy, reducing the chance of her forgetting information on the chosen method, and negating the need for a further appointment.

A method that has been quick started may be continued as an ongoing method of contraception, or it may be used as a temporary ‘bridging’ method until her preferred method can be commenced (e.g., pregnancy excluded).

See summary of additional contraceptive requirements when starting contraception when quick starting contraception. As with every client, all contraceptive methods should be discussed and STI risk assessment performed.

Quick starting contraception and exclusion of pregnancy

a) Quick starting if pregnancy can be excluded

  • Any method of contraception can be quick started at any time in the menstrual cycle if it is reasonably certain that a woman is not pregnant or at risk of pregnancy from recent unprotected sexual intercourse (UPSI). See below.
  • HCPs can be ‘reasonably certain’ that a woman is not currently pregnant if any one or more of the following criteria are met and there are no symptoms or signs of pregnancy:
    • She has had no intercourse since last normal (natural) menses, since childbirth, abortion, miscarriage, ectopic pregnancy or uterine evacuation for gestational trophoblastic disease.
    • She has been correctly and consistently using a reliable method of contraception.
    • Is within the first 5 days of the onset of a normal menstrual period.
    • Is less than 21 days post-partum (non-breast feeding women).
    • Is fully breast feeding, amenorrhoeic and less than 6 months post partum.
    • Is within the first 5 days after abortion, miscarriage, ectopic or uterine evacuation for gestational trophoblastic disease.
    • Has had no intercourse for more than 21 days and has a negative high sensitivity urine pregnancy test (HSUPT; able to detect hcg levels around 20mIU/ml).

 

b) Quick Starting if pregnancy cannot be excluded

  • Women who have a HSUPT but are at risk of pregnancy from recent UPSI should be advised that:
    • Emergency contraception may be indicated.
    • Contraceptive hormones are not thought to cause harm to the fetus and they should not be advised to terminate pregnancy on the grounds of exposure.
    • Additional contraceptive precautions (barrier or abstinence) are required until the quick started contraceptive method becomes effective. See summary of additional contraceptive requirements table, below.
    • A follow up pregnancy test is required no sooner than 21 days after the last UPSI. Provide a pregnancy testing kit or inform of alternative options for pregnancy testing, including local providers of free testing.
    • She should return if there are any concerns or problems with contraception.

Pregnancy diagnosed after Quick starting contraception


FSRH Guidance advises that women should be informed that contraceptive hormones are not thought to cause harm to the fetus and they should not be advised to terminate pregnancy on the grounds of exposure.

 

Wish to continue with the pregnancy (using CHC, POP, IMP, DMPA).

  • CHC or POP should be stopped immediately. Implants should be removed promptly if a pregnancy is diagnosed after starting contraception.

 

Choose not to continue with the pregnancy

  • IMP or DMPA:
    Women can continue the method of contraception with no additional contraception precautions after abortion. If DMPA administered at time of mifepristone there may be a slightly higher risk of continuing pregnancy (failed termination).
  • CHC or POP:
    Women should stop method and restart contraception immediately after abortion with no additional contraception requirements.
  • Using intrauterine contraception (IUC):
    HCPs should advise women whose intrauterine pregnancy is less than 12 weeks gestation that IUC should be removed, as long as the threads are visible or it can be easily removed from the endocervical canal. This is regardless of whether the woman decides to continue with the pregnancy or not. The risk of adverse intrauterine pregnancy events are greater with an IUC insitu compared to those without. IUC removal in first trimester could improve pregnancy outcomes, but it is associated with a small risk of miscarriage.

Documentation

Quick starting hormonal contraception without being reasonably sure pregnancy is excluded is outside the terms of the product license, however, the FSRH support QS contraception as outlined in their guidance.

The General Medical Council advises that, when prescribing a licensed medication for use outside the terms of the product licence: in emergencies or where there is no realistic alternative treatment and such information is likely to cause distress, it may not be practical or necessary to draw attention to the licence. In other cases, where prescribing unlicensed medicines is supported by authoritative clinical guidance, it may be sufficient to describe in general terms why the medicine is not licensed for the proposed use or patient population.

The Nursing and Midwifery Council advises that nurse or midwife independent prescribers may prescribe outside the product licence if they are satisfied that this better serves the patient/client’s needs, and there is a sufficient evidence base. The patient/client should understand the reasons why such medicines are not licensed for this proposed use, and this should be documented accordingly.

The NMC also states it is acceptable for medicines used outside the terms of the licence to be included in patient group directions (PGDs) when such use is justified by current best clinical practice and the direction clearly describes the status of the product.

Summary of methods which can be quick started

Situation

Quick starting

Normal menstruating woman

No pregnancy risk this cycle

All methods can be considered.

Normal menstruating woman

Pregnancy risk this cycle

Not taken Emergency contraception

All methods except any combined hormonal contraception containing cyproterone or any levonorgestrel intra-uterine system.

Following levonorgestrel emergency contraception

All methods except any combined hormonal contraception containing cyproterone or any levonorgestrel intra-uterine system.

Following ulipristal acetate emergency contraception

All methods, but must wait 5 days before starting any hormonal containing contraception.

Summary of additional contraceptive requirements when starting contraception

NB: After ulipristal acetate emergency contraception wait at least 5 days before starting any hormonal contraception

Method

Day of Menstrual Cycle*

Days of additional contraception

required after starting method (condoms/abstinence)

Combined hormonal contraception (except Qlaira/Zoely)

Days 1 to 5

 

Day 6 onwards

None

 

7

Zoely COC

Day 1

 

Day 2 onwards

None

 

7

Qlaira COC

Day 1

 

Day 2 onwards

None

 

9

Progestogen-only pill

Days 1 to 5

 

Day 6 onwards

None

 

2

Implant or

Depot medroxyprogesterone

Days 1 to 5

 

Day 6 onwards

None

 

7

Levonorgestrel intra-uterine system

Days 1 to 7

 

Day 8 onwards

None

 

7

Copper intra-uterine device

(see emergency contraception protocol if this is the indication for insertion)

Any day

none

*Day 1 defined as first day of menstrual bleeding; does not apply to withdrawal or unscheduled bleeding in women already established on hormonal contraception

References

  1. FSRH Clinical Effectiveness Unit. FSRH Clinical Guideline: Quick Starting Contraception [Internet]. The Faculty of Sexual and Reproductive Healthcare; 2017 Apr [cited 2024 May]. https://www.fsrh.org/standards-and-guidance/documents/fsrh-clinical-guidance-quick-starting-contraception-april-2017/
  2. General Medical Council. Good practice in prescribing and managing medicines and devices [Internet]. General Medical Council; 2013 Jan [updated 2021 Apr; cited 2024 May]. Available from: https://www.gmc-uk.org/ethical-guidance/ethical-guidance-for-doctors/good-practice-in-prescribing-and-managing-medicines-and-devices
  3. NMC Standards for medicines management May 2018 https://www.nmc.org.uk/standards/standards-for-post-registration/standards-for-prescribers/standards-for-prescribing-programmes/[cited 2024 May]

Editorial Information

Last reviewed: 31/05/2024

Next review date: 31/05/2026

Author(s): West of Scotland Managed Clinical network for Sexual Health Clinical Guidelines Group .

Version: 8.1

Approved By: West of Scotland Managed Clinical network for Sexual Health