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Prescribed List (Jersey): Changes from 1st November 2019

A formal published “Ministerial Decision” is required as a record of the decision of a Minister (or an Assistant Minister where they have delegated authority) as they exercise their responsibilities and powers.

Ministers are elected by the States Assembly and have legal responsibilities and powers as “corporation sole” under the States of Jersey Law 2005 by virtue of their office and in their areas of responsibility, including entering into agreements, and under any legislation conferring on them powers.

An accurate record of “Ministerial Decisions” is vital to effective governance, including:

  • demonstrating that good governance, and clear lines of accountability and authority, are in place around decisions-making – including the reasons and basis on which a decision is made, and the action required to implement a decision

  • providing a record of decisions and actions that will be available for examination by States Members, and Panels and Committees of the States Assembly; the public, organisations, and the media; and as a historical record and point of reference for the conduct of public affairs

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The Freedom of Information Law (Jersey) Law 2011 is used as a guide when determining what information is be published. While there is a presumption toward publication to support of transparency and accountability, detailed information may not be published if, for example, it would constitute a breach of data protection, or disclosure would prejudice commercial interest.

A decision made on 25 October 2019

Decision Reference:  MD-S-2019-0085

Decision Summary Title :

DS Prescribed list as of 1 Nov 2019

Date of Decision Summary:

23 October 2019

Decision Summary Author:

Policy Principal

Decision Summary:

Public or Exempt?

Public

Type of Report:

Oral or Written?

Written

Person Giving

Oral Report:

NA

Written Report

Title :

WR report PBAC 19 September 2019

Date of Written Report:

22 October 2019

Written Report Author:

Prescribing Advisor

Written Report :

Public or Exempt?

 

Public

Subject: Changes to be made to the Prescribed List (Jersey) as of 1 November 2019

Decision(s): Further to Article 15, paragraphs (11) and (12), of the Health Insurance (Jersey) Law 1967, and having consulted with the Pharmaceutical Benefit Advisory Committee, the Minister decided to make amendments to the Prescribed List with effect from 1 November 2019 as set out in the accompanying report and supporting document.

Reason(s) for Decision: The Pharmaceutical Benefit Advisory Committee met on 19 September 2019 and has provided the Minister with recommendations regarding amendments to the Prescribed List.

 

Items to be added to the Prescribed List

  • Semaglutide 1.34mg/mL solution for injection pre-filled devices
  • Azelastine hydrochloride 125 micrograms/fluticasone propionate 50 micrograms nasal spray (Dymista brand)
  • Hydrocortisone 500mcg/1mg/2mg/5mg granules in capsules for opening (Alkindi) for children
  • Tiotropium 2.5microgram inhalation solution cartridge; tiotropium 2.5microgram/olodaterol 2.5mcg inhalation solution cartridge

 

Following the meeting, the PBAC was asked to urgently consider changes to the Prescribed List in response to the Supply Disruption Alert for ranitidine (a treatment for stomach ulcers and acid reflux) issued on 16th October. Using its agreed procedure, the Committee recommends addition of the following product to provide an alternative to ranitidine while it is out of stock:

 

  • Nizatidine 150mg capsules

 

The recommendations reflect current evidence and expert advice, and ensure that patients in Jersey have access to an appropriate range of modern, safe and effective treatments from their GPs and community prescribers at a proportionate cost to the Fund.

 

Other changes to the Prescribed List

Further minor amendments and deletions will be made to the Prescribed List following a line by line  review of the List and its reformatting to comply with dm+d nomenclature as requested by NHS Business Services Authority.

Resource Implications: The overall financial impact of the above changes is expected to be a small increase in total annual expenditure.  One of the additions to the List has a commercial in confidence price, therefore the exact figure has not been published. 

 

Action required: Health Zone Manager at Customer and Local Services to issue a public notice listing amendments and notify all approved medical practitioners and approved contractors.

Signature:

 

 

Position:

Minister

 

Date Signed:

 

 

Date of Decision (If different from Date Signed):

 

Prescribed List (Jersey): Changes from 1st November 2019

RECOMMENDATIONS OF THE

PHARMACEUTICAL BENEFIT ADVISORY COMMITTEE

 

22 October 2019

 

Summary

 

The Pharmaceutical Benefit Advisory Committee (PBAC) met on 19 September to consider applications for changes to the Prescribed List.

 

The PBAC was unanimous in its recommendations for the following changes to the Prescribed List to be implemented from 1 November 2019.

 

  1. Items to be added to the Prescribed List
    1. Semaglutide 1.34mg/mL solution for injection pre-filled devices
    2. Azelastine hydrochloride 125 micrograms/fluticasone propionate 50 micrograms nasal spray (Dymista brand)
    3. Hydrocortisone 500mcg/1mg/2mg/5mg granules in capsules for opening (Alkindi) for children
    4. Tiotropium 2.5microgram inhalation solution cartridge; tiotropium 2.5microgram/olodaterol 2.5mcg inhalation solution cartridge (change required following notice from manufacturer that a reusable inhaler device will be available)

 

In addition, the PBAC was asked to urgently consider changes to the Prescribed List in response to the Supply Disruption Alert for ranitidine issued on 16th October. The Committee recommends addition of the following product to provide an alternative to ranitidine while it is out of stock:

 

1.5 Nizatidine 150mg capsules

 

 

  1. Other changes to the Prescribed List
    1. A summary list of all amendments and deletions (for discontinued products only) was agreed by the Committee. These were made following a line by line the review of the List and reformatting to comply with dm+d nomenclature, as requested by NHS Business Services Authority.

 

  1. Other considerations
    1. An application for the addition of imiquimod 5% cream, for the treatment of a number of skin conditions, was supported conditionally as a means to reduce hospital waiting times and speed up access to treatment. This support was conditional on views from the hospital dermatologist, to be requested following the meeting. Those views have now been received and do not support making imiquimod cream available in primary care. Therefore, the application will be returned to the Committee for their further consideration.

 

3.2. An application for melatonin 2mg modified-release tablets, for the treatment of insomnia in adults aged over 55 years of age, was the subject of some debate. The Committee acknowledged that the management of insomnia was problematic and that there was misuse of existing treatment options. However, the Committee did not feel that there was compelling support for the addition of another option and, therefore, did not recommend its addition to the List. The Committee indicated that they would review this decision if further information became available.  

 

 

Financial impact

 

The overall financial impact of the above changes is expected to be a small increase in total annual expenditure. However, since one of the additions to the List has a commercial in confidence price, the exact figure cannot be published.  

 

Mrs Alison Creed

Chair, PBAC

 

22 October 2019

 


Recommendations

 

  1. Items to be added to the Prescribed List

 

1.1 Semaglutide 1.34mg/mL solution for injection pre-filled devices

 

  • Semaglutide is licensed for the treatment of type II diabetes mellitus as monotherapy or in combination with other antidiabetic medicines. There are 2 other medicines in the same therapeutic class as semaglutide already included in the List. However, there is evidence that semaglutide may be preferable to these medicines in selected patients. Semaglutide is administered as a weekly injection at a cost similar to other options in its class. Its addition to the List would, therefore, be cost neutral but offer additional choice for patients.

 

1.2 Azelastine hydrochloride 125 micrograms/fluticasone propionate 50 micrograms nasal spray (Dymista brand)

 

  • The addition of the combination nasal spray, Dymista, for the treatment of seasonal allergic rhinitis, has been previously considered but rejected because of the high cost of the product compared with its constituents.
  • The price of Dymista  has since fallen and it now represents a cost saving for patients who require treatment with both azelastine and fluticasone.

 

1.3 Hydrocortisone 500mcg/1mg/2mg/5mg granules in capsules for opening (Alkindi) for children

 

  • This formulation of hydrocortisone was requested by hospital specialists for use in the very small number of children with adrenal insufficiency who need long-term treatment with hydrocortisone but for whom there is no appropriate paediatric formulation.
  • The Alkindi formulation of hydrocortisone is more expensive than standard tablets; at the basic NHS list price, Alkindi is around 3 times more expensive but a confidential discount is available to reduce this gap.

   

1.4 Tiotropium 2.5microgram inhalation solution cartridge; tiotropium 2.5microgram/olodaterol 2.5mcg inhalation solution cartridge (change required following notice from manufacturer that a reusable Respimat inhaler device will be available)

 

  • The manufacturer has given notice that its Respimat inhaler device is to be reusable. The Committee, therefore, recommended that replacement cartridges should be included in the Prescribed List for use with the device.

 

1.5 Nizatidine 150mg capsules (generic only)

 

  • On 15th October, a Supply Disruption Alert was issued by the Department of Health and Social Care in England advising that no further supplied of ranitidine, a treatment for stomach ulcers and acid reflux, would be available until further notice. Around 1,700 people in Jersey are prescribed ranitidine.
  • The Supply Disruption Alert advised that patients taking ranitdine should be reviewed and, if ongoing treatment is needed, an alternative such as omeprazole or lansoprazole is prescribed. These alternatives are already included in the Prescribed List and have a similar cost to ranitidine. However, PBAC members advised that an alternative from the same therapeutic group as ranitidine should also be considered for patients and recommended that nizatidine is added to the List.
  • Nizatidine is around 8-times more expensive that ranitidine.


 

Estimated cost impact of PBAC recommendations

Recommended product

Estimated cost impact

1.1  Semaglutide 1.34mg/mL solution for injection pre-filled devices

No cost impact. Semaglutide is a similar price to other medicines in the same therapeutic group

1.2  Azelastine hydrochloride 125 micrograms/fluticasone propionate 50 micrograms nasal spray (Dymista brand)

 

Cost saving of up to £40,000 is anticipated based on existing use of the constituent products.

1.3  Hydrocortisone 500mcg/1mg/2mg/5mg granules in capsules for opening (Alkindi) for children

 

Confidential price.

Addition of hydrocortisone will increase overall expenditure.

1.4  Tiotropium 2.5microgram inhalation solution cartridge; tiotropium 2.5microgram/olodaterol 2.5mcg inhalation solution cartridge (change required following notice from manufacturer that a reusable Respimat inhaler device will be available)

 

No cost impact anticipated. Cartridges are priced the same as the existing device.

1.5  Nizatidine 150mg capsules

To be added to the List as one of a number of alternatives to ranitidine while it is out of stock. Nizatidine is around 8-times more expensive than ranitidine. If 25% of patients currently taking ranitidine switch to nizatidine, the cost impact will be an increase of around £35,000pa.

 

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