EAHP learning modules

A number of modules for self-assessment are now available online via BMJ Learning. Aimed at hospital pharmacists and based on recordings of satellite events held at the annual European Association of Hospital Pharmacists (EAHP) Congress, they are free to access and accredited by the Accreditation Council for Pharmacy Education (ACPE).

The events were financially supported by different external organisations but totally independent of industry involvement, with the faculty and the topics selected by the EAHP scientific committee.

All users must complete a one-time registration on BMJ Learning and subsequently log in on every visit using their username and password to access modules and their CPD record. Accreditation is only valid for 2 years from the date of publication. Printable CPD certificates are available to users that achieve the minimum pass mark and complete a survey at the end of the course. 1.5-2 ACPE credits will be awarded, depending on the length of the course.



Antibiotic stewardship: advanced

Antibiotic stewardship is at the interface of procurement, clinical pharmacy and patient safety. This advanced course outlines the challenges in antibiotic dosing, discusses the role of clinical pharmacists in antibiotic stewardship, describes new drugs under development, and presents options for handling difficult patient cases.


The Hospital Pharmacist’s role in antithrombotic stewardship

Explains how to determine and manage the reversible risk factors for bleeding in patients taking Direct Oral Anticoagulants (DOACs), establish an antithrombotic stewardship programme to improve adherence to anticoagulant guidelines to minimize complications, and communicate this knowledge to other healthcare professionals. As DOACs are the first-line option for the prevention of stroke in patients with non-valvular atrial fibrillation (AF) and the treatment of venous thromboembolism (VTE), it is essential that hospital pharmacists can balance the benefits and risks of these medications.

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Anticoagulation – from theory to practice

Oral anticoagulant therapy is used to reduce the risk of stroke in patients with atrial fibrillation (AF) and pharmacists have an important role in educating patients about and managing treatment with oral anticoagulants. In this course three pharmacist practitioners members of iPACT (International Pharmacists for Anticoagulation Care Taskforce) present projects outlining how oral anticoagulants can be employed to improve the care of patients suffering from AF.

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Anticoagulants: show me the evidence!

Optimal oral anticoagulant therapy requires careful consideration of patient’s needs and an understanding of the efficacy, safety, pharmacokinetics of the anticoagulants and the methods used to measure their effects. This course enables pharmacists to stay updated with new anticoagulant drugs, educate patients about their drugs, and highlight the importance of adhering to anticoagulant therapy.

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Biologicals and biosimilars

Hospital pharmacists making the difference

Provides insight into how to implement and monitor biosimilars for oncologic therapy, tackles specific issues relating to their optimum use in the hospital arena, and explains how to assess the financial impact on healthcare systems. Hospital pharmacists can play a key role in the use of biosimilars for cancer care if they have a good understanding of their development, regulatory approval processes, and clinical utility.

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Biosimilars in colorectal cancer – what’s your gut feeling?

Outlines the key concepts and facts which support biosimilar approval in the EU and explains how to implement biosimilars of monoclonal antibodies in the treatment of colorectal cancer. As new biosimilars for colorectal cancer are coming to the market, it is important for hospital pharmacists to be able to offer a scientific, unbiased perspective and act as key drivers in the implementation process in order to realise the significant opportunities for cost savings.

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Biosimilars – available yet sometimes missing: the challenge of procurement

Tackles the challenges of switching from a reference biological medicine to a biosimilar, including safety and efficacy concerns, tendering procedures, and medicines shortages. Identifies the problems, shows examples, and discusses the way forward, so that the full potential of biosimilars as enablers of affordable innovation can be fulfilled, with maximum advantages for patients and healthcare providers.

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Biosimilars in cancer care – the next challenge

Provides the key information on biosimilar approval in the EU as applied to cancer therapy. By understanding the concepts and facts, hospital pharmacists will be enabled to provide a scientific, unbiased approach with a focus on patient care in a world of limited resources. By gaining insights on into the regulatory assessment process and the clinician’s perspective in prescribing biosimilars, the ability of hospital pharmacists to advise on how to implement biosimilars of monoclonal antibodies used in cancer therapy will be strengthened.

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The essentials of biologicals: past, present, and future

Offers insights into the evolution of biologicals, which are an essential treatment option for a variety of diseases in current medicine. Course participants will learn about the development and authorisation of biosimilars as well as the quality criteria of biologicals. In addition, issues of switching and interchangeability of biologicals will be addressed to provide an in-depth understanding of key principles regarding quality, safety and efficacy.

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Biosimilars in breast cancer – the next challenge

Biosimilars of targeted breast cancer biologic drugs will soon be introduced into the market, and it will be essential for hospital pharmacists to understand the key concepts in order to manage their implementation. This module gives pharmacists a better understanding of the biosimilar approval process in the EU, the role of biosimilars in reducing therapeutic cost in breast cancer, and how to work with other healthcare providers, stakeholders and patients to manage their implementation.

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Management and leadership

Procurement, tendering, and decision making processes in the hospital setting

Outlines the role of the hospital pharmacist in procurement and tendering, which are essential for managing medication costs at national, regional and local hospital levels. However, price is not the only consideration; value-based tenders include other aspects such as continuity of supply, patient safety, environmental aspects, quality-based factors and innovative characteristics.

Management and leadership

Explores the differences between management and leadership, including topics such as strategic planning, efficiency, team building, process mapping, problem solving and also human factors, vision and buy-in, change management, motivating people and managing resistance. Introduces the use of established management tools that can be used for practical implementation of the principles discussed.

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Politics and healthcare policy

Facing Brexit and FMD – Is Europe ready for the double “storm”?

Discusses how Brexit and the Falsified Medicines Directive will impact the supply of medicines and medicines policy in the EU. Considers what hospital pharmacists can do to prepare for these changes and identify new procedures to prevent the possible negative effects on access to medicines.

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Medicines shortages – Causation and approaches to improvements

Elaborates on the factors that create or exacerbate medicines shortages around the world, and outlines how hospital pharmacists can collaborate with other stakeholders to detect, reduce and avoid shortages, taking into account strategic and quality issues along the medicines supply chain.

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Research methodology

Qualitative research methods

Describes what qualitative is, when it should be used, how to conduct it ethically, the different methods that can be employed and how their results can be analysed. Explains why this research methodology is important in the evaluation of complex interventions and services.

Therapeutic drug monitoring

Therapeutic drug monitoring as a tool for therapy optimisation

Explains how to use therapeutic drug monitoring (TDM) to optimise and individualise therapy. Presents practical advice on identifying drugs that are good candidates for TDM, appropriate indications for TDM, and understanding and interpreting drug concentrations. Emphasises the importance of a multidisciplinary team approach.

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