A dedicated platform for the lymphoedema community

LIMPRINT

LIMPRINT (Lymphoedema IMpact and PRevalence – INTernational Lympoedema Framework) is an international study aimed at capturing the size and impact of chronic oedema in different countries and health services across the world. Focus is to provide evidence to support the development and reimbursement of lymphoedema services.

The project is co-ordinated by the International Lymphoedema Framework (ILF) through its participating national frameworks. This challenging project has demonstrated the possibility of global research within a charitable framework and the power of strong academic partnerships to ensure delivery of robust evidence from each country.

From 2014 to 2017, 9 countries with 40 sites have contributed to an international data set of over 13,000 patients. The study was supported by an electronic data capture system and data collection tools that had been previously validated.  The preliminary analysis has begun to illuminate the burden on acute and community health services across the world and to identify the patient populations most at risk.  

LIMPRINT initial analysis

The initial analysis has shown that chronic oedema is major health care problem and that patients are found throughout the health care system. There are variations in the prevalence rates in acute hospitals internationally with the lowest rates found in Japan and the highest in Denmark. However the importance of risk factors such as obesity, immobility and cellulitis are emerging.  Primary Lymphoedema remains an important group seen in specialist services while secondary patients are seen in many different healthcare settings.  The proportion with cancer as the dominant cause is much lower than frequently reported.  

First results presented at ILF 2017 Conference

First results of the LIMPRINT studies were presented in two key sessions at the 7th ILF conference in Syracuse in 2017. The presentations provided an overview of the results from the study and discussed the implications for health services nationally.

 Data analysis will continue and publishing is being prepared for 2018.

Susie Murray is the study manager responsible for coordinating the activities and liaising with the sites. The project is also supported by an international steering group.