MORPHEO

A study of pain pathways

The pain associated with vaso-occlusive crises is one of the most severe symptoms of sickle cell disease. Every year, thousands of patients attend emergency departments for relief, most often with morphine. However, this essential treatment does not work in the same way for every patient.

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Transforming the lives of people affected by the world’s most common inherited blood disorder is within our reach.

Why does the same dose of morphine relieve some patients… but not others?

The MORPHEO project addresses this key issue.

At present, responses to morphine vary greatly from one patient to another: ineffectiveness, adverse effects or overdose may occur. This variability is due to biological and genetic factors, as well as factors linked to the disease itself.

MORPHEO’s aim is to gain a better understanding of these differences in order to tailor treatments to each patient.

To achieve this, the project combines:

  • detailed analysis of how morphine is metabolised in the body,
  • the study of genetic factors influencing response to treatment,
  • innovative micro-sampling techniques (a single drop of blood),
  • and artificial intelligence models to predict individual responses.

The results should help teams choose morphine doses more accurately, limit adverse effects and improve pain relief in the emergency department.

 

The aim?

A personalised approach to pain management that is more effective and safer.

In the longer term, MORPHEO could help teams anticipate each patient’s needs and provide safer, more effective pain treatment.

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Every donation funds direct action on the ground: equipping a screening centre, training a doctor or developing information tools for patients. Sickle cell disease affects millions of people but remains severely underfunded. Your support changes lives.

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Our projects

We run practical programmes to support earlier diagnosis, better care and wider access to information. Our projects cover research, prevention, therapeutic patient education and access to healthcare in the regions most affected by sickle cell disease.

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Our partners

RED is supported by a strong network of institutional, scientific and community partners. Within the RÊVE consortium and beyond, we combine our strengths to accelerate research and improve care wherever sickle cell disease occurs.