mercredi 6 février 2013

Chickenpox: A highly infectious disease

All parents know. When a child has had chickenpox in the nursery or school, there are all "opportunities" for all his comrades "benefit". Extremely common in children, chickenpox is indeed very ... highly contagious.



Originally chickenpox, a disease most mundane of life, a virus of the family herpes viruses, herpes zoster virus. The same virus herpes zoster can remain dormant for years in the body and determine the occurrence of shingles in adults, generally older, who developed chickenpox in their younger years.

An incubation period of two weeks

   Chickenpox occurs most often in children 2 to 10 years, but it can also be seen in some adults who had previously escaped 1. It is then readily worst home. The virus is transmitted by skin lesions that cause illness, or through saliva droplets 1 and an estimated 600 000 to 700 000 people are infected each year in France by one 4.
The incubation period of chickenpox is between 10 to 21 days, as a rule from 14 to 16 days, and infected children are highly contagious 48 hours before until 5 days after the onset of lesions 2. But the problem is that many young patients have only very discrete lesions that go unnoticed, as they pass though indeed chickenpox!

Telemedicine service sleep apnea

In France, 500,000 people with sleep apnea are treated with a continuous positive airway pressure device (CPAP) to wear at night. Despite its effectiveness, the treatment of choice, very restrictive, is often not observed or abandoned during the first 6 months. Respir @ dom, a telemedicine project, aims to improve monitoring. Explanations.
This remote monitoring treatment of sleep apnea creates a link between the greatest doctor, home health provider and the patient, it makes player treatment.

Sleep apnea: poor adherence

  The sleep apnea affects 5-7% of the population. More than 500,000 people are treated with a continuous positive airway pressure device (CPAP), which sends pressurized air into the airway through a mask applied to the face. This treatment helps to lower cardiovascular risk and metabolic , increased risk in people with sleep apnea syndrome. "The mask must be worn at least 3 to 4 hours per night to ensure long-term effect on cardiovascular prevention in particular," said Dr. Sylvie Royant-Parola, President of the Network and project coordinator Morpheus Respir @ dom. However, "20 to 33% of patients discontinue treatment during the first 4 months and 20 to 50% have insufficient compliance," she informs. "It is not so easy to get used to wearing the mask mandatory every night," says the doctor. Social Security takes into account the duration of use for reimbursement.
In addition, in the current health care system, the health care provider at home that brings equipment home and maintains, was not aware of the technical problems (leaks, insufficient correction of apnea), or health and feelings of the patient between visits. These factors impede adherence. Hence the idea of ​​a telemedicine service which aims to increase the number of people who follow their treatment correctly. "Patients treated well from the start will not over-causing risk of cardiac complications or cerebrovascular accident (CVA) later, "said Dr Royant-Parola.

Sleep apnea: a proposed treatment monitoring through telemedicine

"Respir @ dom is a telemedicine service which involves the remote monitoring of patient treatment apneic" announcement Dr. Royant-Parola. Innovation? "All CPAP machines transmit data on a daily basis on a secure server in the Medical Record Medical Sleep (DMS) Network Morpheus via a GPRS system," said the specialist. These data are available by the doctor, home health provider and the patient. They are analyzed and automatically generate alerts in case of technical defects (malfunction, leakage, insufficient correction of apnea ...). "This allows for greater responsiveness and a more rapid physician and home health provider," said Dr. Royant-Parola. These alerts are sent first to the home health provider that will trigger an action to correct the problem. If it is necessary to modify the treatment, the doctor intervenes.
In parallel with this daily transmission, the patient can return data on its secure space in its DSM: clinical status, tolerance to treatment. "If the patient says he does not feel well, unmotivated, a warning is issued and the clinical health professional will be able to respond," said the physician coordinator of this project. He added: "It telemonitoring offers more personalized services to patients who also become involved in their treatment."

Respir @ dom, better inform the patient

With this project telemedicine, the patient is accompanied also better informed. "Respir @ dom, it is also a community platform supporting a forum moderated by a psychologist or a doctor," said Dr. Royant-Parola. The goal? "Create a dynamic support between patients to advance in the treatment of apnea and better manage their health." "We know the positive discourse of a patient is more convincing than the speech of a health professional," adds Dr. Royant-Parola. This site also informs people with apnea of ​​this disease, treatment, medical advances. There is also a serious game that can involve family and especially children. "With the various aspects of this project, we hope to less désappareillage, better adherence and, ultimately, less over-risk of stroke and heart attack , "says Dr. Royant-Parola.
Part telemonitoring program Respir @ dom is currently restricted to 200 patients included in the study of medico-economic evaluation which will end on 30 November 2013. This program will then be generalized. You can already find out about the site if you are concerned www.respiradom.fr (e).

Curative vaccine against AIDS tested on humans

On January 29, Public Assistance - Hospitals of Marseille (AP-HM) announced the start of clinical trials of a therapeutic vaccine against HIV. Embodying the work of Dr. Erwann Loret, these tests will be supervised by Dr. Isabelle Ravaux, Service of Infectious Diseases, Hospital of the Conception (AP-HM). It retails for around Doctissimo hopes this vaccine cure "Tat Oyi".
Doctissimo: What is the principle of the vaccine that you test?
Dr Isabelle Ravaux: It has been observed in people infected with HIV the presence of Tat protein produced by HIV. This protein is involved in the mechanisms of virus replication but also in extracellular "tricking" the immune system. It will firstly prevent killer cells to launch an attack HIV and secondly, it acts on B cells by reducing the production of antibodies against HIV.
Neutralizing Tat protein in an infected person, it hopes to restore his immunity and block the development of the disease. For this, we need to trigger the production of anti-Tat antibodies sufficient.

Doctissimo: How to successfully induce the immune response?
Dr Isabelle Ravaux: The choice of candidate is the brainchild of Erwann Loret, CNRS researcher. In a cohort of African patients who did not develop the disease (patients called HIV controllers ), in 1996 he discovered that the only abnormality was the virus called the Tat Oyi. In these patients, it was not functional and offered some protection to patients vis-à-vis HIV.
The idea of ​​using this protein "Tat Oty" as a vaccine candidate has naturally imposed. The same team has succeeded in synthesizing this protein. The vaccine "Tat Oty" demonstrated in experiments in vitro and in vivo animal (including macaques) good efficiency, the results of which have been published in leading scientific journals. The next step is testing in humans, for which we received the green light from the National Safety of Medicines (MSNA) January 24, 2013.

Doctissimo: How will unfold clinical trials for this vaccine?
Dr Isabelle Ravaux: Clinical trials will take place in clinical investigation center (CIC) plurithematic 9502 AP-HM. Our biomedical research protocol EVA TAT is divided into two phases.
In a first time, 48 patients treated with HAART with undetectable viral load will be divided into 4 groups. Three receive a dose Tat Oyi different for each group. The latter will receive a placebo. The vaccination consists of three intradermal injections one month apart (on the surface of the skin without penetrating the muscle tissue or vascular). Treatment should be stopped two months to assess the time during which the viral load remains undetectable in patients. Patient recruitment began in February 2013. These Phase I / IIa aim to validate the principle of such a vaccination (it lead to the production of anti-TAT?) Check the safety of these injections transdermal humans and validate the optimal dose, which induces better immune response. The results of this phase will be conducted in December 2013.
If successful (lengthening the time control statistically significant viral load without treatment), 80 patients will be recruited from January 2014 to phase IIb, which will demonstrate the effectiveness of the vaccine. Half of the patients receive the optimal dose of the vaccine and the other half a placebo. The results will be analyzed in March 2015 and should be published around June 2015.
All these tests are "double-blind", that is to say that neither the prescriber nor the patient knows whether the used syringe containing vaccine or placebo (this is the method to ensure results tests by removing the psychological effects of the injection).

Doctissimo: What are the benefits for this therapeutic vaccine?
Dr Isabelle Ravaux: The first potential benefit of this vaccine would be to replace the triple therapy is not without side effects ... or at least be able to do without for a while.
You know you will have difficulty disposing of new classes of antiretroviral drugs in 20 years - it improves the comfort of taking the treatment, reducing the number of tablets including, but laboratories are investing less in AIDS research. It is therefore important to find new strategies to defeat HIV can develop resistance to treatment.
Tomorrow, a combination vaccine could take over the triple and perhaps act on the virus reservoirs (those places where the virus is immune to existing treatments).

Doctissimo: After years of false hopes, vaccines (especially therapeutic vaccines) seem to know a new impetus. Why is this?
Dr Isabelle Ravaux: Therapeutic vaccines aim to stimulate or today "educate" the immune system to fight against HIV. Strategy is no longer targeting surface proteins of the virus, which we now know they are too changeable to induce an effective immune response. The recent encouraging results on therapeutic vaccines explore this route, as the only case of a patient known cure HIV . For this, we need to find the "trick" as held by the two types of HIV virus - HIV-1 and HIV-2 - the target that will not easily mutate. The objective is to obtain an effective immune response and durable. It is our hope with the Tat protein.

Doctissimo: How was funded research?
Dr Isabelle Ravaux: The phases of basic research has been funded by the National Research Agency against AIDS (ANRS). A research protocol was then filed with the agency, which was not accepted as a priority.
To fund this research, it was therefore necessary to conduct a fundraiser, it is for this purpose that the biotechnology company BIOSANTECH was created. It is therefore of private funds but this research would not have been possible without the support of public actors: the University of Aix-Marseille and the CNRS have allowed Dr. Loret continue its research and Assistance Public - Hospitals of Marseille and the South East SATT allowing the conduct of clinical trials.