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Biomedical subjects

A Beauplet

Publications and source records attributed to A Beauplet.

17 recordsLinked to original sources

[Possible actions to guide international cooperation programs].

Transfusion is an essential element of health services. French HCO's are thriving to sustain the transfusional system throughout the world, especially to support low income countries. This article evokes several tentative cooperation experiences and proposes to think over conditions which would make it possible for such actions to become more efficient. The author sets out different aspects making the undertaken restructurizing and implemented support successful operations. First is about the definition of responsibilities, supervision and management as dedicated to the public authorities. Second deals with the management of disposable resources, whatever they be of human, equipment or material nature. A third item is devoted to contributions (supports) that may help the implementation of the product itself. The article finally stresses the importance of the action (program) quality assessment and continuous improvement. Further to his reporting on the cooperation methods, the author presents some of the actions undertaken by the Etablissement Français du Sang (National Blood Agency) in the last few years in Afghanistan, Latin America and Africa.

Blood Banks↗

[Creation and organization of a mobile collection unit].

In France, nearly eighty per cent homologous blood donations are given in mobile settings. The collection site requirements, and particularly premises, are conditioning the security of persons, blood products quality, and blood collection efficiency. They also take a decisive part in the public image of the transfusion network. This paper describes an easy method for evaluating and validating premises used for mobile setting of blood collection.

Blood Donors↗

[Is it possible to organize into a hierarchy blood donation contraindications?].

Because it symbolizes henceforth the sanitary risk and fears which are linked to it, the blood transfusion must master the potential or real risks associated to its practice. The analysis of these risks leads to confirm the initial selection phase of candidates for blood donation as an always original stage of the blood transfusion safety towards the identified infectious risks, but also mainly towards the emergent or modelled risks. The evaluation of the current system of prevention leads to consider two potential dangers: the ineffectiveness of the selection because of the lack of meaning given to this stage, and the donors' disaffection caused by badly accepted or badly justified deferrals. The deficit of meaning can be due to an insufficient information of the population as for the policy of collective prevention of transfusion-transmitted infectious diseases. It can be worsened by the construction of the pre-donation interview which can appear as a succession of questions without visible links. This paper suggests risk analysis to blood transfusion, and a reflection to improve this important stage of blood product safety approach represent by the selection of candidates to a blood donation.

Blood Donors↗

[The transfusion chain: from donor to recipient].

From donor to recipient, raw blood will undergo a succession of processing events before eventually becoming a qualified, recipient-adapted finished product. The integrity of the transfusion chain and its various links will determine the final quality of blood transfusion, a key element for a number of medical disciplines. The recent reform of blood transfusion has brought about a national system based on a single body, the French Blood Institution, with regional branches ensuring effective networking of the entire country. Keeping a permanent scientific watch, this Donor-to-Recipient set-up warrants optimal quality according to current knowledge, and close links with the single hemovigilance network which continually analyses events that may affect transfusion safety and takes immediate action accordingly.

Blood Grouping and Crossmatching↗

[Discovery of a chronic HVC infection without seroconversion in a blood donor in France during 28 months].

The HCV-RNA screening technique developed by the French Fractionation and Biotechnology Laboratory singled out in March 1998 a case of positive HCV-RNA viremia in a blood donor without any anti-HCV antibody. That donor was a 46-year-old woman who had made 54 donations of blood products from 1988 to 1997. She had no history of blood transfusion, no history of hepatitis and no life-style risk factor. Clinical examination was normal. Liver tests (serum alanine amino transferases, gamma glutamyl transpeptidase , alkaline phosphatase, bilirubin , prothrombin and albumin) were normal. Total blood count was normal. Lymphocyte count was normal as well as in vitro functional analysis of lymphocytes (stimulation with different antigens). All screening HCV Elisa tests and immunoblot System available on the French market were unable to detect anti-HCV antibodies. Quantification of serum HCV-RNA (Amplicor Monitor Roche) showed 294,000 copies/mL and HCV genotype 1b determination was performed using Innolipa assay. Further examination of the HCV genotype by direct sequencing of the PCR product showed a classical 1b genotype sequence. The hemovigilance inquiry identified 25 labile products distributed since 1988. Analyzing the records of the recipients that have so far been traced and identified revealed three periods: 1997 to 1995: three recipients were found to be positive for anti-HCV antibodies; two are now cured of hepatitis C. In one recipient, direct sequencing after specific PCR of the hypervariable region coding for the envelope domain showed 100% homology with the donor; 1993 to 1990: four recipients were identified and traced without contamination; in 1988: three of four blood product recipients were anti-HCV negative without HCV-RNA viremia. The forth carried anti-HCV antibodies and genotype 1b HCV-RNA but had a history of multiple surgery. Alter et al. [4] and Bush et al. [5] have previously suggested the possibility of a chronic, immunologically silent state of infection. The case described herein, is the first evidence for this hypothesis. Indeed, the donor has not yet seroconverted 28 months after viremia was discovered. This blood donor was identified by HCV-RNA screening of plasma products. The identification of the same sequence in a recipient of blood from this donor clearly establishes the transmission of the virus by transfusion. The prevalence of such cases of infectious silent chronic HCV carriers has to be determined and the mechanisms responsible for the absence of antibody production need to be clarified.

Amino Acid Sequence↗

[The physician's role in blood donation].

In France, proper transfusion practices impose that the medical pre-donation interview be done by a physician. In Anglo-Saxon countries, it is more often performed by a nurse. The physician's job is not limited to the clinical selection of blood donation volunteers. In the production process, the physician is implicated in the safety and supply of labile blood products. The practice of the profession requires educational and communication skills. As the manager of a medical team working in mobile sites, the physician must ensure the respect of ethics and professional regulations by the staff he or she trains and supervises.

Blood Banks↗

[Quality indicators and dashboards: the experience of a collection department].

Production of labile blood products and pharmaceutical products derived from blood must meet quality and safety requirements set and controlled by regulatory provisions (Guidelines for Transfusion Practices, Characteristics of Labile Blood Products). With its activities exerted at the start of the transfusional chain, collection departments have to meet internal requirements (self-sufficiency, procurement regulation, compliance of blood products as raw materials) as well as external ones (donor and recipient safety). To fit in a dynamics of on-going quality improvement, the quality approach of a department must implement a system to monitor and control its activities. The subject of this work is to report an experience of the implementation of quality indicators and specific dash boards for whole blood collection and related activities in a blood transfusion center.

Blood Banks↗

[Benefits and risks of scheduled autologous transfusion].

Blood transfusion, like any other medical activity, requires an analysis of the risk/benefit ratio for each patient. Autologous blood transfusion does not escape this golden rule. The benefits expected of scheduled autologous transfusion consist of the reduction of the risks inherent in homologous transfusion. Those benefits are indisputable in erythrocyte alloimmunisation and viral or parasitic disease transmission. But the risks attached to such protocols have often been underestimated. The risks for the patient are still linked to the transfusion of autologous labile blood products (haemolysis, bacterial infections) or to consequences of whole blood donations (cardiovascular intolerance, increased use of transfusion, increased operative bleeding). There are also risks for the patient community insofar as autologous blood products which do not all meet the same criteria of clinical and biological validation as homologous blood products are circulated in care institutions.

Anemia↗

[Enzymatic evaluation of blood donors].

Enzymatic, immunologic and hematologic dosages were performed in a group of blood donors. A significant part of this population showed anomalies in the enzymes, either isolated or associated and of variable importance. A systematic serological study of viral hepatitis A (VHA) and viral hepatitis B (VHB) was performed among these donors with biochemical anomalies. A more general biological study (immunology and hematology) completes this work.

Adolescent↗

A new method for monitoring the sterility of blood donation.

Sterility of blood products is a cardinal contributor to patient safety. Bacteriologic controls of stable products comply with strict regulations, but legislation imposes only limited constraints in the case of perishable products, such as packed red cells (RBCs) or fresh-frozen plasma (FFP). Therefore, it is essential to monitor the sterility of aseptic donations from uninfected donors. Such bacteriologic monitoring can now be carried out through a tertiary bag (containing a soybean casein culture medium) connected to the classical double-pack system. This system does not jeopardize the sterility of the whole system, as the connection is tightly stoppered by a membrane. After the blood drawing, this tertiary bag is filled with 5 ml of blood, and separated from the rest of the system. It is then incubated for 3 days at 30 degrees C and for 14 days at 22 degrees C, to test for eventual bacteriologic or fungal contamination. In order to check the feasibility of this technique, we studied 76 blood drawings in the control laboratory of the blood center, and the results confirm the value of this system.

Blood Transfusion↗