MPR is a multispecialty drug information resource for healthcare professionals offering concise prescribing information, point-of-care tools, plus daily news and features on hot topics in pharmacotherapy. Launched in 1985 as the Monthly Prescribing Reference – a concise drug information reference in print – MPR remains a leading authority in prescribing information and has since evolved into an invaluable multichannel resource across print, web, and mobile for drug information and efficient clinical tools for all healthcare professionals.
MPR and its specialty editions are circulated to more than 340,000 healthcare professionals. With a reach of over 1.5 million within the Haymarket Medical Network, the MPR website (www.eMPR.com) is utilized by over 530,000 unique visitors a month and generates 1.3 million page views. The MPR App has been downloaded more than 375,000 times and generates more than 750,000 page views a month.
MPR is a multispecialty drug information resource for
healthcare professionals offering concise prescribing information,
point-of-care tools, plus daily news and features on hot topics in
pharmacotherapy. Launched in 1985 as the Monthly Prescribing Reference –
a concise drug information reference in print – MPR remains a
leading authority in prescribing information and has since evolved into
an invaluable multichannel resource across print, web, and mobile for
drug information and efficient clinical tools for all healthcare
professionals.
MPR and its specialty editions are circulated to more than
340,000 healthcare professionals. With a reach of over 1.5 million
within the Haymarket Medical Network, the MPR website (www.eMPR.com) is utilized by over 530,000 unique visitors a month and generates 1.3 million page views. The MPR App has been downloaded more than 375,000 times and generates more than 750,000 page views a month.
The Food and Drug Administration (FDA) has issued an Emergency Use
Authorization to Spectra Optia Apheresis System and Depuro D2000
Adsorption Cartridge (Terumo BCT Inc. and Marker Therapeutics AG) for
the treatment of patients 18 years of age or older with confirmed
coronavirus disease 2019 (COVID-19) admitted to the intensive care unit
(ICU) with confirmed or imminent respiratory failure to reduce
proinflammatory cytokines levels.
Cytokine levels are typically elevated during infections and can be
associated with a cytokine storm in some COVID-19 patients. The Agency
believes that the ability to manage the cytokine storm associated with
COVID-19 may decrease patient morbidity.
The Spectra Optia Apheresis System is a blood purification system
that operates in conjunction with Depuro D2000 Adsorption Cartridge
devices. The authorized product uses continuous flow centrifugation and
optical detection technology to separate plasma from whole blood,
removing cytokines and other inflammatory mediators, and returning the
filtered blood to the patient. Plasma filtration may be run for up to 4
hours and may be repeated as needed.
“With today’s authorization of a blood purification device, we are
expediting the availability of a treatment option for patients in the
ICU to help reduce the severity of the disease,” said FDA Commissioner
Stephen M. Hahn, MD. “Our staff will continue our around the clock
review of all medical products to expedite the availability of
treatments to help fight this devastating disease.”
For more information visit fda.gov.
Convalescent Plasma Treatment Promising in Severe COVID-19
Researchers found that the level of neutralizing
antibody increased rapidly up to 1:640 in 5 of the 10 cases after
convalescent plasma transfusion.
HealthDay News – One dose of convalescent plasma (CP) therapy is
well tolerated and can potentially improve clinical symptoms in severe
cases with coronavirus disease 2019 (COVID-19), according to a study
published online April 6 in the Proceedings of the National Academy of Sciences.
Kai Duan, from the China National Biotec Group Company Limited in
Beijing, and colleagues prospectively enrolled 10 patients with severe
COVID-19 confirmed by real-time viral RNA tests. Patients received a
transfusion of one dose of CP derived from recently recovered donors
with neutralizing antibody titers above 1:640; patients also received
maximal supportive care and antiviral agents. From onset of illness to CP transfusion, there was a median time of 16.5 days.
The researchers found that the level of neutralizing antibody
increased rapidly up to 1:640 in 5 cases after CP transfusion; in 4
other cases, the high level was maintained (1:640). Significant
improvement was seen in clinical symptoms, with an increase of
oxyhemoglobin saturation within 3 days. Compared with pretransfusion,
several parameters tended to improve, including increased lymphocyte
counts and reduction in C-reactive protein. Varying degrees of
absorption of lung lesions were seen within seven days on radiological
examinations. In seven of the patients who had previous viremia, the
viral load was undetectable after transfusion.
“The optimal dose and treatment time point, as well as the definite
clinical benefits of CP therapy, need to be further investigated in
randomized clinical studies,” the authors write. Abstract/Full Text