Sosa International Consultant Services - SICS

Sosa International Consultant Services - SICS Infectious diseases & Clinical Microbiology in the Developing World

Working with government officials, professional medical societies and other health care practitioners to reduce the disease burden in vulnerable populations. Using comprehensive, cost-effective work plans and approaches that meet the needs and priorities of targeted communities. WORLDWIDE EXPERIENCE Latin America and Caribbean: Mexico, Guatemala, Nicaragua, Costa Rica, Colombia, Ecuador, Peru, Bolivia, Argentina, Paraguay, Brazil, Uruguay, Chile, Venezuela, Dominican Republic, Bahamas, Surinam, Cuba;
Europe and Middle East: Sweden, Russia, United Kingdom, Finland, France, Germany, The Netherlands, Belgium, Czechoslovakia, Denmark, Georgia, Turkey, Greece, Italy, Spain, Portugal, Lebanon. Arab States: Abu Dhabi;
Asia: Bangladesh, Indonesia, Hong Kong, South Korea, Taiwan, Malaysia, Singapore, Thailand, India, Philippines, Japan, Vietnam; North America: USA and Canada;
Africa: Ethiopia, Senegal, The Gambia, Tanzania, Mozambique, South Africa, Namibia, Uganda and Zambia

WHO GLOBAL AMR 2025
10/25/2025

WHO GLOBAL AMR 2025

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Summary of the evidence of CEFTOBIPROLE specifically to treat MRSA pneumonia. Source: Gnoni, Martin. MDCeftobiprole is a...
10/24/2025

Summary of the evidence of CEFTOBIPROLE specifically to treat MRSA pneumonia.
Source: Gnoni, Martin. MD

Ceftobiprole is a fifth-generation cephalosporin with potent activity against methicillin-resistant Staphylococcus aureus (MRSA), and is approved in both the United States and Europe for the treatment of community-acquired pneumonia (CAP) and in Europe - Canada for hospital-acquired pneumonia (HAP), excluding ventilator-associated pneumonia (VAP).[1-2]

Randomized controlled trials and real-world studies have demonstrated that ceftobiprole is non-inferior to standard regimens (e.g., ceftriaxone ± linezolid for CAP, ceftazidime plus linezolid for HAP) in terms of clinical cure rates, including in cases caused by MRSA.[2-4] In a pivotal phase 3 trial for HAP (excluding VAP), ceftobiprole achieved clinical cure rates comparable to ceftazidime plus linezolid (ITT: 59.6% vs 58.8%; CE: 77.8% vs 76.2%), with similar microbiological eradication rates for MRSA (doi:10.1093/cid/ciu219).[4] However, ceftobiprole was less effective in VAP patients.

In vitro studies confirm ceftobiprole’s high activity against MRSA isolates from pneumonia cases in the US and Europe, with susceptibility rates exceeding 95%.[5-7] For example, a US surveillance study found 99.3% of MRSA isolates susceptible to ceftobiprole (MIC50/90, 1/2 mg/L) (doi:10.1128/aac.01402-24), and an Italian survey reported 95.5% susceptibility among MRSA from HAP (doi:10.1093/jac/dkz371).[5][7]

Ceftobiprole’s broad spectrum and favorable safety profile make it a valuable option for empiric and targeted therapy of MRSA pneumonia, especially in settings with multidrug-resistant organisms.[8-11] It is recommended for CAP and HAP (excluding VAP). Still, caution is advised in cases with high risk for ESBL-producing organisms or MDR Pseudomonas, where combination therapy may be needed (doi:10.1080/14787210.2025.2461552).[11]

In summary, ceftobiprole is supported by robust clinical and microbiological evidence for the treatment of MRSA pneumonia in both the US and Europe, with efficacy and safety comparable to standard therapies, except in VAP.[2-4][7]
Reference: Summary of the evidence of CEFTOBIPROLE specifically to treat MRSA pneumonia. 🤔

Ceftobiprole is a fifth-generation cephalosporin with potent activity against methicillin-resistant Staphylococcus aureus (MRSA), and is approved in both the United States and Europe for the treatment of community-acquired pneumonia (CAP) and in Europe - Canada for hospital-acquired pneumonia (HAP), excluding ventilator-associated pneumonia (VAP).[1-2]

Randomized controlled trials and real-world studies have demonstrated that ceftobiprole is non-inferior to standard regimens (e.g., ceftriaxone ± linezolid for CAP, ceftazidime plus linezolid for HAP) in terms of clinical cure rates, including in cases caused by MRSA.[2-4] In a pivotal phase 3 trial for HAP (excluding VAP), ceftobiprole achieved clinical cure rates comparable to ceftazidime plus linezolid (ITT: 59.6% vs 58.8%; CE: 77.8% vs 76.2%), with similar microbiological eradication rates for MRSA (doi:10.1093/cid/ciu219).[4] However, ceftobiprole was less effective in VAP patients.

In vitro studies confirm ceftobiprole’s high activity against MRSA isolates from pneumonia cases in the US and Europe, with susceptibility rates exceeding 95%.[5-7] For example, a US surveillance study found 99.3% of MRSA isolates susceptible to ceftobiprole (MIC50/90, 1/2 mg/L) (doi:10.1128/aac.01402-24), and an Italian survey reported 95.5% susceptibility among MRSA from HAP (doi:10.1093/jac/dkz371).[5][7]

Ceftobiprole’s broad spectrum and favorable safety profile make it a valuable option for empiric and targeted therapy of MRSA pneumonia, especially in settings with multidrug-resistant organisms.[8-11] It is recommended for CAP and HAP (excluding VAP). Still, caution is advised in cases with high risk for ESBL-producing organisms or MDR Pseudomonas, where combination therapy may be needed (doi:10.1080/14787210.2025.2461552).[11]

In summary, ceftobiprole is supported by robust clinical and microbiological evidence for the treatment of MRSA pneumonia in both the US and Europe, with efficacy and safety comparable to standard therapies, except in VAP.[2-4][7]

Gentile, I., Giuliano, S., Corcione, S., De Rosa, F. G., Falcone, M., Giacobbe, D. R., … Bassetti, M. (2025). Current role of ceftobiprole in the treatment of hospital-acquired and community-acquired pneumonia: expert opinion based on literature and real-life experiences. Expert Review of Anti-Infective Therapy, 23(2–4), 217–225. https://doi.org/10.1080/14787210.2025.2461552

The Return of Syphilis - A Warning from 2025
10/23/2025

The Return of Syphilis - A Warning from 2025

Herpes Zoster (Shingle) Vaccine: protection more than skin.
10/23/2025

Herpes Zoster (Shingle) Vaccine: protection more than skin.

Resurgence in Syphilis
10/23/2025

Resurgence in Syphilis

🦠 The Return of Syphilis — A Warning from 2025 The latest JAMA review reveals a striking truth: syphilis is back and rising fast. Between 2019 and 2023, U.S. cases increased by 61%, infections among women doubled, and congenital syphilis rose by 106% — a tragedy that is largely preventable. ....

Chagas Disease in the USA.
09/18/2025

Chagas Disease in the USA.

Chagas disease, a potentially deadly condition caused by a parasite carried by insects called kissing bugs, should now be considered endemic in the United States, experts say – and without recognition that it’s a constant presence in some parts of the country, more people will become ill and die...

A must read!
09/17/2025

A must read!

Decades of immunization progress is backsliding, an NBC News data investigation reveals, threatening the safety of children in America, burdening schools and hindering public health.

08/24/2025

Plastic pollution is now an emerging issue worldwide, and the amount of plastic debris is rapidly increasing day by day in this decade. The surface of plastic contains a wide variety of biofilm-forming microorganisms that can pose a risk to human health. Studies showed that Escherichia coli is resis...

The global epidemiology of carbapenem-resistant Acinetobacter baumanniiCarbapenem-resistant Acinetobacter baumannii (CRA...
07/29/2025

The global epidemiology of carbapenem-resistant Acinetobacter baumannii

Carbapenem-resistant Acinetobacter baumannii (CRAb) is a challenging, environmentally hardy organism with a
propensity to spread within hospitals and a predilection to infect critically ill, vulnerable patients. With its potential
for rapid transmission, limited treatment options, and substantial mortality, CRAb is recognized as a critical,
top-priority pathogen. Since its initial discovery in 1985, CRAb has disseminated globally, presenting a significant
public health threat. CRAb is now endemic in many regions in Europe, South America, Asia, and Africa and globally
contributes to over 50 000 deaths each year. Its ability to adhere to hospital surfaces, withstand desiccation,
and form biofilms leads to widespread outbreaks. At-risk populations include those hospitalized and
ventilated, and the most frequent presentations are respiratory and bloodstream infections. Carbapenem resistance
in CRAb is primarily mediated by plasmid-borne carbapenemase genes, especially blaOXA-23. These genes,
carried by several epidemic international clones, including IC1 and IC2, have facilitated the global dissemination
of CRAb through horizontal gene transfer in healthcare settings. Mortality rates are >20% and vary substantially
by region and by type of infection, with bloodstream infections carrying >40% mortality. Despite its significant
impact, the development of treatments for CRAb remains inadequate. The novel agent sulbactam-durlobactam
holds promise for improved patient outcomes, but ongoing therapeutic development, infection prevention, and
antimicrobial stewardship are critical to combat this formidable pathogen. Here, we review the emergence and
dissemination of CRAb, its molecular epidemiology and resistance mechanisms, summarize contemporary global
clinical epidemiology and patient outcomes, and briefly describe existing and future therapeutics.

05/09/2025

Howard et al. demonstrate that clinical isolates of the opportunistic pathogen Pseudomonas aeruginosa can encode functional plastic-degrading enzymes and that these enzymes can influence bacterial biofilm formation.

Pseudomonas aeruginosa
05/09/2025

Pseudomonas aeruginosa

"We need to understand the impact this had on patient safety," said biomedical scientist Ronan McCarthy.

04/28/2025

Pseudomonas aeruginosa-derived 2-nonyl-4-quinolone N-oxide exerts bactericidal effects on Neisseria gonorrhoea via zeta1–epsilon1 toxin–antitoxin activation in vitro and abrogates experimental infection in mice.

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