Mical Paul

ORCID: 0000-0003-2317-1112
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About
Contact & Profiles
Research Areas
  • Bacterial Identification and Susceptibility Testing
  • Antibiotic Resistance in Bacteria
  • Antibiotic Use and Resistance
  • Antibiotics Pharmacokinetics and Efficacy
  • Pneumonia and Respiratory Infections
  • Neutropenia and Cancer Infections
  • Sepsis Diagnosis and Treatment
  • Antimicrobial Resistance in Staphylococcus
  • Urinary Tract Infections Management
  • Nosocomial Infections in ICU
  • Respiratory viral infections research
  • Meta-analysis and systematic reviews
  • Pneumocystis jirovecii pneumonia detection and treatment
  • Clostridium difficile and Clostridium perfringens research
  • Antifungal resistance and susceptibility
  • Infective Endocarditis Diagnosis and Management
  • Streptococcal Infections and Treatments
  • Hematological disorders and diagnostics
  • Health Systems, Economic Evaluations, Quality of Life
  • Fungal Infections and Studies
  • Influenza Virus Research Studies
  • Blood disorders and treatments
  • Hematopoietic Stem Cell Transplantation
  • Bacterial Infections and Vaccines
  • Emergency and Acute Care Studies

Rambam Health Care Campus
2016-2025

Technion – Israel Institute of Technology
2016-2025

Sylhet Agricultural University
2025

World Health Organization
2025

Northumbria University
2024

Biology of Infection
2020

Haifa Medical Center
2019

Philippine General Hospital
2019

University of the Philippines Manila
2019

Wellcome Trust
2019

The polymyxin antibiotics colistin (polymyxin E) and B became available in the 1950s thus did not undergo contemporary drug development procedures. Their clinical use has recently resurged, assuming an important role as salvage therapy for otherwise untreatable gram-negative infections. Since their reintroduction into clinic, significant confusion remains due to existence of several different conventions used describe doses polymyxins, differences formulations, outdated product information,...

10.1002/phar.2209 article EN Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy 2019-01-01

Gram-negative bacteremia is a major cause of morbidity and mortality in hospitalized patients. Data to guide the duration antibiotic therapy are limited.This was randomized, multicenter, open-label, noninferiority trial. Inpatients with gram-negative bacteremia, who were afebrile hemodynamically stable for at least 48 hours, randomized receive 7 days (intervention) or 14 (control) covering therapy. Patients uncontrolled focus infection excluded. The primary outcome 90 composite all-cause...

10.1093/cid/ciy1054 article EN Clinical Infectious Diseases 2018-12-07

<h3>Importance</h3> Methicillin-resistant<i>Staphylococcus aureus</i>(MRSA) bacteremia is associated with mortality of more than 20%. Combining standard therapy a β-lactam antibiotic has been reduced mortality, although adequately powered randomized clinical trials this intervention have not conducted. <h3>Objective</h3> To determine whether combining an antistaphylococcal effective alone in patients MRSA bacteremia. <h3>Design, Setting, and Participants</h3> Open-label, trial conducted at...

10.1001/jama.2020.0103 article EN JAMA 2020-02-11
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