Cargando…

Single-dose and Steady-state Pharmacokinetics of Vancomycin in Critically Ill Patients Admitted to Medical Intensive Care Unit of India

RATIONALE: Vancomycin remains the standard of care for gram-positive bacterial infections, though there are significant developments in newer antibacterial agents. Efficacy can be improved by linking pharmacokinetic with pharmacodynamic principles, thus leading to optimum antibiotic exposure. There...

Descripción completa

Detalles Bibliográficos
Autores principales:	Mali, Nitin B, Deshpande, Siddharth P, Wandalkar, Poorwa P, Gupta, Vishal A, Karnik, Niteen D, Gogtay, Nithya J, Nataraj, Gita, Mehta, Preeti R, Thatte, Urmila
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Jaypee Brothers Medical Publishers 2019
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6900894/ https://www.ncbi.nlm.nih.gov/pubmed/31911742 http://dx.doi.org/10.5005/jp-journals-10071-23289

Ejemplares similares

Steady-state Pharmacokinetics of Vancomycin in Children Admitted to Pediatric Intensive Care Unit of a Tertiary Referral Center
por: Mali, Nitin B, et al.
Publicado: (2019)

A study comparing trial registry entries of randomized controlled trials with publications of their results in a high impact factor journal: The Journal of the American Medical Association
por: Wandalkar, Poorwa, et al.
Publicado: (2017)

A Multicentric, Prospective, Observational Antibacterial Utilization Study in Indian Tertiary Referral Centers
por: Mali, Nitin Bhagwan, et al.
Publicado: (2018)

A Prospective Antibacterial Utilization Study in Pediatric Intensive Care Unit of a Tertiary Referral Center
por: Mali, Nitin B., et al.
Publicado: (2018)

An analysis of completeness and quality of adverse drug reaction reports at an adverse drug reaction monitoring centre in Western India
por: Mahajan, Manali Mangesh, et al.
Publicado: (2018)

Knowledge about clinical trial agreement and clinical trial related insurance among Ethics Committee members: A cross-sectional survey
por: Sridharan, Kannan, et al.
Publicado: (2016)

Evaluation of pharmacokinetics of single-dose chloroquine in malnourished children with malaria- a comparative study with normally nourished children
por: Kadam, Prashant P., et al.
Publicado: (2016)

Evaluation of cytochrome P450 2D6 phenotyping in healthy adult Western Indians
por: Gogtay, Nithya J., et al.
Publicado: (2014)

A prospective study to assess the association between genotype, phenotype and Prakriti in individuals on phenytoin monotherapy
por: Thaker, Saket J., et al.
Publicado: (2017)

Do clinical trials conducted in India match its healthcare needs? An audit of the Clinical Trials Registry of India
por: Chaturvedi, Mansi, et al.
Publicado: (2017)

Regulatory requirements for clinical trials in India: What academicians need to know
por: Gogtay, Nithya J, et al.
Publicado: (2017)

Compliance of Mumbai-based clinical trial sites with the Quality Council of India guidelines and evaluation of the challenges faced by the investigators
por: Figer, Brinal, et al.
Publicado: (2021)

Pharmacokinetics of single-dose primaquine in patients with chronic kidney dysfunction
por: Kulkarni, Shaunak P., et al.
Publicado: (2013)

Procalcitonin-guided antibiotic usage - addressing heterogeneity in meta-analysis
por: Birajdar, Amit Ravindra, et al.
Publicado: (2018)

An audit of minutes of Subject Expert Committee meetings as a metric to assess the clinical research roadmap of India
por: Shetty, Parvan A., et al.
Publicado: (2019)

A two-year evaluation of the minutes of Investigational New Drug committee meetings
por: Raj, Jeffrey Pradeep, et al.
Publicado: (2021)

Population pharmacokinetics of primaquine and the effect of hepatic and renal dysfunction: An exploratory approach
por: Sridharan, Kannan, et al.
Publicado: (2019)

Investigator preparedness for monitoring and audits
por: Ravi, Renju, et al.
Publicado: (2018)

Investigator-initiated studies: Challenges and solutions
por: Konwar, Mahanjit, et al.
Publicado: (2018)

Recruitment and retention of the participants in clinical trials: Challenges and solutions
por: Chaudhari, Nayan, et al.
Publicado: (2020)

The global initiative for asthma guidelines (2019): change in the recommendation for the management of mild asthma based on the SYGMA-2 trial – A critical appraisal
por: Rajan, Sujeet, et al.
Publicado: (2020)

A comparative study to evaluate quality of data documentation between investigator-initiated and pharmaceutical industry-sponsored studies
por: Figer, Brinal H., et al.
Publicado: (2020)

Evaluation of inter-rater agreement between three causality assessment methods used in pharmacovigilance
por: Thaker, Saket J., et al.
Publicado: (2016)

An audit of colistin use in neonatal sepsis from a tertiary care centre of a resource-limited country
por: Jasani, Bonny, et al.
Publicado: (2016)

Has mandatory prospective registration of all studies brought about a change? A 1-year audit of studies registered in the Clinical Trials Registry of India [CTRI] before and after April 1, 2018
por: Shetty, Nayana S., et al.
Publicado: (2021)

Association between genetic polymorphisms of CYP2C9 and VKORC1 and safety and efficacy of warfarin: Results of a 5 years audit
por: Biswas, Mansij, et al.
Publicado: (2018)

Current status of standardized, quality and ethical oversight of clinical research in the country: An audit of the Central Drugs Standard Control Organization (registration of ethics committees) and national accreditation board for hospital and healthcare providers (accreditation) databases
por: Nishandar, Tushar Bhimrao, et al.
Publicado: (2019)

An audit of reporting of conflict of interest policies among three stakeholders in Indian biomedical journals
por: Bose, Debdipta, et al.
Publicado: (2020)

Evaluation of clinical trials done for orphan drugs versus nonorphan drugs in infectious diseasesan eleven year analysis [2010-2020]
por: Kudyar, Palvi, et al.
Publicado: (2023)

A prospective study to assess the role of paraoxonase 1 genotype and phenotype on the lipid-lowering and antioxidant activity of statins
por: Godbole, Charuta, et al.
Publicado: (2023)

Use of computerized tests to evaluate psychomotor performance in children with specific learning disabilities in comparison to normal children
por: Taur, Santosh, et al.
Publicado: (2014)

An audit of the approval letters issued by Drugs Controller General of India to Ethics Committees in India
por: Bhide, Shruti S., et al.
Publicado: (2016)

An evaluation of the minutes of subject expert committee meetings of novel COVID-19 proposals
por: Raj, Jeffrey Pradeep, et al.
Publicado: (2022)

Authors’ response
por: Taur, Santosh R., et al.
Publicado: (2015)

Evaluation of CYP2C19, P2Y12, and ABCB1 polymorphisms and phenotypic response to clopidogrel in healthy Indian adults
por: Sridharan, Kannan, et al.
Publicado: (2016)

Factors influencing recruitment and retention of participants in clinical studies conducted at a tertiary referral center: A five-year audit
por: Bose, Debdipta, et al.
Publicado: (2020)

An evaluation of drug lag for new drugs approved by the Indian regulator relative to the United States, European Union, and Japanese regulatory agencies: A 15-year analysis (2004–2018)
por: Konwar, Mahanjit, et al.
Publicado: (2021)

An audit of institutional ethics committee queries raised after initial project submission by a single research department at a tertiary referral center in India
por: Raj, Jeffrey Pradeep, et al.
Publicado: (2023)

Audiovisual recording of the consenting process in clinical research: Experiences from a tertiary referral center
por: Shetty, Parvan A, et al.
Publicado: (2018)

Determination of reference intervals from a laboratory database of an academic clinical research unit in a tertiary care teaching hospital and an audit of out of range values
por: Figer, Brinal H., et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_00c45vi866npsos2p2d7orhl3g