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  1. Article ; Online: Cefepime vs Piperacillin-Tazobactam in Adults Hospitalized With Acute Infection: The ACORN Randomized Clinical Trial.

    Qian, Edward T / Casey, Jonathan D / Wright, Adam / Wang, Li / Shotwell, Matthew S / Siemann, Justin K / Dear, Mary Lynn / Stollings, Joanna L / Lloyd, Brad D / Marvi, Tanya K / Seitz, Kevin P / Nelson, George E / Wright, Patty W / Siew, Edward D / Dennis, Bradley M / Wrenn, Jesse O / Andereck, Jonathan W / Han, Jin H / Self, Wesley H /
    Semler, Matthew W / Rice, Todd W

    JAMA

    2023  Volume 330, Issue 16, Page(s) 1557–1567

    Abstract: Importance: Cefepime and piperacillin-tazobactam are commonly administered to hospitalized adults for empirical treatment of infection. Although piperacillin-tazobactam has been hypothesized to cause acute kidney injury and cefepime has been ... ...

    Abstract Importance: Cefepime and piperacillin-tazobactam are commonly administered to hospitalized adults for empirical treatment of infection. Although piperacillin-tazobactam has been hypothesized to cause acute kidney injury and cefepime has been hypothesized to cause neurological dysfunction, their comparative safety has not been evaluated in a randomized clinical trial.
    Objective: To determine whether the choice between cefepime and piperacillin-tazobactam affects the risks of acute kidney injury or neurological dysfunction.
    Design, setting, and participants: The Antibiotic Choice on Renal Outcomes (ACORN) randomized clinical trial compared cefepime vs piperacillin-tazobactam in adults for whom a clinician initiated an order for antipseudomonal antibiotics within 12 hours of presentation to the hospital in the emergency department or medical intensive care unit at an academic medical center in the US between November 10, 2021, and October 7, 2022. The final date of follow-up was November 4, 2022.
    Interventions: Patients were randomized in a 1:1 ratio to cefepime or piperacillin-tazobactam.
    Main outcomes and measures: The primary outcome was the highest stage of acute kidney injury or death by day 14, measured on a 5-level ordinal scale ranging from no acute kidney injury to death. The 2 secondary outcomes were the incidence of major adverse kidney events at day 14 and the number of days alive and free of delirium and coma within 14 days.
    Results: There were 2511 patients included in the primary analysis (median age, 58 years [IQR, 43-69 years]; 42.7% were female; 16.3% were Non-Hispanic Black; 5.4% were Hispanic; 94.7% were enrolled in the emergency department; and 77.2% were receiving vancomycin at enrollment). The highest stage of acute kidney injury or death was not significantly different between the cefepime group and the piperacillin-tazobactam group; there were 85 patients (n = 1214; 7.0%) in the cefepime group with stage 3 acute kidney injury and 92 (7.6%) who died vs 97 patients (n = 1297; 7.5%) in the piperacillin-tazobactam group with stage 3 acute kidney injury and 78 (6.0%) who died (odds ratio, 0.95 [95% CI, 0.80 to 1.13], P = .56). The incidence of major adverse kidney events at day 14 did not differ between groups (124 patients [10.2%] in the cefepime group vs 114 patients [8.8%] in the piperacillin-tazobactam group; absolute difference, 1.4% [95% CI, -1.0% to 3.8%]). Patients in the cefepime group experienced fewer days alive and free of delirium and coma within 14 days (mean [SD], 11.9 [4.6] days vs 12.2 [4.3] days in the piperacillin-tazobactam group; odds ratio, 0.79 [95% CI, 0.65 to 0.95]).
    Conclusions and relevance: Among hospitalized adults in this randomized clinical trial, treatment with piperacillin-tazobactam did not increase the incidence of acute kidney injury or death. Treatment with cefepime resulted in more neurological dysfunction.
    Trial registration: ClinicalTrials.gov Identifier: NCT05094154.
    MeSH term(s) Humans ; Adult ; Female ; Middle Aged ; Male ; Anti-Bacterial Agents/adverse effects ; Cefepime/adverse effects ; Coma ; Piperacillin/adverse effects ; Drug Therapy, Combination ; Retrospective Studies ; Piperacillin, Tazobactam Drug Combination/adverse effects ; Sepsis/complications ; Acute Kidney Injury/etiology ; Kidney ; Delirium
    Chemical Substances Anti-Bacterial Agents ; Cefepime (807PW4VQE3) ; Piperacillin (X00B0D5O0E) ; Piperacillin, Tazobactam Drug Combination (157044-21-8)
    Language English
    Publishing date 2023-10-13
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2958-0
    ISSN 1538-3598 ; 0254-9077 ; 0002-9955 ; 0098-7484
    ISSN (online) 1538-3598
    ISSN 0254-9077 ; 0002-9955 ; 0098-7484
    DOI 10.1001/jama.2023.20583
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Shotgun Kinetic Target-Guided Synthesis Approach Enables the Discovery of Small-Molecule Inhibitors against Pathogenic Free-Living Amoeba Glucokinases.

    Kassu, Mintesinot / Parvatkar, Prakash T / Milanes, Jillian / Monaghan, Neil P / Kim, Chungsik / Dowgiallo, Matthew / Zhao, Yingzhao / Asakawa, Ami H / Huang, Lili / Wagner, Alicia / Miller, Brandon / Carter, Karissa / Barrett, Kayleigh F / Tillery, Logan M / Barrett, Lynn K / Phan, Isabelle Q / Subramanian, Sandhya / Myler, Peter J / Van Voorhis, Wesley C /
    Leahy, James W / Rice, Christopher A / Kyle, Dennis E / Morris, James / Manetsch, Roman

    ACS infectious diseases

    2023  Volume 9, Issue 11, Page(s) 2190–2201

    Abstract: Pathogenic free-living amoebae (pFLA) can cause life-threatening central nervous system (CNS) infections and warrant the investigation of new chemical agents to combat the rise of infection from these pathogens. ...

    Abstract Pathogenic free-living amoebae (pFLA) can cause life-threatening central nervous system (CNS) infections and warrant the investigation of new chemical agents to combat the rise of infection from these pathogens.
    MeSH term(s) Humans ; Amoeba ; Glucokinase ; Naegleria fowleri ; Balamuthia mandrillaris ; Acanthamoeba castellanii
    Chemical Substances Glucokinase (EC 2.7.1.2)
    Language English
    Publishing date 2023-10-11
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ISSN 2373-8227
    ISSN (online) 2373-8227
    DOI 10.1021/acsinfecdis.3c00284
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Conservation of Ancient Genetic Pathways for Intracellular Persistence Among Animal Pathogenic Bordetellae.

    Rivera, Israel / Linz, Bodo / Dewan, Kalyan K / Ma, Longhuan / Rice, Christopher A / Kyle, Dennis E / Harvill, Eric T

    Frontiers in microbiology

    2019  Volume 10, Page(s) 2839

    Abstract: Animal and human pathogens of the ... ...

    Abstract Animal and human pathogens of the genus
    Language English
    Publishing date 2019-12-11
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2587354-4
    ISSN 1664-302X
    ISSN 1664-302X
    DOI 10.3389/fmicb.2019.02839
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: The transcriptome of Balamuthia mandrillaris trophozoites for structure-guided drug design.

    Phan, Isabelle Q / Rice, Christopher A / Craig, Justin / Noorai, Rooksana E / McDonald, Jacquelyn R / Subramanian, Sandhya / Tillery, Logan / Barrett, Lynn K / Shankar, Vijay / Morris, James C / Van Voorhis, Wesley C / Kyle, Dennis E / Myler, Peter J

    Scientific reports

    2021  Volume 11, Issue 1, Page(s) 21664

    Abstract: Balamuthia mandrillaris, a pathogenic free-living amoeba, causes cutaneous skin lesions as well as granulomatous amoebic encephalitis, a 'brain-eating' disease. As with the other known pathogenic free-living amoebas (Naegleria fowleri and Acanthamoeba ... ...

    Abstract Balamuthia mandrillaris, a pathogenic free-living amoeba, causes cutaneous skin lesions as well as granulomatous amoebic encephalitis, a 'brain-eating' disease. As with the other known pathogenic free-living amoebas (Naegleria fowleri and Acanthamoeba species), drug discovery efforts to combat Balamuthia infections of the central nervous system are sparse; few targets have been validated or characterized at the molecular level, and little is known about the biochemical pathways necessary for parasite survival. Current treatments of encephalitis due to B. mandrillaris lack efficacy, leading to case fatality rates above 90%. Using our recently published methodology to discover potential drugs against pathogenic amoebas, we screened a collection of 85 compounds with known antiparasitic activity and identified 59 compounds that impacted the growth of Balamuthia trophozoites at concentrations below 220 µM. Since there is no fully annotated genome or proteome of B. mandrillaris, we sequenced and assembled its transcriptome from a high-throughput RNA-sequencing (RNA-Seq) experiment and located the coding sequences of the genes potentially targeted by the growth inhibitors from our compound screens. We determined the sequence of 17 of these target genes and obtained expression clones for 15 that we validated by direct sequencing. These will be used in the future in combination with the identified hits in structure guided drug discovery campaigns to develop new approaches for the treatment of Balamuthia infections.
    MeSH term(s) Acanthamoeba/genetics ; Amebiasis/drug therapy ; Amoeba/genetics ; Balamuthia mandrillaris/drug effects ; Balamuthia mandrillaris/genetics ; Balamuthia mandrillaris/growth & development ; Base Sequence ; Brain/pathology ; Drug Design/methods ; Drug Discovery/methods ; Encephalitis/pathology ; Gene Expression/genetics ; Naegleria fowleri/genetics ; Transcriptome/genetics ; Trophozoites/drug effects ; Trophozoites/genetics
    Language English
    Publishing date 2021-11-04
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-021-99903-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Activity of doripenem versus comparators in subjects with baseline bacteraemia in six pooled phase 3 clinical trials.

    Rice, Dennis A K / Kaniga, Koné / Lee, Michael / Redman, Rebecca

    International journal of antimicrobial agents

    2013  Volume 41, Issue 4, Page(s) 388–392

    Abstract: An analysis of subjects with concurrent bacteraemia and either nosocomial pneumonia, complicated intra-abdominal infection or complicated urinary tract infection from six phase 3 clinical trials demonstrated similar cure rates and clearance of ... ...

    Abstract An analysis of subjects with concurrent bacteraemia and either nosocomial pneumonia, complicated intra-abdominal infection or complicated urinary tract infection from six phase 3 clinical trials demonstrated similar cure rates and clearance of bacteraemia in patients treated with doripenem and comparator agents.
    MeSH term(s) Anti-Bacterial Agents/therapeutic use ; Bacteremia/drug therapy ; Bacteremia/microbiology ; Carbapenems/therapeutic use ; Cross Infection/drug therapy ; Cross Infection/microbiology ; Female ; Humans ; Imipenem/therapeutic use ; Intraabdominal Infections/drug therapy ; Intraabdominal Infections/microbiology ; Male ; Ofloxacin/therapeutic use ; Pneumonia/drug therapy ; Pneumonia/microbiology ; Thienamycins/therapeutic use ; Treatment Outcome ; Urinary Tract Infections/drug therapy ; Urinary Tract Infections/microbiology
    Chemical Substances Anti-Bacterial Agents ; Carbapenems ; Thienamycins ; Imipenem (71OTZ9ZE0A) ; Ofloxacin (A4P49JAZ9H) ; doripenem (BHV525JOBH) ; meropenem (FV9J3JU8B1)
    Language English
    Publishing date 2013-04
    Publishing country Netherlands
    Document type Clinical Trial, Phase III ; Comparative Study ; Journal Article ; Multicenter Study ; Randomized Controlled Trial ; Research Support, Non-U.S. Gov't
    ZDB-ID 1093977-5
    ISSN 1872-7913 ; 0924-8579
    ISSN (online) 1872-7913
    ISSN 0924-8579
    DOI 10.1016/j.ijantimicag.2012.12.016
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The transcriptome of Balamuthia mandrillaris trophozoites for structure-guided drug design

    Isabelle Q. Phan / Christopher A. Rice / Justin Craig / Rooksana E. Noorai / Jacquelyn R. McDonald / Sandhya Subramanian / Logan Tillery / Lynn K. Barrett / Vijay Shankar / James C. Morris / Wesley C. Van Voorhis / Dennis E. Kyle / Peter J. Myler

    Scientific Reports, Vol 11, Iss 1, Pp 1-

    2021  Volume 13

    Abstract: Abstract Balamuthia mandrillaris, a pathogenic free-living amoeba, causes cutaneous skin lesions as well as granulomatous amoebic encephalitis, a ‘brain-eating’ disease. As with the other known pathogenic free-living amoebas (Naegleria fowleri and ... ...

    Abstract Abstract Balamuthia mandrillaris, a pathogenic free-living amoeba, causes cutaneous skin lesions as well as granulomatous amoebic encephalitis, a ‘brain-eating’ disease. As with the other known pathogenic free-living amoebas (Naegleria fowleri and Acanthamoeba species), drug discovery efforts to combat Balamuthia infections of the central nervous system are sparse; few targets have been validated or characterized at the molecular level, and little is known about the biochemical pathways necessary for parasite survival. Current treatments of encephalitis due to B. mandrillaris lack efficacy, leading to case fatality rates above 90%. Using our recently published methodology to discover potential drugs against pathogenic amoebas, we screened a collection of 85 compounds with known antiparasitic activity and identified 59 compounds that impacted the growth of Balamuthia trophozoites at concentrations below 220 µM. Since there is no fully annotated genome or proteome of B. mandrillaris, we sequenced and assembled its transcriptome from a high-throughput RNA-sequencing (RNA-Seq) experiment and located the coding sequences of the genes potentially targeted by the growth inhibitors from our compound screens. We determined the sequence of 17 of these target genes and obtained expression clones for 15 that we validated by direct sequencing. These will be used in the future in combination with the identified hits in structure guided drug discovery campaigns to develop new approaches for the treatment of Balamuthia infections.
    Keywords Medicine ; R ; Science ; Q
    Subject code 572
    Language English
    Publishing date 2021-11-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: Protocol and statistical analysis plan for the Antibiotic Choice On ReNal outcomes (ACORN) randomised clinical trial.

    Qian, Edward Tang / Casey, Jonathan D / Wright, Adam / Wang, Li / Siemann, Justin / Dear, Mary Lynn / Stollings, Joanna / Lloyd, Bradley Daniel / Seitz, Kevin / Nelson, George / Wright, Patty / Siew, Edward D / Dennis, Bradley / Wrenn, Jesse / Andereck, Jonathan / Self, Wesley H / Semler, Matthew W / Rice, Todd W

    BMJ open

    2023  Volume 13, Issue 3, Page(s) e066995

    Abstract: Introduction: Antibiotics are time-critical in the management of sepsis. When infectious organisms are unknown, patients are treated with empiric antibiotics to include coverage for gram-negative organisms, such as antipseudomonal cephalosporins and ... ...

    Abstract Introduction: Antibiotics are time-critical in the management of sepsis. When infectious organisms are unknown, patients are treated with empiric antibiotics to include coverage for gram-negative organisms, such as antipseudomonal cephalosporins and penicillins. However, in observational studies, some antipseudomonal cephalosporins (eg, cefepime) are associated with neurologic dysfunction while the most common antipseudomonal penicillin (piperacillin-tazobactam) is associated with acute kidney injury (AKI). No randomised control trials have compared these regimens. This manuscript describes the protocol and analysis plan for a trial designed to compare the effects of antipseudomonal cephalosporins and antipseudomonal penicillins among acutely ill patients receiving empiric antibiotics.
    Methods and analysis: The Antibiotic Choice On ReNal outcomes trial is a prospective, single-centre, non-blinded randomised trial being conducted at Vanderbilt University Medical Center. The trial will enrol 2500 acutely ill adults receiving gram-negative coverage for treatment of infection. Eligible patients are randomised 1:1 to receive cefepime or piperacillin-tazobactam on first order entry of a broad-spectrum antibiotic covering gram-negative organisms. The primary outcome is the highest stage of AKI and death occurring between enrolment and 14 days after enrolment. This will be compared between patients randomised to cefepime and randomised to piperacillin-tazobactam using an unadjusted proportional odds regression model. The secondary outcomes are major adverse kidney events through day 14 and number of days alive and free of delirium and coma in 14 days after enrolment. Enrolment began on 10 November 2021 and is expected to be completed in December 2022.
    Ethics and dissemination: The trial was approved by the Vanderbilt University Medical Center institutional review board (IRB#210591) with a waiver of informed consent. Results will be submitted to a peer-reviewed journal and presented at scientific conferences.
    Trial registration number: NCT05094154.
    MeSH term(s) Adult ; Humans ; Anti-Bacterial Agents/therapeutic use ; Cefepime/therapeutic use ; Prospective Studies ; Piperacillin/adverse effects ; Retrospective Studies ; Cephalosporins/therapeutic use ; Piperacillin, Tazobactam Drug Combination ; Kidney ; Acute Kidney Injury/chemically induced ; Penicillins ; Randomized Controlled Trials as Topic
    Chemical Substances Anti-Bacterial Agents ; Cefepime (807PW4VQE3) ; Piperacillin (X00B0D5O0E) ; Cephalosporins ; Piperacillin, Tazobactam Drug Combination (157044-21-8) ; Penicillins
    Language English
    Publishing date 2023-03-10
    Publishing country England
    Document type Clinical Trial Protocol ; Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2599832-8
    ISSN 2044-6055 ; 2044-6055
    ISSN (online) 2044-6055
    ISSN 2044-6055
    DOI 10.1136/bmjopen-2022-066995
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Endovascular thrombectomy versus standard bridging thrombolytic with endovascular thrombectomy within 4·5 h of stroke onset: an open-label, blinded-endpoint, randomised non-inferiority trial.

    Mitchell, Peter J / Yan, Bernard / Churilov, Leonid / Dowling, Richard J / Bush, Steven J / Bivard, Andrew / Huo, Xiao Chuan / Wang, Guoqing / Zhang, Shi Yong / Ton, Mai Duy / Cordato, Dennis J / Kleinig, Timothy J / Ma, Henry / Chandra, Ronil V / Brown, Helen / Campbell, Bruce C V / Cheung, Andrew K / Steinfort, Brendan / Scroop, Rebecca /
    Redmond, Kendal / Miteff, Ferdinand / Liu, Yan / Duc, Dang Phuc / Rice, Hal / Parsons, Mark W / Wu, Teddy Y / Nguyen, Huy-Thang / Donnan, Geoffrey A / Miao, Zhong Rong / Davis, Stephen M

    Lancet (London, England)

    2022  Volume 400, Issue 10346, Page(s) 116–125

    Abstract: Background: The benefit of combined treatment with intravenous thrombolysis before endovascular thrombectomy in patients with acute ischaemic stroke caused by large vessel occlusion remains unclear. We hypothesised that the clinical outcomes of patients ...

    Abstract Background: The benefit of combined treatment with intravenous thrombolysis before endovascular thrombectomy in patients with acute ischaemic stroke caused by large vessel occlusion remains unclear. We hypothesised that the clinical outcomes of patients with stroke with large vessel occlusion treated with direct endovascular thrombectomy within 4·5 h would be non-inferior compared with the outcomes of those treated with standard bridging therapy (intravenous thrombolysis before endovascular thrombectomy).
    Methods: DIRECT-SAFE was an international, multicentre, prospective, randomised, open-label, blinded-endpoint trial. Adult patients with stroke and large vessel occlusion in the intracranial internal carotid artery, middle cerebral artery (M1 or M2), or basilar artery, confirmed by non-contrast CT and vascular imaging, and who presented within 4·5 h of stroke onset were recruited from 25 acute-care hospitals in Australia, New Zealand, China, and Vietnam. Eligible patients were randomly assigned (1:1) via a web-based, computer-generated randomisation procedure stratified by site of baseline arterial occlusion and by geographic region to direct endovascular thrombectomy or bridging therapy. Patients assigned to bridging therapy received intravenous thrombolytic (alteplase or tenecteplase) as per standard care at each site; endovascular thrombectomy was also per standard of care, using the Trevo device (Stryker Neurovascular, Fremont, CA, USA) as first-line intervention. Personnel assessing outcomes were masked to group allocation; patients and treating physicians were not. The primary efficacy endpoint was functional independence defined as modified Rankin Scale score 0-2 or return to baseline at 90 days, with a non-inferiority margin of -0·1, analysed by intention to treat (including all randomly assigned and consenting patients) and per protocol. The intention-to-treat population was included in the safety analyses. The trial is registered with ClinicalTrials.gov, NCT03494920, and is closed to new participants.
    Findings: Between June 2, 2018, and July 8, 2021, 295 patients were randomly assigned to direct endovascular thrombectomy (n=148) or bridging therapy (n=147). Functional independence occurred in 80 (55%) of 146 patients in the direct thrombectomy group and 89 (61%) of 147 patients in the bridging therapy group (intention-to-treat risk difference -0·051, two-sided 95% CI -0·160 to 0·059; per-protocol risk difference -0·062, two-sided 95% CI -0·173 to 0·049). Safety outcomes were similar between groups, with symptomatic intracerebral haemorrhage occurring in two (1%) of 146 patients in the direct group and one (1%) of 147 patients in the bridging group (adjusted odds ratio 1·70, 95% CI 0·22-13·04) and death in 22 (15%) of 146 patients in the direct group and 24 (16%) of 147 patients in the bridging group (adjusted odds ratio 0·92, 95% CI 0·46-1·84).
    Interpretation: We did not show non-inferiority of direct endovascular thrombectomy compared with bridging therapy. The additional information from our study should inform guidelines to recommend bridging therapy as standard treatment.
    Funding: Australian National Health and Medical Research Council and Stryker USA.
    MeSH term(s) Adult ; Australia ; Brain Ischemia/drug therapy ; Endovascular Procedures/methods ; Fibrinolytic Agents/adverse effects ; Humans ; Prospective Studies ; Stroke/drug therapy ; Stroke/surgery ; Thrombectomy/methods ; Treatment Outcome
    Chemical Substances Fibrinolytic Agents
    Language English
    Publishing date 2022-07-04
    Publishing country England
    Document type Equivalence Trial ; Journal Article ; Randomized Controlled Trial
    ZDB-ID 3306-6
    ISSN 1474-547X ; 0023-7507 ; 0140-6736
    ISSN (online) 1474-547X
    ISSN 0023-7507 ; 0140-6736
    DOI 10.1016/S0140-6736(22)00564-5
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  9. Article: Activity of doripenem versus comparators in subjects with baseline bacteraemia in six pooled phase 3 clinical trials

    Rice, Dennis A.K / Kaniga, Koné / Lee, Michael / Redman, Rebecca

    International journal of antimicrobial agents. 2013 Apr., v. 41, no. 4

    2013  

    Abstract: An analysis of subjects with concurrent bacteraemia and either nosocomial pneumonia, complicated intra-abdominal infection or complicated urinary tract infection from six phase 3 clinical trials demonstrated similar cure rates and clearance of ... ...

    Abstract An analysis of subjects with concurrent bacteraemia and either nosocomial pneumonia, complicated intra-abdominal infection or complicated urinary tract infection from six phase 3 clinical trials demonstrated similar cure rates and clearance of bacteraemia in patients treated with doripenem and comparator agents.
    Keywords anti-infective agents ; bacteremia ; clinical trials ; patients ; pneumonia ; urinary tract diseases
    Language English
    Dates of publication 2013-04
    Size p. 388-392.
    Publishing place Elsevier B.V.
    Document type Article
    ZDB-ID 1093977-5
    ISSN 0924-8579
    ISSN 0924-8579
    DOI 10.1016/j.ijantimicag.2012.12.016
    Database NAL-Catalogue (AGRICOLA)

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  10. Article: Practice Recommendations for Transcranial Doppler Ultrasonography in Critically Ill Children in the Pediatric Intensive Care Unit: A Multidisciplinary Expert Consensus Statement.

    O'Brien, Nicole Fortier / Reuter-Rice, Karin / Wainwright, Mark S / Kaplan, Summer L / Appavu, Brian / Erklauer, Jennifer C / Ghosh, Suman / Kirschen, Matthew / Kozak, Brandi / Lidsky, Karen / Lovett, Marlina Elizabeth / Mehollin-Ray, Amy R / Miles, Darryl K / Press, Craig A / Simon, Dennis W / Tasker, Robert C / LaRovere, Kerri Lynn

    Journal of pediatric intensive care

    2020  Volume 10, Issue 2, Page(s) 133–142

    Abstract: Transcranial Doppler ultrasonography (TCD) is being used in many pediatric intensive care units (PICUs) to aid in the diagnosis and monitoring of children with known or suspected pathophysiological changes to cerebral hemodynamics. Standardized ... ...

    Abstract Transcranial Doppler ultrasonography (TCD) is being used in many pediatric intensive care units (PICUs) to aid in the diagnosis and monitoring of children with known or suspected pathophysiological changes to cerebral hemodynamics. Standardized approaches to scanning protocols, interpretation, and documentation of TCD examinations in this setting are lacking. A panel of multidisciplinary clinicians with expertise in the use of TCD in the PICU undertook a three-round modified Delphi process to reach unanimous agreement on 34 statements and then create practice recommendations for TCD use in the PICU. Use of these recommendations will help to ensure that high quality TCD images are captured, interpreted, and reported using standard nomenclature. Furthermore, use will aid in ensuring reproducible and meaningful study results between TCD practitioners and across PICUs.
    Language English
    Publishing date 2020-09-04
    Publishing country Germany
    Document type Journal Article
    ISSN 2146-4618
    ISSN 2146-4618
    DOI 10.1055/s-0040-1715128
    Database MEDical Literature Analysis and Retrieval System OnLINE

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