LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 8 of total 8

Search options

  1. Article: Mismatch of populations between randomised controlled trials of perioperative interventions in major abdominal surgery and current clinical practice.

    Ridgeon, Elliott / Shadwell, Rory / Wilkinson, Alice / Odor, Peter M

    Perioperative medicine (London, England)

    2023  Volume 12, Issue 1, Page(s) 60

    Abstract: ... to reflect the reality of clinical practice (i.e. patients treated by a clinician in their own hospital ...

    Abstract Background: Demographics of patients undergoing major abdominal surgery are changing. External validity of relevant RCTs may be limited by participants not resembling patients encountered in clinical practice. We aimed to characterise differences in age, weight, BMI, and ASA grade between participants in perioperative trials in major abdominal surgery and patients in a reference real-world clinical practice sample. The secondary aim was to investigate whether time since trial publication was associated with increasing mismatch between these groups.
    Methods: MEDLINE and Embase were searched for multicentre RCTs from inception to September 2022. Studies of perioperative interventions in adults were included. Studies that limited enrolment based on age, weight, BMI, or ASA status were excluded. We compared trial cohort age, weight, BMI, and ASA distribution to those of patients undergoing major abdominal surgery at our tertiary referral hospital during September 2021 to September 2022. We used a local, single-institution reference sample to reflect the reality of clinical practice (i.e. patients treated by a clinician in their own hospital, rather than averaged nationally). Mismatch was defined using comparison of summary characteristics and ad hoc criteria based on differences relevant to predicted mortality risk after surgery.
    Results: One-hundred and six trials (44,499 participants) were compared to a reference cohort of 2792 clinical practice patients. Trials were published a median (IQR [range]) 13.4 (5-20 [0-35]) years ago. A total of 94.3% of trials were mismatched on at least one characteristic (age, weight, BMI, ASA). Recruitment of ASA 3 + participants in trials increased over time, and recruitment of ASA 1 participants decreased over time (Spearman's Rho 0.58 and - 0.44, respectively).
    Conclusions: Patients encountered in our current local clinical practice are significantly different from those in our defined set of perioperative RCTs. Older trials recruit more low-risk than high-risk participants-trials may thus 'expire' over time. These trials may not be generalisable to current patients undergoing major abdominal surgery, and meta-analyses or guidelines incorporating these trials may therefore be similarly non-applicable. Comparison to local, rather than national cohorts, is important for meaningful on-the-ground evidence-based decision-making.
    Language English
    Publishing date 2023-11-16
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 2683800-X
    ISSN 2047-0525
    ISSN 2047-0525
    DOI 10.1186/s13741-023-00344-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: The authors reply.

    Ridgeon, Elliott E / Young, Paul J / Bellomo, Rinaldo / Mucchetti, Marta / Lembo, Rosalba / Landoni, Giovanni

    Critical care medicine

    2016  Volume 44, Issue 11, Page(s) e1143

    Language English
    Publishing date 2016
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 197890-1
    ISSN 1530-0293 ; 0090-3493
    ISSN (online) 1530-0293
    ISSN 0090-3493
    DOI 10.1097/CCM.0000000000002045
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: The Fragility Index in Multicenter Randomized Controlled Critical Care Trials.

    Ridgeon, Elliott E / Young, Paul J / Bellomo, Rinaldo / Mucchetti, Marta / Lembo, Rosalba / Landoni, Giovanni

    Critical care medicine

    2016  Volume 44, Issue 7, Page(s) 1278–1284

    Abstract: Objectives: Recent literature has drawn attention to the potential inadequacy of frequentist analysis and threshold p values as tools for reporting outcomes in clinical trials. The fragility index, which is a measure of how many events the statistical ... ...

    Abstract Objectives: Recent literature has drawn attention to the potential inadequacy of frequentist analysis and threshold p values as tools for reporting outcomes in clinical trials. The fragility index, which is a measure of how many events the statistical significance of a result depends on, has been suggested as a means to aid the interpretation of trial results. This study aimed to calculate the fragility index of clinical trials in critical care medicine reporting a statistically significant effect on mortality (increasing or decreasing mortality).
    Data sources: Literature search (PubMed/MEDLINE) to identify all multicenter randomized controlled trials in critical care medicine.
    Study selection: We identified 862 trials; of which 56 fulfilled eligibility criteria and were included in our analysis.
    Data extraction: Calculation of fragility index for trials reporting a statistically significant effect on mortality, and analysis of the relationship between trial characteristics and fragility index.
    Data synthesis: The median fragility index was 2 (interquartile range, 1-3.5), and greater than 40% of trials had a fragility index of less than or equal to 1. 12.5% of trials reported loss to follow-up greater than their fragility index. Trial sample size was positively correlated, and reported p value was negatively correlated, with fragility index.
    Conclusions: In critical care trials reporting statistically significant effects on mortality, the findings often depend on a small number of events. Critical care clinicians should be wary of basing decisions on trials with a low fragility index. We advocate the reporting of fragility index for future trials in critical care to aid interpretation and decision making by clinicians.
    MeSH term(s) Critical Care/statistics & numerical data ; Data Interpretation, Statistical ; Humans ; Mortality ; Multicenter Studies as Topic ; Randomized Controlled Trials as Topic
    Language English
    Publishing date 2016-07
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 197890-1
    ISSN 1530-0293 ; 0090-3493
    ISSN (online) 1530-0293
    ISSN 0090-3493
    DOI 10.1097/CCM.0000000000001670
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Article ; Online: Effect sizes in ongoing randomized controlled critical care trials.

    Ridgeon, Elliott E / Bellomo, Rinaldo / Aberegg, Scott K / Sweeney, Rob Mac / Varughese, Rachel S / Landoni, Giovanni / Young, Paul J

    Critical care (London, England)

    2017  Volume 21, Issue 1, Page(s) 132

    Abstract: Background: An important limitation of many critical care trial designs is that they hypothesize large, and potentially implausible, reductions in mortality. Interpretation of trial results could be improved by systematic assessment of the plausibility ... ...

    Abstract Background: An important limitation of many critical care trial designs is that they hypothesize large, and potentially implausible, reductions in mortality. Interpretation of trial results could be improved by systematic assessment of the plausibility of trial hypotheses; however, such assessment has not been attempted in the field of critical care medicine. The purpose of this study was to determine clinicians' views about prior probabilities and plausible effect sizes for ongoing critical care trials where the primary endpoint is landmark mortality.
    Methods: We conducted a systematic review of clinical trial registries in September 2015 to identify ongoing critical care medicine trials where landmark mortality was the primary outcome, followed by a clinician survey to obtain opinions about ten large trials. Clinicians were asked to estimate the probability that each trial would demonstrate a mortality effect equal to or larger than that used in its sample size calculations.
    Results: Estimates provided by individual clinicians varied from 0% to 100% for most trials, with a median estimate of 15% (IQR 10-20%). The median largest absolute mortality reduction considered plausible was 4.5% (IQR 3.5-5%), compared with a median absolute mortality reduction used in sample size calculations of 5% (IQR 3.6-10%) (P = 0.27).
    Conclusions: For some of the largest ongoing critical care trials, many clinicians regard prior probabilities as low and consider that plausible effects on absolute mortality are less than 5%. Further work is needed to determine whether pooled estimates obtained by surveying clinicians are replicable and accurate or whether other methods of estimating prior probability are preferred.
    MeSH term(s) Critical Care Outcomes ; Hospital Mortality ; Humans ; Patient Selection ; Randomized Controlled Trials as Topic/methods ; Registries/statistics & numerical data ; Research Design/standards ; Statistics, Nonparametric ; Surveys and Questionnaires
    Language English
    Publishing date 2017-06-05
    Publishing country England
    Document type Journal Article ; Review
    ZDB-ID 2051256-9
    ISSN 1466-609X ; 1466-609X
    ISSN (online) 1466-609X
    ISSN 1466-609X
    DOI 10.1186/s13054-017-1726-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article ; Online: Routine radiographs one day after anterior cervical discectomy and fusion are neither necessary nor cost-effective.

    Martin, Sean C / Dabbous, Bassam O / Ridgeon, Elliott E / Magdum, Shailendra A / Cadoux-Hudson, Thomas A D / Pereira, Erlick A C

    British journal of neurosurgery

    2017  Volume 31, Issue 1, Page(s) 50–53

    Abstract: Objectives: Anterior cervical discectomy and fusion (ACDF) is a common operative treatment of compressive pathology of the cervical spinal cord, when caused by one or more degenerated intervertebral discs or related osteophytes. In addition to intra- ... ...

    Abstract Objectives: Anterior cervical discectomy and fusion (ACDF) is a common operative treatment of compressive pathology of the cervical spinal cord, when caused by one or more degenerated intervertebral discs or related osteophytes. In addition to intra-operative radiographs to confirm spinal level before discectomy and implant position after insertion, traditional practice is to obtain post-operative antero-posterior and lateral plain radiographs (XR) before hospital discharge, despite a paucity of evidence supporting their benefit to patient care. Minimising unnecessary radiation to radiosensitive neck structures is desirable, and furthermore, with increasing financial pressure on healthcare resources, routine investigations should be clinically justified and evidence-based. We aim to compare the utility of routine post-operative cervical spine X-rays following ACDF.
    Methods: We compare two groups of consecutive patients undergoing ACDF in a single UK neurosurgical centre. The first group (n = 109) received routine post-operative XR imaging, and the second group (n = 113) received radiographs only when clinically indicated.
    Results: There were no differences in post-operative complication rates (4.6% vs. 5.3%), or requirement for further imaging or of further operative intervention (1.8% vs. 0.9%). The group that did not have routine post-operative radiographs had a significantly shorter stay in hospital (median two days vs. three days). There were no patients in either group where post-operative XR changed clinical management and mandated revision surgery or further imaging. All cases requiring surgery or further imaging were identified by clinical deterioration.
    Conclusions: We suggest that the practice of obtaining routine radiographs of the cervical spine following ACDF should be abandoned, unless there is a clear clinical indication.
    MeSH term(s) Cervical Vertebrae/diagnostic imaging ; Cervical Vertebrae/surgery ; Cost-Benefit Analysis ; Diskectomy/adverse effects ; Diskectomy/economics ; Diskectomy/methods ; Female ; Health Care Costs ; Humans ; Length of Stay ; Male ; Middle Aged ; Neurosurgery/economics ; Neurosurgery/statistics & numerical data ; Postoperative Care/economics ; Postoperative Care/methods ; Postoperative Complications/epidemiology ; Reoperation/statistics & numerical data ; Retrospective Studies ; Spine/diagnostic imaging ; Treatment Outcome ; United Kingdom ; X-Rays
    Language English
    Publishing date 2017-02
    Publishing country England
    Document type Journal Article
    ZDB-ID 639029-8
    ISSN 1360-046X ; 0268-8697
    ISSN (online) 1360-046X
    ISSN 0268-8697
    DOI 10.1080/02688697.2016.1233320
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article ; Online: A comparison of therapeutic hypothermia and strict therapeutic normothermia after cardiac arrest.

    Casamento, Andrew / Minson, Adrian / Radford, Samuel / Mårtensson, Johan / Ridgeon, Elliott / Young, Paul / Bellomo, Rinaldo

    Resuscitation

    2016  Volume 106, Page(s) 83–88

    Abstract: Background and aims: In a recent high-quality randomised controlled trial (RCT), strict therapeutic normothermia (STN) following cardiac arrest with coma resulted in similar outcomes to therapeutic hypothermia (TH). We aimed to test the feasibility, ... ...

    Abstract Background and aims: In a recent high-quality randomised controlled trial (RCT), strict therapeutic normothermia (STN) following cardiac arrest with coma resulted in similar outcomes to therapeutic hypothermia (TH). We aimed to test the feasibility, reproducibility, and safety of the STN protocol outside of its RCT context.
    Methods: In two teaching hospital ICUs, we performed a before-and-after study comparing the previously International Liaison Committee on Resuscitation (ILCOR)-endorsed TH protocol to the recently studied STN protocol. The primary feasibility end point was the percentage of temperature recordings in the prescribed range in the first 24h of treatment. Secondary end points included pharmacological management and complications.
    Results: We studied 69 similar patients in each group. We found no difference in feasibility as shown by the proportion of within range temperatures. However, the median doses of midazolam (37mg vs. 9mg, p=0.02), fentanyl (883μg vs. 310μg, p=0.01) and the use of muscle relaxants (84.1% vs. 59.4%, p=0.001) was greater with the TH protocol. Furthermore, shivering (52.2% vs. 18.8%, p<0.001), a composite of other pre-defined complications (66.7% vs. 47.8%, p<0.03) and fever in the first 96h (55.1% vs. 33.3%, p=0.01) were also more common with the TH protocol.
    Conclusions: The STN protocol was successfully reproduced outside of an RCT and appeared associated with fewer complications than the TH protocol. Our findings imply that the STN protocol may offer clinical advantages over the TH protocol.
    MeSH term(s) APACHE ; Aged ; Analgesics/therapeutic use ; Body Temperature ; Coma/therapy ; Controlled Before-After Studies ; Female ; Heart Arrest/complications ; Heart Arrest/therapy ; Humans ; Hypnotics and Sedatives/therapeutic use ; Hypothermia, Induced/adverse effects ; Intensive Care Units ; Length of Stay ; Male ; Middle Aged ; Muscle Relaxants, Central/therapeutic use ; Reproducibility of Results ; Retrospective Studies
    Chemical Substances Analgesics ; Hypnotics and Sedatives ; Muscle Relaxants, Central
    Language English
    Publishing date 2016-09
    Publishing country Ireland
    Document type Comparative Study ; Journal Article ; Multicenter Study
    ZDB-ID 189901-6
    ISSN 1873-1570 ; 0300-9572
    ISSN (online) 1873-1570
    ISSN 0300-9572
    DOI 10.1016/j.resuscitation.2016.06.019
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  7. Article ; Online: A rapidly enlarging swelling of the left orbit.

    Varughese, Rachel S / Ridgeon, Elliott / Mathew, Anna / Sola-Del Valle, David

    BMJ (Clinical research ed.)

    2015  Volume 350, Page(s) h799

    MeSH term(s) Adolescent ; Female ; Humans ; Orbital Neoplasms/diagnosis ; Rhabdomyosarcoma, Embryonal/diagnosis
    Language English
    Publishing date 2015-02-25
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 1362901-3
    ISSN 1756-1833 ; 0959-8154 ; 0959-8146 ; 0959-8138 ; 0959-535X ; 1759-2151
    ISSN (online) 1756-1833
    ISSN 0959-8154 ; 0959-8146 ; 0959-8138 ; 0959-535X ; 1759-2151
    DOI 10.1136/bmj.h799
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  8. Article: Validation of a classification system for causes of death in critical care: an assessment of inter-rater reliability.

    Ridgeon, Elliott / Bellomo, Rinaldo / Myburgh, John / Saxena, Manoj / Weatherall, Mark / Jahan, Rahi / Arawwawala, Dilshan / Bell, Stephanie / Butt, Warwick / Camsooksai, Julie / Carle, Coralie / Cheng, Andrew / Cirstea, Emanuel / Cohen, Jeremy / Cranshaw, Julius / Delaney, Anthony / Eastwood, Glenn / Eliott, Suzanne / Franke, Uwe /
    Gantner, Dashiell / Green, Cameron / Howard-Griffin, Richard / Inskip, Deborah / Litton, Edward / MacIsaac, Christopher / McCairn, Amanda / Mahambrey, Tushar / Moondi, Parvez / Newby, Lynette / O'Connor, Stephanie / Pegg, Claire / Pope, Alan / Reschreiter, Henrik / Richards, Brent / Robertson, Megan / Rodgers, Helen / Shehabi, Yahya / Smith, Ian / Smith, Julie / Smith, Neil / Tilsley, Anna / Whitehead, Christina / Willett, Emma / Wong, Katherine / Woodford, Claudia / Wright, Stephen / Young, Paul

    Critical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine

    2016  Volume 18, Issue 1, Page(s) 50–54

    Abstract: Objective: Trials in critical care have previously used unvalidated systems to classify cause of death. We aimed to provide initial validation of a method to classify cause of death in intensive care unit patients.: Design, setting and participants: ... ...

    Abstract Objective: Trials in critical care have previously used unvalidated systems to classify cause of death. We aimed to provide initial validation of a method to classify cause of death in intensive care unit patients.
    Design, setting and participants: One hundred case scenarios of patients who died in an ICU were presented online to raters, who were asked to select a proximate and an underlying cause of death for each, using the ICU Deaths Classification and Reason (ICU-DECLARE) system. We evaluated two methods of categorising proximate cause of death (designated Lists A and B) and one method of categorising underlying cause of death. Raters were ICU specialists and research coordinators from Australia, New Zealand and the United Kingdom.
    Main outcome measures: Inter-rater reliability, as measured by the Fleiss multirater kappa, and the median proportion of raters choosing the most likely diagnosis (defined as the most popular classification choice in each case).
    Results: Across all raters and cases, for proximate cause of death List A, kappa was 0.54 (95% CI, 0.49-0.60), and for proximate cause of death List B, kappa was 0.58 (95% CI, 0.53-0.63). For the underlying cause of death, kappa was 0.48 (95% CI, 0.44-0.53). The median proportion of raters choosing the most likely diagnosis for proximate cause of death, List A, was 77.5% (interquartile range [IQR], 60.0%-93.8%), and the median proportion choosing the most likely diagnosis for proximate cause of death, List B, was 82.5% (IQR, 60.0%-92.5%). The median proportion choosing the most likely diagnosis for underlying cause was 65.0% (IQR, 50.0%-81.3%). Kappa and median agreement were similar between countries. ICU specialists showed higher kappa and median agreement than research coordinators.
    Conclusions: The ICU-DECLARE system allowed ICU doctors to classify the proximate cause of death of patients who died in the ICU with substantial reliability.
    MeSH term(s) Australia ; Cause of Death ; Critical Care ; Humans ; New Zealand ; Reproducibility of Results ; United Kingdom
    Language English
    Publishing date 2016-03
    Publishing country Australia
    Document type Journal Article ; Validation Studies
    ZDB-ID 2401976-8
    ISSN 1441-2772
    ISSN 1441-2772
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top