Evidence map›Paper›PMID 25888496›Full record

ArticleCritical care (London, England)2015

A pilot study of change in fracture risk in patients with acute respiratory distress syndrome.

Jaikitry Rawal, Mark J W McPhail, Gamumu Ratnayake, Pearl Chan, John Moxham, Stephen D R Harridge, Nicholas Hart, Hugh E Montgomery, Zudin A Puthucheary

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Critical care (London, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01106300 (Assessment of Peripheral Muscle and Bone Mass in the Critically Ill and Its Response to External Muscle Stimulation), which is not on this map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01106300 completednot on this map

Assessment of Peripheral Muscle and Bone Mass in the Critically Ill and Its Response to External Muscle Stimulation

TypeobservationalSponsorUniversity College, LondonRan2009 to 2015Enrolled63ConditionsCritical Illness, Septic Shock, Trauma, Organ Failure
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 23 citations in OpenAlex.

  1. Trial
  2. Protocol summary and statistical analysis plan for the bone loss prevention with zoledronic acid or denosumab in critically ill adults (BONE ZONE) trial.Critical care and resuscitation : journal of the Australasian Academy of Critical Care Medicine · 2026
    Article
  3. Identifying risk factors for systemic complications following fracture-related infection.European journal of orthopaedic surgery & traumatology : orthopedie traumatologie · 2025
    Article
  4. Article
  5. Risks of incident major osteoporotic fractures following SARS-CoV-2 infection among older individuals: a population-based cohort study in Hong Kong.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Article
  6. Observational
  7. Bone - a casualty of ICU survival?Critical care (London, England) · 2015
    Article
  8. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 2 countries.

Jaikitry RawalInstitute of Health and Human Performance, University College London, Room 443, 74 Huntley Street, London, WC1E 6AU, UK. jrawal@mac.com.
Mark J W McPhailDepartment of Hepatology and Gastroenterology, St Mary's Hospital, Imperial College London, praed street, London, W2 1NY, UK. mark.mcphail@csc.mrc.ac.uk.
Gamumu RatnayakeNIHR Comprehensive Biomedical Research Centre, Guy's and St Thomas' NHS Foundation Trust and King's College London, Westminster Bridge Road, London, SE17EH, UK. rgamrat@googlemail.com.
Pearl ChanInstitute of Health and Human Performance, University College London, Room 443, 74 Huntley Street, London, WC1E 6AU, UK. pearlchan@doctors.org.uk.
John MoxhamKing's College London School of Medicine, denmark hill, London, SE59RS, UK. john.moxham@nhs.net.
Stephen D R HarridgeCentre of Human and Aerospace Physiological Sciences, King's College London, Great Maze Pond, London, SE1 9RT, UK. s.harridge@kcl.ac.uk.
Nicholas HartNIHR Comprehensive Biomedical Research Centre, Guy's and St Thomas' NHS Foundation Trust and King's College London, Westminster Bridge Road, London, SE17EH, UK. Nicholas.hart@gstt.nhs.uk.
Hugh E MontgomeryInstitute of Health and Human Performance, University College London, Room 443, 74 Huntley Street, London, WC1E 6AU, UK. h.montgomery@ucl.ac.uk.
Zudin A PuthuchearyInstitute of Health and Human Performance, University College London, Room 443, 74 Huntley Street, London, WC1E 6AU, UK. Zudin_amilka_puthucheary@nuhs.edu.sg.
King's College London · GBUniversity College London · GBGuy's and St Thomas' NHS Foundation Trust · GBNational University Hospital · SGSt Mary's Hospital · GB

Funding

Department of Health DRF-2010-03-114Wellcome Trust
6 · The paper itself

Abstract

introductionAcute skeletal muscle wasting is a major contributor to post critical illness physical impairment. However, the bone response remains uncharacterized. We prospectively investigated the early changes in bone mineral density (BMD) and fracture risk in critical illness.

methodsPatients were prospectively recruited ≤24 hours following intensive care unit (ICU) admission to a university teaching or a community hospital (August 2009 to April 2011). All were aged >18 years and expected to be intubated for >48 hours, spend >7 days in critical care and survive ICU admission. Forty-six patients were studied (55.3% male), with a mean age of 54.4 years (95% confidence interval (CI): 49.1 to 59.6) and an APACHE II score of 23.9 (95% CI: 22.4 to 25.5). Calcaneal dual X-ray absorptiometry (DXA) assessment of BMD was performed on day 1 and 10. Increase in fracture risk was calculated from the change in T-score.

resultsBMD did not change between day 1 and 10 in the cohort overall (0.434 (95% CI: 0.405 to 0.463) versus 0.425 g/cm(2) (95% CI: 0.399 to 0.450), P = 0.58). Multivariable logistical regression revealed admission corrected calcium (odds ratio (OR): 1.980 (95% CI: 1.089 to 3.609), P = 0.026) and admission PaO2-to-FiO2 ratio (OR: 0.916 (95% CI: 0.833 to 0.998), P = 0.044) to be associated with >2% loss of BMD. Patients with acute respiratory distress syndrome had a greater loss in BMD than those without (-2.81% (95% CI: -5.73 to 0.118%), n = 34 versus 2.40% (95% CI: 0.204 to 4.586%), n = 12, P = 0.029). In the 34 patients with acute respiratory distress syndrome, fracture risk increased by 19.4% (95% CI: 13.9 to 25.0%).

conclusionsPatients with acute respiratory distress syndrome demonstrated early and rapid bone demineralisation with associated increase in fracture risk.

Indexed as

Absorptiometry, PhotonAdultAgedBone Demineralization, PathologicBone DensityCalcaneusCalciumFemaleFractures, BoneHumansIntensive Care UnitsMaleMiddle AgedPilot ProjectsProspective StudiesRespiration, ArtificialCalciumSerum Albumin

Identifiers

PMID25888496
PMCPMC4411936
OpenAlexW2033682858

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.