Evidence map›Paper›PMID 42331585›Full record

ArticleBMJ open2026

Preoperative Risk Evaluation for Cancer Treatment (PREdiCT): protocol for an international cohort study evaluating a trimodal screening tool to predict outcomes following gastrointestinal cancer surgery.

Jack Reeves, Cherry Koh, Kate Alexander, Michael Solomon, Sascha Karunaratne, Alexandria Petridis, Sharon Carey, Haryana Dhillon, Kate White, Neil Pillinger and 44 more

Abstract readMulticenter Study
In one paragraph

Article in BMJ open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

54 authors.

Jack ReevesSurgical Outcomes Research Centre (SOuRCe), Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.ORCID http://orcid.org/0009-0009-2851-5501
Cherry KohSurgical Outcomes Research Centre (SOuRCe), Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Kate AlexanderSurgical Outcomes Research Centre (SOuRCe), Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.ORCID http://orcid.org/0000-0002-7163-097X
Michael SolomonSurgical Outcomes Research Centre (SOuRCe), Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Sascha KarunaratneSurgical Outcomes Research Centre (SOuRCe), Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.ORCID http://orcid.org/0000-0001-7518-0307
Alexandria PetridisSurgical Outcomes Research Centre (SOuRCe), Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Sharon CareySurgical Outcomes Research Centre (SOuRCe), Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Haryana DhillonSchool of Psychology, Centre for Medical Psychology & Evidence-Based Decision Making, The University of Sydney Faculty of Science, Sydney, New South Wales, Australia.ORCID http://orcid.org/0000-0003-4039-5169
Kate WhiteSurgical Outcomes Research Centre (SOuRCe), Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.ORCID http://orcid.org/0000-0003-4763-1734
Neil PillingerCentral Clinical School, The University of Sydney Faculty of Medicine and Health, Sydney, New South Wales, Australia.
Chelsia GillisSchool of Human Nutrition, McGill University, Montreal, Québec, Canada.
Nicholas HirstSurgical Outcomes Research Centre (SOuRCe), Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Zaid ShadidSurgical Outcomes Research Centre (SOuRCe), Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Md Ishraque RahmanSurgical Outcomes Research Centre (SOuRCe), Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Ianthe BodenPhysiotherapy Department, Launceston General Hospital, Launceston, Tasmania, Australia.ORCID http://orcid.org/0000-0002-9283-4779
Alison MahoneyPhysiotherapy Department, The Prince Charles Hospital, Brisbane, Queensland, Australia.
John WoodfieldDepartment of Surgery and Critical Care, Dunedin Hospital, Dunedin, Otago, New Zealand.
Daniel VaggGeneral Surgical Department, Nepean Hospital, Penrith, New South Wales, Australia.
Hans D De BoerDepartment of Anesthesiology Pain Medicine and Procedural Sedation and Analgesia, Martin General Hospital, Groningen, The Netherlands.
Paul SuttonColorectal and Peritoneal Oncology Centre, The Christie NHS Foundation Trust, Manchester, UK.
Leani PereiraPostgraduate Program in Health Sciences, Faculdade de Ciências Médicas de Minas Gerais, Belo Horizonte, Brazil.
Ana Paula Drummond-LagePostgraduate Program in Health Sciences, Faculdade de Ciências Médicas de Minas Gerais, Belo Horizonte, Brazil.
Santiago McloughlinAnaesthesia Department, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
Adrian AlvarezAnaesthesia Department, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
Katrina PirieDepartment of Anaesthesiology and Perioperative Medicine, Alfred Hospital, Melbourne, Victoria, Australia.
Michael W HiiHepatobiliary and Upper Gastrointestinal Unit, St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
Alsadig SulimanSudan Medical Specialisation Board, Department of General Surgery, Al-Waleedeen Specialised Hospital, Gezira State, Sudan.
Burak UçanerDepartment of General Surgery, University of Health Sciences Gülhane Training and Research Hospital, Ankara, Turkey.
Dimitrios SchizasFirst Department of Surgery, National and Kapodistrian University of Athens, Laikon General Hospital, Athens, Greece.ORCID http://orcid.org/0000-0002-7046-0112
Kyrillos NassimIntensive Care Medicine Department, Nasser Institute Hospital for Research and Treatment, Cairo, Egypt.
Raga'a AlbatoolDepartment of General Surgery, Al Jumhuri Hospital, Sana'a, Yemen.
Khloud AliDepartment of Surgery, Althawra Hospital, Sana'a, Yemen.
Tania TriantafyllouDepartment of Propaedeutic Surgery, Hippocrateio Hospital of Athens, Athens, Greece.
Apostolaki StylianaDepartment of Anesthesiology, General Hospital Saint George, Chania, Greece.
Ilenia MerliniGeneral Surgery Unit, Madonna del Soccorso Hospital, San Benedetto del Tronto, Italy.
Elke Van DaeleDepartment of Gastrointestinal Surgery, University Hospital Ghent, Ghent, Belgium.
Francesk MulitaDepartment of General Surgery, General Hospital of Eastern Achaia, Agio, Greece.
Max BellPerioperative Medicine and Intensive Care Medicine, Karolinska University Hospital, Stockholm, Sweden.
Graciela Martinez-PalliDepartment of Anesthesiology, Hospital Clinic de Barcelona, Barcelona, Spain.ORCID http://orcid.org/0000-0002-7163-8090
Christian KochDepartment of Anesthesiology, Intensive Care Medicine and Pain Therapy, Justus Liebig University Giessen, Giessen, Germany.
Massimo FalconiDivision of Pancreatic and Transplant Surgery, San Raffaele Hospital, Milan, Italy.
Tatiana GarmanovaFaculty of Medicine, Lomonosov Moscow State University, Moscow, Russian Federation.
Niantao DengRoyal Prince Alfred Hospital, Sydney Local Health District, Camperdown, New South Wales, Australia.
Flavio TirelliDepartment of Medical and Surgical Sciences, Fondazione Policlinico Universitario, Rome, Italy.
Tim LubbersDepartment of General Surgery, Maastricht University Medical Centre+, Maastricht, The Netherlands.
Carina ChwatHospital Universitario Austral, Buenos Aires, Argentina.
Alfredo CostalesBritish Hospital of Buenos Aires, Buenos Aires, Argentina.
Nader M HannaDepartment of Surgery, Southlake Regional Health Centre, Newmarket, Ontario, Canada.
Andriana PetrovaBarts Health NHS Trust, London, UK.
Almu'atasim KhameesDepartment of General Surgery, King Hussein Cancer Center, Amman, Jordan.ORCID http://orcid.org/0000-0002-6282-8351
David BeardNHMRC Clinical Trails Centre, The University of Sydney, Sydney, New South Wales, Australia.
Catherine L GrangerDepartment of Physiotherapy, The University of Melbourne, Parkville, Victoria, Australia.ORCID http://orcid.org/0000-0001-6169-370X
PREdiCT Study Investigators
Daniel SteffensSurgical Outcomes Research Centre (SOuRCe), Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia Daniel.Steffens@health.nsw.gov.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionGastrointestinal cancer surgery commonly leads to postoperative complications and other adverse outcomes. While prehabilitation shows promise in reducing adverse postoperative outcomes, most hospitals have resource limitations that preclude its use as standard of care. Additionally, the need to expedite surgery from diagnosis often creates a narrow window for prehabilitation initiatives. Online, self-reported screening tools may address these challenges by facilitating early identification of high-risk patients and enabling targeted preoperative interventions, thereby allowing equitable allocation of limited resources. Therefore, the primary aim of this study is to evaluate the predictive utility of a tri-modal (physical, nutritional, psychological) screening tool for patients undergoing gastrointestinal cancer surgery.

methodsThis prospective international cohort study will recruit 1214 adults undergoing elective gastrointestinal cancer surgery across 35 sites from 19 countries. Participants will complete an online screening tool developed through a comprehensive, multistep, predefined process. The screening tool comprises the Duke Activity Status Index, Patient-Generated Subjective Global Assessment Short Form and the Patient Health Questionnaire-4, in English, Spanish, French or Portuguese. These tools were selected based on a scoping review, followed by an international Delphi consensus process. The primary outcomes include rate of postoperative complications, major complications (Clavien-Dindo Classification grade III-V) and overall complication severity assessed by the Comprehensive Complications Index; all assessed 30 days postoperatively. Secondary outcomes include hospital length of stay, readmission rate within 30 days, discharge destination (home vs other), days at home and alive in 30 days postsurgery, 30-day all-cause mortality and 12-month survival. Primary analyses will establish optimal screening tool cut-points to stratify patients into clinically actionable risk categories for postoperative complications and examine the independent predictive value of these screening scores after adjusting for established clinical risk factors. ETHICS AND DISSEMINATION: This study has received ethical approval from the Sydney Local Health District Human Research and Ethics Committee (X25-0333 and 2025/ETH02465) and has been registered on the Open Science Framework (10.17605/OSF.IO/HVCGD). The results of Preoperative Risk Evaluation for Cancer Treatment will be submitted to reputable journals and presented at national and international conferences.

Indexed as

Gastrointestinal NeoplasmsPostoperative ComplicationsPreoperative CareAdultFemaleHumansProspective StudiesResearch DesignRisk AssessmentSurveys and QuestionnairesExerciseNutritionONCOLOGY

Identifiers

PMID42331585
PMCPMC13289133

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.