Evidence map›Paper›PMID 31605179›Full record

Observational studyWorld journal of surgery2020

Investigating Wilms' Tumours Worldwide: A Report of the OxPLORE Collaboration-A Cross-Sectional Observational Study.

K Ford, S Gunawardana, E Manirambona, G S Philipoh, B Mukama, A Kanyamuhunga, P Cartledge, M J Nyoni, D Mwaipaya, J Mpwaga and 7 more

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in World journal of surgery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
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

17 authors.

K FordDepartment of Pediatric Surgery, Oxford University Hospital, Headley Way, Headington, Oxford, OX3 9DU, UK.
S GunawardanaOxford University, Oxford, UK.
E ManirambonaUniversity of Rwanda, Centre Hospitalier Universitaire de Kigali, Kigali, Rwanda.
G S PhilipohMuhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
B MukamaUniversity of Rwanda, Centre Hospitalier Universitaire de Kigali, Kigali, Rwanda.
A KanyamuhungaDepartment of Pediatric Oncology, Centre Hospitalier Universitaire de Kigali, Kigali, Rwanda.
P CartledgeUniversity of Rwanda, Centre Hospitalier Universitaire de Kigali, Kigali, Rwanda.
M J NyoniMuhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
D MwaipayaMuhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
J MpwagaMuhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.
Z BokharyDepartment of Pediatric Surgery, Muhimbili National Hospital, Dar es Salaam, Tanzania.
T ScanlanDepartment of Pediatric Oncology, Muhimbili National Hospital, Dar es Salaam, Tanzania.
T HeinsohnOxford University, Oxford, UK.
H HathawayOxford University, Oxford, UK.
R MansfieldOxford University, Oxford, UK.
S WilsonDepartment of Paediatric Oncology, Oxford University Hospitals, Oxford, UK.
K LakhooDepartment of Pediatric Surgery, Oxford University Hospital, Headley Way, Headington, Oxford, OX3 9DU, UK. kokila.lakhoo@paediatrics.ox.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChildhood cancer is neglected within global health. Oxford Pediatrics Linking Oncology Research with Electives describes early outcomes following collaboration between low- and high-income paediatric surgery and oncology centres. The aim of this paper is twofold: to describe the development of a medical student-led research collaboration; and to report on the experience of Wilms' tumour (WT).

methodsThis cross-sectional observational study is reported as per STROBE guidelines. Collaborating centres included three tertiary hospitals in Tanzania, Rwanda and the UK. Data were submitted by medical students following retrospective patient note review of 2 years using a standardised data collection tool. Primary outcome was survival (point of discharge/death).

resultsThere were 104 patients with WT reported across all centres over the study period (Tanzania n = 71, Rwanda n = 26, UK n = 7). Survival was higher in the high-income institution [87% in Tanzania, 92% in Rwanda, 100% in the UK (X

conclusionsThis study demonstrates novel research methodology involving medical students collaborating across the global south and global north. The comparison of outcomes advocates, on an institutional level, for development in access to services and multidisciplinary treatment of WT.

Indexed as

Biomedical ResearchChildChild, PreschoolCross-Sectional StudiesFemaleHumansInfantIntersectoral CollaborationKidney NeoplasmsMaleRetrospective StudiesStudents, MedicalWilms Tumor

Identifiers

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.