Evidence map›Paper›PMID 34592787›Full record

ArticleJournal of applied clinical medical physics2021

Investigation of optimum minimum segment width on VMAT plan quality and deliverability: A comprehensive dosimetric and clinical evaluation using DVH analysis.

Ab Mohamed Yoosuf, Muhammad Bilal Ahmad, Salem AlShehri, Abdulrahman Alhadab, Mamdouh Alqathami

Abstract read
In one paragraph

Article in Journal of applied clinical medical physics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Dosimetric impact of MLC positional errors on dose distribution in IMRT.Journal of applied clinical medical physics · 2024
    Article
  3. Article
  4. Article
  5. Article
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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

5 authors.

Ab Mohamed YoosufDepartment of Radiation Oncology, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.
Muhammad Bilal AhmadDepartment of Radiation Oncology, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.
Salem AlShehriDepartment of Radiation Oncology, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.
Abdulrahman AlhadabDepartment of Radiation Oncology, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.
Mamdouh AlqathamiDepartment of Radiation Oncology, Ministry of National Guard-Health Affairs, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMinimum segment width (MSW) plays a fundamental role in the shaping of optimized apertures and creation of segments of varying sizes and shapes in complex radiotherapy treatment plans. The purpose of this work was to study the effect of MSW on dose distribution in patients planned with VMAT for various treatment sites using dose volume histogram (DVH) analysis. MATERIALS AND

methodsFor the validation of optimum MSW, 125 clinical treatment plans were evaluated. Five groups were identified (brain, head and neck, thorax, pelvis, and extremity), and five cases were chosen from each group. For each case, five plans were created with different MSW (0.5, 0.8, 1.0, 1.25, and 1.5 cm). The quality of treatment plans created using different MSW were compared using dosimetric indicators such as target coverage (D

resultsA total of 125 plans were created and compared across five groups. In terms of treatment plan quality, the plans using MSW of 0.5 cm was found to be superior in all groups. PTV coverage (D

conclusionDose volume histogram (DVH) analysis demonstrated that treatment plans with minimal MSW showed better plan quality and deliverability and provided clinical relevance as compared to gamma index analysis.

Indexed as

Radiotherapy, Intensity-ModulatedHumansOrgans at RiskRadiometryRadiotherapy DosageRadiotherapy Planning, Computer-AssistedDVHIMRTplan qualitysegment widthVMAT

Identifiers

PMID34592787
PMCPMC8598144

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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.