Evidence map›Paper›PMID 38205458›Full record

ArticleCureus2023

A Prospective Randomized Controlled Trial Comparing Clinical Equivalence of PD Synth and PDS Polydioxanone Sutures.

Amritha Prabha Shankar, Stanley Mathew, V S S Nagababu Tippana, Keerthi B R, Saleem Naik, Ravinder K Pandita, Badareesh L, Naveen Kumar An, Venkata Narasimha Rao V, Bharath Kumar Bhat and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Cureus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 35% 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.

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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

12 authors at 1 institution in 2 countries.

Amritha Prabha ShankarDepartment of Surgical Oncology, Vydehi Institute of Medical Sciences and Research Centre, Bengaluru, IND.
Stanley MathewDepartment of General Surgery, Kasturba Medical College and Kasturba Hospital, Manipal, IND.
V S S Nagababu TippanaDepartment of General Surgery, King George Hospital/Andhra Medical College, Visakhapatnam, IND.
Keerthi B RDepartment of Surgical Oncology, Vydehi Institute of Medical Sciences & Research Centre, Bengaluru, IND.
Saleem NaikDepartment of General Surgery, Batra Hospital and Medical Research Center, New Delhi, IND.
Ravinder K PanditaDepartment of General Surgery, Batra Hospital and Medical Research Center, New Delhi, IND.
Badareesh LDepartment of General Surgery, Kasturba Medical College and Kasturba Hospital, Manipal, IND.
Naveen Kumar AnDepartment of Surgical Oncology, Kasturba Medical College, Manipal, IND.
Venkata Narasimha Rao VDepartment of Surgical Oncology, Kasturba Medical College and Kasturba Hospital, Manipal, IND.
Bharath Kumar BhatDepartment of Gastrosurgery, Kasturba Medical College and Kasturba Hospital, Manipal, IND.
Ashok K MoharanaDepartment of Clinical Affairs, Healthium Medtech Limited, Bengaluru, IND.
Deepak TsDepartment of Clinical Affairs, Healthium Medtech Limited, Bengaluru, IND.
Kasturba Medical College Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction Incisional hernia is a common complication of midline laparotomy that may develop even after several years of surgery. Abdominal fascia closure with ideal suture material reduces the incidence of incisional hernia. This study compared the clinical equivalence of PD Synth (Healthium Medtech Limited) and PDS (Ethicon, Johnson & Johnson) slowly absorbed polydioxanone suture with respect to the occurrence of incisional hernia, following elective/emergency midline laparotomy. Methods Eighty-eight subjects undergoing elective/emergency midline laparotomy were randomized to PD Synth (n=45) and PDS (n=43) groups of this prospective, multicenter, randomized (1:1), single-blind, two-arm, parallel-group study (December 2020-May 2023). Primary endpoint was incidence of incisional hernia, occurring within six and 12 months of surgery. Secondary endpoints included incidence of fascial dehiscence, surgical site infection (SSI), suture sinus, seroma, hematoma, scar tenderness, and re-suturing, and evaluation of operative data, hospital stay, intra-operative suture handling, pain, time to return to normal day-to-day activities and work, overall patient satisfaction score, and adverse events. Results One subject in both PD Synth and PDS groups (p>0.05) developed incisional hernia at umbilicus 12 months post-laparotomy. In PDS

Indexed as

absorbable suturefascial dehiscenceincisional herniamidline laparotomypolydioxanone suture

Identifiers

PMID38205458
PMCPMC10776896
OpenAlexW4389569667

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.