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Single Site Thoracic Surgery for Pediatric Pneumothorax

Pain Versus Gain: Multiport Versus Single-Port Thoracoscopic Surgery for Pediatric Pneumothorax a Case Series

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05034640
Enrollment
7
Registered
2021-09-05
Start date
2021-04-05
Completion date
2021-04-28
Last updated
2024-02-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric Disorder, Pneumothorax, Spontaneous, Thoracic Diseases, Thoracic Surgery

Brief summary

Video-Assisted Thoracoscopic Surgery (VATS) has become a standard of care in adults, pediatric surgeons have been slower to undertake this approach. There are limitations for working in children. The site of a chest tube becomes the working site for thoracoscopic surgery and the only scar. We propose this study to do a retrospective review comparing the conventional multiport thoracic surgery with the newer single port site.

Detailed description

While Video-Assisted Thoracoscopic Surgery (VATS) has become a standard of care in adults, pediatric surgeons have been slower to undertake this approach. The limitations for working in children are decreased working space, unknown thoracoscopic effects on body physiology, and instrument accommodation. Especially as the field for minimally invasive surgery expands, using the single port approach has unique implications in children. The site of a chest tube becomes the working site for thoracoscopic surgery and the only scar. Despite some learning curve, the preliminary outcomes are similar to the multiport surgeries with better cosmesis. The learning curves for single port site surgery have been well described and our group recently performed a similar study for appendectomies. We propose this study to do a retrospective review comparing the conventional multiport thoracic surgery with the newer single port site.

Interventions

PROCEDUREConventional multiport thoracoscopic surgery

Use 2 or more incisions for multiple instrument entry during the surgery and chest tube placement at the end of the operation.

PROCEDURESingle port site thoracoscopic surgery

Using only 1 incision for multiple instrument entry during the surgery and chest tube placement at the end of the operation. Single port - GelPOINT Mini® port (Applied Medical, Rancho Santa Margarita, California, USA)

Sponsors

Loma Linda University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 19 Years
Healthy volunteers
No

Inclusion criteria

* Age \< 19 years old * pneumothorax * underwent surgery for pneumothorax

Exclusion criteria

* Age =/\> 19 years old * history of prior thoracic surgery * history of cancer

Design outcomes

Primary

MeasureTime frameDescription
Total amount of opioid doses in 24 hours post-op24 hours post-operative VATS procedurePain medication records will be reviewed for all opioids dispensed during the post-operative period until time of discharge. The name of the opioid, the dosage, the route, and the frequency will be recorded.period until time of discharge. The name of the opioid, the dosage, the route, and the frequency will be recorded.
Assessment of length of time of chest tube insertionTime from surgery until chest tube removalTime will be recorded from surgery until chest tube removal post operation.

Secondary

MeasureTime frameDescription
Assessment of operation timeThe time from surgery incision start to surgery closing will be the end time.The length of surgery will be recorded.
Assessment of pneumothorax reoccurrenceWithin 48 hours post-operative period after surgery.If a pneumothorax occurs in the post-operative period, this will be recorded.
Total opioid dose from surgery until dischargeWithin 72 hours post-operative period after surgery.Pain medication records will be reviewed for all opioids dispensed during the period from start of surgery through time of hospital discharge. The name of the opioid, the dosage, the route, and the frequency will be recorded.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026