Qualitative Study of Surgeons With Prospective Patient Follow-up

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 4
SponsorUniversity Hospital Southampton NHS Foundation Trust

About this trial

Necrotising enterocolitis (NEC) is a devastating disease which causes severe bowel inflammation resulting in babies becoming critically unwell. It mainly affects premature babies (who can be born as early as 22 weeks) in the first few weeks of life. A quarter of babies don't respond to intensive care treatment and require surgery to remove bowel which has died to prevent them from getting sicker. Sadly, about a third of the most unwell babies don't survive and those that do have a high incidence of significant long-term health problems.

Deciding which babies will benefit from surgery is challenging and there are no objective methods used to do this currently. Surgeons must weigh up the risks and benefits of performing major surgery on a tiny baby in the knowledge that surgery itself may cause harm. This uncertainty causes delays in performing surgery. Those that have a delay are more likely to have a poor outcome.

In order to improve these unfavourable outcomes it is essential to understand and define current practice in detail (i.e. indications and timing for surgery) and understand how this may be associated with outcome. These outcomes are both short term, including mortality and ability to tolerate enteral nutrition, and long term which include neurodevelopmental outcomes at 2 years of life.

To do this the investigators will undertake a multicentre mixed methods study with qualitative interview of consultant paediatric surgeons shortly after making a decision to operate, or not, on a baby with NEC. The investigators will then take consent from the parents/guardian of the infant to follow-up their clinical outcomes using data linkage to routinely collected data, within the national neonatal research database. Outcomes of interest include survival, feeding outcomes, further surgical procedures and neurodevelopment at 2 years.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Infant with suspected or confirmed NEC undergoing review by surgeon, regardless of outcome of that review (I.e. surgery indicated or not).

Disqualifiers

Lack of consent from surgeon to undertake interview.

Lack of consent from parents to follow-up outcomes of infant.

Trial population

Infant with necrotising enterocolitis undergoing review by paediatric surgeon.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

75 Participants
are grouped into 1 trial group
Group A: Infants with necrotising enterocolitis reviewed by a surgeon

Trial outcomes

Primary outcomes

1

Mortality

Mortality

Time frame
At 52 weeks corrected gestational age and at 2 years age.

Secondary outcomes

1

Death or parental nutrition dependence

Death or parental nutrition dependence versus survivors not requiring parental nutrition

Time frame
Hospital discharge (up to 52 weeks corrected gestational age)

Other outcomes

Sponsors and contacts

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