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Imaging Modalities in Diagnosing Necrotizing Enterocolitis in Preterm Infants.

The Use of Different Imaging Modalities in Diagnosing Necrotizing Enterocolitis in Preterm Infants.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03188380
Enrollment
200
Registered
2017-06-15
Start date
2021-01-01
Completion date
2022-12-31
Last updated
2020-05-14

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

Conditions

Necrotising Enterocolitis

Keywords

nec, abdominal ultrasound, abdominal radiograph, preterm

Brief summary

Background Necrotizing enterocolitis (NEC) is one of the most serious conditions in newborns, affecting up to 10% of very low birth weight infants (VLBW). In the most premature population mortality rates can rise as high as 60%. Typical findings on abdominal radiography (AR) include pnuematosis intestinalis (PI), portal vein gas (PVG) and pneumoperitoneum, but are sometimes not present even in severe cases. Abdominal ultrasound (AUS) can depict PI, PVG and pnuemoperitoneum (in some cases a head of AR), but it also provides other crucial information such as bowel wall viability (thickness or thinning) and free abdominal fluid. These additional findings are helpful in expediting diagnosis and management of NEC. Methods and analysis The hypothesis being tested is that preforming an AUR in patients with clinical symptoms of NEC but inconclusive/normal AR will enhance detection rates, and expedite treatment in infants born at \<32 weeks. Discussion The use of AUS together with AR as an add-on test may increase the accuracy of diagnosing NEC, and precipitate treatment. Swift implementation of antibiotics and bowel rest is extremely important. To our best knowledge, our study will be the first to focus only on VLBW, who are most prone to NEC. It will also be the first multi-centre study evaluating the use of AUS as an add-on test, enabling us to recruit a significantly higher number of patients compared to published studies.

Interventions

DIAGNOSTIC_TESTPlain abdominal radiography

After meeting enrolment criteria each patient will have an AR performed. One image will be obtained with a vertical beam and a horizontal beam, with the patient supine.

DIAGNOSTIC_TESTAbdominal ultrasound

If the AR is inconclusive or no abnormalities typical for NEC are recorded, an AUS will be ordered.

Sponsors

Jagiellonian University
CollaboratorOTHER
Ujastek Obstetrics and Gynaecology Hospital
CollaboratorUNKNOWN
University Children's Hospital of Cracow
CollaboratorUNKNOWN
Princess Anna Mazowiecka Hospital, Warsaw, Poland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
22 Weeks to 32 Weeks
Healthy volunteers
No

Inclusion criteria

* Abdominal distension * Visible bowels loops * Feeding intolerance (defined as emesis ≥ 2 consecutive feeds, or gastric residuals of \>50% per feed in ≥ 2 consecutive feeds, bilious residuals, bilious emesis) * Temperature instability (defined as ≥ 2 consecutive measurements) * Frank bloody stools * Cardiovascular instability (hypotension; defined as MAP \< 30mmHg, tachycardia \>160/' or bradycardia \< 80/') * Recurrent apnea * Increase of abdominal girth \> 2cm (allowing inter-observer variability of 1 cm) within 12 h * Abdominal wall erythemia And/or at least 2 of the below laboratory findings5: * Thrombocytopenia \< 50 x103/uL * Leukopenia \<6 x106/uL * CRP \> 10 mg/L * PCT \> 1 ng/ml * Coagulopathy

Exclusion criteria

* • \< 22 weeks of gestational age or \> 32 weeks (estimated by ultrasound) * Congenital abnormalities * No parental consent

Design outcomes

Primary

MeasureTime frameDescription
Intervention timeuntil 40 weeks of post-conceptional ageThe time required to initiate conservative and/or surgical treatment after diagnosing NEC with AR versus AR and AUS

Secondary

MeasureTime frameDescription
Sensitivity and specificityuntil 40 weeks of post-conceptual ageSensitivity and specificity of a diagnostic strategy involving a combination of AR (reference test) followed by AUS (index test) as compared to AR (reference test) in diagnosing NEC.

Countries

Poland

Contacts

Primary ContactJoanna Seliga-Siwecka, MD PhD
seliga.joanna@gmail.com+48225966155

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026