FLIRPED: Thermal Imaging and Pediatric Burns

Sponsor
Assistance Publique - Hôpitaux de Paris (Other)
Overall Status
Unknown status
CT.gov ID
NCT03702972
Collaborator
(none)
40
1
3
13.2

Study Details

Study Description

Brief Summary

The need to cover a burn with a skin graft is determined primarily by its depth. In fact only burns of the second deep degree or the third degree are likely to be grafted. However, if the diagnosis is obvious in the case of third degree burns, second degree burns are often "mixed" with more or less deep areas, especially in pediatrics.

Clinical experience and daily observation of the burn since its occurrence currently determine the indication for surgery. In practice, it is rare to be able to determine with certainty whether a second degree mixed burn will require a graft before the 10-12th day of evolution. There are currently devices that can help refine the diagnosis such as laser Doppler, but they are expensive devices, and not 100% reliable. The thermal camera Flir-one® attaches to a smartphone or tablet and allows thanks to a free application, to obtain a thermogram of the pointed area. This is a device used to detect insulation deficits in the building sector. Knowing that a deep burn, by devascularization, will have an external temperature lower than a superficial burn, a thermogram would thus make it possible to better identify the deep zones and the superficial zones of the burn. One study showed a good sensitivity and specificity of the device but it was a population of adult patients. This determined that a difference in skin temperature between a deep burned area and healthy skin should be at least 1.15 ° C in favor of healthy skin, to retain a burn as deep, and not to operate so-called superficial burn if this difference was below this threshold. However, further studies would be needed to demonstrate the validity of this method in clinical practice.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    All patients under 18, with acute burns (<10 days of development), surface area <10%, second degree, hospitalized from 22/01/18 in the plastic surgery department and burns Trousseau Hospital in Paris, subject to the non-opposition of parental authority. 500000 pediatric burns are counted each year in France. In 2005, they resulted in 5109 hospital stays 2. Improving the accuracy of the diagnosis before 10 days of evolution would make it possible to graft the children who needed it more quickly and thus shorten the length of hospital stay. It is therefore a public health issue, with a significant medical and economic impact.

    Description of the item (s) being researched

    It involves collecting, through a thermal camera, a temperature difference between a second-degree burn zone and an adjacent healthy zone, in order to prove that this difference, can make it possible to retain the burn as deep, and can therefore guide a surgical decision.

    Justification of the duration of the research.

    According to the same study in adults1, the number of patients to be included was 41 to obtain sufficient power for a statistical analysis of the same data collected in this study, and according to the same methodology. A duration of 4 months seems compatible with such recruitment in the specialized center for treating pediatric burns at the Trousseau Hospital in Paris.

    Goal of the study: Objectively determine the depth of pediatric acute burns using a thermal imaging camera.

    METHOD AND POPULATION

    Main evaluation criterion Measurement of Δ T = temperature difference between the burned area and an adjacent healthy area of 3cm, or contralateral if extremity burns, with the thermal camera, by a blind surgeon the final evaluation of the depth (between D10 and D14 ).

    The thermograms will be read at three different times, from the moment of admission to hospital or after the patient has been cured by:

    • T1: D1 to D4 of the burn

    • T2: D4 to D7 of the burn

    • T3: D7 to D10 of the burn.

    Secondary evaluation criteria Interest of the repeated measurements to determine if the evolution of ΔT is also an index reflecting the depth of the burn.

    Recruitment of the population Hospitalized patients from 22/01/18 in the Pediatric Burn Surgery Department of Trousseau Hospital in Paris.

    Eligibility criteria (inclusion and non-inclusion criteria) Inclusion criteria: All patients <18 years of age, with acute burns (<10 days of progression) of the second degree of body surface area burned <10%, hospitalized from 22/01/18 in the plastic surgery department and burns at the Trousseau Hospital in Paris, subject to the non-opposition of parental authority.

    Criteria for non-inclusion: First-degree burns, third-degree burns, fever episode not caused by burns, burn surgery before measurement, inability to communicate with the persons having parental authority.

    Population monitoring Patients will be followed as usual as part of the nurse consultation consultation treatment every 2 days initially at the Trousseau Hospital Pediatric Burn Treatment Center, with surgical advice on how to proceed with care. local, as was already the case, then the pace will adapt to the pathology, with iterative appointments specialized consultation with the surgeon from 15 days after discharge and every 2 months until complete healing and definitive in the event of satisfactory evolution. In the case of surgery necessary for healing during hospitalization, the follow-up may last for a period of 2 years.

    Risks AND VIGILANCE

    Non-interventional research involving the human person presents no risk to patients.

    The adverse effects observed in the patients participating in the research are notified by the investigators according to the local vigilance plans put in place as part of the care activities.

    Terms of data collection

    The collection of thermograms on thermal camera is performed by a blind surgeon of the operative decision of the burn. The thermograms will be read at three different times, from the moment of admission to hospital or after the patient has been cured by:

    • T1: D1 to D4 of the burn

    • T2: D4 to D7 of the burn

    • T3: D7 to D10 of the burn

    An operative decision or a continuation of the surgical care is recorded in the database at D10-14 in blind of the registered thermograms, by the only expertise of a surgeon different from that having measured the ΔT thus without modification of the care usually dispensed for each patient included.

    The research does not foresee the use of data extracted from existing information systems or study bases already carried out.

    Data circuit The collection of thermograms on a thermal camera is done by a surgeon who uses himself to transfer them by connectivity on the centralized computer database, protected, anonymized with a number given to each patient which only the surgeon having collected the thermograms knows the correspondence with the real identity. This surgeon does not participate in the operative decision of the patient and records it if necessary in the patient database after it is taken by the rest of the surgical team who remains blind thermograms and Δ T measured.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    40 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Contribution of Thermal Imaging in Determining the Depth of Pediatric Acute Burns: a Prospective Observational Study
    Anticipated Study Start Date :
    Oct 1, 2018
    Anticipated Primary Completion Date :
    Jan 1, 2019
    Anticipated Study Completion Date :
    Jan 1, 2019

    Outcome Measures

    Primary Outcome Measures

    1. Temperature difference between burned zone and adjacent or contralateral healthy zone at time T3 [day 7 to day 10 from the day of the burn occurrence]

      Δ T3 will be recorded from day 7 to day 10 once by the Flir One Thermal Imager

    Secondary Outcome Measures

    1. Temperature difference between burned zone and adjacent or contralateral healthy zone at time s T1 [day 1 to day 4 from the day of the burn occurrence]

      Δ T1 will be recorded from day 1 to day 4 once by the Flir One Thermal Imager

    2. Temperature difference between burned zone and adjacent or contralateral healthy zone at time s T2 [day 4 to day 7 from the day of the burn occurrence]

      Δ T2 will be recorded from day 4 to day 7 once by the Flir One Thermal Imager

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A to 18 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age <18 years,

    • Acute burns (<10 days of evolution) of the second degree

    • Body surface burned <10% of total body area

    • Hospitalized patients for a period of 4 months and 15 days in the plastic surgery and burns department at Trousseau Hospital in Paris.

    • Affiliates to the general system of social security as having the right of the holders of parental authority

    Exclusion Criteria:
    • Burns of the first degree,

    • Third degree burns,

    • fever episode not caused by burning,

    • Surgical procedure on burn before measurement,

    • Impossibility to communicate with the holders of the parental authority or opposition formulated to the participation

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Service de chirurgie plastique et des brûlés Paris Ile De France France 75012

    Sponsors and Collaborators

    • Assistance Publique - Hôpitaux de Paris

    Investigators

    • Principal Investigator: Sophie CASSIER, Doctor, Assistance Publique - Hôpitaux de Paris

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Assistance Publique - Hôpitaux de Paris
    ClinicalTrials.gov Identifier:
    NCT03702972
    Other Study ID Numbers:
    • NI18021J
    • 2018-A01154-51
    First Posted:
    Oct 11, 2018
    Last Update Posted:
    Oct 11, 2018
    Last Verified:
    Aug 1, 2018
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Assistance Publique - Hôpitaux de Paris
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 11, 2018