HBO in the acute treatment of thermal
burn wounds
COST B14 study project
Intended participants
(as per February 2000):
- Military Hospital
"Queen Astrid"
Depts of Burn Care and Hyperbaric Oxygen Therapy
Brussels - BELGIUM
- BerufsGenossenschafts
Unfallklinikum Murnau
Dept of Intensive Care, Burn Care and Hyperbaric Medicine
Murnau - GERMANY
- Rigshospitalet
Dept of Anaesthesia and National Burn Unit
Kopenhagen - DENMARK
- Karolinska Institut
Burn Care Unit and Dept of Anesthesia
Stockholm - SWEDEN
- Allgemeines
Krankenhaus Wien
Dept of Anesthesia and Burn Center
Vienna - AUSTRIA
Objective of study
To evaluate possible
effect of HBO on the conversion of 2nd degree burn wounds to 3rd
degree burn wounds during the 1st 24 hours after the burn.
To evaluate possible
effect of HBO on oedema formation after the burn, as evaluated during the first
three days.
Evaluation of effect
of HBO on other parameters:
- total weight
loss during first 3 days of hospitalisation
- fluid resuscitation
requirements (total volume infused during 1st week)
- duration of
ICU stay
- need for and
duration of intubation
- incidence of
infection
- incidence of
general complications
- total epithelialisation
time (need for daily wound dressings)
Patient group
- 20%-80% TBSA
burned
- at least 50%
of TBSA = 2nd degree burn
- no restriction
as to site burned
- age group: 18
to 70 years
- concomitant
pathology: diseases to be excluded (cardiac insufficiency, renal insufficiency,
pulmonary insufficiency)
- stratification
to be made for
- age groups
(18-45, 45-70)
- cause of burn
wound (flame, surface, water)
- inhalation
injury yes/no
- site burned:
face/neck, chest, hands
Intake
- evaluation of
TBSA burned (9% rule)
- evaluation of
TBSA 2nd degree burn: clinical evaluation, based upon 5 parameters
(NB table does
not exist yet, scores to be discussed)
Parameter
|
3
|
2
|
1
|
Remarks
|
- color
|
white, black
|
pink
|
red
|
|
sensitivity
|
no
|
|
yes
|
|
capillary refill
|
none
|
> 10 secs
|
< 10 sec
|
|
blistering
|
yes
|
|
no
|
|
humidity
|
|
humid
|
dry
|
|
Sum
|
|
|
|
If > 10 = 3rd degree
If < 6 = 1st degree
|
- escharotomies
as necessary
- weighing
- parameters,
incl. CVP
- fluid resuscitation:
1st 24hrs: 3ml/kg/% of Hartmann® solution, first 50% in 8hrs
– on day 2 and further: on guidance of diuresis (minimal 0.5ml/min)
- no systematic
ATB given
- cardiac support:
(dopamine), dobutamine, levorenine, adrenaline
- wound dressing:
flammazine®, daily dressing changes in sterile bath (hibitane® in
water)
Intervention
- after randomisation:
- HBO : 2.0
ATA 3x25minutes, 2x /day for 3 days – 1st HBO < 12hrs after
burn wound infliction, > 8 hrs interval between HBO sessions
- Non-HBO: standard
care
- re-evaluation
daily (% TBSA 3rd, 2nd degree), scoring system, weight,
CVP
Excision/grafting policy
- hands: after
< 1 week if deep 2nd degree or 3rd degree
- rest of body:
after 1-2 weeks depending on stability of patient
- if TBSA burned
is high: first excision of 3rd degree zones, coverage with homografts
(cadaver skin)
- if mainly deep
2nd degree and moderate TBSA burned: autograft coverage
- no use of artificial
skin or keratocyte cultures (may be used if TBSA > 80% = exclusion from
study)
Secondary exclusion
- superficial
or systemic infection with other than Staphylococcus epidermidis during first
week
- ARDS (defined
as: X-ray diffuse bilateral interstitial and alveolar infiltration, PaO2 <
60mmHg despite 10lpm 100% O2 in face mask) , renal failure (defined as: uremia
> 100mg/dl, serum creatinin > 8 mg/dl) during first week
Outcome parameters:
- % TBSA 2nd
and 3rd degree burn on day 1 (intake)
- % TBSA 2nd
and 3rd degree burn on day 2
- % TBSA 2nd
and 3rd degree burn on day 3
- % TBSA 2nd
and 3rd degree burn on day 4
- % TBSA grafted,
as compared to assessment of % TBSA deep 2nd and 3rd
degree burn on day 4
- weight gain
evolution
- total fluid
volume infused during 1st week
- duration of
ICU stay
- need for and
duration of intubation
- number of excision/grafting
procedures performed
- time to complete
(> 95%) epithelialisation
- incidence of
infection
- incidence of
general complications (ARDS, renal failure)
Estimated patient sample
needed : ?
Study protocol NOT finalised !!!
Send comments or expressions of interest to: Peter
Germonpré
|