Introduction
On March 11, 2020, the COVID-19 pandemic was declared, caused by the new
coronavirus. On March 30, 2020, when 320 cases had been registered in Brazil,
the Division of Plastic Surgery and Burns of the largest hospital complex in
Latin America was physically aimed at the infected; burned patients were
transferred to another burn center, and health professionals were relocated.
In this context, we had the challenge of treating a large burned and multiple
trauma patient with arterial thrombosis in the right lower limb, a rare
complication associated with the burn. His treatment was carried out in one of
the complex’s institutes, which is not specialized in trauma care, but
where the structure was temporarily moved to these services, and where he
remained hospitalized due to the need for specialized multidisciplinary
care.
CASE REPORT
An 18-year-old male patient, without comorbidities, truck collision victim,
followed by an explosion of a gasoline tank on his motorcycle, had predominantly
3rd degree burns with an estimated burned body surface (BBS) of 50% in the lower
limbs, abdomen, lower back and left forearm, and second-degree burns on the
right forearm (Figure 1).
Computed tomography (CT), subarachnoid hemorrhage, hemoventriculus (IV ventricle)
and signs of diffuse axonal lesion are identified. On CT control, there were
signs of worsening of cerebral edema; we opted for external ventricular drain
(EVD) and passage of intracranial pressure catheter (ICP) by the neurosurgery
team.
After 24 hours, he presented edema, decreased temperature and non-fixed cyanosis
of the right lower limb with little improvement of possible venous congestion
post-escharotomy. After 12 hours with worsening of the perfusion, he was
submitted to angiotomography (CTA) (Figure 2), evidencing filiform flow and sometimes an absence of flow in the
anterior and posterior tibial artery, tibiofibular trunk, fibular and difficult
characterization in the more distal segments, evolving with fixed cianosis.
Because of vascular injury’s situation not yet delimited, extensive deep
burn and severe neurotrauma, amputation after clinical compensation was
chosen.
After the withdrawal of EVD and ICP with an improvement of the clinical picture,
open transtibial amputation was performed on the 13th day of hospitalization.
After six days, the stump was ischemic with necrosis (Figure 3), requiring enlargement of the amputation level to
transfemoral.
Figure 1 - Initial care of patients with 50% BBS predominantly of third-degree
by direct flame.
Figure 1 - Initial care of patients with 50% BBS predominantly of third-degree
by direct flame.
Figure 2 - A. Arterial reconstruction; B and
C. Lower limb CTA evidencing bottleneck and obstruction
of flow in the anterior tibial artery (orange arrow) and posterior
tibial artery (red arrow), and difficult characterization of the more
distal segments in the right lower limb.
Figure 2 - A. Arterial reconstruction; B and
C. Lower limb CTA evidencing bottleneck and obstruction
of flow in the anterior tibial artery (orange arrow) and posterior
tibial artery (red arrow), and difficult characterization of the more
distal segments in the right lower limb.
From there, we perform weekly serial operations with debridement and mesh skin
grafting. Table 1 summarizes our surgical
interventions. Neurologically, the patient showed improvement in the level of
consciousness and motor coordination, also having areas of ulceration
(Figure 4) for future
grafting.
In the 27th IHL, molecular test (RT-PCR) was collected for COVID-19, which had
been negative, for investigation of febrile peaks without other symptoms,
treated with antibiotic therapy by bloodstream infection. In the 41st IHL, a
COVID-19 serological test was performed from all hospitalized patients in the
same intensive care unit (ICU) due to one of the patients’ infections. In
this, there was positivity for immunoglobulin G.
Figure 3 - Necrotic aspect of a right flap of open transtibial amputation of the
right leg and visualization of an extensive and deep burn in the left
lower limb.
Figure 3 - Necrotic aspect of a right flap of open transtibial amputation of the
right leg and visualization of an extensive and deep burn in the left
lower limb.
Figure 4 - All burn necrotic tissue were excised and covered with partial skin
graft in a 3: 1 mesh. The upper limbs were used twice as a skin donor
area after 15 days of restoration. There are still ulcerated areas that
a skin graft will cover.
Figure 4 - All burn necrotic tissue were excised and covered with partial skin
graft in a 3: 1 mesh. The upper limbs were used twice as a skin donor
area after 15 days of restoration. There are still ulcerated areas that
a skin graft will cover.
Table 1 - Summary of surgeries performed according to the day of
hospitalization and its results.
#Surgery - Day of hospitalization (IHL) |
Evolution |
#1 -
2nd IHL EVD by the neurosurgery team.
|
Withdrawal at 5º IHL after intracranial pressure remains
normal with CLOSED EVD for 72 hours.
|
#2 - 12th IHL Right open
transtibial amputation by vascular surgery (VC): the
muscle presented little bleeding, presence of hematomas,
thrombosed vessels; it was then decided to keep open muscle flap
without skin coverage to evaluate viability, and installed
subatmospheric pressure therapy (VAC).
|
VAC dressing removed after 6 days
showing muscle stump flap with necrosis and ischemic aspect
(Figure 2).
|
#3 -
18th IHL Right transfemoral amputation by VC.
Debridement and grafting on the abdomen and left forearm.
|
Opening of graft dressing after 6 days: integration
>90%.
|
#4 -
24th IHL Left transtibial amputation by VC due to
the extent and depth of the burn in the foot, leading to the
unviability of limb reconstruction. Debridement and grafting on
the right transfemoral stump.
|
Opening
of graft dressing after 6 days: integration >90%.
|
#5 -
31st IHL Debridement and grafting on the back, inguinal region
and gluteus on the right.
|
Opening of graft dressing after 7 days: integration ~60%. |
#6 -
32nd IHL Tracheostomy by thoracic surgery for
airway protection after extubation failure (neurological status
+ psychomotor agitation).
|
|
#7 -
38th IHL Debridement and grafting on the left stump.
|
Opening of graft dressing after 7 days: integration ~80%. |
#8 -
45th IHL Debridement and grafting on the back and glutes.
|
Opening
of graft dressing after 7 days: integration ~80%.
|
Table 1 - Summary of surgeries performed according to the day of
hospitalization and its results.
DISCUSSION
Extensive burn is one of the most severe and complex forms of trauma1. In this case, there was a
beneficial sharing of the assistance team’s performance of the
non-specialized institute with the team of the burn division. There was a need
for nursing, not affected by the treatment of burn patients, to be quickly
trained in applying the dressings, and joint efforts with the plastic surgery
team to integrate the grafts and restore the donor area (reused after 15 days)
were essential.
Early activation of uncontrolled coagulation and fibrinolysis may be consequences
of endothelial injury and systemic inflammatory response2. Current evidence suggests that
the uncontrollable increase in the coagulation system is proportional to BBS,
burn depth, inhalation injury, and hemodilution in the volume resuscitation
phase3.
A severe burn can cause thrombosis of capillaries and small-caliber veins, but
rarely medium and large caliber4.5. Few cases of
burn-induced arterial thrombosis have been reported, although well described in
necropsies of burned patients5.
Among these cases, most patients had risk factors such as atherosclerotic
disease or artery catheterization6. In this case, the patient without comorbidities presented
early laboratory alterations (Table 2)
associated with hemoconcentration with increased hemoglobin and hematocrit
(increased blood viscosity, risk factor for thrombosis); blood dyscrasia with
increased prothrombin time (PT) and activated partial thromboplastin time (aTTP)
and platelet intake, suggesting disseminated intravascular coagulation (IVC). In
the IVC, there is a continuous procoagulant activity with fibrin deposition in
small and medium vessels that consume and deplete coagulation factors, which may
cause thrombosis and bleeding7.
Kinetic studies with fibrinogen and marked platelets reveal that, in addition to
this systemic consumption, significant local consumption occurs in burned
areas8. In this case,
CTA suggested native arterial thrombus, which could be caused by
atherosclerosis, aneurysm, dissection or hypercoagulability9. The trauma could lead to
arterial thrombosis subsequent to a pseudoaneurysm or arterial dissection, which
was not seen on imaging10.
Thus, the most likely etiology of thrombosis was due to hypercoagulability
associated with IVC secondary to the large burned systemic inflammatory
response.
Neurotrauma11 contraindicated
the use of thrombolytics, and embolectomy was deprecated, as it would need to be
performed early when the patient still needed clinical and neurological
compensation. For this reason, and the depth and extent of the burns, we opted
for limb amputation.
Table 2 - Laboratory tests of the first 5 days of hospitalization showing:
hemoconcentration by increased hemoglobin (Hb) and hematocrit (Ht);
blood dyscrasia with increased prothrombin time (INR) and activated
partial thromboplastin time (aTTP) with platelet consumption suggesting
CIVD; systemic inflammatory condition suggested by c-reactive protein
(CRP) increase.
|
Hb (g/dL)/Ht
(%)
|
Platelets |
INR |
ATTP |
CRP |
11/04/20 |
19.9 / 55 |
565.000 |
1.6 |
1.3 |
|
12/04/20 |
23 / 65 |
309.999 |
1.9 |
1.17 |
39 |
13/04/20 |
20.0 / 61 |
183.000 |
2.2 |
1.39 |
117 |
14/04/20 |
12.2 / 35 |
76.999 |
1.5 |
1.22 |
87.68 |
15/05/20 |
11.6 / 32 |
77.000 |
1.2 |
1.2 |
103.54 |
Table 2 - Laboratory tests of the first 5 days of hospitalization showing:
hemoconcentration by increased hemoglobin (Hb) and hematocrit (Ht);
blood dyscrasia with increased prothrombin time (INR) and activated
partial thromboplastin time (aTTP) with platelet consumption suggesting
CIVD; systemic inflammatory condition suggested by c-reactive protein
(CRP) increase.
Despite the absence of local infectious complications, we considered the surgical
approach late. In addition to waiting for better clinical conditions, the
physical loss of our specialized structure for burns caused logistical
difficulties, from obtaining an operating room to the availability of our
specific equipment and supplies. Fortunately, after the reorganization of the
hospital complex, we were able to perform weekly surgical interventions.
To prevent COVID-19, patients hospitalized were allocated according to their
infectious status, with wards for suspects, infected and uninfected. Every
patient treated in the emergency room performs RT-PCR infectious screening and
is considered suspicious, remaining in isolation with droplet precaution. After
the result, the patient is referred to his/her respective ward, where constant
surveillance of infectious signs (fever and respiratory symptoms) is performed.
If present, they are re-transferred to the suspect ward until thorough
investigation with imaging and new RT-PCR for COVID-19. Besides, there was an
impediment to any patient’s visitation, either in the ward or ICU.
Despite these efforts, the patient was infected during hospitalization and,
fortunately, did not present any respiratory complication or other thrombotic
complication.
CONCLUSION
Despite the knowledge of burn-related coagulopathy, we still need evidence of
diagnostic criteria, prophylaxis and treatment. COVID-19 caused important
changes in our clinical-surgical practice. Thus, the sharing of knowledge and
skills, interaction between professionals from various areas, and the search for
solutions adapted to the crisis situation can emerge as a positive legacy in the
pandemic face.
REFERENCES
1. Zuo KJ, Medina A, Tredget EE. Important developments in burn care.
Plast Reconstr Surg. 2017 Jan;139(1):120e-38e. DOI: https://doi.org/10.1097/PRS.0000000000002908
2. Glas GJ, Levi M, Schultz MJ. Coagulopathy and its management in
patients with severe burns. J Thromb Haemost. 2016
Mai;14(5)865-74.
3. Marsden NJ, Van M, Dean S, Azzopardi EA, Hemington GS, Evans PA, et
al. Measuring coagulation in burns: an evidence-based systematic review. Scars
Burn Heal. 2017 Set;3:2059513117728201. DOI: https://doi.org/10.1177/2059513117728201
4. Counce JS, Cone JB, McAlister L, Wallace B, Caldwell Junior FT.
Surgical complications of thermal injury. Am J Surg. 1988 Dez;156(6):556-7. DOI:
https://doi.org/10.1016/s0002-9610(88)80552-x
5. Sevitt S. A review of the complications of burns, their origin and
importance for illness and death. J Trauma. 1979 Mai;19(5):358-69. DOI:
https://doi.org/10.1097/00005373-197905000-00010
6. Barret JP, Dziewulski PG. Complications of the hypercoagulable
status in burn injury. Burns. 2006;32(8):1005-8. DOI: https://doi.org/10.1016/j.burns.2006.02.018
7. Pintão MCT, Franco RF. Coagulação intravascular
disseminada. Medicina (Ribeirão Preto). 2001
Dez;34:282-91.
8. Levi M, Van Der Poll T. Disseminated intravascular coagulation: a
review for the internist. Intern Emerg Med. 2013 Set;8(1):23-32. DOI: https://doi.org/10.1007/s11739-012-0859-9
9. Leung LLK. Clinical features and diagnosis of acute lower extremity
ischemia. Waltham, MA: UpToDate; 2020.
10. Mitchell ME, Carpenter JP. Clinical features and diagnosis of acute
lower extremity ischemia. Waltham, MA: UpToDate; 2020.
11. Braun JD. Embolism to the lower extremities. Waltham, MA: UpToDate;
2020.
1. Hospital das Clínicas, Faculty of
Medicine, University of São Paulo, Department of Plastic Surgery and
Burns, São Paulo, SP, Brazil.
Corresponding author: Rafael Eiki
Takemura, Avenida Doutor Enéas Carvalho de Aguiar, 255,
Cerqueira César, São Paulo, SP, Brazil., Zip Code: 05403-000,
E-mail: eikitakemura@gmail.com
Article received: July 06, 2020.
Article accepted: January 10, 2021.
Conflicts of interest: none
Institution: Hospital das Clínicas, Faculty of Medicine, University of
São Paulo, Department of Plastic Surgery and Burns, São Paulo,
SP, Brazil.