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Revista Brasileira de Anestesiologia

Print version ISSN 0034-7094

Rev. Bras. Anestesiol. vol.59 no.1 Campinas Jan./Feb. 2009

http://dx.doi.org/10.1590/S0034-70942009000100009 

CLINICAL REPORT

 

Transfusion-related acute lung injury (Trali) after mastectomy with microsur-gical breast reconstruction*

 

Aparecimiento de lesión pulmonar aguda relacionada con la transfusión (TRALI - Transfusion Related Acute Lung Injury) en postoperatorio de mastectomía con reconstrucción micro quirúrgica de mama

 

 

Beatriz Garcia Sluminsky, TSA, M.D.I; Ranger Cavalcante da Silva, TSA, M.D.II

ICo-Responsável pelo CET do Hospital de Clínicas da UFPR e Anestesiologista dos Hospitais Vita Curitiba
IIMestre em Medicina e Cirurgia pela UFPR; Co-Responsável pelo CET do Hospital de Clínicas da UFPR; Anestesiologista e Coordenador do Serviço de Anestesiologia do Hospital Vita Curitiba

Correspondence to

 

 


SUMMARY

BACKGROUND AND OBJECTIVES: After its description more than 20 years ago, TRALI Transfusion Related Acute Lung Injury became the main cause of transfusion-related morbidity and mortality in the United States and England. Since reliable data on its epidemiology in Brazil are not available, the difficulty to diagnose, varied clinical presentation, and absence of specific laboratory data, case reports are important. This is the first report of this transfusion reaction indexed in the LILACS data base.
CASE REPORT: A 36-year old female underwent mastectomy with microsurgical breast reconstruction under general anesthesia. Immediately after the transfusion of one unit of packed red blood cells in the post-anesthetic recovery room, she developed respiratory failure, which did not require reintubation. Supportive treatment was instituted in the intensive care unit after other diagnostic hypotheses were ruled out. She had a favorable evolution and was discharged from the hospital without sequelae.
CONCLUSION: The importance of judicious blood transfusion is emphasized since, although disease transmission is rare, TRALI is not, but it is underestimated due to the diversity of diagnostic hypotheses. Therefore, the knowledge of this disorder and its dissemination, especially in our country, is important.

Key Words: BLOOD: Transfusion; COMPLICATIONS: acute lung injury; SURGERY, Plastic: mammoplasty.


RESUMEN

JUSTIFICATIVAS Y OBJETIVOS: Después de su descripción hace más de 20 años, la TRALI - Transfusion Related Acute Lung Injury se convirtió, en los Estados Unidos de América y en Inglaterra, en la principal causa de morbidez y mortalidad relacionada con la transfusión sanguínea. Por el hecho de no haber datos confiables con relación a su epidemiología en Brasil, su difícil diagnóstico, al cuadro clínico variado y la ausencia de datos de laboratorio específicos, los relatos de casos son importantes. Es el primer relato de esta reacción transfusional indexado a la base de datos del LILACS.
RELATO DEL CASO: Paciente femenino, de 36 años, sometida a la mastectomía con reconstrucción micro quirúrgica de mama bajo anestesia general. Inmediatamente después del término de la transfusión de un concentrado de hematíes, en la sala de recuperación postanestésica, evolucionó con insuficiencia respiratoria no necesitando re-intubación traqueal. Fue realizado el tratamiento de soporte en la unidad de cuidados intensivos después de descartar otras hipótesis diagnósticas. Evolucionó bien y recibió el alta al cuarto día del postoperatorio, sin secuelas.
CONCLUSIONES: Resaltamos la importancia de la realización con criterio de la transfusión sanguínea, ya que a pesar de que la transmisión de enfermedades sea algo raro, el aparecimiento de TRALI es muy frecuente, sin embargo, se subestima por la diversidad de hipótesis diagnósticas. Por eso, es saludable que conozcamos y divulguemos esa enfermedad, sobre todo en nuestro medio.


 

 

INTRODUCTION

After its description more than 20 years ago, TRALI — Transfusion-Related Acute Lung Injury — became the main cause of transfusion-related morbidity and mortality in the United States and England 1,2. However, since reliable data on its epidemiology in Brazil are not available, the difficulty to diagnose, varied clinical presentation, and absence of specific laboratory data, case reports are important. The authors report a case of TRALI in a patient who underwent a mastectomy with microsurgical breast reconstruction. This is the first report of this transfusion reaction indexed in the LILACS data base.

 

CASE REPORT

This is a 36 years old female, ASA I, scheduled for a mastectomy with microsurgical reconstruction of the breast. During the pre-anesthetic evaluation, done the day before, the patient stated she had undergone two breast surgeries under general anesthesia for removal of nodes without intercurrences. She was taking clonazepam for two months and denied using any other medication, smoking, or alcohol, as well as any systemic diseases. The physical exam was normal. Laboratory exams showed Hb 12.7 g.dL-1 and MCV 37.6%; all other results were normal. The electrocardiogram showed altered right bundle branch conduction and the chest X-ray was normal. Since the surgery was expected to be lengthy, significant bleeding was a possibility and the red blood cell count was in the lower normal limit, two units of packed-red blood cells were requested.

The patient underwent the proposed procedure, which lasted four and a half hours, under balanced general anesthesia and controlled mechanical ventilation with tracheal intubation. The surgery evolved without intercurrences, the patient remained hemodynamically stable, with effective urine output, and intraoperative losses were compensated by the administration of 2,500 mL of NS and 500 mL of hetastarch. At the end of the surgery, blood for the determination of Hb and MCV was drawn, and the patient was extubated without intercurrences. She was transferred to the post-anesthetic recovery room (PARR) with blood pressure 100 x 70 mmHg, HR 84 bpm, RR 12 bpm, which were similar to preoperative parameters. She had a SpO2 99% with O2 via a face mask, which was maintained in the PARR. Approximately 20 minutes after admission to the PARR, the results of her blood work revealed Hb 8 mg.dL-1 and MCV 24%. Although the patient remained hemodynamically stable without any complaints it was decided to transfuse one unit of PRBCs because she was actively bleeding through the drain and to avoid transfusion in the room.

The PRBC was transfused in approximately 25 minutes and, immediately after the transfusion, the patient developed dyspnea, tachypnea (30 bpm), and progressive reduction of SpO2, down to 82% with 6 L.min-1 of O2 via face mask. On auscultation, she had rare crackles and rales bilaterally, more prominent on the bases. A chest X-ray revealed interstitial infiltrate and diffuse and confluent alveolar opacities on the lower two thirds of the lung fields bilaterally (Figure 1).

 

 

Meanwhile, the patient developed coughing productive of frothy secretion approximately 90 minutes after the transfusion. Blood for arterial blood gases was drawn and a bed in the intensive care unit was requested (ICU). Assuming a diagnosis of pulmonary edema, despite effective diuresis, normal blood pressure, and jugular veins on the posterior limits of the sternocleidomastoideo muscle, it was decided to administer 20 mg of furosemide with the hypothesis of volume overload. Among the differential diagnoses the possibility of acute lung injury (ALI) by sepsis or bronchoaspiration, and due to the cause-effect relationship, transfusion-related acute lung injury (TRALI) was included. The last hypothesis was considered more likely and, therefore, 500 mg of hydrocortisone IV was administered and the blood bank was contacted to make the proper arrangements with the donor. Arterial blood gases revealed hypoxemia and metabolic acidosis (PaO2 90 mmHg; SatO2 91%; pH 7.25; bicarbonate 19.3 mEq.L-1), with a PaO2:FiO2 225. Three hours later, the condition of the patient had improved and she was transferred to the ICU with the diagnosis of TRALI. There, treatment with 100 mg of hydrocortisone IV every eight hours continued, along with ipratropium bromide and fenoterol. To rule out cardiogenic pulmonary edema, an echocardiogram was done, which was normal as well as the ECG. Twelve hours after her admission to the ICU the patient referred improvement of dyspnea, RR 16 bpm, SpO2 96% under mist mask. Auscultation revealed improvement of the breath sounds, with rare crackles in the bases. The chest X-ray had improved, with residual basilar opacities (Figure 2).

 

 

The patient showed progressive improvement and was discharged from the ICU 36 hours after her admission to the unit. Two days after the surgery the patient was asymptomatic, SpO2 97% in room air, and her chest X-ray was normal (Figure 3); she was discharged from the hospital on the same day. The patient returned to the hospital seven months later for retouch and symmetrization of the breast and underwent the same anesthetic technique. Blood transfusion was not necessary, and the surgery and postoperative period evolved without intercurrences. Currently the patient is asymptomatic with normal pulmonary function.

 

 

DISCUSSION

Transfusion-related acute lung injury is the most common transfusion-related cause of morbidity and mortality in the United States and England, which has increased the interest on its precise diagnosis and research of its pathophysiology and prevention 1,2. Although the first reports go back to 1951 3, only in 1983 Popovski and Moore described the presentation and pathophysiology of this disorder, calling it "transfusion-related acute lung injury" — TRALI 4.

In general, TRALI presents with symptoms of respiratory distress, which begin during or up to six hours after transfusion. However, some cases might develop up to 48 hours after transfusion 5. Since most transfusions are surgery-related 6, if transfusion is done during the surgery, this disorder may develop early, hindering the diagnosis, which might not even be made. Thus, it is considered as a transitory hypoxemia because anesthesia restricts the spectrum of symptoms and since it is a self-limited process it might, depending on the severity of the case, have resolved by the end of the surgery 5. In the case presented here, transfusion was done in the PARR with the patient awake and oriented allowing proper diagnosis despite the very early development of symptoms.

Dyspnea is another characteristic symptom of this reaction, which usually develop over a few minutes due to acute pulmonary edema leading to reduction in arterial oxygen saturation and in many cases cyanosis. On the chest X-ray, edema begins on dependent lung regions and perihilar region, similar to cardiogenic pulmonary edema 5. The radiologic aspect progresses rapidly to a generalized form (white-out) affecting the entire lung. Auscultation has discrete changes that do not explain the reduction in oxygen saturation and radiographic images 5. The interstitial nature of the fluid, in contrast with the intra-alveolar fluid of cardiogenic pulmonary edema, despite the lack of scientific evidence to support this affirmation could possibly explain the paucity of auscultation 5. During general anesthesia the elimination through the trachea tube of frothy secretion can be seen especially in cases with rapid progression 5. In the present case, since the patient was awake, she developed cough and eliminated frothy material through the mouth, which indicated the diagnosis of pulmonary edema. If the patient is intubated and under mechanical ventilation it might present with difficulty to ventilate, increased endotracheal pressure, and abrupt reduction in blood pressure. However, the clinical presentation is characterized by a constellation of non-specific signs and symptoms common to several disorders, making for a difficult differential diagnosis. Even with the presentation of this patient, TRALI can be mistaken with ALI (Acute Lung Injury) caused by sepsis, trauma, aspiration of gastric contents, disseminated intravascular coagulation, or ventilation-related pulmonary lesion.

Consensus on its pathophysiology is lacking, although HLA class I (Human Leukocyte Antigen) and HLA class II antigens in the donor blood have been implicated. Less than 10% of the cases are due to leukocyte antigens in the blood of the receptor6. This explains the need to contact the blood bank to take proper measures regarding other blood products involving the donor that might be still in storage. Along with the high prevalence of HLA antigens in blood products implicated in TRALI, the high incidence of multiparous donors, sensitized during pregnancy by fetal antigens, is also associated with this disorder. Despite the apparent association between prior sensitization during pregnancy and TRALI, blood with high HLA sensitization of up to 26.7% in 332 multiparous donors has not been implicated in the development of TRALI 3. Recent studies indicated the need of antigen-antibody concordance, as well as some specificity of the antibodies for combinations. In the present case, the donor was male, healthy, the blood was compatible (ABO and RH), and other blood products with his blood had been previously transfused without intercurrences (one unit of fresh frozen plasma and one unit of platelets). Data regarding the patient, as well as the complication resulting from the transfusion, were recently included in the data bank of a health agency.

Acute pulmonary edema, despite most of the time the radiologic characteristics suggest non-cardiogenic pulmonary edema, as in the case presented here, is the main differential diagnosis and the exclusion of a cardiac cause is paramount. Treatment of TRALI consists of supportive measures and up to 72% of the patients require intubation and mechanical ventilation5. When intubation is not necessary, supportive measures include oxygen administration. Hypotension can be treated with the administration of fluids or, in refractory cases, vasopressors. Fluid administration presupposes the exclusion of fluid overload and cardiogenic pulmonary edema. Diuretics are not recommended when volume overload is not present. The use of corticosteroids is empirical, and data supporting or contraindicating their administration do not exist.

When compared to ALI, TRALI has a low mortality rate (6 to 10%), and it does not lead to late pulmonary dysfunction 5. In the case presented here, despite the early development and rapid progression of symptoms, the patient did not require tracheal intubation, allowing fast and complete recovery of pulmonary function.

The present case report emphasized the importance of judicious care when transfusing blood, since the inherent risks go beyond the transmission of viral diseases, the most feared complication although rare in countries with elevated human development index. On the other hand, TRALI is common and notoriously underestimated due to the diversity of diagnostic hypotheses, justifying the dissemination of the knowledge of this disorder, especially in our country, where the anesthesiologist is involved directly in blood transfusions.

 

REFERENCES

01. United States Government Food and Drug Administration, 2004 http://www.fda.org/        [ Links ]

02. SHOT, 2003. http://www.shotuk.org        [ Links ]

03. Barrett NA, Kam PC — Transfusion-related acute lung injury: a literature review. Anaesthesia, 2006;61:777-785.         [ Links ]

04. Popovski MA, Abel MD, Moore SB — Transfusion-related acute lung injury associated with passive transfer of anti-leukocyte antibodies. Am Rev Respir Dis, 1983;128:185-189.         [ Links ]

05. Moore SB — Transfusion-related acute lung injury (TRALI): clinical presentation, treatment, and prognosis. Crit Care Med, 2006;34(5/Suppl):s114-s117.         [ Links ]

06. Curtis BR, McFarland JG — Mechanisms of transfusion-related acute lung injury (TRALI): anti-leukocyte antibodies. Crit Care Med, 2006;34(5/Suppl):s118-s123.         [ Links ]

07. Densmore TL, Goodnough LT, Ali S et al — Prevalence of HLA sensitization in female apheresis donors. Transfusion, 1999;39: 103-106.         [ Links ]

 

 

Correspondence to:
Dra. Beatriz Garcia Sluminsky
Rua Reinaldo Hecke, 453/301-A— Abranches
82210-300 Curitiba, PR
E-mail: garciame@terra.com.br

Submitted em 25 de março de 2008
Accepted para publicação em 27 de outubro de 2008

 

 

* Received from Serviço de Anestesiologia do Hospital Vita Curitiba, Curitiba, PR