| Transfusion related acute lung injury |
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Micrograph of diffuse alveolar damage, the histologic correlate of TRALI. H&E stain.
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| Classification and external resources |
| ICD-9 |
518.7 |
Chest X-ray of transfusion-related acute lung injury (TRALI) compared to chest X-ray of the same subject afterwards.
In medicine, transfusion related acute lung injury (TRALI) is a serious blood transfusion complication characterized by the acute onset of non-cardiogenic pulmonary edema following transfusion of blood products.[1]
Although the incidence of TRALI has decreased with modified transfusion practices, it is still the leading cause of transfusion-related fatalities in the United States from fiscal year 2008 through fiscal year 2012.[2]
Contents
- 1 Definition
- 2 Incidence
- 3 Etiology and risk factors
- 4 Pathophysiology
- 5 Clinical Features
- 6 Mortality & morbidity
- 7 Treatment
- 8 See also
- 9 References
- 10 External links
Definition
TRALI is defined as an acute lung injury that is temporally related to a blood transfusion; specifically, it occurs within the first six hours following a transfusion.[3]
It is typically associated with plasma components such as platelets and Fresh Frozen Plasma, though cases have been reported with packed red blood cells since there is some residual plasma in the packed cells. The blood component transfused is not part of the case definition. Transfusion-related acute lung injury (TRALI) is an uncommon syndrome that is due to the presence of leukocyte antibodies in transfused plasma. TRALI is believed to occur in approximately one in every 5000 transfusions. Leukoagglutination and pooling of granulocytes in the recipient's lungs may occur, with release of the contents of leukocyte granules, and resulting injury to cellular membranes, endothelial surfaces, and potentially to lung parenchyma. In most cases leukoagglutination results in mild dyspnea and pulmonary infiltrates within about 6 hours of transfusion, and spontaneously resolves;
Occasionally more severe lung injury occurs as a result of this phenomenon and Acute Respiratory Distress Syndrome (ARDS) results. Leukocyte filters may prevent TRALI for those patients whose lung injury is due to leukoagglutination of the donor white blood cells, but because most TRALI is due to donor antibodies to leukocytes, filters are not helpful in TRALI prevention. Transfused plasma (from any component source) may also contain antibodies that cross-react with platelets in the recipient, producing usually mild forms of posttransfusion purpura or platelet aggregation after transfusion.
Another nonspecific form of immunologic transfusion complication is mild to moderate immunosuppression consequent to transfusion. This effect of transfusion is not completely understood, but appears to be more common with cellular transfusion and may result in both desirable and undesirable effects. Mild immunosuppression may benefit organ transplant recipients and patients with autoimmune diseases; however, neonates and other already immunosuppressed hosts may be more vulnerable to infection, and cancer patients may possibly have worse outcomes postoperatively.
Incidence
The true incidence of TRALI is unknown because of the difficulty in making the diagnosis and because of underreporting. It is estimated to occur in 1:1300 to 1:5000 transfusions of plasma-containing products. TRALI is the leading reported cause of death related to transfusion in the United States; more than 20 cases were reported per year from 2003 to 2005.
Etiology and risk factors
The etiology of TRALI is currently not fully understood. TRALI is thought to be immune mediated.[4][5] Antibodies directed toward Human Leukocyte Antigens (HLA) or Human Neutrophil Antigens (HNA) have been implicated. Women who are multiparous (have had more than one child) develop these antibodies through exposure to fetal blood; transfusion of blood components obtained from these donors is thought to carry a higher risk of inducing immune-mediated TRALI.[5] Previous transfusion or transplantation can also lead to donor sensitization. To be at risk of TRALI via this mechanism, the blood recipient must express the specific HLA or neutrophil receptors to which the implicated donor has formed antibodies. A two-hit hypothesis has been suggested[citation needed] wherein pre-existing pulmonary pathology (i.e. the first-hit) leads to localization of neutrophils to the pulmonary microvasculature. The second hit occurs when the aforementioned antibodies are transfused and attach to and activate neutrophils, leading to release of cytokines and vasoactive substances that induce non-cardiac pulmonary edema.
A non-immune mechanism has been studied and proposed by Silliman, involving the accumulation of bioactive lipids in stored blood components (red cells, platelets, plasma) that possess neutrophil priming capabilities.
TRALI is typically associated with plasma products such as FFP, but can also occur in recipients of packed red blood cells due to the residual plasma present in the unit. The AABB (formerly the American Association of Blood Banks) recommended on 11/03/2006 in association bulletin 06-07 that blood banks use high plasma volume components from female donors for further manufacturing instead of transfusion due to the higher risk of TRALI.
Pathophysiology
The precise mechanisms of the capillary leak syndrome in TRALI have not been fully determined, but two main hypotheses have been proposed. One involves white cell antibody-mediated TRALI and the other cytokine-mediated TRALI. The former suggests that TRALI is often a result of infusion of antibodies to HLA class I or class II or human neutrophil antigens (HNAs). Following transfusion, these antibodies react with neutrophils in the pulmonary microvasculature. Activated neutrophils damage the endothelium. Vascular leakage into the alveolar space with pulmonary edema ensues. In 90 percent of reported cases, antibodies were present in the donor plasma; in 10 percent of the cases antibodies were present in the recipient plasma. The second hypothesis suggests that neutrophils accumulate and are primed in the patient's pulmonary microvasculature as a result of preexisting systemic inflammation. Activation of these neutrophils by lipids or other mediators, such as CD40L, which accumulate in cellular blood components during storage, contributes to endothelial damage in susceptible patients, leading to vascular leaks and pulmonary edema. Because 20 percent of blood components contain HLA antibodies yet TRALI is relatively uncommon, it is conceivable that additional factors play a role in the development of TRALI.
Clinical Features
It is often impossible to distinguish TRALI from adult respiratory distress syndrome. The typical presentation of TRALI is the sudden development of dyspnea, severe hypoxemia (O2 saturation <90% in room air), hypotension, and fever that develop within 6 hours after transfusion and usually resolve with supportive care within 48 to 96 hours. Although hypotension is considered one of the important signs in diagnosing TRALI, hypertension can occur in some cases.
Mortality & morbidity
The immune mediated form of TRALI occurs approximately once every 5000 transfusions and has a mortality of 6-9%.[6]
Treatment
Supportive care is the mainstay of therapy in TRALI. Oxygen supplementation is employed in all reported cases of TRALI and aggressive respiratory support is needed in 72 percent of patients. Intravenous administration of fluids, as well as vasopressors, are essential for blood pressure support. Use of diuretics, which are indicated in the management of transfusion associated circulatory overload (TACO), should be avoided in TRALI. Corticosteroids can be beneficial.
See also
References
- ^ Gajic O, Moore SB. Transfusion-related acute lung injury. Mayo Clin Proc. 2005 Jun;80(6):766-70. PMID 15945528.
- ^ U.S. Food and Drug Administration, Center for Biologics Evaluation and Research. Fatalities Reported to FDA Following Blood Collection and Transfusion: Annual Summary for Fiscal Year 2012. Bethesda, Md: U.S. Food and Drug Administration.
- ^ Toy P, Popovsky MA, Abraham E, Ambruso DR, Holness LG, Kopko PM, McFarland JG, Nathens AB, Silliman CC, Stroncek D; National Heart, Lung and Blood Institute Working Group on TRALI. Transfusion-related acute lung injury: definition and review. Crit Care Med. 2005 Apr;33(4):721-6. PMID 15818095.
- ^ Dykes A, Smallwood D, Kotsimbos T, Street A. Transfusion-related acute lung injury (TRALI) in a patient with a single lung transplant. Br J Haematol. 2000 Jun;109(3):674-6. PMID 10886228.
- ^ a b Muller JY. [TRALI: from diagnosis to prevention] Transfus Clin Biol. 2005 Jun;12(2):95-102. PMID 15894508.
- ^ Bux J. Transfusion-related acute lung injury (TRALI): a serious adverse event of blood transfusion. Vox Sang. 2005 Jul;89(1):1-10. PMID 15938734.
External links
- Transfusion Related Acute Lung Injury - US Food and Drug Administration (FDA).
- Neutrophil Antigens and Antibodies - American Society of Histocompatibility and Immunogenetics.
- TRALI (ABBA)
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Transfusion medicine
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| General concepts |
- Apheresis (plasmapheresis, plateletpheresis, leukapheresis)
- Blood transfusion
- Coombs test (direct and indirect)
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- International Society of Blood Transfusion
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- ISBT 128
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blood types |
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Blood products /
blood donation |
- Whole blood
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Index of cells from bone marrow
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| Description |
- Immune system
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| Treatment |
- Transfusion
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Complications of surgical and medical care (T80–T88, 996–999)
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| Transfusion reactions |
- Transfusion hemosiderosis
- TRALI
- TACO
- TA-GvHD
- FNHTR
- Acute/Delayed hemolytic transfusion reaction
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| Vaccine injury |
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| Other |
- Serum sickness
- Malignant hyperthermia
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また、HTLV-116)、CMV17)、エプスタイン・バーウイルス(EBV)18)、ヒトパルボウイルスB1919)、マラリア原虫20)、E型肝炎ウイルス(HEV)21)等に感染することがあり、その他血液を介するウイルス、細菌、原虫等に感染する危険性も否定できない。観察を十分に行い、感染が確認された場合には適切な処置を行うこと。
