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Canadian Journal of Anesthesia 52:30-37 (2005)
© Canadian Anesthesiologists' Society, 2005

General Anesthesia

Perioperative platelet transfusion: recommendations of the Agence française de sécurité sanitaire des produits de santé (AFSSaPS) 2003

[Transfusion périopératoire de plaquettes : recommandations de l’Agence française de sécurité sanitaire des produits de santé (AFSSaPS) 2003]

Charles Marc Samama, MD PhD*, Rachid Djoudi, MD{dagger}, Thomas Lecompte, MD PhD{ddagger}, Nathalie Nathan-Denizot, MD PhD§, Jean-François Schved, MD PhD ¶ and the AFSSAPS Expert Group

* From the Département d’Anesthésie-Réanimation, Hôpital Avicenne, Bobigny;
{dagger} Site transfusionnel Saint-Antoine, EFS Ile-de-France, Paris;
{ddagger} Service d’Hématologie Biologique, CHU de Nancy, Nancy;
§ Département d’Anesthésie-Réanimation Chirurgicale, Centre Hospitalier Universitaire Dupuytren, Limoges; Département d’Hématologie/Biologie, CHU Saint Eloi, Montpellier, France.

Address correspondence to: Pr. Charles Marc Samama, Département d’Anesthésie-Réanimation, Hôpital Avicenne, 125, route de Stalingrad, 93009 Bobigny cedex, France. Phone: +33-1-48955591; Fax: +33-1-48955589; E-mail: cmsamama{at}invivo.edu


    Abstract
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 Abstract
 Introduction
 Perioperative platelet...
 Platelet transfusion before an...
 Platelet transfusion during an...
 APPENDIX 1
 References
 
Purpose: To present the recommendations of the Agence Française de Sécurité Sanitaire des Produits de Santé (AFSSaPS; French Safety Agency for Health Products).

Methods: A panel of experts reviewed and graded the literature on platelet transfusions; recommendations were formulated.

Main findings: Threshold platelet counts (PC) for transfusions in the perioperative context have not been clearly defined and should be determined by the existence of hemorrhagic risk factors. In the case of commonly practiced invasive procedures, the recommendation is to transfuse in order to achieve PC > 50,000·µL–1. In the absence of platelet dysfunction, regardless of the type of surgery, the standard hemorrhagic risk threshold for surgery is 50,000·µL–1. It has not been proven that the risk threshold is different according to the type of surgery. For neurosurgery and ophthalmologic surgery involving the posterior segment of the eye, a PC of 100,000·µL–1 is required. For axial regional anesthesia, a PC of 50,000·µL–1 is sufficient for spinal anesthesia; a PC of 80,000·µL–1 has been proposed for epidurals. During massive transfusion, prophylactic platelet infusion cannot be recommended beyond a loss of two blood volumes in less than 24 hr (Professional Consensus). As for the therapeutic transfusion of plasma and/or platelets, as much as possible, platelet deficit should be documented with test results (PC and fibrinogen) before transfusing. In the event of bleeding, platelet transfusion may precede plasma infusion. However, although this recommendation has been the subject of several professional consensus agreements, it is not based on any randomized studies.

Conclusion: Threshold PC for perioperative transfusions have not been clearly defined and most recommendations are the result of a professional consensus.


    Introduction
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 Abstract
 Introduction
 Perioperative platelet...
 Platelet transfusion before an...
 Platelet transfusion during an...
 APPENDIX 1
 References
 
IN 2003, the Agence Française de Sécurité Sanitaire des Produits de Santé (AFSSaPS; French Safety Agency for Health Products) issued new recommendations on platelet transfusion to update the previous recommendations issued in 1997. A large working group was constituted, composed of several experts originating from different medical fields (anesthesiology, intensive care, transfusion medicine, hematology, immunology, pediatrics). The litterature was screened extensively, using several databases (Medline, Embase, etc) and after one year of intensive work and several meetings, an extensive review of the subject and the related recommendations became available. The texts were reviewed by a multidisciplinary reading committee whose comments were implemented in the final version. Recommendations were classified (grade) according to the evidence level of the studies supporting them (Table IGo). Finally, the texts were validated by the "Comité de validation des recommanda-tions et Références médicales de l’AFSSaPS." Members of these three groups are listed in Appendix 1.


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TABLE I Levels of evidence and grades of recommendations
 
We have chosen to extract the perioperative section of these recommendations for the information of clinical anesthesiologists.

The original, integral version of the recommendations on platelet transfusions can be found on the website of the Agence Française de Sécurité Sanitaire des Produits de Santé: AFSSaPS (French Safety Agency for Health Products): http://www.agmed.sante.gouv.fr/htm/5/rbp/indrbp.htm


    Perioperative platelet transfusions: recommendations
 TOP
 Abstract
 Introduction
 Perioperative platelet...
 Platelet transfusion before an...
 Platelet transfusion during an...
 APPENDIX 1
 References
 
Threshold platelet counts (PC) for perioperative transfusions have not been clearly defined and should be determined by the existence of hemorrhagic risk factors:

- The existence and severity of spontaneous bleeding syndrome or bleeding caused by a minor trauma.
- A history of bleeding or transfusions during previous minor surgery or invasive procedures.
- Associated hemostatic abnormality, particularly in the case of disseminated intravascular coagulation.
- Changes in platelet function induced by drugs or associated diseases: blood diseases (monoclonal gammopathy, myelodysplasia), kidney disease.
- Hypothermia, anemia, splenomegaly.
- Persistent shock, infection.
- Hypertension.

Regardless of the hemorrhagic risk assessment:

- The procedure should always be performed by an experienced practitioner.
- The rapid availability of blood products should be ensured.
- Hemorrhagic risk factors should be corrected.

It is recommended, particularly for surgery, that non-specific methods of reduction of bleeding be used, i.e., (Professional Consensus):

- First choose the method that provides the best surgical control of hemostasis.
- Maintain normothermia.1
- Limit hemodilution.2–4
- Ensure the early detection of a hemorrhagic syndrome requiring complementary surgical hemosta-sis.5
- Limit therapies interfering with hemostasis (anticoagulants, antiplatelet agents...) to strict indications.6


    Platelet transfusion before an invasive procedure or surgery in the event of thrombocytopenia
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 Introduction
 Perioperative platelet...
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 APPENDIX 1
 References
 
Invasive procedure
For common invasive procedures (transparietal liver biopsy, lumbar puncture, transbronchial endoscopic biopsy, gastrointestinal endoscopy with biopsy, placement of catheter, etc.) performed in thrombocy-topenic patients, the recommendation is to transfuse platelets to achieve a PC > 50,000·µL–1 (Grade C).7,8 Post-transfusion PC should be monitored prior to the procedure. It is not necessary to systematically check the bleeding time.9,10

Surgery
In the absence of platelet dysfunction, regardless of the type of surgery, there is no hemorrhagic risk associated with thrombocytopenia alone for PC > 50,000·µL–1. The risk is low for PC between 50,000 to 100,000·µL–1. The standard threshold for hemorrhagic risk for surgery is therefore 50,000·µL–1, including cardiac surgery with cardiopulmonary bypass (Professional Consensus).11–15

There is no proof that the risk threshold is different according to the type of surgery. Nonetheless, for neu-rosurgery and ophthalmologic surgery involving the posterior segment of the eye, a PC of 100,000·µL–1 is required.16

For axial regional anesthesia:

a PC of 50,000·µL–1 is deemed sufficient for spinal anesthesia.

a PC of 80,000·µL–1 has been proposed for epidurals, but other hemorrhagic risk factors must be taken into account, particularly those cited previously, as well as the progressive nature of the thrombocytope-nia.17–21

Aside from cases of massive transfusion, platelet transfusion is considered useful in cardiac surgery and major liver surgery (particularly liver transplantation and portocaval shunt).

In cardiac surgery, therapeutic platelet transfusion is justified if the PC < 50,000·µL–1 (Professional Consensus). Platelet transfusion is justified in the event of microvascular bleeding associated with PC < 100,000·µL–1 (Grade B evidence).

In liver surgery, particularly transplantation, therapeutic platelet transfusion is justified if the PC is 50,000·µL–1 (Grade C). Correction of other factors that foster bleeding such as hypovolemia, hypothermia and anemia is imperative and is an integral part of the platelet transfusion process.

In obstetrics, there is no indication for platelet transfusion in the case of gestational thrombocytope-nia22 in late pregnancy (also known as idiopathic thrombocytopenic purpura (Professional Consensus).

In the event of thrombocytopenia associated with hemolysis, elevated liver enzymes, and low platelets syndrome (HELLP) or preeclampsia, platelet transfusion is recommended immediately before a Cesarean section for a PC of less than 50,000·µL–1 and immediately before vaginal delivery for a PC < 30,000·µL–1 (Professional Consensus).

In autoimmune thrombocytopenic purpura, transfused platelets are very rapidly destroyed, as are the patient’s own platelets. Therefore, there is no indication for platelet transfusion, aside from life-threatening hemorrhagic emergencies (Professional Consensus). In this case, they should be combined with intravenously administered immunoglobulin and high doses of corticosteroids.


    Platelet transfusion during an invasive procedure or surgery in the event of thrombopathy
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 Abstract
 Introduction
 Perioperative platelet...
 Platelet transfusion before an...
 Platelet transfusion during an...
 APPENDIX 1
 References
 
Hematologic thrombopathy
Constitutional or acquired thrombopathy should be managed by specialists for an in-depth investigation. There is no proof that any specific test (particularly the bleeding time) can predict hemorrhagic risk in these patients.

Drug-induced thrombopathy
Drug-induced thrombopathies are the most frequent cause of acquired thrombopathy.23–30 The main drugs involved are platelet function inhibitors and nons-teroidal anti-inflammatory drugs, which have an effect on platelet functionA (depending on the drug and the dosage).

Drugs involved6
The hemorrhagic risks by type of surgery are presented in Appendix 2Go.


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APPENDIX 2 Drugs most often involved in abnormal platelet function in surgical patients
 
Prophylaxis
Prophylactic platelet transfusion before an invasive procedure, when platelet inhibitor therapy has not been discontinued in a timely manner, is not recommended (Professional Consensus).

Role of transfusion
There are no clinical studies validating the benefits of platelet transfusion in reducing the risk of bleeding (prophylactic administration) or in limiting bleeding when it occurs (therapeutic administration) in patients with drug induced thrombopathy. However, this is the only therapeutic option that can be envisaged in the event of severe hemorrhage (Professional Consensus).

Platelet transfusion in the event of massive transfusion
Several definitions for massive transfusion have been proposed:5,31–35

- Replacement of the loss of more than one blood volume in less than 24 hr.
- Replacement of the loss of more than 50% of blood volume in less than three hours.
- Blood loss of more than 150 mL·min–1.

Treatment priorities are:

- Restore blood volume to maintain tissue perfusion and oxygenation.
- Control hemostasis by treating the cause of bleeding and by correcting the coagulopathy with an appropriate choice of blood products.

Prophylactic platelet transfusions based on volume replaced
Prophylactic infusion of platelets is not recommended beyond the replacement of two blood volumes in less than 24 hr (Professional Consensus).

It is important to consider the individual clinical situation and reasons for bleeding. It is likely but not certain that the preventive administration of platelets is not useful if the patient is not bleeding.

Fresh frozen plasma (FFP) should be transfused at the same time as platelets.

Therapeutic platelet transfusion
Abnormal bleeding is bleeding that is unexpected and does not respond either to compression or to electro-coagulation. Although clinical assessment remains an important element in the decision making process, alone is not a sufficient indication for transfusion.

Transfusion of FFP or platelets
As much as possible, it is desirable to document platelet deficits with test results (PC and fibrinogen) before transfusing.

It is also desirable to closely monitor PC and fibrinogen and to begin with platelet concentrates (Professional Consensus). A number of authors suggest using point of care coagulation monitors for surgical bleeding.36

Other elements involved in increased hemostatic problems during massive transfusion
Hypothermia interferes with hemostasis. It is imperative that all available techniques be used to warm the patient as well as the infusion and transfusion products.1,37,38 A drop in hematocrit increases the risk of bleeding, particularly in the presence of thrombocy-topenia. Infusion of packed red blood cells should not be delayed.2–4 Hemostatic problems observed during massive transfusion are increased by shock. Optimization of the patient’s hemodynamic status is an essential objective.39 If a multiple trauma victim with multiple transfusions has a head injury, perioper-ative hemostasis should be controlled even further (earlier infusion of plasma, platelets).

Table IIGo summarizes the available information and proposes a therapeutic transfusion protocol based on the presence/absence of clinical bleeding and the results of laboratory tests.


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TABLE II Proposals to help with therapeutic decision making
 

    APPENDIX 1
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 Abstract
 Introduction
 Perioperative platelet...
 Platelet transfusion before an...
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 APPENDIX 1
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Working group
Pr MICHALLET Mauricette, President, Lyon

Dr NOUYRIGAT Emmanuel, Afssaps

Dr DUMARCET Nathalie, Afssaps

Dr BOURHIS Hean-Henri, Villejuif

Pr CAZENAVE Jean-Pierre, Strasbourg

Pr CLARIS Olivier, Lyon

Dr DAVID Bernard, Afssaps

Dr DECONINCK Eric, Besançon

Dr DENIS Catherine, Afssaps

Dr DJOUDI Rachid, Paris

Pr DUFOUR Patrick, Strasbourg

Dr FOLLEA Gilles, Nantes

Dr KAPLAN-GOUET Cécile, Paris

Pr LECOMPTE Thomas, Vandoeuvre les Nancy

Dr LEFRERE François, Paris

Pr MARIE Jean-Pierre, Paris

Dr MERCADIER Anne, Paris

Pr NATHAN-DENIZOT Nathalie, Limoges

Dr OUNNOUGHENE Afssaps

Pr SAMAMA Marc, Bobigny

Dr SANDID Afssaps

Pr SCHVED Jean-François, Montpellier

Dr SUTTON Laurent, Paris

Dr TRAINEAU Richard, Paris

Dr VEY Norbert, Marseille

Review group
Dr CHABERNAUD Jean-Louis, Clamart

Dr CLUET-DENNETIERE Sophie, Compiègne

Dr DENNINGER Marie-Hélène, Clichy

Dr FAVIER Rémi, Paris

Dr FORESTIER François, Bordeaux

Pr HARDY Jean-François, Montréal

Dr HERNANDORENA José-Xavier, Bayonne

Pr HERVE Patrick, Besançon

Pr IFRAH Norbert, Angers

Pr JANVIER Gérard, Pessac

Pr JOUSSEMET Marcel, Clamart

Dr LAPIERRE Valérie, Besançon

Dr LASNE Dominique, Paris

Dr LEPEU Gérard, Avignon

Pr LONGROIS Dan, Nancy

Pr MILPIED Noël, Nantes

Pr MULLER Jean-Yves, Nantes

Dr PIGNON Bernard, Reims

Pr RIOU Bruno, Paris

Dr SENSEBE Luc, Tours

Pr SIE Pierre, Toulouse

Pr SIMEONI Umberto, Marseille

Pr STEIB Annick, Strasbourg

Pr VAN DER LINDEN Philippe, Jumet

Pr TCHERNIA Gilbert, Le Kremlin Bicêtre

Validation Commmittee
Pr BOUVENOT Gilles, President, Marseille

Pr BERGMANN Jean-François, Vice-President, Paris

Dr CARON Jacques, Lille

Pr CAULIN Charles, Paris

Pr CHOUTET Patrick, Tours

Pr DUPUIS Bernard, Lille

Pr JOLLIET Pascale, Nantes

Dr AMBROSI Pierre, Marseille

Dr ATLAN Pierre, Paris

Pr BANNWARTH Bernard, Bordeaux

Dr CAMELLI Bruno, Paris

Dr CUCHERAT Michel, Lyon

Dr DEMOLIS Pierre, le Kremlin Bicêtre

Dr DENIS Catherine, Afssaps

Pr DIQUET Bertrand, Angers

Dr DUMARCET Nathalie, Afssaps

Dr GUEYFFIER François, Lyon

Dr HANSLIK Thomas, Boulogne Billancourt

Dr LE ROUX Gérard, Epinay sous Sénart

Dr LIEVRE Michel, , Lyon

Dr MEYER François, Afssaps

Pr PETIT Michel, Sotteville-lès-Rouen

Dr REVEILLAUD Olivier, Bièvres

Pr RICHÉ Christian, Brest

Dr ROSTOKER Guy, Afssaps

Dr TREMOLIERES François, Mantes-la-Jolie

Pr TROUVIN Jean-Hugues, Afssaps

Dr WONG Olivier, Paris


    Footnotes
 
Accepted for publication October 10, 2004.

A See experts’ conference organized at the initiative of the Société française d’anesthésie et de réanimation (SFAR; the French Society of Anesthesiology and Intensive Care) on "Antiplatelet agents in the perioperative period", available at www.Sfar.org. Back


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 Abstract
 Introduction
 Perioperative platelet...
 Platelet transfusion before an...
 Platelet transfusion during an...
 APPENDIX 1
 References
 
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