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您所在的位置:首頁 > 專業交流 > Lancet:術前輸血能降低鐮狀細胞病患者圍手術期并發癥

Lancet:術前輸血能降低鐮狀細胞病患者圍手術期并發癥

2013-02-16 15:09 閱讀:1889 來源:medlive.cn 作者:網* 責任編輯:網絡
[導讀] 近期在線發表于《柳葉刀》的一項研究表明,術前輸血能降低鐮狀細胞病患者圍手術期并發癥的發生。
近期在線發表于《柳葉刀》的一項研究表明,術前輸血能降低鐮狀細胞病患者圍手術期并發癥的發生。
目前對于術前輸血能否給鐮狀細胞病患者帶來獲益尚無統一的意見。由于圍手術期并發癥常見于鐮狀細胞患者,英國Guy’s and St Thomas醫院的Jo Howard博士等評估選擇術前輸血患者的其圍手術期并發癥發生率。
該前瞻性多中心隨機對照研究在四個國家22家醫院進行開展。入組的受試者為年齡至少為1歲、鐮狀細胞貧血(SS)或鐮狀β°-地中海貧血(Sβ°)、并且準備進行低危(如腹股溝疝修補術、腺樣體切除術)或中危(如膽囊切除術、關節置換術)手術。排除符合上述入組標準的患者被隨機分為兩組,一組在術前不進行輸血,另一組在術前10天內進行輸血。研究的主要結局是在隨機化和術后30天出現重要并發癥的患者所占的比例。采用意向治療對研究結果進行分析。
研究納入了70名患者,最終分析了67名患者數據,其中33名未進行術前輸血,34名在術前進行了輸血。納入分析的67名患者中,65名患者的血紅蛋白為SS亞型,54名患者擬進行中危手術。術前未輸血組中13人發生了臨床重要并發癥,而術前輸血組中僅5人,所占比例分別為39%和15%。在出現并發癥患者中,兩組分別有10人(30%)和1人(3%)出現嚴重不良反應。沒有調整的臨床重要并發癥的比值比為3.8%,95%可信區間為1.2~12.2。這11名出現嚴重不良反應的患者中有10人(91%)出現了急性胸痛綜合征,其中9人術前未輸血,1人進行術前輸血。在兩組間,研究者們并未發現存在住院天數和再次入院率的差別。
研究結果指出,在鐮狀細胞病患者中進行術前輸血能降低患者圍手術期并發癥的發生率,特別是能改善擬進行低危和中危手術的血紅蛋白SS亞型的患者在圍手術期并發癥的產生。
The Transfusion Alternatives Preoperatively in Sickle Cell Disease (TAPS) study: a randomised, controlled, multicentre clinical trial.
BACKGROUND: No consensus exists on whether preoperative blood transfusions are beneficial in patients with sickle-cell disease. We assessed whether perioperative complication rates would be altered by preoperative transfusion. METHODS: We did a multicentre, randomised trial. Eligible patients were aged at least 1 year, had haemoglobin SS or Sβ(0)thalassaemia sickle-cell-disease subtypes, and were scheduled for low-risk or medium-risk operations. Patients were randomly assigned no transfusion or transfusion no more than 10 days before surgery. The primary outcome was the proportion of clinically important complications between randomisation and 30 days after surgery. Analysis was by intention to treat. FINDINGS: 67 (96%) of 70 enrolled patients-33 no preoperative transfusion and 34 preoperative transfusion-were assessed. 65 (97%) of 67 patients had the haemoglobin SS subtype and 54 (81%) were scheduled to undergo medium-risk surgery. 13 (39%) of 33 patients in the no-preoperative-transfusion group had clinically important complications, compared with five (15%) in the preoperative-transfusion group (p=0·023). Of these, 10 (30%) and one (3%), respectively, had serious adverse events. The unadjusted odds ratio of clinically important complications was 3·8 (95% CI 1·2-12·2, p=0·027). 10 (91%) of 11 serious adverse events were acute chest syndrome (nine in the no-preoperative-transfusion group and one in the preoperative-transfusion group). Duration of hospital stay and readmission rates did not differ between study groups. INTERPRETATION: Preoperative transfusion was associated with decreased perioperative complications in patients with sickle-cell disease in this trial. This approach could, therefore, be beneficial for patients with the haemoglobin SS subtype who are scheduled to undergo low-risk and medium-risk surgeries. FUNDING: NHS Blood and Transplant.

 


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