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Similar efficacy of oral TXA to IA TXA in total knee arthroplasty without a tourniquet
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ARTHROPLASTY
Similar efficacy of oral TXA to IA TXA in total knee arthroplasty without a tourniquet .

OrthoEvidence Journal (OE Journal) - ACE Report

OE Journal. 2022;10(10):7 BMC Musculoskelet Disord. 2018 Mar 15;19(1):85
Autori che hanno contribuito

FX Pei ZK Zhou HY Wang D Wang H Zhu WK Meng ZY Luo Q Li

150 patients scheduled for total knee arthroplasty were randomized to either perioperative oral tranexamic acid or intraarticular tranexamic acid. Patients were assessed perioperatively for total blood loss, intraoperative blood loss, the incidence of transfusion, number of transfused units, and postoperative complications. At the 1-month and 3-month follow-ups, patients were also assessed for knee circumference, health-related quality of life, mortality, and readmission. No significant differences were observed between groups in the perioperative measures, including total blood loss, intraoperative blood loss, transfusion rate, and complication rate. Additionally, there were no significant differences between groups in outcomes at follow-up.


Dettagli sul finanziamento della pubblicazione +
Finanziamento:
Not Reported
Conflicts:
None disclosed

Rischio di pregiudizio

9/10

Criteri di segnalazione

20/21

Indice di fragilità

N/A

Was the allocation sequence adequately generated?

Was allocation adequately concealed?

Blinding Treatment Providers: Was knowledge of the allocated interventions adequately prevented?

Blinding Outcome Assessors: Was knowledge of the allocated interventions adequately prevented?

Blinding Patients: Was knowledge of the allocated interventions adequately prevented?

Was loss to follow-up (missing outcome data) infrequent?

Are reports of the study free of suggestion of selective outcome reporting?

Were outcomes objective, patient-important and assessed in a manner to limit bias (ie. duplicate assessors, Independent assessors)?

Was the sample size sufficiently large to assure a balance of prognosis and sufficiently large number of outcome events?

Was investigator expertise/experience with both treatment and control techniques likely the same (ie.were criteria for surgeon participation/expertise provided)?

Sì = 1

Incerto = 0,5

Non rilevante = 0

No = 0

La valutazione dei criteri di segnalazione valuta la trasparenza con cui gli autori riportano le caratteristiche metodologiche e sperimentali dello studio all'interno della pubblicazione. La valutazione è suddivisa in cinque categorie che vengono presentate di seguito.

4/4

Randomization

4/4

Outcome Measurements

4/4

Inclusion / Exclusion

4/4

Therapy Description

4/5

Statistics

Detsky AS, Naylor CD, O'Rourke K, McGeer AJ, L'Abbé KA. J Clin Epidemiol. 1992;45:255-65

L'Indice di Fragilità è uno strumento che aiuta l'interpretazione dei risultati significativi, fornendo una misura della forza di un risultato. L'Indice di Fragilità rappresenta il numero di eventi consecutivi che devono essere aggiunti a un risultato dicotomico per rendere il risultato non più significativo. Un numero piccolo rappresenta un risultato più debole, mentre un numero grande rappresenta un risultato più forte.

Perché questo studio era necessario ora?

Tranexamic acid has been the subject of investigation for reducing blood loss in total knee arthroplasty. Early studies have focused on the intravenous and intra-articular application of tranexamic acid in these procedures. More recently, interest has grown in the application of oral tranexamic acid. While results from placebo-controlled trials have demonstrated efficacy, comparisons to other forms of tranexamic acid are needed.

Qual era la domanda di ricerca principale?

In total knee arthroplasty, is there a significant difference in total blood loss between oral tranexamic acid administration and intraarticular tranexamic acid administration?

Caratteristiche dello studio +
Population:
150 patients, 18 years of age or older, scheduled for primary, unilateral total knee arthroplasty due to primary osteoarthritis. All cases were completed under general anesthesia, through a medial parapatellar approach. Chemothromboprophylaxis was administered using low-molecular-weight heparin (Clexane; Sanofi-Aventis) and rivaroxaban.
Intervention:
Oral TXA group: Patients were administered four oral tranexamic acid 500mg tablets at approximately 2 hours prior to incision, and subsequent 1g doses at 6 and 12 hours postoperatively. (n=75; 74 analyzed) (Mean age: 65.0+/-13.1)
Comparison:
IA TXA group: Patients were administered a solution of 3g tranexamic acid in 100mL saline intraoperatively via intraarticular infiltration. (n=75; 73 analyzed) (Mean age: 63.6+/-11.5)
Outcomes:
The primary outcome was total blood loss, calculated using the Gross formula. Secondary outcomes included intraoperative blood loss, transfusion rate, number of units transfused, postoperative hemoglobin and hematocrit levels, the incidence of postoperative complications, quality of life on the QoR-40 measure, range of motion, pain, the Knee Society Score, knee circumference, 30-day mortality, and 90-day readmission.
Methods:
RCT; Patient- and assessor-blind
Time:
Patients were assessed perioperatively, and at 1 and 3 months post-operation.
Quali erano i risultati importanti?
  • Total blood loss did not significantly differ between the oral TXA group (788.8+/-349.1mL) and the IA TXA group (872.4+/-393.1mL) (p=0.21).
  • Intraoperative blood loss and transfusion rate did not significantly differ between the oral TXA group and the IA TXA group (p=0.58 and 0.73, respectively).
  • Hemoglobin and hematocrit level at 72 hours post-operation did not significantly differ between the oral TXA group and the IA TXA group (p=0.22 and 0.20, respectively).
  • The incidence of complications did not significantly differ between the oral TXA group (2/74) and the IA TXA group (1/73). Complications included one case of DVT in the oral TXA group, one case of wound secretion in the oral TXA group, and one case of hematoma in the IA TXA group.
  • QoR-40, knee range of motion, and pain scores did not significantly differ between the oral TXA group and the IA TXA at 1 month or 3 months postoperatively.
  • No case of all cause 30-day mortality was observed in either group.
  • No case of all cause 90-day readmission was observed in either group.
Che cosa devo ricordare di più?

In total knee arthroplasty, oral tranexamic acid and intraarticular tranexamic acid demonstrated no significant differences in total blood loss, transfusion rate, incidence of postoperative complications, or postoperative clinical and functional outcomes up to 3 months postoperatively.

Come influenzerà l'assistenza ai miei pazienti?

The results of this study suggest that oral tranexamic acid may offer similar effects to intraarticular tranexamic acid on blood loss, transfusion rate, postoperative outcomes, and complications following total knee arthroplasty.

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Come citare questo documento ACE Report

OrthoEvidence. Similar efficacy of oral TXA to IA TXA in total knee arthroplasty without a tourniquet. OE Journal. 2022;10(10):7. Available from: https://myorthoevidence.com/AceReport/Show/

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