Xarelto (rivaroxaban) - recommendation for holding prior to injection?

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ctts

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Just saw my first patient on Xarelto. Not aware of any guidelines on how long to hold prior to ESI and when it can be restarted. Any thoughts on this? Thanks!

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An epidural catheter should not be removed earlier than 18 hours after the last administration of XARELTO®. The next XARELTO® dose is not to be administered earlier than 6 hours after the removal of the catheter. Delay the administration of XARELTO® for 24 hours if traumatic puncture occurs
 
Just my first patient on Xarelto-

Are people treating this like Pradaxa?

3 days off for most patients, 5 days off for renal dysfunction?
 
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An epidural catheter should not be removed earlier than 18 hours after the last administration of XARELTO®. The next XARELTO® dose is not to be administered earlier than 6 hours after the removal of the catheter. Delay the administration of XARELTO® for 24 hours if traumatic puncture occurs

The information above is from the package insert. Also, it is contraindicated in renal impairment (creatinine clearance < 15 mL/min), moderate and severe hepatic impairment with elevated INR.

I recommend to my patients to hold for 24 hours.
 
The information above is from the package insert. Also, it is contraindicated in renal impairment (creatinine clearance < 15 mL/min), moderate and severe hepatic impairment with elevated INR.

I recommend to my patients to hold for 24 hours.

Why only 24 hours? It seems like it would take more than 24 hours for the body to completely replace the Factor Xa, (and that's once the drug has left the body).

It seems that a few years after every new blood thinner is introduced, the required time to hold it for neuroaxial procedures is increased, (after unexpected bleeds are reported).

I'd rather skip that possibility in my patient needing a cervical ESI.
 
From the PI:

WARNINGS: (A) DISCONTINUING XARELTO® IN PATIENTS WITH NONVALVULAR ATRIAL FIBRILLATION INCREASES RISK OF STROKE,
(B) SPINAL/EPIDURAL HEMATOMA
A. DISCONTINUING XARELTO® IN PATIENTS WITH NONVALVULAR ATRIAL FIBRILLATION

Discontinuing XARELTO® places patients at an increased risk of thrombotic events. An increased rate of stroke was observed following XARELTO® discontinuation in clinical trials in atrial fibrillation patients. If anticoagulation with XARELTO® must be discontinued for a reason other than pathological bleeding, consider administering another anticoagulant.

B. SPINAL/EPIDURAL HEMATOMA

Epidural or spinal hematomas have occurred in patients treated with XARELTO® who are receiving neuraxial anesthesia or undergoing spinal puncture. These hematomas may result in long-term or permanent paralysis. Consider these risks when scheduling patients for spinal procedures. Factors that can increase the risk of developing epidural or spinal hematomas in these patients include:

Use of indwelling epidural catheters

Concomitant use of other drugs that affect hemostasis, such as non-steroidal anti-inflammatory drugs (NSAIDs), platelet inhibitors, other anticoagulants, see Drug Interactions

A history of traumatic or repeated epidural or spinal punctures

A history of spinal deformity or spinal surgery

Monitor patients frequently for signs and symptoms of neurological impairment. If neurological compromise is noted, urgent treatment is necessary.

Consider the benefits and risks before neuraxial intervention in patients anticoagulated or to be anticoagulated for thromboprophylaxis.



Increased Risk of Stroke After Discontinuation in Nonvalvular Atrial Fibrillation: Discontinuing XARELTO®, in the absence of adequate alternative anticoagulation, increases the risk of thrombotic events. An increased rate of stroke was observed during the transition from XARELTO® to warfarin in clinical trials in atrial fibrillation patients. If XARELTO® must be discontinued for a reason other than pathological bleeding, consider administering another anticoagulant.



A specific antidote for rivaroxaban is not available. Because of high plasma protein binding, rivaroxaban is not expected to be dialyzable. Protamine sulfate and vitamin K are not expected to affect the anticoagulant activity of rivaroxaban. There is no experience with antifibrinolytic agents (tranexamic acid, aminocaproic acid) in individuals receiving rivaroxaban. There is neither scientific rationale for benefit nor experience with systemic hemostatics (desmopressin and aprotinin) in individuals receiving rivaroxaban. Use of procoagulant reversal agents such as prothrombin complex concentrate (PCC), activated prothrombin complex concentrate (APCC), or recombinant factor VIIa (rFVIIa) may be considered, but has not been evaluated in clinical trials.


Spinal/Epidural Anesthesia or Puncture: When neuraxial anesthesia (spinal/epidural anesthesia) or spinal puncture is employed, patients treated with anticoagulant agents for prevention of thromboembolic complications are at risk of developing an epidural or spinal hematoma, which can result in long-term or permanent paralysis.

An epidural catheter should not be removed earlier than 18 hours after the last administration of XARELTO®. The next XARELTO® dose is not to be administered earlier than 6 hours after the removal of the catheter. Delay the administration of XARELTO® for 24 hours if traumatic puncture occurs.



I'm guessing that there was 1+ epidural hematoma's during the study of the drug in Phase 3 trials. Also guessing that there were a number of CVA's when the drug was stopped for whatever reason. Because of the labeling, I'd defer the anticoagulation regimen to the Cardiologist. I'd also use a different informed consent for this drug that includes all the info above.
 
Why only 24 hours? It seems like it would take more than 24 hours for the body to completely replace the Factor Xa, (and that's once the drug has left the body).

It seems that a few years after every new blood thinner is introduced, the required time to hold it for neuroaxial procedures is increased, (after unexpected bleeds are reported).

I'd rather skip that possibility in my patient needing a cervical ESI.

Due to it's pharmacokinetics, and PI, I treat it as other Xa inhibitors such as LMWH and follow the ARSA Guidelines for therapeutic doses -> hold for 24 hours.
 
Due to it's pharmacokinetics, and PI, I treat it as other Xa inhibitors such as LMWH and follow the ARSA Guidelines for therapeutic doses -> hold for 24 hours.


So is everyone just having patients hold Xarelto for 24 hrs before procedures?

Not many people chimed on this thread.
 
So nobody has an opinion on this besides NOSFAN?

No one ever sees patients on Xarelto besides me?
It depends on when surgery is scheduled. It's supposed to be taken with the heaviest meal of the day (typically dinner), so it could be closer to 30+ hours if you take it with dinner Wednesday night and surgery is Friday morning.
 
:confused::confused:
Due to it's pharmacokinetics, and PI, I treat it as other Xa inhibitors such as LMWH and follow the ARSA Guidelines for therapeutic doses -> hold for 24 hours.
Has anyone heard of using for surgeries other than knee/hip replacement? Just curious of outcomes/types of surgery where experience is being gained (no locations, just patient type/outcomes).
 
Thought I'd bump this thread since I just saw my first referral on Xarelto. Some of the stories I've seen from surgeons are horrifying.

Anything new?
 
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Thought I'd bump this thread since I just saw my first referral on Xarelto. Some of the stories I've seen from surgeons are horrifying.

Anything new?

I've bumped it several times and nobody wants to say a damn thing......




What are the horror stories from the surgeons?

Excessive bleeding in patient that were off for several days, excessive bleeding in emergency surgeries where the patients wasn't off for several day?

Spontaneous bleeding?
 
All of the above.

One surgeon said it helped him make an early dx of rectal CA because the pt started bleeding.
 
All of the above.

One surgeon said it helped him make an early dx of rectal CA because the pt started bleeding.

Ah,

I only had the one patient on it so far, cervical radic of course. I had him hold it for 4 days. Did fine, great response to ESI, and no problems, but I"m really hoping he never comes back....
 
Why only 24 hours? It seems like it would take more than 24 hours for the body to completely replace the Factor Xa, (and that's once the drug has left the body).

It seems that a few years after every new blood thinner is introduced, the required time to hold it for neuroaxial procedures is increased, (after unexpected bleeds are reported).

I'd rather skip that possibility in my patient needing a cervical ESI.

Xarelto reversibly binds Xa and does not deplete it. It has a plasma half-life of 5 to 9 hours in healthy subjects (ages 20 to 45 years) and 11 to 13 hours in the elderly. Therefore, the anticoagulant effect is only present when the drug is taken.
 
Our protocol for Xarelto is a hold time of 48 hrs prior to neuraxial blockade and do not resume Xarelto until 6 hours post-procedure.
 
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Any guidelines about when each antiplatelet/anticoagulant can be restarted post epidural ?
 
Great Question.

Here's what we use as guidelines to restart agents post-injection:

Most Anti-platlet agents: 2 hours post injection
Pradaxa : 6 hours
Thrombolytics: 10 days (except for catheter clearance doses there are no restrictions)
Xarelto: 6 hours
Heparin, Coumadin, Arixtra: 2 hours
Lovenox: 24 hours (which I do not agree with btw, IMHO)
 
And to clarify, those times were for minumum time between single neuraxial injection OR catheter removal until first dose of anticoagulant.
 
48 hours is what the cardiologist say for eliquis
 
48 hours is what the cardiologist say for eliquis

Cardiologist always underestimate these things, because their priority is different from ours. 10 years ago they would say you only need to hold plavix for 3 days, lovenox for 10 hrs, etc.

I always at least double whatever time period the cardiologist thinks
 
Cardiologist always underestimate these things, because their priority is different from ours. 10 years ago they would say you only need to hold plavix for 3 days, lovenox for 10 hrs, etc.

I always at least double whatever time period the cardiologist thinks

Any new thoughts on xarelto?
 
http://www2.kenes.com/asraspring201..._Neuraxial Anesthesia and Anticoagulation.pdf

According to European guidelines, 22-26 hours should elapse between discontinuation of rivaroxaban and neuraxial block (22). Longer intervals are required in patients with renal insufficiency. Indwelling neuraxial catheters are contraindicated due to the “boxed warning”. Given the potential for overestimation of renal function with estimated creatinine clearance, it is recommended that a minimum of two days (and ideally four days) elapse between discontinuation of rivaroxaban and neural blockade. Likewise, indwelling neuraxial catheters should be removed four to six hours prior to initiation of rivaroxaban therapy postoperatively(22).
 
we had a patient who ws on ASA 81 and Xarelto- both held for 5 d for cervical MBB procedure and she had a fair amount of bleeding noted subcutaneously after first injection. The rest of procedure aborted, I would rather be conservative and these are elective procedures.... however 5 days shoulder be plenty. Granted MBB is not neuroaxial its still close enough.
How long would you hold it for...
 
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we had a patient who ws on ASA 81 and Xarelto- both held for 5 d for cervical MBB procedure and she had a fair amount of bleeding noted subcutaneously after first injection. The rest of procedure aborted, I would rather be conservative and these are elective procedures.... however 5 days shoulder be plenty. Granted MBB is not neuroaxial its still close enough. Cards is giving push back to hold for longer.. she is in a fib. also I am not too excited about wanting to proceed w this one.
How long would you hold it for...

Would not hold anticoag for MBB or SIJ. Not in the neuraxis. Skin bleeding is not predictive of internal bleeding.
 
Would not hold anticoag for MBB or SIJ. Not in the neuraxis. Skin bleeding is not predictive of internal bleeding.[/quote

It was not skin bleeding topically, more of subcutaneous pooling in a 2 inch area . Notable bruising on post procedure followup as well.
 
Would not hold anticoag for MBB or SIJ. Not in the neuraxis. Skin bleeding is not predictive of internal bleeding.


Totally agree. I only hold anticoagulants for injection in the neuraxis, stellate ganglion and other sympathetic blocks, and anterior intra articular hips.

For Xarelto, I hold for 5 days, I haven't seen any solid evidence one way or another, but until ASRA includes it in guidelines, I figure better safe than sorry. I always get cardiology or prescribing doc clearance to hold it and other anticoagulants.
 
only need 2 days for xarelto and maybe 4 with renal insufficiency
 
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