Can you get a DVT if your INR is 2.3. I have APS and my range should be 3.5 -4.
Woke up this morning with a niggle at top of my calf. I self tested and my INr is 2.3.
Rang my doctor all appointments have gone even though I stressed the urgency.
They advised me to ring 111. (UK) Done this and they were very helpful and I am waiting for a clinician to ring me back. But that I would check with everyone on here first.
Many thanks
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Molly100
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At the hospital they took a Venus blood test and my INR was actually 1.8! Anyway they gave me clexane injection and 10mg Warfarin. I go back tomorrow for a scan even though my blood test I did not have a DVT. Glad they checking because years ago when I was having recurrent DVT's I never had the obvious symptoms.
Short answer is "it depends" - on you. Real question is can YOU get a DVT at 2.3.
For me, 2.3 is in range and theoretically not a problem, I could still get a DVT but it would not be a particularly high risk (I clot arterially anyway). For YOU 2.3 is way below your range, which means your risk would be far far higher than mine (there will be a reason your range is higher). Hopefully it isn't one, but you've done the right thing.
Hi Molly hope you are okay, what is your normal medication if any? If you are on warfarin there is less than a 2% chance of clotting (caveat this with being taken correctly/no missed dosages/other illness etc) but didn't stop me panicking! Got sent to DVT clinic as had pain in my leg and vein inflamed. Turns out I also have edema (fluid in leg) as well as APS! And the NHS guidance is water tablets or drink more coffee as it is a natural duretic!
Oh gosh that sounds awful. I am on warfarin for 30 odd years due to APS. So it was a complete surprise to see that I have had another one. I am just glad that the hospital were so on the ball.
Hi everyone just to let you all know I do have a DVT!! Even though blood test said I didn't yesterday they had me back for a scan today. Thank god they did!! I cant praise Eastbourne DGH enough. They have been great. Just waiting to see Dr.
Glad you are being sorted out by Eastbourne hospital. It's good to know as I live near Battle. I note that you self tested yesterday when used first suspected a clot. Are you not able to self medicate as well? I am under St Thomas's with a range of 3.5 to 4. If I go below 3 I inject myself with Clexane. Perhaps you could discuss this route with your doctors.
Hi Stella. I'm not sure my brain could cope with that. I get awful brain fog . I feel happier leaving it to professional s. My partner gives me the clexane at home if needed . I'm just glad I did test and didn't leave it.
Hi Molly100, I’d agree with Ray, it’s all very personal to you. My understanding is that your range is assigned based on your risk, and being in range doesn’t guarantee zero event, but should lower the risk to the point that events are either unnoticeable or of minimal consequence.
Sharing experiences - because it’s good that we do - my INR range is 2.0-3.0, but I’ve still had a couple of repeat TIAs, however, they’re just that and very minor in comparison to a stroke. Message from my consultant is that this is life for me now, but that as long as I keep taking the pills and closely monitor my INR, and keep within my range then events should never escalate to the dangerous level.
So, and going back to Ray’s post, it’s great that you are checking your INR and getting the venous test done if any doubt exists at all - this is the best action you can take. The meters are known to read a bit high for APS (certainly the CoaguChek), so if in doubt then get checked fully, and make sure to communicate your concerns / niggles / symptoms to the doctor or clinic. I’m also working with them to try and keep my INR in the top half of the range, as the risk of a low reading is worse than the risk of a high one.
It can also be possible to get a bit of brain fog or memory issue when you’re INR is low, and obvs you have your own identifiers like your calf niggle. If so always then try and be aware of this, don’t ignore it, use it as a reason to do a test and check.
Above all, and I know it’s easy to say, but try hard not to worry too much, maybe just enough to make yourself test and check, and to then take the necessary action.
And if you’re lucky enough to have a great consultant, and get to see them occasionally, write all these uncertainties, questions, doubts and fears down, and then don’t leave the appointment until you’re happy with the responses!
Thank you for your reply. I have not had a DVT for 30 years and so it def came as a shock. I dread to think what would have happened if I had left it until Monday when I am due to send my test in to the Nurse who deals with it. Thank you all for your comments I am so glad we have each other on here to answer our problems.
On a side note, after reading all the lovely responses from all of our friends here, I would only add that it’s important to figure out if you are going to be a reliable,”finger sticker.”
Some of really aren’t, and that’s a shame.
You might be one who needs a blood draw once a week perhaps from your local clinic for a few months to make sure you are in your therapeutic range. ( you might even test each blood draw against your home coagu check for comparison.)
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