Low Potassium and tachycardia

Posted , 24 users are following.

Hi, im a active normally healthy 17 year old female. I eat well, at a good weight, have no eating disorders etc.

On the 9th of december last year, i started having chest pain and tachycardia. I was admitted to hospital and was told i have a potassium level of 2.7, my heart was going at 170bpm and had a bag of potassium fluids and 3 doses of a drug to slow my heart rate down.

A similair incident then occured on the 29th of december, potassium at 2.7 and required the drug to again slow my heart.

Now on the 26th of this month it happened again, but my potassium had dropped to 2.2 and i required 2 bags of fluids and 2 oral medicanol drinks before i was dicharged.

i have had numerous blood tests but no abnormal results, the doctors are still baffled on whats happening. 

When it happens, i feel the palpitations start and i get a sharp shooting pain up and down my chest. Since the first incident i am constantly tired and feel really sick, i keep suffering with bad headaches and joint pains. Due to my hospital being down 1 doctor, my treatment appears to keep getting delayed. When im in A&E after being admitted i am normally in there around 16+ hours before my heart rate begins to slow, i then have to finish my fluids from the iv administraation before going home.

It feels as though we are getting no where with the hospital as they cannot find whats wrong with me. 

Last night (29th Jan) i got mild chest pain and tachycardia. i was able to control it at home and slow it down myself after most the night by using the valsalvic maneovor, my heart was going around 130bpm. 

I have a blood test coming up on monday however my results always return normal. Has anyone got any feedback/input thats relevant and may help?

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  • Posted

    Its reassuring to know that you are following our discussions,zzappd. I recently found out that the doctor I saw was only a GP with a special interest in heart conditions so I asked my doctor to refer me to an Electrophysiologist who is  mentioned on the Arrhythmia Alliance website. I am a carer to my husband(he has Parkinsons Disease) so its not good for me to be having these attacks. I have gone as long as six months without one so I don't want to take regular medication. I just want something that will slow my heart back down when I have one. Something I am noticing though is that the day before an attack my stomach plays up and I don't think its coincidence. I had one in November and the day before I had been to the doctor over my stomach and I was given an h-pylori test. I woke with an attack at five in the morning and nothing would stop it and after four hours I had to go to A&E.
    • Posted

      There can be a number of triggers for people but usually if it's an svt it's random. The best and safest treatment is an ablation. In the meantime, try some of the maneuvers I mentioned earlier. I don't know without seeing the EKG, but if this is an svt, it poses absolutely no danger to you. But I'd need to see the monitor results to know for sure
  • Posted

    My first question is to inquire whether your magnisium level is within normal limits. If your magnisium is too low, you will not be able to raise your potassium. The second question is whether your physicians checked your aldosterone level and renin activity level, which is a simple blood test and 24 hour urine. Hyperaldosteronism will cause severe hypokalemia that will not be relieved until the excess aldosterone is eliminated. Just some suggestions.
  • Posted

    Can you explain what I do about thse potassium levels? I have had two SVT's within a month and four in three months.
    • Posted

      There can be several causes of SVT and hypokalemia is one. My first recommendation is that you see a cardiologist to determine if the cause of SVT. If your problem is just SVT and not hypokalemia, than a cardiologist is definitely recommended. The usual course of determining the cause of SVT, in addition to a detailed lifestyle assesment (caffeine consumption, etc), would be to have you wear a halter monitor for several weeks to a month. This will allow the cardiologist to monitor what type of arrhythmias you are having, how often, how long,  etc. It you have hypokalemia than the cause of your SVT may be potassium related.

      Severe hypokalemia (potassium levels below 2.5), cannot be left untreated. In addition to cardiac abnormalities, your kidneys are very sensitive to changes in potassium and do no respond well to prolonged hypokalemia.  While a general practitioner can discover low potassium, you should be referred to a specialist if the hypokalemia cannot be corrected with a potassium supplement. This usually means there is an underlying cause for your low potassium that must be addressed that could be multifaceted. 

      I would not recommend you try and treat this on your own. In addition to a cardiologist, you may wish to seek the help of an endocrinologist as your probem may be endocrine in nature. 

      Hope this helps. 

  • Posted

    Thank you. I have arranged to see my GP next week for a potassium test.

    I only saw a consultant at the end of March despite having SVT's for 5 years. He suggested an Ablation but I have never had ant tests. I have had to go to hospital five times over this period and never once has potassium levels been mentioned.

    Thanks for your kind advice.

    • Posted

      Good luck!

      While an ablation is certainly one way to fix isolated tachycardias, You first need to know the cause. This is an invasive procedure that is not without risks. 

      I certainly hope you can get your problem fixed! I know this must be worrisome to you and having the answers will go a long way in relieving your concerns.

  • Posted

    Thought I'd better add a few things from my experience after seeing all the comments. 

    I'm 50 and having been diagnosed with SVT since birth.

    When you have any kind of arythmia or tachycardia condition (racing heart, missed beats, palpatations, heart not pumping correctly e.g.top & bottom pump at the same time) I have found taking in natural potassium sources works very well for me (bananas, dried apricots, coconut water - organic sources work best) and the people I know with these conditions.

    The val salva maneuver (spelling), coughing and splashing cold water on your face work well to calm the episode.  The potassium ingestion takes it away.  I probably eat 2-3 bananas a day, as well as dried apricots, baked potatoes, avocados and raisins (all good sources of potassium).  Taking potassium pills triggers an episode.  Go figure (maybe because its a synthetic source).

    When I was young, laying on my heart side in bed would help an episode.  Now at 50 laying on my heart side causes an episode.  Laying on my opposite side abates it.  I think a neutral position is best.

    If I have an episode cooling my body helps a lot.  Heating my body up makes it worse.

    Find all your trigger foods/drinks and eliminate those from your diet.  Mine are coffee (caffeine), alcohol, chocolate, any herbs that stimulate e.g. st. john's wort, guarana, ginseng, watch out for cold remedies with ephedrine in them!  Even Coenzyme Q10 is a trigger for me (supposed to be good for your heart).  Unfortunately I've found my list of trigger foods expanding as I age. It was only caffeine when I was young.

    Stress affects the heart terribly (does me) and causes episodes of my SVT easily since I was 40.  In my 20s and 30s no problem.  In your early years you stress out when you get an episode and that makes the problem twice as worse.  When you age you know it will pass with time and you know what to do about it.  So you calm down.  You watch your breathing.  This calming helps a lot. 

    I have to watch my sleep too.  I have to get a solid 6-8 hours.  Anything shorter and I can guarantee an episode the next day (heart fluttering & racing up to 180bpm).

    So how do I cope?  I over-compensate with all the good stuff: I follow a strict routine getting good sleep, I avoid all trigger foods/drinks (gave up cofee & alcohol), I eat loads of veges. & no junk food, I lost loads of weight and I exercise 6 days per week.  It took years to get this way.  Not over night.  But you gotta start...

    The result: I now live a "normal" life.  I have minor episodes now only.  No major ones.  In 2000 a major one required defribilation.  That will wake you up - literally :-)

    The alternative is to become a victim to your illness and then you have to go down the medical remedy route of beta blockers, catheter ablation surgery and pacemaker.  Give the natural apporach a go first.  Any decent cardiologist will recommend it.

    Before I did all this: I was in a pretty dire situation the last 10 years.  There was so much I could no longer do.

    For those of you in their 20s and 30s I wish you can start the good habits now.  Follow a life of balance.  No extremes.  You only get one heart and those heart cells are not  replaced.  Make exercise a habit.  Find something you enjoy.  Eat well.  Sleep well.  Avoid stressful jobs and relationships.

    But if you do all that you can have your health and still be happy.  I am.  I experimented with all kinds of different things over the years to find out what's best for me.

    • Posted

      Please please please get your aldosterone and renin checked. Any of you who've had low potassium and tachycardia. And Google "Conn's" and "Primary Hyperaldosteronism".

      I wish someone had told me that before I had to go to ER/A&E nine times... with BP up to 255 and pulse up to 177.

      Oh, and if you get diagnosed, join the Facebook Hyperaldosteronism Support Group, great advice there

  • Posted

    I have had episodes of palpitation since I was your age nd it seemed to be linked to my menstrual cycle.I have never had any pain or breathlessness and the longest attack I have had was 25 minutes. Am now 57. They have recently become more unpredictable and a good friend suggested I asked for a referral to an electro cardiologist not a cardionlogist to sort it out. I wish this had happened before. You have every right to do this and I would strongly advise it as they were the first people who took it really seriously and made sense of it. I have taken potassioum supplements for ages and am not sure if theu helped or not. I have never takn any medication for this as am a bit of a health junkie. There are goos electro cardiologists at the Royal Brompton hosptial in London. I am seeing Dr Ernst who is very good and she deals with this sort of thinhg all the time and is a specialist in it. 
    • Posted

      I found potassium supplements actually made my condition worse - they triggered arythmias (irregular heartbeats).  You say you're a health food junkie so just consider that man made supplements are not health person.  Nature makes health food.  There's so many other support nutirents required for mineral absorbtion.  There's chemistry and physics at play.  I have found through experimentation its best to get your supplementation needs from foods, especially organic sources.

      For example, before exercise I eat half a banana and some dried apricots.  Half way through exercise I sip a little coconut water.  The result?  No arythmia or tachycardia.  Without these, a guaranteed episode during and after exercise.

      These foods are not a cure.  But I'm a strong believer in the need to over-compensate for one's genetic flaw.  So do more of the good stuff than normal folk do.  Doing so allows you to be "normal."

  • Posted

    I have svt and I just turned 21. I went to the hospital with a blood pressure of 78 over 42 and a heart rate over 160. Now I had it bother me before but it took 2 hours to get my heart rate down. They did an eco and found out I have an extra electrical pathway. I used to run cross country and play soccer in high school, but the electrical pathway is something you are born with that just decides to act up. So if you have not found a reason behind this yet tell your doctor you want an eco done in search of an extra electical pathway which can be fixed. I'm also pregnant so I have to wait til after baby arrives to get this small procedure. Anyway hope this can help people.
  • Posted

    I have magnesium and potassium supplements to help with this problem and if i miss any doses it acts up. I also take another pill flecanide to control my heart rate. And my blood tests were all normal. It can't be caught without further investigation.
    • Posted

      I found the supplements don't work as well as natural sources.  In fact as I aged the supplements induced episodes.  I find bananas, coconut water & dried apricots work best.
  • Posted

    Hi there, I'm a 35 yearold man. I found out about a potassium problem I was having when I turned 31. Well it took me until recently, this year actually to finally find a partial remedy to this problem. I read it from another website and decided to give it a go: V8 Juice. If I feel my potassium level dipping (which usually kicks in a feeling like asthma [can't get a deep breath]) I drop a cup or two of the juice and within a few minutes I'm back to normal. You need the LOW SODIUM stuff though and it costs next to nothing to buy at the grocery store, maybe $5 for a big bottle.

    I've tried Potassium Pills and various other things but what really helped is drinking ALOT of Orange Juice and the odd glass of V8. Recently, I've been having frequent urination problems so I have to remind myself to drink more V8, at least a glass per day. This will unfortunately cause a bit of diahrrea but, the pros outweigh the cons. If you don't have either of those available then you need to be taking in lots of coconut water (generally expensive) and eating bananas like nobody's business. Its important to get that hit of potassium each day. 

    • Posted

      The best potassium remedy I've found is from banana skins.  Boil them then simmer for 10 mins.  Strain the skinds and drink.  Gives me a good night's sleep if I have tachycardia.  Great remedy.
    • Posted

      No not much now. Before it was really bad but the addition to frequent shots of orange juice and V8 have completely cleared up my problems. Whenever I feel the symptoms kicking in, I drink a couple glasses of V8 and follow it with a bit of orange juice the next day.  Seriously, try it. 

       

    • Posted

      Thanks for the tip pal, I'll try that when I'm in a pinch. Sometimes there are no places to get V8, but Bananas are virtually everywhere you go and CHEAP. Great work. 
    • Posted

      Thing is iv gastritis that's why it's all so difficult to treat so oj n tomotao juice not good on me but I'm taking coco water instead just very expensive
    • Posted

      Please please please get your aldosterone and renin checked. Any of you who've had low potassium and tachycardia. And Google "Conn's" and "Primary Hyperaldosteronism".

      I wish someone had told me that before I had to go to ER/A&E nine times... with BP up to 255 and pulse up to 177.

      Oh, and if you get diagnosed, join the Facebook Hyperaldosteronism Support Group, great advice there

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