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?
1 like, 53 replies
Pwincess26 welshgirl13
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zzappd Pwincess26
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mtngirl929 welshgirl13
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Pwincess26 welshgirl13
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mtngirl929 Pwincess26
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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.
Pwincess26 welshgirl13
Posted
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.
mtngirl929 Pwincess26
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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.
chrisfox welshgirl13
Posted
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.
david36153 chrisfox
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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
Susan1985 welshgirl13
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chrisfox Susan1985
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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."
kaylee9695 welshgirl13
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kaylee9695 welshgirl13
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chrisfox kaylee9695
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PotassiumGuy welshgirl13
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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.
chrisfox PotassiumGuy
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melissa89834 PotassiumGuy
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PotassiumGuy melissa89834
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PotassiumGuy chrisfox
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melissa89834 PotassiumGuy
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david36153 PotassiumGuy
Posted
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