Blood platelets up and down

Common Questions and Answers about Blood platelets up and down


I recently found out i have genital herpes but i havnt known until 3 months after the incident. Anyways since then when i get my cbc <span style = 'background-color: #dae8f4'>blood</span> count my <span style = 'background-color: #dae8f4'>blood</span> platelets always come <span style = 'background-color: #dae8f4'>up</span> as too high. My doctor says it may be because you have a virus running in your body, and keeps testing my blood monthly to see if it goes back down. He doesn't seem too concerned, but i am just wondering if the high platelets could have anything to do with a herpes recently being exposed in my body??
but, my platelets keep going down <span style = 'background-color: #dae8f4'>and</span> <span style = 'background-color: #dae8f4'>down</span>. they went to 50 <span style = 'background-color: #dae8f4'>and</span> every two months have <span style = 'background-color: #dae8f4'>blood</span> tests with my oncologist.and he mentioned that we don't want them at 30 or that meant a plasma transplant.. so thank the LORD.. last week they stayed the same 'adequate' as they would say.. geez, now ,maybe I won't be able to begin the meds until they do something with these platelets.... hmm... don't like this.
5 and blood TEST WAS goOD PLATELETS WAS AT 51 <span style = 'background-color: #dae8f4'>and</span> AT 9 WEEKS RED <span style = 'background-color: #dae8f4'>and</span> WHitE CELLS WERE TO LOW <span style = 'background-color: #dae8f4'>and</span> PLATELETS AT 31 <span style = 'background-color: #dae8f4'>and</span> SHE CALL MONDAY 15 th SAID STOP FOR NOW SHE WONT LET ME go NO LOWER .the RED and WHitE CELLS I CAN GET NEAPOGEN. PROCRit .BUT WERE CAN YOU GET OR TRY NEW DRUG FOR BOOSTING PLATETLET .
the obstructed flow of blood through the portal vein (portal hypertension) causes the spleen to enlarge by causing an increase in pressure inside the vessels of the spleen. the spleen stores red <span style = 'background-color: #dae8f4'>and</span> white <span style = 'background-color: #dae8f4'>blood</span> cells <span style = 'background-color: #dae8f4'>and</span> platelets (fragment of cells that are used to clot blood). An enlarged spleen traps platelets lowering levels in the blood which can lead to the inability of blood to clot. This is called Thrombocytopenia and is common in people with cirrhosis.
Before treatment my platelets were 65 and during treatment they went up to 84 but now 12 weeks after treatment they're <span style = 'background-color: #dae8f4'>down</span> to 75. My white <span style = 'background-color: #dae8f4'>blood</span> cells are also a bit <span style = 'background-color: #dae8f4'>down</span> <span style = 'background-color: #dae8f4'>and</span> never have been before. Everything else is normal. AST, ALT, All Phos are all very normal and down from being very high before treatment.
Now I am afraid that he will do this again, but I will only do half dose tomorrow <span style = 'background-color: #dae8f4'>and</span> then hopefully, platelets will come <span style = 'background-color: #dae8f4'>up</span> enough for final two weeks. they have been in the 60 range since beginning treatment and are usually low anyway without tx.
Keep those platelets up and you will be fine. the values for platelets, WBC, <span style = 'background-color: #dae8f4'>and</span> RBC will change over time within a range. going <span style = 'background-color: #dae8f4'>up</span> sometimes <span style = 'background-color: #dae8f4'>and</span> going down at others. As long as you can keep them from a constant free fall you should be good to continue treatment. Can't wait to see viral load results to see how the meds are working on your HCV! Keep up the good work! Hang in there!
I have had low platelets, but not too low. Mine have been <span style = 'background-color: #dae8f4'>down</span> to 60, but it's the WBC (anc) that has been to .4 <span style = 'background-color: #dae8f4'>and</span> I take Neulasta, another nasty rescue drug. At least it kept me on tx at full dose. Now my platelets last week were 137 which is higher than before tx. I am happy and would like to think that it is because the reversal of liver damage. I too have heard Nemenga is brutal. I think Missmiss took it once for platelets. Platelets do bounce around quite a bit and I would get a dr.
the spleen enlarges with advance cirrhosis <span style = 'background-color: #dae8f4'>and</span> will affect your platelets. I'm post transplant <span style = 'background-color: #dae8f4'>and</span> my platelets are always on the low side as the spleen does not return to normal size after a liver transplant. I don' think this has anything to do with the virus, my guess is it's about the condition of your liver whether the virus is still present or not. Have you had any other testing since your biopsy in 2004 ? Do you see a hepatologist ? what do they tell you about these results ?
I also am feeling splitting headaches <span style = 'background-color: #dae8f4'>and</span> insomnia, <span style = 'background-color: #dae8f4'>and</span> hoping symptoms calm <span style = 'background-color: #dae8f4'>down</span> in a month or two... I am glad to have found this site and this thread... it is good to know there are others going through this and having the same side effects, and to hear from others who are progressing through the treatment... good luck to all of us who are fighting this hepc battle!!!!! god bless and happy holidays...
called and said everything looked normal and that her platelet count was at 215k. I looked it <span style = 'background-color: #dae8f4'>up</span> on the web <span style = 'background-color: #dae8f4'>and</span> see that the normal range is 150 to 400. I know if the Dr. says it's normal I probably shouldn't worry but I can't help it. She seems to be at the lower end of normal and for a young healthy person it seems like she should be at the higher end. Should I be concerned at all? Should I ask for follow up bloodwork in the future? This whole thing just came out of the blue.
A platelet infusion will not work if the problem is related to backup in the spleen. the platelets just back <span style = 'background-color: #dae8f4'>up</span> <span style = 'background-color: #dae8f4'>and</span> are removed from the system very quickly, 6-10 hours. If the problem is due to bone marrow suppression, then the infusion might be an alternative. I hope this information helps.
have allowed 2 weeks of peg <span style = 'background-color: #dae8f4'>and</span> rivin <span style = 'background-color: #dae8f4'>and</span> go back in for <span style = 'background-color: #dae8f4'>blood</span> work on the 29 of Dec.. Tomorrow night shot #5 for this genotype 2B. Drs. are optimistic but I'm reserving myself to cheer when this roller coaster stops. Isn't it best to wait and see? Any thoughts... I'm trying to smile!
but since finished treatment my platelets have dropped from an average 170-190 the past years,to 160 <span style = 'background-color: #dae8f4'>and</span> i worried this trend continues. my bili is still jumping <span style = 'background-color: #dae8f4'>up</span> <span style = 'background-color: #dae8f4'>and</span> <span style = 'background-color: #dae8f4'>down</span> 1-2 mg/dl. albumin is alwyas around 45-50,inr is 1.02. my docs doesent seem to worry alltough i keep telling them i feel sick all the time,with pain in joints,and muscles.and no appetite. any suggestions if this low platelets are a sign of portal hypertension,alltough my spleen is not enlarged.
Today I received my lab work <span style = 'background-color: #dae8f4'>and</span> it showed my platelets came <span style = 'background-color: #dae8f4'>down</span> to 115. I wanted to know if they can be this low without Cirrhosis?.
He said that when you have low platelets your body makes more to keep <span style = 'background-color: #dae8f4'>up</span> so what you have circulating is newer <span style = 'background-color: #dae8f4'>and</span> bigger platelets <span style = 'background-color: #dae8f4'>and</span> they funtion pretty well.(Don't go skydiving or anything) I was pretty relieved that he's doen't want to adjust my meds. Hanging in there...
Only persons with cirrhosis need to worry about their platelet count becoming too low to during hepatitis therapy. there are treatments to boost platelet counts, transfusion of platelets <span style = 'background-color: #dae8f4'>and</span> Eltrombopag/Promacta a drug that raises the platelet count.
So if I understand you correctly... when you are not on treatment your platelets are about 70k is that correct? My platelets are also about 70k when not on treatment. I have cirrhosis; stage 4 liver disease with an enlarged spleen and moderate varices. Do you have cirrhosis? Low platelets can be a common symptom of cirrhosis. 2 weeks ago when I was at week 12 of tx my platelets when down to 26k. I was running out of platelets to lose!
which makes the spleen continue to enlarge....<span style = 'background-color: #dae8f4'>and</span> the platelet count continue to drop. Platelets in the <span style = 'background-color: #dae8f4'>blood</span> causes your <span style = 'background-color: #dae8f4'>blood</span> to clot if a blood vessel is cut. they have no affect on how you feel. If a person's platelets count goes down below 25,000 is there may need to intervention. Intervention is only a temporary fix. Platelets will start to drop again a day or two after treatment. the only treatment is either a platelet transfusion or drugs that can raise platelets. You need neither.
"what can I do to get/keep this up and what are some of the causes of it?" A low platelet count usually is an indication of an underlying health issue. As with most conditions there are many causes. it is up to a doctor to diagnose the cause. there are no recommended solutions for thrombocytopenia before treatment. Transfusions are not indicated before hepatitis C therapy or during therapy unless patients have active bleeding and platelet counts > 50,000 cells/μL.
I'm being treated by a hepatologist thru an NP at a transplant hospital here in Charleston, <span style = 'background-color: #dae8f4'>and</span> yet again they are wanting me to reduce riba from 800mg to 600mg already went <span style = 'background-color: #dae8f4'>down</span> from 1000mg to 800 weeks ago, also pegintron to almost half because of these latest numbers. I'm ready to keep on going to 24 weeks but I want to give myself the best possible chance to achieve und and with these reductions I'm not sure that it would help.
what foods or drugs are good for low platelets
) thank you for the input, hope your doing well ! I just had another CBC <span style = 'background-color: #dae8f4'>and</span> my platelets went <span style = 'background-color: #dae8f4'>up</span> from 57 to 63 - Kinda good news !
I think that we started close to the same time. Are you doing 48 weeks? I have had low platelets for 3years <span style = 'background-color: #dae8f4'>and</span> have been in the 20's <span style = 'background-color: #dae8f4'>and</span> haven't had alot of symptoms. Occationally a nose bleed and gums bleeding. the fatique is from hvc and treatment I think. Let me know how you are doing.
My husband has been on Pegasys/Riba treatment for 17 weeks the first 12 weeks being double shots. He reached UND at 12 weeks <span style = 'background-color: #dae8f4'>and</span> his last 2 <span style = 'background-color: #dae8f4'>blood</span> tests showed platelets of 53 ,000 <span style = 'background-color: #dae8f4'>and</span> 52, 000 the last test being done on July 30 His doctor recommended taking a half a shot for the next 2 weeks to see if his platelets increase His platelets were around 75,000 pre-treatment.
Ive been in the hospital 8 times since 4/2012, for vomitting blood and bloody diarrhea. I end <span style = 'background-color: #dae8f4'>up</span> getting <span style = 'background-color: #dae8f4'>blood</span> transfusions <span style = 'background-color: #dae8f4'>and</span> discharged with propranalol <span style = 'background-color: #dae8f4'>and</span> vitamins,iron, folic acid. they banded first admission, but said the other admissions that the blood vessels were too small to band. Any ideas on folic acid and 1,000 units of irons daily ?
and I laughed so hard and thought to myself,,,I wish so bad it was though! I wish I would just wake <span style = 'background-color: #dae8f4'>up</span> <span style = 'background-color: #dae8f4'>and</span> it was a dream but all you guys were really a part of my life <span style = 'background-color: #dae8f4'>and</span> just good friends,,,No hep c! Wouldn't that be wonderful! You are a great friend Chevy!!
People with cirrhosis start out with a lower platelet count than others with less liver damage. Usually less than 125,000 <span style = 'background-color: #dae8f4'>and</span> many times less then 100,000 platelets. Only people with cirrhosis or other platelet issues need to worry about platelets dropping dangerously low. 20,000 or less. Interferon causes all treating persons platelets to drop to some degree. Obviously the more platelets you start with before treatment, the higher the platelet count will stay.
My platelets went <span style = 'background-color: #dae8f4'>up</span> to 293 during preload than straight back to where they were with first INF shots.Still today if I increase Riba platelets go up slightly. Data for geno 4s is always skimpy. BTW that is another reason why I keep going the extra mile when given a choice. Overall several studies show improved SVR with extending tx starting with Sanchez Tapias. I see it like higher Riba dose produces better SVR rates.