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How Long Does Blood In Urine Associated With Sickle Cell Trait Last
See below: Painless gross hematuria occurs with a higher frequency in sickle trait than in sickle cell disease and likely results from infarctive episodes in the renal medulla. Functional tubule abnormalities such as nephrogenic diabetes insipidus result from marked reduction in vasa recta blood flow, combined with ischemic tubule injury. ...Read more
Urine is the product of the kidneys, which is produced to eliminate the waste products of metabolism, manage body fluid balance, &maintain acid-base balance. The blood is first filtered by the kidneys, and the composition of the resulting fluid is then altered depending on the body's needs. It is composed of mostly water, and breakdown products from blood cells impart ...Read more
Variable : Urinary tract infections are more common in individuals with sickle cell syndromes. These are caused by the "usual" organisms seen in the general population. Asymptomatic urinary tract infections may be a precipitating event for a pain crisis. Pyelonephritis may precipitate life threatening complications in sickle cell patients. ...Read more
Sickle in low oxygen: A person with sickle cell trait only, is ok at sea level, but at high altitudes can get sickling in his red blood cells due to the lower concentration of oxygen at high altitudes. The problem of sickled cells clogging off the spleen is rare, but has happened to some people exercising above 10, 000 feet. Good hydration and avoiding over-exertion might decrease the chances of problems starting. ...Read more
Had recent trouble with severe anemia. Red blood cell count went down to a six. I ended up in the hospital getting transfused with three units of blood. Does sickle cell trait effect anemia?
Sickle cell trait...: Will not produce the anemia that you describe. You should work with your dr. To identify the cause and to correct it. I hope that you are feeling better after the care you received, and together with your dr you will get to the bottom of it. Good luck to you. Keep us posted. ...Read moreSee 2 more doctor answers
Less than a week: Depends on how severe the intussusception was. Usually after successful radiographic reduction, blood in the stool should resolve within a week. If there is persistent lower GI bleeding, then need to consider other causes (eg polyps, meckel diverticulum, etc) that could account for both problems. ...Read moreSee 2 more doctor answers
Depends: Up to 120 days is possible but it depends on the age of the blood donated. Most often 60-90 days is considered as most likely. ...Read more
I'm anemic, with mild thrombocytosis and rouleaux formation . Is this dangerous ? My blood test also came with suspicion with thalesemian blood trait
FInd cause: Your physician owes a duty to you to answer these questions. Are you iron deficient? If so, is it from your diet (vegetarian?) or are you losing blood? The thrombocytosis suggests it. Is the rouleaux real or a lab overread? (the latter is common.) do you in fact have thalassemia minor? A look at the smear and indices should give a presumptive answer. Iron deficiency warns of possible latent bad dz. ...Read more
I just took a sickle cell screen and result was negative. Does that mean i'm not a sickle cell carrier-aa genotype?
Means no Hgb S: This test is specifically looking for HGB s. It will detect sickle trait (hgb as) or sickle cell disease (hgb ss). If the test is negative it means there is no sickle hemoglobin present, but it does not mean aa. There are many abnormal hemoglobins that are not aa, but would also test negative on a sickle screen. ...Read moreSee 1 more doctor answer
Depends: COPD is progressive, histiocytosis is more indolent. Pulm rehab and bronchodilator rx can prolong life, but consideration for lung transplant should be under consideration for progressive disease. The life span of advanced COPD with hystiocytosis is around 5-6 yr. ...Read moreSee 1 more doctor answer
NOT AS BAD: Precludes you from certain activities.Get a more detailed answer ›
Was tested for sickle cell and the trait. I do not have either one. But I have high hemoglobin s & low a. What other than sickle cell can cause this?
Sickle beta thal: If you have high HGB s and low HGB a, then you have sickle beta-plus thalassemia ( if you have HGB a1), or sickle beta-zero thalassemia. ( if you have HGB a2 not HGB a1). These are both forms of sickle cell disease not trait. Beta zero is just as severe as homozygous sickle cell anemia (hgb ss); beta plus is milder in terms of symptoms. ...Read moreSee 1 more doctor answer
It doesn't always...: Patients with sickle cell disease can be immunocompromised because the disease causes the loss of your spleen, an important organ that helps the body fight certain infections. Fevers in patients with sickle cell disease are usually caused by infections. Fevers usually don't accompany pain crises. ...Read moreSee 1 more doctor answer
6-8 months for beta: Alpha thalassemia major is generally fatal before birth, with just rare cases born alive. Beta thalassemia major babies look normal at birth because fetal hemoglobin doesn't need beta globulin. As fetal hemoglobin goes away and adult hemoglobin starts being made, the baby will feel the effects of his lack of beta globulin. Symptoms start after the first 6-8 months of life. ...Read moreSee 1 more doctor answer
What can happen with untreated high hematocrit, red blood cell counts, and blood calcium levels? I do live at high altitude in SLC, Utah.
Nothing for high HCT: Your hematocrit is high due to living on high altititude which may be normal physiological reaction to O2 level being low.But we do not know how high it is to comment High Calcium level needs to be further investigated as it may be due Primary Hyperparathyroidism or Secondary Hyperparathyroidism You need to have blood level of Calcium,Parathyroid Hormone Level,25 Hydroxy VitD level as well Consult ...Read moreSee 1 more doctor answer
If a person has a little higher than normal hgb f result, but no symptoms, does that confirm thalassemia b minor? No sickle cell in the family.
No. : Beta thalassemia would be suggested by an elevated HGB a2. There are many different genetic abnormalities that cause thalassemia. Some may increase HGB f, though this is not the norm. Also, thalassemia causes small red blood cells and an related red blood cell count with variable degrees of anemia due to low hemoglobin. ...Read moreSee 1 more doctor answer
Hematuria is the presence of blood in the urine. When you can see the blood, it's called gross hematuria. When the blood can only be seen under a microscope it is known as microscopic hematuria. Hematuria can be caused by kidney stones, kidney infections, urinary tract infections, an enlarged prostate, cancer, certain medications, and ...Read more
An inherited blood disease causing red blood cells to be sickle (curved) shaped instead of round. It shortens life expectancy, and can result in bacterial infections, painful swelling of the hands and feet, fever, arthritis, leg ulcers, fatigue, anemia, eye damage, and ...Read more
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