Polycystic kidney disease (PKD) is a disease that causes cysts to grow on the kidney. You can see the cysts in the picture above. The disease can cause pain, headaches, high blood pressure, and can even make cysts spread to other organs such as the liver. In extreme cases, a kidney transplant may be required. The disease can be inherited from a parent or can be caused from spontaneous gene mutations. PKD can also be contracted if the person had serious kidney problems in the past.
PKD has a wide variety of treatments depending on the symptoms of the person who has it. Treatments for pain start out as simple pain medications, but if the pain becomes severe, surgery will be required. Prolonged cases of PKD may cause kidney failure, so a kidney
There is no cure for CKD however it can be treated to relieve symptoms and give the patient a better life and to stop the condition becoming worse. During the early stages of CKD treatments can be given by your GP and mainly involve lifestyle changes such as becoming healthy, doing more exercise and taking certain medicines to assist in controlling blood pressure which then prevents further damage to the kidneys. However if the disease gets worse to the point where the kidneys stop working and functioning properly either a kidney transplant or dialysis which will be explained more in D2 more and it can impact a patient’s life a lot.
Medical procedures that people endure that could cause physical and mental pain include blood transfusion, major surgery and organ transplants.
All the symptoms that were described were based on the kidney functions, so more and further
Chronic Kidney Disease (CKD) is a disease that is described as a loss of kidney function gradually over time. As kidney function decreases, the waste collection in the body’s blood becomes high and makes the individual feel sick. This disease can lead to other complications in the body such as anemia, poor nutritional health, high blood pressure, and nerve damage. These complications will begin to progress and show as CKD progresses to advanced stages. Early detection of this disease is essential when it comes to treatment. If CKD is diagnosed early enough the disease progression can be slowed down and managed. This disease will eventually lead to failure of the kidneys
Primary treatments include antibiotic therapy, Fluid resuscitation, and crystalloid. Potential treatments depending on patient status include vasopressors and steroids, ventilator, renal dialysis, blood transfusion, and surgery.
I chose to write about PCOS because I myself suffer from this disease. PCOS is short for Polycystic Ovarian Syndrome. PCOS is a type of disease where your ovaries fill up with follicles filled with fluid (cyst). It causes mainly infertility and type 2 diabetes. This disease is more common in women who are in the reproductive stage. Not only can it cause the infertility and type 2 diabetes, but it can also cause an irregular menstrual cycle and can cause your body to produce more of a male hormone called androgen. Some other things it may cause is depression, anxiety, high blood pressure, sleep apnea, high blood sugar and many other health problems. The cause of this disease has not been yet identified, but it is said one of the ways could be
Polycystic Kidney Disease (PKD) is a genetic disorder primarily affecting the kidneys. It is characterized by growth of numerous cysts on the kidneys (McPhee, Papadakis & Rabow, 2014). The kidneys primary job is to filter the waste products from the blood into urine and ultimately out of the body. The cysts are primarily fluid filled and when they become enlarged, they interfere the normal functioning of the kidneys, leading to enlarged kidney (McPhee et al., 2014). When the enlarged kidney stops properly functioning leading kidney failure. It may take years before the kidneys totally loose function and then require dialysis, which is in only about half of the patients diagnosed with PKD. According to National Kidney and Urologic Diseases Information Clearing House (NKUDIC)(2007), mutations in genes PKD1, PKD2 and PKHD1 cause polycystic kidney disease. Defects in the formation of epithelial cells and their cilium result in cyst formation and obstruction that is followed by destruction of renal parenchyma, interstitial fibrosis, and loss of functional nephrons (McCance, Heuther, Brasher, 2014). The renal, gastrointestinal, cardiovascular and cerebrovascular organs are the most common systems affected by PKD (McPhee et al., 2014).
Injury to the glomerulus and the tubules presents the onset of Intra-renal failure (Matzke, 2011). Some of the frequent causes for Intra-renal failure are glomerulonephritis; pyelonephritis; and tubular injury. Post-renal failure develops from things like ureteroliths, tumors, or anatomic impediments. Opposite of the acute form, the chronic form has a slow onset that has no early stage symptoms. It is important to know that following an acute episode a chronic renal episode often follows, and at this juncture the damage is irreversible. Glomerulonephritis and pyelonephritis combined, has been reported to be the forerunner in as much as half the cases from acute to chronic renal failure. Diabetes mellitus, renal vascular disease, such as atherosclerosis, hypertension, polycystic kidney disease, drug damage, and nephrolith are all examples of other causes of CKD (Pradeep, 2014). Biopsies of kidneys that suffered with CKD reveal smaller kidneys with scarring on the tubules.
There are three kinds of ways to test for polycystic kidney disease. They are ultrasound tests, CT tests, and magnetic resonance imaging. There are many ways to treat this disease. They can include simple over the counter pain medications, these are used when symptoms are not too bad. Sometimes, a kidney transplant will be needed if the kidney fails. The only other way to get this disease is from already
I’m sorry to inform you that your prospective baby boy has Autosomal Recessive Polycystic Kidney Disease (ARPKD). ARPKD is inherited recessively so you are both most likely carriers of the disease. There is no good way to say this but that means you have a 50% chance of having a child with ARPKD. From our last ultrasound we saw that his kidney was abnormally large for a fetus his age and we believe we’ve also located a cyst. ARPKD causes cysts to grow in your kidney. Cysts a sac that contains fluid and can interfere with the filtering of waste in the blood. The cysts cause the kidney is become abnormally large. Some of the symptoms for ARPKD are: liver scarring, trouble breathing, kidney failure, kidney stones, and high blood pressure. I’m
Polycystic ovarian syndrome (PCOS) is the most prevalent endocrine abnormality of reproductive-aged women, occurring between 10 and 21% (March et al., 2010). Due to its complexity, PCOS is associated with a spectrum of symptoms, including amenorrhea, anovulation, hirsutism, acne, and obesity. All of which are subjective and do not allow for a definitive diagnosis. Long term complications, such as infertility, insulin resistance, dyslipidemia, depression, and anxiety require an early diagnosis; but establishing a comprehensive diagnostic criterion has been difficult (Teede et al., 2011). Historically, Stein and Leventhal first identified PCOS in 1935 when they associated it with hirsutism, chronic anovulation, obesity, and bilateral ovarian
There is no cure for polycystic kidney disease. Scientific research, in fact, failed to identify therapies that could be decisive. However your doctor may prescribe drugs or treatment to relieve certain symptoms. You have to treat hypertension with medications with ACE inhibitors or low-salt diet, the same way as kidney failure can be slowed with a lifestyle healthier, doing physical activity, and not smoking, eating fat-free foods.
There are treatment options for the disorder but none that will diminish all of the effects PKU has. Treatment include genetic testing, regular primary care visits , and clinical Psychologist visits for help with social delays at a younger age. Self care is definitely a large part of living with the disorder, people with PKU have a diet restricting them from aspartame , any meats , fish , chicken , eggs, nuts , beans, milk, and all other dairy product.
This condition can be treated at anytime by an antibiotic like penicillin. Since this condition can damage the organs, it is better to get it treated sooner than later. It is also important to keep going back to the doctors to get blood work done repeatedly to make sure that the infection is totally cleared up.
The need for intervention in this disease is obvious, without it patient’s quality of life is greatly depleted. Finding a cure to completely prevent ADPKD at the moment is out of the question due to the complexity of the disease, and due to the amount of information we know being limited. But I think there is an opportunity in the cyst