Rebecca S. Tuetken, MD

  • Associate Professor of Rheumatology
  • Department of Internal Medicine
  • Roy J. and Lucille A. Carver College of Medicine
  • University of Iowa
  • Iowa City, Iowa

Safety of long-term treatment with cabergoline on cardiac valve disease in patients with prolactinomas bad cholesterol in quail eggs purchase 160mg fenofibrate overnight delivery. Cardiac valve disease and low-dose dopamine agonist therapy: an artefact of reporting bias Long-term cabergoline therapy is not associated with valvular heart disease in patients with prolactinomas does cholesterol medication make you lose weight cheap fenofibrate 160 mg. Your doctor will analyze your lab work and symptoms cholesterol zvyseny discount 160mg fenofibrate free shipping, and prescribe you any necessary ancillary medications recommended in the chart below (when your symptoms and/or blood values warrant it) cholesterol test do you need to fast cheap fenofibrate 160mg. They will also discuss the potential side efects of these medica tions and their ramications before you start taking them. First and foremost, its Receptor Tablet most common use is for the Modulator) prevention of gynecomastia. Nolvadex binds to the receptor site in breast tissue, safely preventing estrogen formation. Estrogen is important for a properly functioning immune system, while maintaining healthy joints. Some (Selective (Clomiphene men do not respond Estrogen Citrate or well to Clomid. For an excellent summary on understanding the pharmacodynamics of Clomid, see Lee Myers article The Half Life of Clomid216. A daily dose of 30 mg for two to three days in a row (until libido and feelings of sexual desire are restored) has been efective for some patients. Role of 5a-reductase inhibitors and selective estrogen receptor modulators as potential chemopreventive agents for prostate cancer. Raloxifene has about 10x the binding afnity for the estrogen receptor in breast tissue compared to Nolvadex220. In other words, it binds much more strongly to the receptor site and virtually eliminates the possibility of any estrogen reaching a receptor and exerting an undesired efect221. Benecial efects of raloxifene and tamoxifen in the treatment of pubertal gynecomastia. Raloxifene on the Risk of Developing Invasive Breast Cancer and Other Disease Outcomes. Arimidex works by actively blocking the aromatase enzyme from binding to an androgen (testosterone), thereby blocking the bodys ability to produce estrogen. An Inhibitors) Tablet optimal dosing protocol 1 mg Tablet of Arimidex while on continued. This could have terrible consequences for your good cholesterol prole, bone mineral density, libido, and overall feel ings of well-being. There is no sex drive or function, and you often ex perience lethargy and overall lifelessness. A serious limitation of the use of aromatase inhibitors in isolation in aging men is that the stimulating efect on testosterone levels may be too weak, especially in men with the lowest baseline testosterone levels who would potentially benet the most from stimulation235. There is normally a narrow therapeutic window in reg ulating estrogen (estradiol/E2) levels before you even tually start negatively impacting your health and your libido. Merrill Matschke in Chapter 12 on maintaining fertility through hormonal optimization. This is to get estrogen levels within an acceptable ther apeutic range where hormonal balance is achieved and side efects are alleviated. A much safer and efective strategy is to either reduce the testosterone dosage, or alter the dosing schedule to deal with the symptoms of excess estrogen. Robert Kominiarek sees patients in his practice with osteoporo sis (breakdown of the bones) in the spine and hips after being on Arimidex for 6-12+ con secutive months (or longer). As aromatase inhibition is dose-dependent, it has been suggested that aromatase is less suppressed in the testes than in adipose and muscle tissue, which explains the incomplete efectiveness of aromatase inhibition in men. Additionally, ongoing blood draws done regularly and honest patient feedback are crucial for both the patient and the doctor to achieve (and maintain) an optimal hormonal balance. Metabolic Syndrome, Obesity, Insulin Resistance, Aromatase and Estrogen Testosterone levels are low er in men with obesity, met abolic syndrome, and type 2 diabetes240. You can see this just by looking around, as obesity is increasing dra matically across most of the world. We all know the rea sons behind this: poor diet, and a lack of exercise are literally killing us. Low Testosterone Associated With Obesity and the Metabolic Syndrome Contributes to Sexual Dysfunction and Cardiovascular Disease Risk in Men With Type 2 Diabetes. And if youre already an obese man, a very recent study244 says that being testosterone decient will dramatically increase your risk of death. It would also make sense for men with Type 2 diabetes and metabolic syndrome to consider having their testosterone levels measured. Aromatase, the enzyme responsible for converting testosterone to estrogen, is more abundant in fat tissue245. This conversion happens more often in stubborn body fat246 deposit areas (which contain specic stubborn fat receptor cells with poor blood ow), such as the fat tissue found in the love handles, chest, and upper and lower back. In other words, the higher your body fat percentage, the more likely you are to be susceptible to negative estrogen induced side efects like poor erectile strength, moodiness, water retention, increased fat deposition, and so on (from high estrogen levels). Always discuss this with your physician and make sure to regularly monitor sensitive E2 (estrogen) levels throughout therapy until balance. Rob Kominiarek249 loves using transdermal testosterone delivery systems in a lipiderm base for obese men sufering from metabolic disorder and insulin resistance. When this is combined with the use of peptide hormones like Tesamorelin250, the fat-burning efect is greatly enhanced. Efects of Growth Hormone Releasing Hormone on Visceral Fat, Metabolic and Cardiovascular Indices in Human Studies. We tell you the normal dosages used by physicians, and the side efects associated with each of them. With the average male becoming more overweight over time, men are experiencing breast tissue growth that is made worse by poor nutrition, stress, additional body fat and a combination of high estrogen and low testosterone. This is an issue that extends way beyond aesthetics and looking good without your clothes on. Unfortunately, most men will sufer from gynecomastia in silence because of how growing breasts negatively afects a mans self-condence. With condence completely stripped away, many men are too afraid to remove their shirt in public. Men need to physically recover from this condition, while treating the psychological component at the same time. There is no reason that modern-day men dealing with the shame and taboo surrounding gyno shouldnt be able to work with elite physicians who can treat and eliminate this condition for good. To provide you with insights from the worlds foremost subject matter expert on gynecomastia, we interviewed Dr. Cruise is a Board Certied Plastic Surgeon in Newport Beach, California and a recognized world authority252 in the treatment of gynecomastia. Cruise has worked with more than 3000 gyno patients and successfully performed more than 2000 gyno removal surgeries. His stories about the emotional devastation sufered by many of his patients was heartbreaking. If there is no excess breast tissue left to hold, this loss of elasticity is relatively unnoticed. However, if that skin is holding the weight of gynecomastia, it will eventually fail. In this case, a patient has gone from a Type 1 or 2 (which requires incisions that are not noticeable) to Type 3 or Type 4 (which requires progressively higher levels of skin tightening and hence, longer incisions are necessary). Cruise was kind enough to ofer some important take away points regarding gyno treatment. Often times, this leads them to be bullied, teased, and sometimes become suicidal. There are stories of bad outcomes, useless medications, contradictory opinions, and its hard to make sense of it all. Cruise originally coined this term to highlight what he would often see in his gyno patients. They often wear 2 shirts at the same time, and have the outer shirt oversized to make sure their chest contour is not revealed.

Any illness or injury in the last 5 years A driver must report any condition for which he/she is currently under treatment cholesterol lowering diet plan ireland buy fenofibrate 160 mg online. The driver is also asked to report any illness/injury he/she has sustained within the last 5 years cholesterol medication beginning with a best buy for fenofibrate, whether or not currently under treatment low cholesterol foods grocery list fenofibrate 160 mg fast delivery. Seizures hdl cholesterol foods to eat generic fenofibrate 160 mg visa, epilepsy Ask questions to ascertain whether the driver has a diagnosis of epilepsy (two or more unprovoked seizures), or whether the driver has had one seizure. Gather information regarding type of seizure, duration, frequency of seizure activity, and date of last seizure. Eye disorders or impaired vision (except corrective lenses) Ask about changes in vision, diagnosis of eye disorder, and diagnoses commonly associated with secondary eye changes that interfere with driving. Complaints of glare or near-crashes are driver responses that may be the first warning signs of an eye disorder that interferes with safe driving. Ear disorders, loss of hearing or balance Ask about changes in hearing, ringing in the ears, difficulties with balance, or dizziness. Loss of balance while performing nondriving tasks can lead to serious injury of the driver. Obtain heart surgery information, including such pertinent operative reports as copies of the original cardiac catheterization report, Page 29 of 260 stress tests, worksheets, and original tracings, as needed, to adequately assess medical fitness for duty. High blood pressure Ask about the history, diagnosis, and treatment of hypertension. In addition, talk with the driver about his/her response to prescribed medications. The likelihood increases, however, when there is target organ damage, particularly cerebral vascular disease. As a medical examiner, though, you are concerned with the blood pressure response to treatment, and whether the driver is free of any effects or side effects that could impair job performance. Muscular disease Ask the driver about history, diagnosis, and treatment of musculoskeletal conditions, such as rheumatic, arthritic, orthopedic, and neuromuscular diseases. Does the diagnosis indicate that the driver is at risk for sudden, incapacitating episodes of muscle weakness, ataxia, paresthesia, hypotonia, or pain However, most commercial drivers are not short of breath while driving their vehicles. Feel free to ask other questions to help you gather sufficient information to make your qualification/disqualification decision. Lung disease, emphysema, asthma, chronic bronchitis Ask about emergency room visits, hospitalizations, supplemental use of oxygen, use of inhalers and other medications, risk of exposure to allergens, etc. Even the slightest impairment in respiratory function under emergency conditions (when greater oxygen supply is necessary for performance) may be detrimental to safe driving. Page 30 of 260 Kidney disease, dialysis Ask about the degree and stability of renal impairment, ability to maintain treatment schedules, and the presence and status of any co-existing diseases. Digestive problems Refer to the guidance found in Regulations You must review and discuss with the driver any "Yes" answers. Diabetes or elevated blood glucose controlled by diet, pills, or insulin Ask about treatment, whether by diet, oral medications, Byetta, or insulin. Loss of or altered consciousness Loss of consciousness while driving endangers the driver and the public. Your discussion with the driver should include cause, duration, initial treatment, and any evidence of recurrence or prior episodes of loss of or altered consciousness. Fainting, dizziness Note whether the driver checked Yes due to fainting or dizziness. Ask about episode characteristics, including frequency, factors leading to and surrounding an episode, and any associated neurologic symptoms. Sleep disorders, pauses in breathing while asleep, daytime sleepiness, loud snoring Ask the driver about sleep disorders. Also ask about such symptoms as daytime sleepiness, loud snoring, or pauses in breathing while asleep. Page 31 of 260 Stroke or paralysis Note any residual paresthesia, sensory deficit, or weakness as a result of stroke and consider both time and risk for seizure. Missing or impaired hand, arm, foot, leg, finger, toe Determine whether the missing limb affects driver power grasping, prehension, or ability to perform normal tasks, such as braking, clutching, accelerating, etc. Spinal injury or disease Refer to the guidance found in Regulations You must review and discuss with the driver any "Yes" answers. How does the pain affect the ability of the driver to perform driving and nondriving tasks You should refer the driver who shows signs of a current alcoholic illness to a specialist. Narcotic or habit-forming drug use Explore the use of the medication, whether or not it is prescribed, and the medications effect on driver reaction time, ability to focus, and concentration. Include a copy of any supplementary medical reports obtained to complete the health history. Specialist Vision Certificationthe vision testing and certification may be completed by an ophthalmologist or optometrist. When the vision test is done by an ophthalmologist or optometrist, that provider must fill in the date, name, telephone number, license number, and State of issue, and sign the examination form. Additionally, ensure that any attached specialist report includes all required examination and provider information listed on the Medical Examination Report form. The forced whisper test was administered first, and hearing measured by the test failed to meet the minimum five feet requirement in both ears. This three-month certificate is a one-time issuance for the recertification period and is not intended to mean once in the drivers lifetime. The medical examiner may use his/her clinical expertise and results of the individual driver examination to determine the length of time between recertification examinations. Figure 10 Medical Examination Report Form: Blood Pressure/Pulse Rate Recommendation Tablethe following table corresponds to the first two columns of the recommendation table in the Medical Examination Report form. Column one has the blood pressure readings, and column two has the category classification.

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Grows well in Organic Minor toxins No data Maxillary Sinusitis No data White to dark materials grey greenish to black Epicoccum Red or Acidic Fruit and None No toxins Infection of skin and No data orange environment Vegetables; lung cholesterol emboli in eyes definition generic fenofibrate 160mg free shipping. Summary of Key Health Effects by Organism bad cholesterol levels nz discount fenofibrate online mastercard, Based on Animal and Human Data 1 Bolded entries are based on human data cholesterol medication diabetes discount 160 mg fenofibrate with amex, while the bolded and italicized entry means that the human data support effects seen in animal studies 16 3 cholesterol ratio values order fenofibrate overnight. Alternaria can also be found on the conjunctiva (the moist membranes on the inner surface of the eyelids). The routes of entry are by inhalation, dermally (through breaks in the skin), and ocularly, after corneal trauma. Alternaria infections are more prevalent in patients with immunosuppression (Pastor and Guarro, 2008). The incidence of Alternaria infections in onychomycosis (fungal infections of the nails) was very low (<2. The most frequent and common Alternaria infections are infections of the skin, with approximately 90% being cutaneous infections and characterized by erythema, desquamation of the skin, red papules and ulceration. Approximately 30% of the patients with cutaneous infections were on immunosuppressive treatment (Pastor and Guarro, 2008). Oculomycosis (fungal infections of the eye), onychomycosis and invasive and non-invasive rhinosinusitis (long-term nasal congestion and thick mucus secretions) are other Alternaria effects reported. Contact with the soil and/or garbage are common exposure scenarios in cases of oculomycosis and onychomycosis (Pastor and Guarro, 2008). Many of these cases were related to ocular trauma and exposure to soil and/or garbage (Pastor and Guarro, 2008). The most common fungi isolated from sinusitis are Aspergillus but Alternaria is commonly associated with this disease as well (Shin et al. Immunosuppression does not appear to be a risk factor in chronic rhinosinusitis (Pastor and Guarro, 2008). The mean serum IgG levels specific for Alternaria were fivefold higher in chronic rhinosinusitis patients as compared to healthy patients (Ponikau et al. Type I allergies (allergies that are antibody-mediated) can be caused by Alternaria alternata and A. Children and young adults have a high risk of allergic respiratory condition if they have skin reactions to the antigens of A. The respiratory conditions present themselves as severe asthma (Heibling and Reimers, 2003). Approximately 10 % of patients with respiratory allergies had been sensitized to Alternaria and/or Cladosporium (Martinez-Canavate et al. Airway hyper-responsiveness, the exaggerated narrowing of the airways after the inhalation of allergenic stimuli, is a key feature of asthma. In the United States, 80% of individuals with confirmed asthma have positive allergic reaction to Alternaria (Nasser and Pulimood, 2009). In school aged children, sensitization to Alternaria correlated with asthma (Perzanowski et al. Thunderstorm induced asthma is increasing and also has been associated with sensitization to Alternaria spores (Nasser and Pullimood, 2009). Allergic bronchopulmonary mycosis caused by Alternaria has been reported (Singh and Denning, 2012). These effects can not be definitively associated with the Alternaria exposure, in light of the mixed exposure and subjective nature of the symptoms. Systemic infections with Alternaria are rare and found primarily in immunosuppressed people. For example, phaeohyphomycosis (presenting as a deep subcutaneous fungal infection caused by Alternaria) was observed in a renal transplant patient (Salido-Vallejo 2014). The presence of scaling on the skin of dogs and cats plus the possibility of the aerosolization of Alternaria spores can increase the frequency and intensity of an asthmatic attack in patients already sensitized to Alternaria (Singh and Denning, 2012; Jang et al. Utility of molecular identification in opportunistic Mycotic infections: A case of cutaneous Alternaria infectoria infection in a cardiac transplant recipient. A European multicenter study promoted by the Subcommittee on Aerobiology and Environmental Aspects of Inhalant Allergens of the European Academy of Allergology and Clinical Immunology. Cutaneous Alternaria infectoria infection in a dog in association with therapeutic immunosuppression for the management of immune-mediated haemolytic anaemia. Alternaria alternata invasive fungal infection in a patient with Fanconis Anemia after an unrelated bone marrow transplant. Association of sensitization to Alternaria allergens with asthma among school-age children. Subcutaneous phaeohyphomycosis due to Alternaria infectoria in a renal transplant patient: Surgical treatment with no long-term relapse. Aspergillus adapts well to a broad range of environmental conditions, including heat, which makes it a successful pathogen. It also produces small airborne conidia, which are easily dispersed in the environment and respired (Binder and Lass-Florl, 2013). Respired conidia are scrubbed from the airway via cilia in the respiratory epithelium (mucociliary clearance), but some conidia may still pass into the lung (Binder and Lass-Florl, 2013). In healthy individuals, these fungal conidia are generally eliminated through phagocytic defenses, but infection of the lung is more likely to occur in persons with depressed immune systems (Binder and Lass-Florl, 2013; Brakhage, 2005). Invasive infection occurs in the lung and sinus tissues after the mucosal surfaces are breached, resulting in tissue damage and, eventually, dissemination through the blood stream (Hope et al. These infections are classified into three categories: non-invasive infection (colonization of mucosal surfaces), invasive infection (the growth of fungi in tissues), and allergic or hypersensitivity diseases (Binder and Lass-Florl, 2013). Aspergillus can also cause corneal infections (keratitis) following ocular injury with subsequent contamination, particularly among agricultural workers (De Lucca, 2007). Aspergilloma (chronic mycetoma), a generally benign fungus ball (Binder and Lass Florl, 2013; Kilch, 2009), is generally found in the lung and is commonly found in people with pre-existing damage to the lung. Symptoms 21 include mild hemoptysis (coughing up bloody mucus), chronic cough, weight loss, and sometimes fever (Kilch, 2009). However, aspergillomas have also been reported in the sinus cavity and in immunocompetent people, although rarely (Binder and Lass-Florl, 2013). Acute pulmonary aspergillosis has also been reported in healthy men after spreading contaminated bark chips (Kilch, 2009). In persons with a weakened immune system, the inhaled Aspergillus conidia germinate and produce hyphae that invade pulmonary tissue (De Lucca, 2007). Other risk factors include prolonged neutropenia (abnormally low levels of neutrophils in the blood), broad spectrum antibiotic treatment, severe immunosuppression, inherited immune defects, underlying diseases and conditions, biological factors. The associative nature of some risk factors, such as corticosteroid treatment and infection with cytomegalovirus, are not agreed upon (Binker and Lass-Florl, 2013; Brakhage, 2005). Sino-orbital aspergillosis is another, usually fatal, progressive and opportunistic Aspergillus infection in immunocompromised. Aspergilli can also cause fungal rhinosinusitis, which can lead to invasive Aspergillus sinusitis, a fatal, but uncommon, disease (Binder and Lass-Florl, 2013; Kilch, 2009). However, Aspergillus has been reported to cause chronic sphenoid sinusitis, or an infection of the sphenoid sinuses, in healthy individuals (De Lucca, 2007). There is some limited evidence of an association between Aspergillus exposure and disease of the lower respiratory tract. Environmental exposure to Aspergillus spores is less likely to be the cause of allergy than exposure to Aspergillus that has germinated in the respiratory tract (Sporik et al. Epidemiology studies have identified an increase in allergy, allergic rhinitis, asthma, and asthma like symptoms. However, positive skin prick tests for patients in the study were common (36% for A. Environmental exposure to Aspergillus spores is not significantly associated with an increase in the number of hospital admissions among children with asthma (Atkinson et al. Restrictive and obstructive respiratory impairments, specifically post-shift decrements in pulmonary function tests, allergic symptoms, and high IgE levels, were identified in grain storage workers and associated with spores of Aspergillus, Alternaria, Drechslera, Epicoccum, Nigrospora, and Periconia (Chattopadhyay et al. This disease is not invasive, but is instead caused by colonization of the respiratory tract (Mazur and Kim, 2006) and exposure to conidia or aspergillus-antigens, usually A.

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Other causes: congenital cholesterol medication pain buy fenofibrate 160mg amex, thrombus cholesterol numbers vs ratio buy cheap fenofibrate line, atrial myxoma cholesterol levels and pregnancy 160mg fenofibrate, calcification of annulus/leaflets cholesteryl ester transfer protein generic fenofibrate 160 mg online. Course: stenosis impedes filling left atrial enlargement left ventricular failure pulmonary hypertension right-sided failure. Increased demands may precipitate symptoms (pregnancy, Endocarditis/Pericarditis/Myocarditis/Valvular Heart Disease Page 37 Notes anemia, infection). Opening snap early diastole followed by low-pitched rumble at apex (mid-diastole), accentuated in left lateral decubitus position. Loud murmur: crescendo-decrescendo systolic murmur ending before S2 heard best at the apex. Treatment: cardiac cath to assess severity and need for emergent surgery, treat pulmonary edema, possible intra aortic balloon pump. Murmur: raspy, low-pitched crescendo-decrescendo systolic murmur heard best at the base, radiates to carotids. May be acute in infective endocarditis, aortic dissection at root, Marfans, syphilis, trauma. Austin-Flint murmur (soft diastolic rumble regurgitant stream hitting mitral valve). Myocarditis should be considered in any patient with a viral syndrome and signs of cardiac disease. Staph is now the most common cause of native valve endocarditis (no longer streptococci). Prophylaxis for endocarditis is recommended in high risk patients that are undergoing a dental procedure that involve manipulation of the gingival tissue. Prevention of Bacterial Endocarditis: Recommendation by the American Heart Association. Hamptons Hump: Triangular pleural-based density with rounded apex that points towards the hilum. May radiate to the back (interscapular) and then the mid and low back as the dissection propagates distally. Pseudo-hypotension due to compression of the true lumen by the false lumen resulting in reduced blood flow to the subclavian arteries with a difference in blood pressures between the arms (systolic difference of >15 mmHg is significant). Renal artery occlusion may result in uncontrolled hypertension, decreased urinary output and rising creatinine. Esmolol (Brevibloc) 500 mcg/kg bolus, 50-200 mcg/kg/min infusion (nice due to rapid onset and only has a 5 minute half life). Ideal study to evaluate symptomatic, but you need a hemodynamically stable patient. Option for elective or emergent repair includes percutaneous trans-femoral intraluminal graft for patients with co morbidities. Pathogenesis: intimal tear with dissection into the media resulting in 2 channels true and false lumen. Classification: Stanford Type A ascending (75%) managed surgically; Stanford Type B distal (25%) managed medically. Transesophageal echocardiography: Demonstrates involvement of ascending aorta, aortic insufficiency, pericardial effusion. Pathogenesis: localized dilation resulting from weakening of vessel wall; 98% infrarenal. Clinical Policy: Critical issues in the evaluation and management of adult patients with suspected acute nontraumatic thoracic aortic dissection. Mulcare M, Sharma R: Abdominal Aortic Aneurysms; Critical Decisions in Emergency Medicine; Lesson 30; January 2013. Clinical manifestations of and diagnostic strategies for acute pulmonary embolism. Partial thrombosis of the false lumen in patients with acute type B aortic dissection. Delayed hemolytic reaction: Minor blood group incompatibility resulting in extravascular (liver, spleen) hemolysis days later. Potential bleeding below 50,000 with a high risk of spontaneous bleeding below 20,000. May have severe (< 1% activity), moderate (1-5% activity), or mild (5-30% activity) disease. An imbalance between hemostasis (excessive clotting) and fibrinolysis (excessive bleeding). Due to activation of the Hematology/Oncology Page 70 Notes clotting cascade with consumption of clotting factors and platelets with fibrinolysis and fibrin deposition in the microvasculature causing tissue ischemia. Multiple etiologies: trauma, burns, sepsis, cancer, snake bites, obstetric complications (amniotic fluid embolism, abruptio placenta, retained products of conception), transfusion rxn. Splenic sequestration: shock in children due to microvascular obstruction resulting in splenomegaly, hypovolemia. Painful occlusive crisis: extremity, chest, abdominal pain often precipitated by dehydration, hypoxia, infection, trauma, stress. Obstruction of the lumen by extrinsic compression, vein wall invasion by tumor or intraluminal thrombosis. Symptoms: headache, hoarseness, nausea, dyspnea, visual and mental status changes. Nausea/vomiting, anorexia, polyuria, polydipsia, dehydration, weakness, lethargy, coma, constipation and abdominal pain. Consider bisphosphonates (etidronate, pamidronate), gallium, steroids, calcitonin, mithramycin, and dialysis. Decompressive laminectomy only if a tissue diagnosis is needed, the spine is unstable or the patient has failed radiation therapy. Pericardial fluid compresses the heart, resulting in decreased diastolic filling and circulatory collapse. Subxiphoid pericardial window with catheter placement for drainage and sclerotherapy. Fever may develop due to infection (60%), chemotherapeutic agents, tumor necrosis, transfusions or antibiotics. Impaired inflammatory response from neutropenia makes it difficult to localize the source of infection. Examine for sinusitis, dental abscess, perirectal abscess (do not perform rectal exam), meningismus, cellulitis. Retinopathy with sausage-link or boxcar segmentation due to venous hemorrhage. Occurs 1-5 days following chemotherapy in rapidly growing tumors such as leukemia and lymphoma. Cell lysis results in hyperuricemia, hyperkalemia, hyperphosphatemia and subsequent hypocalcemia. Chemotherapy pretreatment with hydration and allopurinol or rasburicase (recombinant urate oxidase enzyme). Urinary alkalinization is controversial as it improves uric acid diuresis, but may worsen hypocalcemic tetany. Von Willebrands disease is due to platelet dysfunction resulting in a prolonged bleeding time. Patients with sickle cell disease are prone to infections by encapsulated organisms. Acute chest syndrome is the most common cause of death in patients with sickle cell anemia. Superior vena cava syndrome presents with facial plethora, dilated veins over the chest and arms, headache, visual difficulty and dyspnea, but does not require emergent treatment. Initial therapy of neoplastic spinal cord compression is intravenous steroids and radiation therapy. Pain is the most common complaint with spinal cord compression; weakness and sensory changes are late findings. The incidence of infection increases in neutropenic patients when the 3 neutrophil count drops below 500/mm. Remember to consider autotransfusion of blood in patients with traumatic hemothoraces. Kahn, S, Ander D: Trauma Updates-Fluid resuscitation in traumatic hemorrhagic shock; Trauma Reports, Mar/April 2013.