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Alzheimer’s Disease

July 26, 2010 By: crashell44 Category: Uncategorized

Alzheimer’s disease (AD) affects approximately twice as many women as men. Because the risk for AD increases with age, part of this sex difference is accounted for by the fact that women live longer than men. However, additional factors likely contribute to the increased risk for AD in women, including sex differences in brain size, structure, and functional organization. There is emerging evidence for sex-specific differences in gene expression, not only for genes on the X and Y chromosomes but also for some autosomal genes. Estrogens have pleiotropic genomic and nongenomic effects on the central nervous system, including neurotrophic actions in key areas involved in cognition and memory. Women with AD have lower endogenous estrogen levels compared to women without AD. These observations have led to the hypothesis that estrogen is neuroprotective.

Some studies have suggested that estrogen administration improves cognitive function in nondemented postmenopausal women as well as in women with AD, and several observational studies have suggested that postmenopausal hormone therapy (PHT) may decrease the risk of AD. However, recent placebo-controlled trials have found no improvement in disease progression or cognitive function after up to 15 months of PHT in women with AD. Further, the Women’s Health Initiative Memory Study (WHIMS), an ancillary study in the Women’s Health Initiative (WHI), found no benefit compared to placebo of estrogen alone [combined continuous equine estrogen (CEE), 0.625 mg qd] or estrogen with progestin [CEE, 0.625 mg qd, and medroxyprogesterone acetate (MPA), 2.5 mg qd] on cognitive function or the development of dementia in women 65 years and older. Indeed, there was a significantly increased risk for both dementia and mild cognitive impairment in women receiving hormone therapy. The possible explanations for the discrepant results between the observational studies and the randomized clinical trials remain unclear.

What are three different forms of crystal-induced arthritis, and what are the crystals involved?

June 17, 2010 By: crashell44 Category: Case Discussion

Gout is a crystal-induced arthritis due to the deposition of monosodium urate (MSU) crystals. Pseudogout results from the formation and release of calcium pyrophosphate dihydrate (CPPD) crystals. The deposition of hydroxyapatite crystals can induce acute inflammatory arthritides such as calcific periarthritis/tendinitis and the Milwaukee shoulder syndrome, a destructive arthropathy of the shoulder associated with rotator cuff defects.

What five diseases are classified as seronegative spondyloarthropathies?

June 17, 2010 By: crashell44 Category: Case Discussion

The spondyloarthropathies consist of AS, reactive arthritis (formerly known as Reiter’s syndrome), psoriatic arthritis, arthritis secondary to inflammatory bowel disease, and undifferentiated spondyloarthropathy.

What is the definition of sciatica, and what are three possible causes of it?

June 17, 2010 By: crashell44 Category: Anatomy

Sciatica is defined as back pain that radiates laterally down one leg below the knee. The pain is usually sharp or burning. Sciatica usually occurs as a consequence of lumbar spondylosis (degenerative disc or facet joint disease) and can be associated with a ruptured intervertebral disc or an idiopathic sciatic nerve irritation. Infectious, neoplastic, and infiltrative disorders should always be considered.

What are three possible causes of LBP in young men?

June 17, 2010 By: crashell44 Category: Case Discussion

Three possible causes of back pain in young men include lumbosacral muscle spasm, a ruptured intervertebral disc, and AS or another seronegative spondyloarthropathy. Forms of common autoimmune and chronic inflammatory diseases, such as rheumatoid arthritis (RA) or systemic lupus erythematosus (SLE), rarely involve the joints of the low back. Therefore, LBP is not one of the initial symptoms of these disorders.

Neurogenetics

June 16, 2010 By: crashell44 Category: Neurology

The landscape of neurology has been transformed by modern molecular genetics . More than 350 different disease-causing genes have now been identified, and >1000 neurologic disorders have been genetically mapped to various chromosomal locations. The vast majority of these represent highly penetrant mutations that cause rare neurologic disorders; alternatively, they represent rare monogenic causes of common phenotypes. Examples of the latter include mutations of the amyloid precursor protein in familial Alzheimer’s disease, the Read the rest of this entry →

Eating Disorders: Introduction

June 16, 2010 By: crashell44 Category: Nutrition

Anorexia nervosa and bulimia nervosa are characterized by severe disturbances of eating behavior. The salient feature of anorexia nervosa (AN) is a refusal to maintain a minimally normal body weight. Bulimia nervosa (BN) is characterized by recurrent episodes of binge eating followed by abnormal compensatory behaviors, such as self-induced vomiting. AN and BN are distinct clinical syndromes but share certain features in common. Both disorders occur primarily among previously healthy young women who become overly concerned with body shape and weight. Many patients with BN have past histories of anorexia nervosa, and many patients with AN engage in binge eating and purging behavior. In the current diagnostic system, the critical distinction between AN and BN depends on body weight: patients with AN are, by definition, significantly underweight, whereas patients with BN have body weights in the normal range or above.

Binge eating disorder (BED) is a more recently described syndrome characterized by repeated episodes of binge eating, similar to those of BN, in the absence of inappropriate compensatory behavior. Patients with BED are typically middle-aged men or women with significant obesity. They have an increased frequency of anxiety and depression compared to similarly obese patients without BED. It is not established that patients with BED are at increased risk for medical complications or that they require specific treatment interventions.

Nutritional Requirements and Dietary Assessment: Introduction

June 15, 2010 By: crashell44 Category: Nutrition

Nutrients are substances that must be supplied by the diet because they are not synthesized in the body in sufficient amounts. Nutrient requirements for groups of healthy persons have been determined experimentally. For good health we require energy-providing nutrients (protein, fat, and carbohydrate), vitamins, minerals, and water. Specific nutrient requirements include 9 essential amino acids, several fatty acids, 4 fat-soluble vitamins, 10 water-soluble vitamins, and choline. Several inorganic substances, including 4 minerals, 7 trace minerals, 3 electrolytes, and the ultratrace elements, also must be supplied in the diet.

The required amounts of the essential nutrients differ by age and physiologic state. Conditionally essential nutrients are not required in the diet but must be supplied to individuals who do not synthesize them in adequate amounts, such as those with genetic defects, those having pathologic states with nutritional implications, and developmentally immature infants. Many organic phytochemicals and zoochemicals present in foods have health effects. For example, dietary fiber has beneficial effects on gastrointestinal function. Other bioactive food constituents or contaminants such as lead may have negative health effects.

Diagnostic Hypothesis Generation

June 15, 2010 By: crashell44 Category: Uncategorized

Cognitive scientists studying the thought processes of expert clinicians have observed that clinicians group data into packets, or “chunks,” which are stored in their memories and manipulated to generate diagnostic hypotheses. Because short-term memory can typically hold only 7–10 items at a time, the number of packets that can be actively integrated into hypothesis-generating activities is similarly limited. The cognitive shortcuts discussed above play a key role in the generation of diagnostic hypotheses, many of which are discarded as rapidly as they are formed. Read the rest of this entry →

The Use of Cognitive Shortcuts

June 15, 2010 By: crashell44 Category: Uncategorized

Cognitive shortcuts or rules of thumb, sometimes referred to as heuristics, can help solve complex problems, of the sort encountered daily in clinical medicine, with great efficiency. Clinicians rely on three basic types of heuristics. When assessing a particular patient, clinicians often weigh the probability that this patient’s clinical features match those of the class of patients with the leading diagnostic hypotheses being considered. In other words, the clinician is searching for the diagnosis for which the patient appears to be a representative example; this cognitive shortcut is called the representativeness heuristic.

It may take only a few characteristics from the history for an expert clinician using the representativeness heuristic to arrive at a sound diagnostic hypothesis. For example, an elderly patient with new-onset fever, cough productive of copious sputum, unilateral pleuritic chest pain, and dyspnea is readily identified as fitting the pattern for acute pneumonia, probably of bacterial origin. Evidence of focal pulmonary consolidation on the physical examination will increase the clinician’s confidence in the diagnosis because it fits the expected pattern of acute bacterial pneumonia. Knowing this allows the experienced clinician to conduct an efficient, directed, and therapeutically productive patient evaluation since there may be little else in the history or physical examination of direct relevance. The inexperienced medical student or resident, who has not yet learned the patterns most prevalent in clinical medicine, must work much harder to achieve the same result and is often at risk of missing the important clinical problem in a sea of compulsively collected but unhelpful data.

However, physicians using the representativeness heuristic can reach erroneous conclusions if they fail to consider the underlying prevalence of two competing diagnoses (i.e., the prior, or pretest, probabilities). Consider a patient with pleuritic chest pain, dyspnea, and a low-grade fever. A clinician might consider acute pneumonia and acute pulmonary embolism to be the two leading diagnostic alternatives. Using the representativeness heuristic, the clinician might judge both diagnostic candidates to be equally likely, although to do so would be wrong if pneumonia was much more prevalent in the underlying population. Mistakes may also result from a failure to consider that a pattern based on a small number of prior observations will likely be less reliable than one based on larger samples.

A second commonly used cognitive shortcut, the availability heuristic, involves judgments made on the basis of how easily prior similar cases or outcomes can be brought to mind. For example, the experienced clinician may recall 20 elderly patients seen over the past few years who presented with painless dyspnea of acute onset and were found to have acute myocardial infarction. The novice clinician may spend valuable time seeking a pulmonary cause for the symptoms before considering and then confirming the cardiac diagnosis. In this situation, the patient’s clinical pattern does not fit the expected pattern of acute myocardial infarction, but experience with this atypical presentation, and the ability to recall it, can help direct the physician to the diagnosis.

Errors with the availability heuristic can come from several sources of recall bias. For example, rare catastrophes are likely to be remembered with a clarity and force out of proportion to their value, and recent experience is, of course, easier to recall and therefore more influential on clinical judgments.

The third commonly used cognitive shortcut, the anchoring heuristic, involves estimating a probability by starting from a familiar point (the anchor) and adjusting to the new case from there. Anchoring can be a powerful tool for diagnosis but is often used incorrectly. For example, a clinician may judge the probability of coronary artery disease (CAD) to be very high after a positive exercise thallium test, because the prediction has been anchored to the test result (“positive test = high probability of CAD”). Yet, as discussed below, this prediction would be inaccurate if the clinical (pretest) picture of the patient being tested indicates a low probability of disease (e.g., a 30-year-old woman with no risk factors). As illustrated in this example, anchors are not necessarily the same as the pretest probability (see “Measures of Disease Probability and Bayes’ Theorem,” below).



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