Preamble About 20% of strokes are due to cerebral haemorrhage; the rest are due to ischaemic cerebral infarction. Cerebral haemorrhage is frequently difficult to distinguish from cerebral infarction. The clinical symptoms depend on the site of the infarction. When infarction and haemorrhage cannot be distinguished, the term stroke should be used. Definition Cerebral haemorrhage is haemorrhage into the cerebrum. Basic requirement for use of the term Demonstration of haemorrhage by an appropriate method such as computer tomography CT ; or magnetic resonance imaging MRI ; or histopathology. Reference 11.
Topic: Renal Physiology 1997, Exam 2, Question 55 Author: David Williams 314. The major transport mechanism initiating proton secretion in the kidney is the apical . There are three major recipients for these protons during an acid load, the usual physiological state on a Western diet. The vast majority only serve to recapture that has been filtered, and they therefore result in no net acid secretion. Of the net secreted protons, those associated with the production of NEW , the vast majority associate with and are trapped in the lumen as a charged, but not measurably acid, species. A smaller portion associate with filtered and actually acidify the urine, forming the acids. Answer: ? Reason: Na H antiporter, bicarbonate, bicarbonate, Ammonia NH3 ; , phosphate, titratable.
PKC was first identified almost 20 years ago 25, 26 ; and has been implicated in key cellular responses such as the regulation of proliferation and apoptosis 27 ; . In relation to this study, PKC is one of the PKCs that has been implicated in cardiac myocyte hypertrophy 28 ; and ischemic preconditioning cardioprotection 29 ; , although equally its inhibition has been reported to be beneficial in cardiac ischemia 30 ; . However, the regulation of this kinase is still not well understood. Like all c nPKCs, PKC interacts with DAG, which brings the kinase to the plasma membrane, and this plays a part in its activation. More recent studies indicate that other events, including phosphorylation, are associated with activation of PKC 8 ; . In addition, PKC interacts with other proteins e.g. receptors for activated C kinase ; , which are assumed to play a role in subcellular targeting of the enzyme for activation and or substrate phosphorylation 28 ; . How this relates to DAG production is rarely considered. The identification of phorbol esters as "DAG mimetics, " and therefore activators of c nPKCs, resulted in wide usage of these compounds for the investigation of the mode of activation and function of c nPKCs within cells. However, although PMA for example ; obviously does activate c nPKCs, activation of PKC by PMA does not necessarily resemble the activation by physiological generation of DAG. Specifically, in cardiac myocytes as in other cells ; , PMA promotes sustained translocation of PKC to the particulate fraction of the cell followed by downregulation of the protein 14 ; , whereas physiological agonists, including ET-1, induce transient translocation 15 ; , and we have failed to detect any significant subsequent to down-regulation.4 This transient translocation raises the question of whether PKC is active only when tethered by DAG to the membrane. Alternatively, like other protein kinases e.g. protein kinase B 31 ; and c-Raf 32 , PKC may be recruited to the membrane for activation and then retain its activity presumably now independent of DAG PtdSer ; as it migrates to other areas of the cell. Here, potentially following interaction with targeting proteins, PKC phosphorylates specific substrates. Our data are strongly supportive of the latter scenario because PKC recovered after 10 min of stimulation with ET-1 showed an increase in lipid-independent activity Fig. 8, D, F, and G ; , which would be required for the enzyme to remain active in other areas of the cell. We have attempted to study the subcellular localization of PKC in cardiac myocytes by immunostaining using antibodies to the total enzyme and the different phosphorylated forms. However, these experiments have proved unsuccessful because we suspect ; the levels of expression of endogenous PKC are below the threshold for detection. An increase in lipid-independent activity was also seen in response to PMA Fig. 8, C, F, and G ; , but it is possible that the detergent used to prepare whole cell extracts for FPLC resulted in extraction of PKC associated with PMA and membrane lipids. A similar argument could apply for ET-1, but for this physiological agonist, there was retrotranslocation of PKC back into the soluble fraction of the cell by 10 min Fig. 1D ; . This coincided with an increase in lipidindependent activity in the soluble extract Fig. 10E ; in addition to the particulate extract Fig. 10F ; . The mechanisms by which PKC attains.
The meclizine antivert ; will help with the vertigo and a different antiemetic will help with the nausea and vomiting.
A drug called antivert was prescribed for her.
Comparable in placeboand fluoxetine-treated patients, it most likely represented a "placebo" effect. However, by days 4-6 there were significant subjects. energy differences between placebosubjects kJ d 2365 days 600 and fluoxetine-treated their overall Fluoxetine-treated intake from 565 1 794 kcal d ; of 143 kJ d that start have for decreased kcal d and colace.
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In an eight week period there are an approximately 6, 600 people hospitalized in Middlesex-London. It will be assumed that all hospitalized individuals are part of a high-risk group, except women admitted for delivery. There are approximately 750 deliveries in an eight week period. Therefore approximately 5, 850 individuals will be eligible for prophylaxis. It will be assumed that they take prophylactic drugs for the entire 6 or 8 weeks. According to the Ontario Pandemic Influenza Plan, there are approximately 97, 256 individuals in this category 65 year olds 55, 730; high risk 19-64 year olds 39, 298; high risk 13-18 year olds 2, 228 ; . Excluding ill high-risk individuals seeking outpatient care 12, 846 ; , hospitalized individuals 5, 850 ; and residents of long-term care facilities 4, 317 ; reduces this estimate to 74, 343. This is still an overestimate of the true number, though, since people represented in other categories of this table would also need to be excluded and depakote.
Nausea and Vomiting, Age 4 and Older: Home Treatment Home treatment may be all that is needed to treat occasional nausea. Watch for dehydration and treat it early. Older adults and young children can quickly be come dehydrated. Use acetaminophen, such as Tylenol or Panadol, instead of aspirin or a nonsteroidal anti-in flammatory drug NSAID ; , such as ibuprofen, if you need to treat a fever or abdominal pain. Take a nonprescription antinausea medicine, such as meclizine Atnivert or Bonine ; or dimenhydrinate Dramamine ; , or an antihistamine, such as Benadryl. Try acupressure: - Place the tip of your right index finger on the underside of your left wrist, about 1.5 in. 4 cm ; from your hand. - Apply moderate pressure for 2 to 3 minutes. - Repeat as needed. - Acupressure bands, which are available for motion sickness, may help reduce nausea. Suck on peppermint candy or chew a stick of peppermint gum. Peppermint is an antispasmodic that will help decrease the stomach contractions that may be causing your nausea. If you are vomiting: Rest in bed until you are feeling better. If vomiting lasts longer than 24 hours, sip a rehydration drink to restore lost fluids and nutrients. After vomiting has stopped for one hour, drink 1 fl oz ml ; of a clear liquid every 20 minutes for one hour. Clear liquids include apple or grape juice mixed to half strength with water, rehydration drinks, weak tea with sugar, clear broth, and gelatin dessert. Avoid orange juice, grapefruit juice, tomato juice, or lemonade. Do not drink milk products, alcohol, or carbonated drinks such as sodas. If you do not have any more vomiting, increase the amount of fluid you drink to 8 fl 237 ml ; during the.
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Patient A Patient A was diagnosed with left ear endolymphatic hydrops possibly secondary to labyrinthine otosclerosis in 1980 at the age of 32 . Initial symptoms included left ear tinnitus, fluctuating left ear hearing loss, and vertigo with nausea and vomiting. Typical episodes persisted from 1 to 2 hours. Hearing testing revealed a severe rising to mild sensorineural hearing loss in the left ear. See Table 1 for documentation of pure-tone threshold measurements and word recognition testing. Patient A also reported visual blurring and difficulties with gait and hand-eye coordination . His gait was described as ataxic . Antivret provided minimal control of the vertigo. Sodium fluoride was prescribed to treat the otosclerosis. Aneurologic examination was negative . The severity and duration of vertiginous attacks increased in 1981, with episodes persisting from 4 hours to 3 days . Left ear tinnitus and hearing fluctuations continued. Audiometric testing on May 5, 1981 revealed a relatively flat, moderate sensorineural hearing loss in the left ear. Aleft ear Cody tack sacculotomy was performed in July 1981 Cody, 1969, 1973 ; Cody and McDonald, 1983 ; . Following surgery, patient A experienced no vertigo until 1991, 10 years later. However, onset of right ear aural fullness and tinnitus was reported in 1987 . Table 1 documents minor fluctuations in right ear hearing. With recurrence of the vertigo, patient A also experienced unsteadiness and loudness discomfort . A tentative diagnosis of early right ear hydrops was made . In 1992, he reported continued episodes of vertigo with nausea and vomiting, right ear hearing fluctuations, and increased right ear tinnitus . Audiometric testing documented a mild, low-frequency sensorineural hearing loss in the right ear see Table 1 ; . Bilateral endolymphatic hydrops was diagnosed, and a course of prednisone was prescribed in an effort to improve and cytoxan!
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BRAIN NATRIURETIC PEPTIDE LEVELS CORRELATE WITH SIX MINUTE WALK DISTANCE AND WORLD HEALTH ORGANIZATION FUNCTIONAL CLASSIFICATION IN PATENTS WITH CONNECTIVE TISSUE DISEASE -ASSOCIATED PULMONARY ARTERIAL HYPERTENSION Shiromino Hearth MD Edward L. Salerno MD * Naomi Rothfield MD W. D. Hager MD Raymond Foley MD University of Connecticut Health Center, Farmington, CT PURPOSE: Previous clinical studies have demonstrated that brain natriuretic peptide BNP ; levels correlate with functional capacity via the six minute walk test in patients with idiopathic pulmonary arterial hypertension PAH ; . We sought to determine whether BNP levels correlated with six minute walk distance and World Health Organization WHO ; Functional Class in a unique population of patients with connective tissue disease associated- pulmonary arterial hypertension. METHODS: A retrospective analysis of 14 patients with connective tissue disease-associated PAH 10 with systemic sclerosis and 4 with mixed connective tissue disease ; was undertaken. All patients had a right heart catheterization for diagnostic confirmation. BNP levels, six minute walk distances, and WHO functional classification were extracted from the medical record while patients were receiving therapy with an endothelin antagonist, prostanoid, or a combination thereof. Statistical analysis was performed to determine if BNP levels correlated with six minute walk distance and WHO functional class. RESULTS: There were 30 data points for BNP verses the six minute walk test. Pearson's correlation for these variables was -0.574 with a P value of P 0.001. For BNP versus WHO functional classification there were 34 variables. The Pearson's correlation was 0.586 with a P value of P 0.001 Table 1 ; . CONCLUSION: BNP levels correlate with six minute walk distance and WHO functional class in a population of patients with connective tissue disease-associated PAH. CLINICAL IMPLICATIONS: In patients with pulmonary arterial hypertension secondary to systemic sclerosis or mixed connective tissue disease, BNP may be a useful marker of exercise capacity and functional class. Additional studies with larger sample size are necessary to confirm these findings and levothroid.
Sulfosalicylic acid test, the nitric acid ring test, and the heat and acetic acid test. A total of 3408 values were obtained over a period of several weeks, with a few tests being done each day with each method. It will be observed that the results obtained with the tablet test in this series were satisfactory, being slightly superior to those obtained with the other three tests. A second series of comparative blind tests, using negative urines and samples which contained added bovine albumin, was carried out, using inexperienced operators who were unfamiliar with all of the tests. The procedure for each test was provided in written form to each operator. Results obtained in this series are shown in Fig. 2. It is evident that the precision with all 4 tests is considerably less than that obtained by the experienced operators. The inexperienced operators classified more of the negative urines as "trace" with the tablet test than with any of the other procedures. In urines with 10 mg. per 100 ml. of added protein the detection of protein was more readily achieved with the tablet test than with any of the three turbidimetrio procedures. Significantly better detection of protein at the 20 mg. per 100 ml. level and at the 30 mg. per 100 ml. level was also obtained with the tablet test. Classification of 300 mg. per 100 ml. of protein as a large amount was more consistent with the tablet than with the turbidity tests.
Eric Campbell is an assistant professor at Harvard Medical School, where David Blumenthal is a professor of medicine and health policy. Joshua Powers is an assistant professor and coordinator of the Ph.D. Program in Higher Education Leadership, Department of Educational Leadership, School of Education, Indiana State University, in Terre Haute. Brian Biles is a professor of health policy in the George Washington University Department of Health Policy, Washington, D.C and purinethol.
The comedian was good. Busy as I was, I had to stop several times to laugh. Greg and I made eye contact often from across the room, but I didn't get much time to speak to any of them. After the comedian they rose up and adjourned to the bar area, in what was clearly becoming a nightly custom. I wondered briefly whether Greg would become part of another of Rob and Toni's demonstrations. When midnight came I was physically tired, but still feeling better emotionally than I had since we'd left homeport. I made my way below decks to the crew quarters, opened my door, and got one more happy surprise: a rollaway bed had been pulled up next to mine, and Greg was sacked out in it. As I closed the door he stirred and sat up. "Where'd you get that?" I asked, dumbfounded. "Housekeeping, " he replied with a shrug. "Rob and Toni said you shouldn't be alone tonight, so here I am." I rewarded his self-sacrifice with a very hot kiss, and started undressing for bed. As I pulled off my underwear, I saw Greg lift his head and start sniffing the air. "Do you smell cinnamon buns?.
In cultured, non-human mammalian cells, no DNA strand breakage or induction of unscheduled DNA synthesis was observed. Although mutations were induced in some studies, the inconsistent positive results were weak and not clearly associated with a particular locus; both positive and negative results were obtained in experiments at the Tk and Hprt loci and tests for ouabain resistance. Similarly, results for the induction of both sister chromatid exchange and chromosomal aberrations were equally divided between positive and negative in different laboratories. Single studies in cultured mammalian cells for the induction of micronuclei and aneuploidy did not show any effect of phenobarbital treatment. Variable results were also obtained in assays for cell transformation conducted in different laboratories, but the differences may have been due partly to the different transformation assays used. Assays for gap-junctional intercellular communication, however, also gave variable results in different laboratories even when the same Chinese hamster lung V79 cell system was used in five of six studies. In a single study with Djungarian hamster fibroblasts, cell-to-cell communication was actually enhanced. The negative result with NRK-52E cells, a rat kidney epithelial cell line, was interpreted by the authors as being consistent with the lack of effect of phenobarbital which does not promote renal tumours ; on the kidney, since barbital, a renal tumour promoter, did inhibit gap-junctional intercellular communication in these cells Konishi et al., 1990 ; . In cultured human lymphoblastoid cells, no significant increase in the frequency of mutations was observed in one study, while, in cultured human lymphocytes, chromosomal aberrations were induced in two studies; sister chromatid exchange was not induced in another study. In vivo, phenobarbital did not form adducts with DNA in mouse liver after either a single oral dose 200 mg kg bw ; or when given for 2 weeks in the diet 1000 mg kg ; . A study of mutation induction in mice carrying the Escherichia coli lacI transgene as the target did not show any effect of phenobarbital. Studies of the bone-marrow cells of mice treated in vivo also did not show induction of sister chromatid exchange, micronuclei or chromosomal aberrations after treatment with phenobarbital alone. A significant response was observed in the single-cell gel electrophoresis assay with cells from the liver of mice given phenobarbital 140 mg kg bw ; by intraperitoneal injection 24 h before sacrifice, but not effect was seen with treatment 3 h before being killed; no effect was observed in a number of other organs. The frequency of morphologically abnormal sperm was not increased in mice treated with phenobarbital. Phenobarbital was reported to induce chromosomal abnormalities, including translocations, in male mouse primary spermatocytes after oral administration for 5 or 60 days. [The Working Group noted that the level of the effects reported was little influenced by either the dose or the treatment regimen.] A positive response was reported in a test for dominant lethal mutation in male Swiss mice Nandan & Rao, 1983 ; . [The Working Group noted that there was a significant response of all germ-cell stages, and a greater response in treated spermatogonial cells and requip.
Combinatorial chemistry and high-throughput screening have been the rage in drug discovery since the late 1990s, but plant and animal sources still hold promise. In particular, venoms have proven to be rich areas for exploitation. Drugs derived from snakes, vampire bats, and Gila monsters are all nearing regulatory review and potentially, approval. But in September, a Food and Drug Administration advisory panel voted against approval of AstraZeneca's Exanta, a cobra venom-derived anticoagulant. These products face the same and possibly higher hurdles as other molecules when it comes to reaching the market. One of the most successful products derived from venom was the first FDA-approved angiotensin converting enzyme ACE ; inhibitor, captopril. John Vane, a researcher at the Royal College of Surgeons, and a Brazilian fellow in his lab discovered that a peptide in Brazilian viper venom blocked the formation of angiotensin II. That drug went on to become Bristol-Myers Squibb's captopril, which was approved in 1981. In 2002, worldwide sales of ACE inhibitors totaled .8 billion US ; . A more recent success is Integrilin, an antiplatelet drug approved in 1998 to treat acute coronary syndrome. Integrilin binds to glycoprotein IIb IIIa, inhibiting platelet aggregation. It is a synthetic analog of barbourin, which is found in the venom of the Southeastern pygmy rattlesnake. The drug was developed by San Francisco-based COR Therapeutics, which merged with Millennium Pharmaceuticals of Cambridge, Mass. COR screened venoms from 62 snakes to find the right compound, according to COR executive Robert Scarborough.1 The drug is sold by Millennium and Schering-Plough. Integrilin sales were 5.8 million in 2003, according to Millennium. The company is studying two new uses for the drug: the management of ST-segment elevation myocardial infarction, and the prevention of bleeding and heart attacks during coronary artery bypass surgery. If approved, Exanta ximelagatran ; could capture an even bigger market--an estimated billion per year by competing with the oral anticoagulant warfarin. Exanta can be given twice daily, and there's no need for the tricky blood level monitoring the older drug requires. Potential uses include post-surgical prevention of venous thrombosis or pulmonary embolism, as well as stroke prevention in patients with atrial fibrillation which affects two million people in the United States ; . Only about 35% of patients with atrial fibrillation receive therapy, and many aren't being treated within the correct therapeutic range, says Jonathan Halperin, an AstraZeneca consultant and professor at Mount Sinai Medical Center in New York. Exanta has European approval for preventing venous thromboembolism in major orthopedic surgery and was launched in Germany in June. However, an FDA advisory panel cited concerns about the drug's efficacy and risks primarily liver toxicity ; and recommended against approval of the drug on Sept. 10. At press time, the company declined to comment on its future plans for the drug. Other venom-based drugs are at an earlier phase of development. Francis Markland, a biochemistry professor at the University of Southern California USC ; Keck School of Medicine in Los Angeles, has been looking at venom's potential for almost 40 years. His research led to the discovery of fibrolase, a clot-busting compound from the southern copperhead that is now in Phase II studies at Nuvelo in Sunny- vale, Calif. The company was formed through the merger of Hyseq Pharmaceuticals and Variagenics, which closed on Jan. 31, 2003. Nuvelo has created a recombinant form of the protein, alfimeprase, and is testing its ability to restore blood flow in blocked peripheral arteries.
What should your blood pressure be if you are diabetic? 140 90? 135 High blood pressure is very common in diabetics as over 75% of diabetics are also hypertensive. There is a clear correlation between blood pressure and cardiovascular disease; the higher the blood pressure, the more likely a diabetic is to have a heart event. This relationship between high blood pressure and heart disease is much stronger in diabetics as opposed to nondiabetics. Do we have evidence to show that lowering blood pressure in diabetics can reduce the risk of heart disease? Absolutely! The ideal blood pressure recommended by the American Diabetes Association is 130 80 or less. There is also evidence to suggest that lower is better. Is there any particular type of blood pressure medication that is better than another for diabetics? About ten years ago, a class of medications came out called ACE inhibitors. These medications have Over 80 percent of patients been shown to also protect with Type II diabetes are diabetics against heart disease and obese. kidney disease. Five years ago another group of related medications were developed called ARBs. Several studies were published over the past year to show that in Type II "adult onset" ; diabetics, ARBs reduce heart disease and can prevent kidney failure. These drugs are now recommended as first line treatment for high blood pressure in diabetic patients. The METABOLIC RESEARCH INSTITUTE is currently involved in a clinical trial comparing two ARBs that are already FDA approved in diabetics who have high blood pressure and sustiva.
Nutritional concerns: Just as it chelates a variety of other minerals, penicillamine can bind zinc and interfere with the absorption of both penicillamine and zinc. nutritional support: Some nutritionally oriented physicians have begun treating individuals with Wilson's disease with zinc instead of penicillamine. This type of combined therapy using large-dose zinc sulfate and low-dose penicillamine has become recognized as an safe, effective and inexpensive treatment for children with hepatolenticular degeneration. However, individuals taking penicillamine should avoid zinc-containing supplements unless specifically recommended by their prescribing physician or another nutritionally trained healthcare professional.13.
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Data extracted from hankey, 199861 the risk of vascular ischaemic events in patients with various clinical manifestations of atherothrombosis: data from caprie ; using data on validated outcome events for the itt population, the author analysed the risk of 1 ; fatal or non-fatal is; 2 ; fatal or non-fatal mi; and 3 ; fatal or non-fatal mi other vascular death excluding fatal is ; in the patients whose qualifying condition was is n 6431 ; and in patients whose qualifying condition was pad n 6452.
Nocardia can be identified by Gram stain in wound drainage or tissue specimens as delicate branching gram positive rods; filaments may appear beaded on Gram stain Figure 2 most species are acid fast when stained with a modified Ziehl-Neelsen stain. The diagnosis can be confirmed by isolation of the organism; however, it may require longer incubation 5-7 days ; rather than the 48 hours plates are usually held Figure 3 ; . The majority of isolates 95% ; causing this syndrome are due to N. brasiliensis. In Queensland N. brasiliensis accounts for approximately 30% of all Nocardia isolations from all sites and methotrexate.
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1013. Takishima, T., S. Suzuki, K. Sekizawa, Y. Hirose, H. Sasaki, M. Sugiyama, Y. Shimizu, Y. Akaizawa, and C. Shindo. 1982. Laryngeal narrowing measured with low frequency sound. Tohoku J.Exp.Med. 137: 463-464. Abstract: We measured laryngeal resistance with 800 Hz sound in human subjects. 800 Hz sound was forced into the mouth and the intensities of sound above and below vocal cord were detected by two microphones on the anterior neck. Respiratory resistance Rrs ; was simultaneously measured by an oscillation method. When the subject voluntarily controlled the glottis aperture at functional residual capacity, the percent increase of difference of intensity of sound between two microphones Y % ; was curvilinearly proportional to the increase of Rrs X ; from the control state; Y 20.8 X X 1.24. Since Rrs below the larynx was constant at a given lung volume, we could estimate the increase of laryngeal resistance from the control state by knowing the percent increase of difference of intensity of sound. The present method would be clinically applicable to measure Rrs independent from laryngeal artifact 1014. Thacker, R. E. and S. S. Kraman. 1982. The prevalence of auscultatory crackles in subjects without lung disease. Chest 81: 672-674. Abstract: Crackles heard during auscultation of the lungs are generally considered an abnormal physical finding. This study was done to see if crackles could be induced to occur in the lungs of normal subjects. We studied 52 nonsmoking normal subjects by listening at the right and left posterior bases and over the lower right anterior chest during inspiration from functional residual capacity FRC ; and then during inspiration from residual volume RV ; . Crackles were recorded on magnetic tape for subsequent time-expanded waveform analysis. No crackles were heard at any of the three sites during inhalation from FRC. Of 52 subjects, 26 had crackles over the anterior site when inhaling from RV. These crackles were often profuse, loud, and easily recorded. Waveform analysis revealed these crackles in normal subjects to be similar to those occurring in patients with interstitial lung diseases. We conclude that crackles, heard over the anterior chest during inspiration from low lung volumes, are not necessarily adventitious sounds 1015. Wilson, A. J. and B. H. Brown. 1982. Wideband compander system for biological signals. Med.Biol.Eng Comput. 20: 512-516. 1016. Workum, P., S. K. Holford, E. A. DelBono, and R. L. Murphy. 1982. The prevalence and character of crackles rales ; in young women without significant lung disease. Am.Rev.Respir.Dis. 126: 921-923. Abstract: Although some investigators have reported that crackles are present only in persons with lung disease, others say they also occur in normal persons. In order to clarify this difference of opinion, we determined the prevalence of crackles in 56 women without significant lung disease. The subjects ranged from 19 to 33 age mean, 21.3 ; . They all had a FVC greater than 80% predicted and a FEV1 FVC ratio greater than 75%. None had a history of acute or chronic lung disease. During slow inspirations from residual volume, midinspiratory fine crackles were heard at the anterior bases in 35 of subjects by a physician using an acoustic stethoscope, whereas a bioengineer using an 800 Hertz high pass filtered stethoscope heard crackles in 53 subjects. Crackles during tidal breathing were heard in 2 subjects. It is postulated that the crackles noted after expiration to residual volume are nonpathologic, and occur when basilar airways, which close at the end of a forced expiration, suddenly open during inspiration. Examination of the quality, timing, and anatomic distribution of the crackles in apparently normal subjects suggests that they can often be distinguished from those resulting from diseases such as bronchitis, interstitial fibrosis, and congestive heart failure 1017. Cegla, U. H. and C. Navarro. 1981. [Are changes in airway resistance revealed by the pneumosonogram sufficiently specific?]. Med.Klin. 76: 324-325. 1018. Chowdhury, S. K. and A. K. Majumder. 1981. Digital spectrum analysis of respiratory sound. IEEE Trans.Biomed.Eng 28: 784-788. 1019. Fredberg, J. J. 1981. Acoustic determinants of respiratory system properties. Ann.Biomed.Eng 9: 463-473. 1020. Gavriely, N., Y. Palti, and G. Alroy. 1981. Spectral characteristics of normal breath sounds. J.Appl.Physiol 50: 307-314. Abstract: An objective and accurate measurement and characterization of breath sounds was carried out by a fast-Fourier-transform frequency-domain analysis. Normal vesicular breath sounds, picked up over the chest wall of 10 healthy subjects showed a characteristic pattern: the power of the signal decreased exponentially as frequency increased. Since the log amplitude vs. log frequency relationships were linear, they could be characterized by the values of the slope and the maximal frequency. The average slope of the power spectrum curves was found to be in oct + - SD ; 13.0 + - 1.4 over the base of the right lung, 12.6 + - 2.4 over the base of the left lung, 9.8 + - 1.4 over the interscapular region, and 14.4 + - 4.3 over the right anterior chest. The maximal frequencies of inspiratory and expiratory breath sounds, picked up over the base of the right lung, were in Hz + - 446 + - 143 and 286 + - 53 P less than 0.01 ; , over the base of the left lung 475 + - 115 and 284 + - 47 P less than 0.01 ; , over the interscapular region 434 + - 130 and 338 + - 77 P less than 0.05 ; , and over the right anterior chest 604 + 204.
M2. AL-FITURI MEDAL LECTURE 2008: MUSCULOSKELETAL RHEUMATIC COMPLICATIONS OF DIABETES MELLITUS: AN OVERVIEW. Rida Saleh BARUNI, Division of Physical Medicine, Rehabilitation and Pain, Department of Medicine, Sheikh Khalifa Medical City, Abu Dhabi, UAE.
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