Pub Date : 2019-08-26DOI: 10.1002/9781119409861.ch10
S. Goland, U. Elkayam
—Peripartum cardiomyopathy is a potentially life-threatening pregnancy-associated disease that typically arises in the peripartum period and is marked by left ventricular dysfunction and heart failure. The disease is relatively uncommon, but its incidence is rising. Women often recover cardiac function, but long-lasting morbidity and mortality are not infrequent. Management of peripartum cardiomyopathy is largely limited to the same neurohormonal antagonists used in other forms of cardiomyopathy, and no proven disease-specific therapies exist yet. Research in the past decade has suggested that peripartum cardiomyopathy is caused by vascular dysfunction, triggered by late-gestational maternal hormones. Most recently, information has also indicated that many cases of peripartum cardiomyopathy have genetic underpinnings. We review here the known epidemiology, clinical presentation, and management of peripartum cardiomyopathy, as well as the current knowledge of the pathophysiology of the disease. ( Circulation . 2016;133:1397-1409. DOI: 10.1161/ CIRCULATIONAHA.115.020491.) peripartum
{"title":"Peripartum cardiomyopathy.","authors":"S. Goland, U. Elkayam","doi":"10.1002/9781119409861.ch10","DOIUrl":"https://doi.org/10.1002/9781119409861.ch10","url":null,"abstract":"—Peripartum cardiomyopathy is a potentially life-threatening pregnancy-associated disease that typically arises in the peripartum period and is marked by left ventricular dysfunction and heart failure. The disease is relatively uncommon, but its incidence is rising. Women often recover cardiac function, but long-lasting morbidity and mortality are not infrequent. Management of peripartum cardiomyopathy is largely limited to the same neurohormonal antagonists used in other forms of cardiomyopathy, and no proven disease-specific therapies exist yet. Research in the past decade has suggested that peripartum cardiomyopathy is caused by vascular dysfunction, triggered by late-gestational maternal hormones. Most recently, information has also indicated that many cases of peripartum cardiomyopathy have genetic underpinnings. We review here the known epidemiology, clinical presentation, and management of peripartum cardiomyopathy, as well as the current knowledge of the pathophysiology of the disease. ( Circulation . 2016;133:1397-1409. DOI: 10.1161/ CIRCULATIONAHA.115.020491.) peripartum","PeriodicalId":73992,"journal":{"name":"Journal of the Tennessee Medical Association","volume":"77 1 1","pages":"29-31, 33"},"PeriodicalIF":0.0,"publicationDate":"2019-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/9781119409861.ch10","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44362471","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2019-07-09DOI: 10.4135/9781412963848.n77
J. H. Wolaver
{"title":"Drug abuse.","authors":"J. H. Wolaver","doi":"10.4135/9781412963848.n77","DOIUrl":"https://doi.org/10.4135/9781412963848.n77","url":null,"abstract":"","PeriodicalId":73992,"journal":{"name":"Journal of the Tennessee Medical Association","volume":"62 7 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2019-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70539152","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2018-09-29DOI: 10.1007/978-3-319-61421-2
Gregory H. Reaman, G. Kupfer, Franklin O. Smith
{"title":"Bone Marrow Failure","authors":"Gregory H. Reaman, G. Kupfer, Franklin O. Smith","doi":"10.1007/978-3-319-61421-2","DOIUrl":"https://doi.org/10.1007/978-3-319-61421-2","url":null,"abstract":"","PeriodicalId":73992,"journal":{"name":"Journal of the Tennessee Medical Association","volume":"26 9","pages":""},"PeriodicalIF":0.0,"publicationDate":"2018-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/978-3-319-61421-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"51026531","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Aguila Aguila Elementary School Adelante Healthcare 50023 N 514th Ave 50023 N 514th Ave 85320 623-386-6114 Ajo Desert Senita Dental Center Desert Senita Community Health Center 140 W Estrella Ave 140 W Estrella Ave 85321 520-387-4500 Ajo Main Clinic/dental Center Desert Senita Community Health Center 410 N Malacate St 85321 520-387-5651 520-387-5347 Amado Amado Clinic United Community Health Center, Inc. 28720 S Nogales Hwy 28720 S Nogales Hw 85645 Amado Sopori Elementary School United Community Health Center, Inc. 5000 W Arivaca Rd 5000 W Arivaca Rd 85645 520-625-3502 Apache Junction Apache Junction Clinic Pinal County Health Department 575 N Idaho Rd Ste 301 575 N Idaho Rd Ste 3 85119 480-982-0230 Apache Junction Desert Vista Elementary School Banner Health Foundation 3701 E Broadway Ave 3701 E Broadway Av 85119 602-495-4348 Apache Junction Mountain Health & Wellness M Mountain Health & Wellness 2805 S Ironwood Dr 2805 S Ironwood Dr 85120 4809834866 Apache Junction Mountain Health and Wellness Mountain Health and Wellness 625 N Plaza Dr 625 N Plaza Dr 85120 623-583-3001 Apache Junction Sun Life Family Health Center Sun Life Family Health Center, Inc. 2080 W Southern Ave 2080 W Southern Av 85120 520-381-0341 Arivaca United Community Health Center United Community Health Center, Inc. 17388 W 3rd St 17388 W 3rd St 85601 520-398-2621 520-398-2613 Arlington Arlington Elementary Adelante Healthcare 9410 S 355th Ave 9410 S 355th Ave 85322 623-386-6114 Ash Fork Ash Fork Clinic North Country HealthCare 112 Park Ave 112 Park Ave 86320 928-637-2305 928-637-2343 Ash Fork Ashfork Health Center North Country HealthCare PO Box 191 Po Box 191 86320 928-637-2305 Ashburn Smallwood Prison Dental Service 44031 Pipeline Plaza Ste 300 44031 Pipeline Plaza 20147 703-729-9464 703-729-1227 Avondale Adelante Healthcare OB/GYN Av Adelante Healthcare 3400 N Dysart Rd Ste F121 85392 Avondale AMDx, Ltd. Dba NeuroDiagnosti AMDx, Ltd. Dba NeuroDiagnostics Labor 10320 W McDowell Rd Ste 10320 W McDowell 85392 602-424-4450 602-424-4451 Avondale Avondale Elem School Banner Health Foundation 45 S 3rd Ave 45 S 3rd Ave 85323 602-495-4348 Avondale Avondale Family Health Center Maricopa Integrated Health System 950 E Van Buren St 950 E Van Buren St 85323 623-344-6800 623-344-6801
阿奎拉阿奎拉小学阿德兰特医疗保健50023北514大道50023北514大道85320 623-386-6114阿乔沙漠塞尼塔牙科中心沙漠塞尼塔社区卫生中心140西埃斯特雷拉大道140西埃斯特雷拉大道85321 520-387-4500阿乔主要诊所/牙科中心沙漠塞尼塔社区卫生中心410北Malacate街85321 520-387-5651 520-387-5347阿马多阿马多诊所联合社区卫生中心，28720 S Nogales Hw 85645 Amado Sopori小学联合社区卫生中心，公司，5000 W Arivaca路5000 W Arivaca路85645 520-625-3502阿帕奇交界处阿帕奇交界处诊所皮纳尔县卫生部575北爱达荷州路301号575北爱达荷州路3号85119 480-982-0230阿帕奇交界处沙漠Vista小学Banner健康基金会3701东百老汇大道3701东百老汇大道85119 602-495-4348阿帕奇交界处山健康与保健M山健康与保健2805 S铁木博士2805 S铁木博士85120 4809834866阿帕奇交界处山健康与保健阿帕奇枢纽永明家庭健康中心永明家庭健康中心有限公司南大街2080号西侧阿灵顿阿灵顿小学阿德兰特医疗保健9410 S 355大街9410 S 355大街85322 623-386-6114灰叉灰叉诊所北部国家医疗保健112公园大道112公园大道86320 928-637-2305 928-637-2343灰叉阿什福克健康中心北部国家医疗保健邮政信箱191邮政信箱191 86320 928-637-2305阿什本斯莫伍德监狱牙科服务44031管道广场街300 44031管道广场20147 703-729-9464 703-729-1227Avondale Adelante Healthcare, 3400 N dyart Rd Ste F121 85392。Dba neurodiagnostics AMDx有限公司Dba NeuroDiagnostics Labor 10320 W McDowell Rd Ste 10320 W McDowell 85392 602-424-4450 602-424-4451 Avondale Avondale Elem学校Banner健康基金会45 S 3rd Ave 45 S 3rd Ave 85323 602-495-4348 Avondale Avondale家庭健康中心Maricopa综合健康系统950 E Van Buren St 950 E Van Buren St 85323 623-344-6800 623-344-6801
{"title":"Primary care clinics.","authors":"Amado Amado Clinic","doi":"10.1201/b10406-31","DOIUrl":"https://doi.org/10.1201/b10406-31","url":null,"abstract":"Aguila Aguila Elementary School Adelante Healthcare 50023 N 514th Ave 50023 N 514th Ave 85320 623-386-6114 Ajo Desert Senita Dental Center Desert Senita Community Health Center 140 W Estrella Ave 140 W Estrella Ave 85321 520-387-4500 Ajo Main Clinic/dental Center Desert Senita Community Health Center 410 N Malacate St 85321 520-387-5651 520-387-5347 Amado Amado Clinic United Community Health Center, Inc. 28720 S Nogales Hwy 28720 S Nogales Hw 85645 Amado Sopori Elementary School United Community Health Center, Inc. 5000 W Arivaca Rd 5000 W Arivaca Rd 85645 520-625-3502 Apache Junction Apache Junction Clinic Pinal County Health Department 575 N Idaho Rd Ste 301 575 N Idaho Rd Ste 3 85119 480-982-0230 Apache Junction Desert Vista Elementary School Banner Health Foundation 3701 E Broadway Ave 3701 E Broadway Av 85119 602-495-4348 Apache Junction Mountain Health & Wellness M Mountain Health & Wellness 2805 S Ironwood Dr 2805 S Ironwood Dr 85120 4809834866 Apache Junction Mountain Health and Wellness Mountain Health and Wellness 625 N Plaza Dr 625 N Plaza Dr 85120 623-583-3001 Apache Junction Sun Life Family Health Center Sun Life Family Health Center, Inc. 2080 W Southern Ave 2080 W Southern Av 85120 520-381-0341 Arivaca United Community Health Center United Community Health Center, Inc. 17388 W 3rd St 17388 W 3rd St 85601 520-398-2621 520-398-2613 Arlington Arlington Elementary Adelante Healthcare 9410 S 355th Ave 9410 S 355th Ave 85322 623-386-6114 Ash Fork Ash Fork Clinic North Country HealthCare 112 Park Ave 112 Park Ave 86320 928-637-2305 928-637-2343 Ash Fork Ashfork Health Center North Country HealthCare PO Box 191 Po Box 191 86320 928-637-2305 Ashburn Smallwood Prison Dental Service 44031 Pipeline Plaza Ste 300 44031 Pipeline Plaza 20147 703-729-9464 703-729-1227 Avondale Adelante Healthcare OB/GYN Av Adelante Healthcare 3400 N Dysart Rd Ste F121 85392 Avondale AMDx, Ltd. Dba NeuroDiagnosti AMDx, Ltd. Dba NeuroDiagnostics Labor 10320 W McDowell Rd Ste 10320 W McDowell 85392 602-424-4450 602-424-4451 Avondale Avondale Elem School Banner Health Foundation 45 S 3rd Ave 45 S 3rd Ave 85323 602-495-4348 Avondale Avondale Family Health Center Maricopa Integrated Health System 950 E Van Buren St 950 E Van Buren St 85323 623-344-6800 623-344-6801","PeriodicalId":73992,"journal":{"name":"Journal of the Tennessee Medical Association","volume":"68 3 1","pages":"213"},"PeriodicalIF":0.0,"publicationDate":"2018-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42526802","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2017-09-17DOI: 10.1542/9781610021128-rocky
C. E. Kossmann
{"title":"Rocky Mountain spotted fever.","authors":"C. E. Kossmann","doi":"10.1542/9781610021128-rocky","DOIUrl":"https://doi.org/10.1542/9781610021128-rocky","url":null,"abstract":"","PeriodicalId":73992,"journal":{"name":"Journal of the Tennessee Medical Association","volume":"76 11 1","pages":"730-6"},"PeriodicalIF":0.0,"publicationDate":"2017-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49341584","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
F. Bärtschi, M. Zuber, M. Namdar, B. Seifert, R. Jenni
Background: Management of patients with aortic stenosis is challenging since only few data exists indicating the rate of progression and the correlation to relevant determinants. We investigated whether analysis of the long-term progression, etiology and vascular risk factors could help to define optimal control intervals. Methods: We included 77 patients (age 51.1 ± 14.3 years) in one referral centre with an echocardiographyproven aortic stenosis (mean gradient >12 mm Hg) and a long-term follow-up of three echocardiographic examinations. Missing clinical data were supplemented by a questionnaire to the general practitioner. Two retrospective examination time intervals were defined as a second interval of <2 years (1.3 ± 0.4) and a first interval of >2 years (6.0 ± 2.4) dating back to the initial examination (maximum of 10.6 years prior to the last examination). Results: During 6.0 ± 2.4 years, the mean pressure gradient increased from 24.2 ± 13.6 to 38.1 ± 20.4 mm Hg (p <0.0001); respectively 2.1 ± 3.0 mm Hg/year in the first time period and 4.2 ± 8.2 mm Hg/year in the second time period (p = 0.049), for the entire population. According to severity, patients with mild or moderate aortic stenosis showed an increase from 2.0 ± 2.7 to 4.0 ± 6.6 mm Hg/year (p = 0.04) or from 2.2 ± 3.2 to 3.5 ± 10.9 mm Hg/year respectively (p = 0.66). The group with severe aortic stenosis had an increase of 9.6 ± 12.0 mm Hg/year (group too small for statistical analysis). During the total examination period, left ventricular mass index increased from 149 ± 60 g/m2 to 168 ± 63 g/m2 (p <0.0001), which corresponds to an increase of 3.2 to 7.8 g/m2 per annum (p = 0.52), and the relative wall thickness increased from 40.0 ± 8.5 to 43.0 ± 9.8% (p = 0.002). Ejection fraction remained stable and we found no correlation between etiology, vascular risk factors and progression of the disease. Conclusions: Progression of the mean pressure gradient in patients with aortic stenosis went from 2 mm Hg/year for mild stenosis, to 4 mm Hg/year for moderate stenosis. We found no correlation to conventional vascular risk factors. In patients with mild aortic stenosis and preserved left ventricular ejection fraction, echocardiographic follow-up every 3 to 5 years, until a mean transvalvular pressure gradient of 30 mm Hg is reached, might be a safe and cost-effective follow-up strategy. In patients with more severe aortic stenosis, follow-up has to be more frequent.
背景:主动脉瓣狭窄患者的管理是具有挑战性的，因为只有很少的数据表明进展率和相关决定因素的相关性。我们研究了对长期进展、病因和血管危险因素的分析是否有助于确定最佳控制时间间隔。方法:我们在一个转诊中心纳入77例超声心动图证实主动脉狭窄的患者(年龄51.1±14.3岁)(平均梯度>12 mm Hg)，并进行了三次超声心动图检查的长期随访。通过对全科医生的问卷调查来补充缺失的临床数据。两次回顾性检查时间间隔定义为第二次间隔为2年(6.0±2.4年)，可追溯到首次检查(最长10.6年，最后一次检查)。结果:在6.0±2.4年期间，平均压力梯度从24.2±13.6 mm Hg增加到38.1±20.4 mm Hg (p <0.0001);第一个时间段为2.1±3.0 mm Hg/年，第二个时间段为4.2±8.2 mm Hg/年(p = 0.049)。根据严重程度，轻、中度主动脉狭窄患者分别从2.0±2.7 mm Hg/年增加到4.0±6.6 mm Hg/年(p = 0.04)或从2.2±3.2 mm Hg/年增加到3.5±10.9 mm Hg/年(p = 0.66)。重度主动脉瓣狭窄组升高9.6±12.0 mm Hg/年(组太小，无法统计分析)。在整个检查期间，左室质量指数从149±60 g/m2增加到168±63 g/m2 (p <0.0001)，相当于每年增加3.2 ~ 7.8 g/m2 (p = 0.52)，相对壁厚从40.0±8.5增加到43.0±9.8% (p = 0.002)。射血分数保持稳定，我们发现病因、血管危险因素和疾病进展之间没有相关性。结论:主动脉狭窄患者的平均压力梯度的进展从轻度狭窄的2 mm Hg/年，到中度狭窄的4 mm Hg/年。我们发现与常规血管危险因素无相关性。对于轻度主动脉瓣狭窄并保留左心室射血分数的患者，每3 - 5年进行一次超声心动图随访，直到平均经瓣压力梯度达到30 mm Hg，这可能是一种安全且具有成本效益的随访策略。对于主动脉瓣狭窄更严重的患者，随访必须更频繁。
{"title":"Natural history of aortic stenosis.","authors":"F. Bärtschi, M. Zuber, M. Namdar, B. Seifert, R. Jenni","doi":"10.4414/CVM.2010.01507","DOIUrl":"https://doi.org/10.4414/CVM.2010.01507","url":null,"abstract":"Background: Management of patients with aortic stenosis is challenging since only few data exists indicating the rate of progression and the correlation to relevant determinants. We investigated whether analysis of the long-term progression, etiology and vascular risk factors could help to define optimal control intervals. Methods: We included 77 patients (age 51.1 ± 14.3 years) in one referral centre with an echocardiographyproven aortic stenosis (mean gradient >12 mm Hg) and a long-term follow-up of three echocardiographic examinations. Missing clinical data were supplemented by a questionnaire to the general practitioner. Two retrospective examination time intervals were defined as a second interval of <2 years (1.3 ± 0.4) and a first interval of >2 years (6.0 ± 2.4) dating back to the initial examination (maximum of 10.6 years prior to the last examination). Results: During 6.0 ± 2.4 years, the mean pressure gradient increased from 24.2 ± 13.6 to 38.1 ± 20.4 mm Hg (p <0.0001); respectively 2.1 ± 3.0 mm Hg/year in the first time period and 4.2 ± 8.2 mm Hg/year in the second time period (p = 0.049), for the entire population. According to severity, patients with mild or moderate aortic stenosis showed an increase from 2.0 ± 2.7 to 4.0 ± 6.6 mm Hg/year (p = 0.04) or from 2.2 ± 3.2 to 3.5 ± 10.9 mm Hg/year respectively (p = 0.66). The group with severe aortic stenosis had an increase of 9.6 ± 12.0 mm Hg/year (group too small for statistical analysis). During the total examination period, left ventricular mass index increased from 149 ± 60 g/m2 to 168 ± 63 g/m2 (p <0.0001), which corresponds to an increase of 3.2 to 7.8 g/m2 per annum (p = 0.52), and the relative wall thickness increased from 40.0 ± 8.5 to 43.0 ± 9.8% (p = 0.002). Ejection fraction remained stable and we found no correlation between etiology, vascular risk factors and progression of the disease. Conclusions: Progression of the mean pressure gradient in patients with aortic stenosis went from 2 mm Hg/year for mild stenosis, to 4 mm Hg/year for moderate stenosis. We found no correlation to conventional vascular risk factors. In patients with mild aortic stenosis and preserved left ventricular ejection fraction, echocardiographic follow-up every 3 to 5 years, until a mean transvalvular pressure gradient of 30 mm Hg is reached, might be a safe and cost-effective follow-up strategy. In patients with more severe aortic stenosis, follow-up has to be more frequent.","PeriodicalId":73992,"journal":{"name":"Journal of the Tennessee Medical Association","volume":"2 7582 1","pages":"1334"},"PeriodicalIF":0.0,"publicationDate":"2010-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70752385","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2009-01-01DOI: 10.1017/CBO9780511635663
M. Avram, Nicole E. Rogers
{"title":"Hair Transplantation: Frontmatter","authors":"M. Avram, Nicole E. Rogers","doi":"10.1017/CBO9780511635663","DOIUrl":"https://doi.org/10.1017/CBO9780511635663","url":null,"abstract":"","PeriodicalId":73992,"journal":{"name":"Journal of the Tennessee Medical Association","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2009-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"57085868","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2005-10-01DOI: 10.1001/jama.1991.03460140096034
S. Quintana, R. Font, I. Sandalinas, M. Mañas
{"title":"Guidelines for the appropriate use of do-not-resuscitate orders.","authors":"S. Quintana, R. Font, I. Sandalinas, M. Mañas","doi":"10.1001/jama.1991.03460140096034","DOIUrl":"https://doi.org/10.1001/jama.1991.03460140096034","url":null,"abstract":"","PeriodicalId":73992,"journal":{"name":"Journal of the Tennessee Medical Association","volume":"64 7","pages":"240-4"},"PeriodicalIF":0.0,"publicationDate":"2005-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1001/jama.1991.03460140096034","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"50826264","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 1996-04-01DOI: 10.1177/109135059600100102
F. Cole
{"title":"President's Page.","authors":"F. Cole","doi":"10.1177/109135059600100102","DOIUrl":"https://doi.org/10.1177/109135059600100102","url":null,"abstract":"","PeriodicalId":73992,"journal":{"name":"Journal of the Tennessee Medical Association","volume":"62 5 1","pages":"433"},"PeriodicalIF":0.0,"publicationDate":"1996-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1177/109135059600100102","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"65383272","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Non-diphtheria corynebacteria are normal commensals of the skin and mucous membranes of humans. Increasingly, however, these saprophytic organisms are being recognized as pathogens. Patients infected with these bacteria typically have an underlying immunosuppressive process and/or an indwelling venous catheter. Pleuropulmonary infection with Corynebacterium striatum is rare. We present a patient with diabetes mellitus who developed an intrapulmonary abscess due to C. striatum.
{"title":"Pulmonary abscess due to Corynebacterium striatum.","authors":"J H Batson, R Mukkamala, R P Byrd, T M Roy","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Non-diphtheria corynebacteria are normal commensals of the skin and mucous membranes of humans. Increasingly, however, these saprophytic organisms are being recognized as pathogens. Patients infected with these bacteria typically have an underlying immunosuppressive process and/or an indwelling venous catheter. Pleuropulmonary infection with Corynebacterium striatum is rare. We present a patient with diabetes mellitus who developed an intrapulmonary abscess due to C. striatum.</p>","PeriodicalId":73992,"journal":{"name":"Journal of the Tennessee Medical Association","volume":"89 4","pages":"115-6"},"PeriodicalIF":0.0,"publicationDate":"1996-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19832034","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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