14 results on '"S. Villavicencio"'
Search Results
2. CARDIOGRAFIA POR IMPEDANCIA (CI) MONITOREO HEMODINÁMICO NO INVASIVO
- Author
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Daniel S. Villavicencio León
- Subjects
Cardiografía por Impedancia ,Monitoreo Hemodinámico ,Education ,Medicine - Abstract
Un nuevo método de diagnóstico no invasivo, utiliza la Cardiografía por impedancia (CI) para rápidamente obtener una información del estado hemodinámico que permita un mejor control clínico para evaluación, diagnóstico, pronóstico y tratamiento de nuestros pacientes. (1) El método registra el flujo sanguíneo, la resistencia vascular, la contractilidad cardíaca y el estado de los líquidos corporales, completando 17 parámetros o más dependiendo del tipo de equipo que se utilice. La CI nos permite evaluar mejor al paciente para controlar el tratamiento de la: Insuficiencia Cardíaca (2-3), Hipertensión Arterial Sistémica (4), Disnea (5), Optimización del uso de marcapasos (6) y otras muchas aplicaciones en las diferentes especialidades Médicas.
- Published
- 2019
3. LA CARDIOGRAFÍA POR IMPEDANCIA APLICADA EN UN PACIENTE HIPERTENSO RESISTENTE
- Author
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Daniel S. Villavicencio León
- Subjects
Cardiografía por impedancia ,Estado Hemodinamico ,Hipertensión Arterial ,Education ,Medicine - Abstract
Revisamos el caso de una paciente del sexo femenino de 41 años de edad, procedente y residente en Cuenca, de estado civil casada que recibe tratamiento desde hace 3 años para Hipertensión arterial pero que no se ha podido normalizar sus valores. Hace 24 horas acude a consulta de facultativo por presentar sin causa aparente intensa cefalea occipital acompañada de nausea, mareos, trastornos visuales (fosfenos). En la exploración y examen general se le encuentra con cifras tensionales muy elevadas 170/110 mmHg, por lo que se le administra Captopril Sub lingual de emergencia y se envía para control de especialista. Después de la evaluación clínica, se realiza exámenes complementarios como laboratorio clínico, electrocardiograma y cardiografía por impedancia y se hace la estratificación del riesgo cardiovascular. Se decide tratamiento con terapia combinada con calcioantagonista (CA). Antagonista de los receptores de la Angiotensina ARA II, y un Alfa-beta bloqueador. Los controles a la semana, un mes y dos meses posteriores muestran una paciente controlada y sin la presencia de daños de órgano blanco. Cuatro años más tarde acude a control porque se siente bien, pero quiere una valoración de su estado de salud. Se realizan los exámenes de control, en particular una cardiografía por impedancia y se verifica la normalidad de su estado hemodinámico.
- Published
- 2019
4. Observatorio de Financiamiento para el Desarrollo. Nota T��cnica N�� 1
- Author
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Katiuska King, Carranza-Barona, Cesar, Salazar, Nicol��s Villavicencio, Yamel Cede��o, Serrano, Carol, Abad, Nicole, and Herrera, Isaac
- Published
- 2021
- Full Text
- View/download PDF
5. Oxidative Stress and Cardiovascular Risk in Type 1 Diabetes Mellitus: Insights From the DCCT/EDIC Study
- Author
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W.H. Wilson Tang, Paula McGee, John M. Lachin, Daniel Y. Li, Byron Hoogwerf, Stanley L. Hazen, D.M. Nathan, B. Zinman, O. Crofford, S. Genuth, J. Brown‐Friday, J. Crandall, H. Engel, S. Engel, H. Martinez, M. Phillips, M. Reid, H. Shamoon, J. Sheindlin, R. Gubitosi‐Klug, L. Mayer, S. Pendegast, H. Zegarra, D. Miller, L. Singerman, S. Smith‐Brewer, M. Novak, J. Quin, Saul Genuth, M. Palmert, E. Brown, J. McConnell, P. Pugsley, P. Crawford, W. Dahms, N.S. Gregory, M.E. Lackaye, S. Kiss, R. Chan, A. Orlin, M. Rubin, D. Brillon, V. Reppucci, T. Lee, M. Heinemann, S. Chang, B. Levy, L. Jovanovic, M. Richardson, B. Bosco, A. Dwoskin, R. Hanna, S. Barron, R. Campbell, A. Bhan, D. Kruger, J.K. Jones, P.A. Edwards, J.D. Carey, E. Angus, A. Thomas, A. Galprin, M. McLellan, F. Whitehouse, R. Bergenstal, M. Johnson, K. Gunyou, L. Thomas, J. Laechelt, P. Hollander, M. Spencer, D. Kendall, R. Cuddihy, P. Callahan, S. List, J. Gott, N. Rude, B. Olson, M. Franz, G. Castle, R. Birk, J. Nelson, D. Freking, L. Gill, W. Mestrezat, D. Etzwiler, K. Morgan, L.P. Aiello, E. Golden, P. Arrigg, V. Asuquo, R. Beaser, L. Bestourous, J. Cavallerano, R. Cavicchi, O. Ganda, O. Hamdy, R. Kirby, T. Murtha, D Schlossman, S. Shah, G. Sharuk, P. Silva, P. Silver, M. Stockman, J. Sun, E. Weimann, H. Wolpert, L.M. Aiello, A. Jacobson, L. Rand, J. Rosenzwieg, M.E. Larkin, M. Christofi, K. Folino, J. Godine, P. Lou, C. Stevens, E. Anderson, H. Bode, S. Brink, C. Cornish, D. Cros, L. Delahanty, eManbey, C. Haggan, J. Lynch, C. McKitrick, D. Norman, D. Moore, M. Ong, C. Taylor, D. Zimbler, S. Crowell, S. Fritz, K. Hansen, C. Gauthier‐Kelly, F.J. Service, G. Ziegler, A. Barkmeier, L. Schmidt, B. French, R. Woodwick, R. Rizza, W.F. Schwenk, M. Haymond, J. Pach, J. Mortenson, B. Zimmerman, A. Lucas, R. Colligan, L. Luttrell, M. Lopes‐Virella, S. Caulder, C. Pittman, N. Patel, K. Lee, M. Nutaitis, J. Fernandes, K. Hermayer, S. Kwon, A Blevins, J. Parker, J. Colwell, D. Lee, J. Soule, P. Lindsey, M. Bracey, A. Farr, S. Elsing, T. Thompson, J. Selby, T. Lyons, S. Yacoub‐Wasef, M. Szpiech, D. Wood, R. Mayfield, M. Molitch, D. Adelman, S. Colson, L. Jampol, A. Lyon, M. Gill, Z. Strugula, L. Kaminski, R. Mirza, E. Simjanoski, D. Ryan, C. Johnson, A. Wallia, S. Ajroud‐Driss, P. Astelford, N. Leloudes, A. Degillio, B. Schaefer, S. Mudaliar, G Lorenzi, M. Goldbaum, K. Jones, M. Prince, M. Swenson, I. Grant, R. Reed, R. Lyon, O. Kolterman, M. Giotta, T. Clark, G. Friedenberg, W.I. Sivitz, B. Vittetoe, J. Kramer, M. Bayless, R. Zeitler, H. Schrott, N. Olson, L. Snetselaar, R. Hoffman, J. MacIndoe, T. Weingeist, C. Fountain, R. Miller, S. Johnsonbaugh, M. Patronas, M. Carney, S. Mendley, P. Salemi, R. Liss, M. Hebdon, D. Counts, T. Donner, J. Gordon, R. Hemady, A. Kowarski, D. Ostrowski, S. Steidl, B. Jones, W.H. Herman, C.L. Martin, R. Pop‐Busui, D.A. Greene, M.J. Stevens, N. Burkhart, T. Sandford, J. Floyd, J. Bantle, N. Flaherty, J. Terry, D. Koozekanani, S. Montezuma, N. Wimmergren, B. Rogness, M. Mech, T. Strand, J. Olson, L. McKenzie, C. Kwong, F. Goetz, R. Warhol, D. Hainsworth, D. Goldstein, S. Hitt, J. Giangiacomo, D.S Schade, J.L. Canady, M.R. Burge, A. Das, R.B. Avery, L.H. Ketai, J.E. Chapin, M.L. Schluter, J. Rich, C. Johannes, D. Hornbeck, M. Schutta, P.A. Bourne, A. Brucker, S. Braunstein, S. Schwartz, B.J. Maschak‐Carey, L. Baker, T. Orchard, L. Cimino, T. Songer, B. Doft, S. Olson, D. Becker, D. Rubinstein, R.L. Bergren, J. Fruit, R. Hyre, C. Palmer, N. Silvers, L. Lobes, P. Paczan Rath, P.W. Conrad, S. Yalamanchi, J. Wesche, M. Bratkowksi, S. Arslanian, J. Rinkoff, J. Warnicki, D. Curtin, D. Steinberg, G. Vagstad, R. Harris, L. Steranchak, J. Arch, K. Kelly, P. Ostrosaka, M. Guiliani, M. Good, T. Williams, K. Olsen, A. Campbell, C. Shipe, R. Conwit, D. Finegold, M. Zaucha, A. Drash, A. Morrison, J.I. Malone, M.L. Bernal, P.R. Pavan, N. Grove, E.A. Tanaka, D. McMillan, J. Vaccaro‐Kish, L. Babbione, H. Solc, T.J. DeClue, S. Dagogo‐Jack, C. Wigley, H. Ricks, A. Kitabchi, E. Chaum, M.B. Murphy, S. Moser, D. Meyer, A. Iannacone, S. Yoser, M. Bryer‐Ash, S. Schussler, H. Lambeth, P. Raskin, S. Strowig, M. Basco, S. Cercone, A. Barnie, R. Devenyi, M. Mandelcorn, M. Brent, S. Rogers, A. Gordon, N. Bakshi, B. Perkins, L. Tuason, F. Perdikaris, R. Ehrlich, D. Daneman, K. Perlman, S Ferguson, J. Palmer, R. Fahlstrom, I.H. de Boer, J. Kinyoun, L. Van Ottingham, S. Catton, J. Ginsberg, C. McDonald, J. Harth, M. Driscoll, T. Sheidow, J. Mahon, C. Canny, D. Nicolle, P. Colby, J. Dupre, I. Hramiak, N.W. Rodger, M. Jenner, T. Smith, W. Brown, M. May, J. Lipps Hagan, A. Agarwal, T. Adkins, R. Lorenz, S. Feman, L. Survant, N.H. White, L. Levandoski, G. Grand, M. Thomas, D. Joseph, K. Blinder, G. Shah, D. Burgess, I. Boniuk, J. Santiago, W. Tamborlane, P. Gatcomb, K. Stoessel, P. Ramos, K. Fong, P. Ossorio, J. Ahern, L. Meadema‐Mayer, C. Beck, K. Farrell, J Quin, P. Gaston, R. Trail, J. Lachin, J. Backlund, I. Bebu, B. Braffett, L. Diminick, X. Gao, W. Hsu, K. Klumpp, H. Pan, V. Trapani, P. Cleary, P. McGee, W. Sun, S. Villavicencio, K. Anderson, L. Dews, Naji Younes, B. Rutledge, K. Chan, D. Rosenberg, B. Petty, A. Determan, D. Kenny, C. Williams, C. Cowie, C. Siebert, M. Steffes, V. Arends, J. Bucksa, M. Nowicki, B. Chavers, D. O'Leary, J. Polak, A. Harrington, L. Funk, R Crow, B. Gloeb, S. Thomas, C. O'Donnell, E.Z. Soliman, Z.M. Zhang, Y. Li, C. Campbell, L. Keasler, S. Hensley, J. Hu, M. Barr, T. Taylor, R. Prineas, E.L. Feldman, J.W. Albers, P. Low, C. Sommer, K. Nickander, T. Speigelberg, M. Pfiefer, M. Schumer, M. Moran, J. Farquhar, C. Ryan, D. Sandstrom, M. Geckle, E. Cupelli, F. Thoma, B. Burzuk, T. Woodfill, R. Danis, B. Blodi, D. Lawrence, H. Wabers, S. Gangaputra, S. Neill, M. Burger, J. Dingledine, V. Gama, R. Sussman, M. Davis, L. Hubbard, M. Budoff, S. Darabian, P. Rezaeian, N. Wong, M. Fox, R. Oudiz, L Kim, R. Detrano, K. Cruickshanks, D. Dalton, K. Bainbridge, J. Lima, D. Bluemke, E. Turkbey, der Geest, C. Liu, A. Malayeri, A. Jain, C. Miao, H. Chahal, R. Jarboe, V. Monnier, D. Sell, C. Strauch, S. Hazen, A. Pratt, W. Tang, J. Brunzell, J. Purnell, R. Natarajan, F. Miao, L. Zhang, Z. Chen, A. Paterson, A. Boright, S. Bull, L. Sun, S. Scherer, T.J. Lyons, A. Jenkins, R. Klein, G. Virella, A. Jaffa, R. Carter, J. Stoner, W.T. Garvey, D. Lackland, M. Brabham, D. McGee, D. Zheng, R.K. Mayfield, J. Maynard, H. Wessells, A Sarma, R. Dunn, S. Holt, J. Hotaling, C. Kim, Q. Clemens, J. Brown, and K. McVary
- Subjects
medicine.medical_specialty ,endocrine system diseases ,030209 endocrinology & metabolism ,Disease ,030204 cardiovascular system & hematology ,Lower risk ,medicine.disease_cause ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,Diabetes mellitus ,medicine ,Diseases of the circulatory (Cardiovascular) system ,Coronary Heart Disease ,Glycemic ,Original Research ,free radical ,Inflammation ,Type 1 diabetes ,biology ,business.industry ,Paraoxonase ,medicine.disease ,paraoxonase ,3. Good health ,RC666-701 ,Cohort ,diabetes mellitus ,biology.protein ,Cardiology and Cardiovascular Medicine ,business ,Oxidant Stress ,Oxidative stress ,F2Isoprostane ,Biomarkers - Abstract
Background Hyperglycemia leading to increased oxidative stress is implicated in the increased risk for the development of macrovascular and microvascular complications in patients with type 1 diabetes mellitus. Methods and Results A random subcohort of 349 participants was selected from the DCCT / EDIC (Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications) cohort. This included 320 controls and 29 cardiovascular disease cases that were augmented with 98 additional known cases to yield a case cohort of 447 participants (320 controls, 127 cases). Biosamples from DCCT baseline, year 1, and closeout of DCCT , and 1 to 2 years post‐ DCCT ( EDIC years 1 and 2) were measured for markers of oxidative stress, including plasma myeloperoxidase, paraoxonase activity, urinary F 2α isoprostanes, and its metabolite, 2,3 dinor‐8 iso prostaglandin F 2α . Following adjustment for glycated hemoblobin and weighting the observations inversely proportional to the sampling selection probabilities, higher paraoxonase activity, reflective of antioxidant activity, and 2,3 dinor‐8 iso prostaglandin F 2α , an oxidative marker, were significantly associated with lower risk of cardiovascular disease (−4.5% risk for 10% higher paraoxonase, P iso prostaglandin F 2α , P =0.0092). In contrast, the oxidative markers myeloperoxidase and F 2α isoprostanes were not significantly associated with cardiovascular disease after adjustment for glycated hemoblobin. There were no significant differences between DCCT intensive and conventional treatment groups in the change in all biomarkers across time segments. Conclusions Heightened antioxidant activity (rather than diminished oxidative stress markers) is associated with lower cardiovascular disease risk in type 1 diabetes mellitus, but these biomarkers did not change over time with intensification of glycemic control. Clinical Trial Registration URL : https://www.clinicaltrials.gov . Unique identifiers: NCT 00360815 and NCT 00360893.
- Published
- 2018
6. Case Report: Pancreas Graft With a Duodenal Complication Rescued Using Total Duodenectomy
- Author
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Domingo Casadei, I. C. Cabrera, Pablo Uva, S. Villavicencio Fornaciari, and A.E. Giunippero
- Subjects
Male ,medicine.medical_specialty ,Duodenum ,Fistula ,medicine.medical_treatment ,Postoperative Complications ,Laparotomy ,medicine ,Humans ,Digestive System Surgical Procedures ,Transplantation ,business.industry ,Anastomosis, Surgical ,Middle Aged ,medicine.disease ,Kidney Transplantation ,Surgery ,medicine.anatomical_structure ,Diabetes Mellitus, Type 2 ,Pancreatic fistula ,Duodenal Fistula ,Drainage ,Kidney Failure, Chronic ,Pancreas Transplantation ,Complication ,Pancreas ,business - Abstract
Simultaneous pancreas-kidney (SPK) transplantation is the treatment of choice for type 1 diabetics with end-stage renal disease. Recently patients with type 2 diabetes have been considered for transplantation. Despite that the patient and graft survival rates have improved over the past years, it continues to be a procedure with high surgical complication rates. We herein report a case of a pancreatic graft with a duodenal complication rescued using a total duodenectomy, a procedure that is seldom used. A 57-year-old type 2 diabetic underwent a SPK transplantation with systemic-enteric drainage. He was converted to a Roux en Y at day 7 for a small duodenal fistula without peritonitis. At day 13, with good graft function, he presented with gastrointestinal and abdominal bleeding. At laparotomy he had a congestive duodenum with intraluminal bleeding and an anastomotic fistula. We performed a total duodenectomy with enteric drainage. The patient was discharged home on day 39 with a pancreatic fistula on intramuscular Octretotide that lasted for 3 months. He was never readmitted and has good pancreas and kidney function at 16 months of follow-up. We think this is an option to rescue a pancreas graft with duodenal complications in selected cases.
- Published
- 2014
- Full Text
- View/download PDF
7. 702 Quality of life in male extrophy-epispadias patients: Long term follow up
- Author
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C. Centeno, S. Villavicencio, M. Enrike, J. Caffaratti, A. Bujons, and B. Jose
- Subjects
Pediatrics ,medicine.medical_specialty ,Quality of life ,Long term follow up ,business.industry ,Urology ,medicine ,Epispadias ,medicine.disease ,business - Published
- 2016
- Full Text
- View/download PDF
8. Computer-aided teaching of thermoelectrical power plant operation
- Author
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S. Villavicencio and G. Rodriguez
- Subjects
Computer graphics ,Engineering drawing ,Electricity generation ,Power station ,Computer science ,Control system ,Electronic engineering ,Computer-aided ,Instrumentation (computer programming) ,Animation ,Graphics - Abstract
A computer aided system (SADCOM: Sistema de Apoyo Didactico Computarizado) to teach power plant principles of operation to new plant operators is described. SADCOM usex text, graphics, colors and animation to illustrate the basic processes of a power plant. The presentations are controlled by the instructor who explains how the different systems, equipment and processes work. SADCOM teaches the following topics: tube and instrumentation diagrams, operation procedures, failure analysis, and generation unit thermal balances where mass, pressures and temperatures can be modified to see how they affect the efficiency of the unit.
- Published
- 2002
- Full Text
- View/download PDF
9. [Acute renal insufficiency in severe dehydration in infants]
- Author
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L, Del Rio, E, Cassorla Levy, and S, Villavicencio
- Subjects
Diagnosis, Differential ,Male ,Dehydration ,Diarrhea, Infantile ,Infant, Newborn ,Humans ,Infant ,Female ,Mannitol ,Acute Kidney Injury - Published
- 1966
10. National population-based estimates for major birth defects, 2016-2020.
- Author
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Stallings EB, Isenburg JL, Rutkowski RE, Kirby RS, Nembhard WN, Sandidge T, Villavicencio S, Nguyen HH, McMahon DM, Nestoridi E, and Pabst LJ
- Subjects
- Humans, Maternal Age, United States epidemiology, Female, Down Syndrome, Gastroschisis epidemiology, Heart Defects, Congenital epidemiology, Transposition of Great Vessels
- Abstract
Background: We provide updated crude and adjusted prevalence estimates of major birth defects in the United States for the period 2016-2020., Methods: Data were collected from 13 US population-based surveillance programs that used active or a combination of active and passive case ascertainment methods to collect all birth outcomes. These data were used to calculate pooled prevalence estimates and national prevalence estimates adjusted for maternal race/ethnicity for all conditions, and maternal age for trisomies and gastroschisis. Prevalence was compared to previously published national estimates from 1999 to 2014., Results: Adjusted national prevalence estimates per 10,000 live births ranged from 0.63 for common truncus to 18.65 for clubfoot. Temporal changes were observed for several birth defects, including increases in the prevalence of atrioventricular septal defect, tetralogy of Fallot, omphalocele, trisomy 18, and trisomy 21 (Down syndrome) and decreases in the prevalence of anencephaly, common truncus, transposition of the great arteries, and cleft lip with and without cleft palate., Conclusion: This study provides updated national estimates of selected major birth defects in the United States. These data can be used for continued temporal monitoring of birth defects prevalence. Increases and decreases in prevalence since 1999 observed in this study warrant further investigation., (© 2024 Wiley Periodicals LLC. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.)
- Published
- 2024
- Full Text
- View/download PDF
11. Case report: pancreas graft with a duodenal complication rescued using total duodenectomy.
- Author
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Uva PD, Villavicencio Fornaciari S, Giunippero AE, Cabrera IC, and Casadei DH
- Subjects
- Anastomosis, Surgical adverse effects, Digestive System Surgical Procedures methods, Drainage methods, Humans, Kidney Failure, Chronic surgery, Male, Middle Aged, Postoperative Complications surgery, Diabetes Mellitus, Type 2 surgery, Duodenum surgery, Kidney Transplantation adverse effects, Pancreas Transplantation adverse effects
- Abstract
Simultaneous pancreas-kidney (SPK) transplantation is the treatment of choice for type 1 diabetics with end-stage renal disease. Recently patients with type 2 diabetes have been considered for transplantation. Despite that the patient and graft survival rates have improved over the past years, it continues to be a procedure with high surgical complication rates. We herein report a case of a pancreatic graft with a duodenal complication rescued using a total duodenectomy, a procedure that is seldom used. A 57-year-old type 2 diabetic underwent a SPK transplantation with systemic-enteric drainage. He was converted to a Roux en Y at day 7 for a small duodenal fistula without peritonitis. At day 13, with good graft function, he presented with gastrointestinal and abdominal bleeding. At laparotomy he had a congestive duodenum with intraluminal bleeding and an anastomotic fistula. We performed a total duodenectomy with enteric drainage. The patient was discharged home on day 39 with a pancreatic fistula on intramuscular Octretotide that lasted for 3 months. He was never readmitted and has good pancreas and kidney function at 16 months of follow-up. We think this is an option to rescue a pancreas graft with duodenal complications in selected cases.
- Published
- 2014
- Full Text
- View/download PDF
12. The association of skin intrinsic fluorescence with type 1 diabetes complications in the DCCT/EDIC study.
- Author
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Orchard TJ, Lyons TJ, Cleary PA, Braffett BH, Maynard J, Cowie C, Gubitosi-Klug RA, Way J, Anderson K, Barnie A, and Villavicencio S
- Subjects
- Adolescent, Adult, Diabetic Nephropathies metabolism, Diabetic Retinopathy metabolism, Female, Fluorescence, Glycated Hemoglobin metabolism, Humans, Male, Young Adult, Diabetes Complications metabolism, Diabetes Mellitus, Type 1 complications, Diabetes Mellitus, Type 1 metabolism, Skin metabolism
- Abstract
Objective: To determine whether skin intrinsic fluorescence (SIF) is associated with long-term complications of type 1 diabetes (T1D) and, if so, whether it is independent of chronic glycemic exposure and previous intensive therapy., Research Design and Methods: We studied 1,185 (92%) of 1,289 active Diabetes Control and Complications Trial (DCCT)/Epidemiology of Diabetes Interventions and Complications (EDIC) participants from 2010 to 2011. SIF was determined using a fluorescence spectrometer and related cross-sectionally to recently determined measures of retinopathy (stereo fundus photography), cardiac autonomic neuropathy (CAN; R-R interval), confirmed clinical neuropathy, nephropathy (albumin excretion rate [AER]), and coronary artery calcification (CAC)., Results: Overall, moderately strong associations were seen with all complications, before adjustment for mean HbA1c over time, which rendered these associations nonsignificant with the exception of sustained AER>30 mg/24 h and CAC, which were largely unaffected by adjustment. However, when examined within the former DCCT treatment group, associations were generally weaker in the intensive group and nonsignificant after adjustment, while in the conventional group, associations remained significant for CAN, sustained AER>30 mg/24 h, and CAC even after mean HbA1c adjustment., Conclusions: SIF is associated with T1D complications in DCCT\EDIC. Much of this association appears to be related to historical glycemic exposure, particularly in the previously intensively treated participants, in whom adjustment for HbA1c eliminates statistical significance.
- Published
- 2013
- Full Text
- View/download PDF
13. Clinical and technical factors associated with skin intrinsic fluorescence in subjects with type 1 diabetes from the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Study.
- Author
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Cleary PA, Braffett BH, Orchard T, Lyons TJ, Maynard J, Cowie C, Gubitosi-Klug RA, Way J, Anderson K, Barnie A, and Villavicencio S
- Subjects
- Adult, Aging pathology, Analysis of Variance, Biomarkers blood, Blood Glucose metabolism, Diabetes Mellitus, Type 1 blood, Diabetes Mellitus, Type 1 physiopathology, Diabetic Angiopathies blood, Diabetic Angiopathies physiopathology, Diabetic Nephropathies blood, Diabetic Nephropathies physiopathology, Female, Forearm, Glycated Hemoglobin metabolism, Glycation End Products, Advanced blood, Humans, Hyperglycemia blood, Hypoglycemic Agents therapeutic use, Insulin therapeutic use, Male, Middle Aged, Phenotype, Predictive Value of Tests, Risk Factors, Skin chemistry, Skin metabolism, Smoking pathology, Diabetes Mellitus, Type 1 pathology, Diabetic Angiopathies pathology, Diabetic Nephropathies pathology, Skin pathology, Spectrometry, Fluorescence methods
- Abstract
Background: The Diabetes Control and Complications Trial (DCCT)/Epidemiology of Diabetes Interventions and Complications(EDIC) studies have established multiyear mean hemoglobin A1c (HbA1c) as predictive of microvascular complications in persons with type 1 diabetes. However, multiyear mean HbA1c is not always available in the clinical setting. Skin advanced glycation end products (AGEs) are thought to partially reflect effects of hyperglycemia over time, and measurement of skin AGEs might be a surrogate for multiyear mean HbA1c. As certain AGEs fluoresce and skin fluorescence has been demonstrated to correlate with the concentration of skin AGEs, noninvasive measurement by skin intrinsic fluorescence(SIF) facilitates the exploration of the association of mean HbA1c and other clinical/technical factors with SIF using the detailed phenotypic database available in DCCT/EDIC., Subjects and Methods: Of the subjects, 1,185 (53% male) had measurements of SIF during years 16/17 of EDIC with mean age and diabetes duration of 51.5 and 29.8 years, respectively. SIF measurements were obtained on the underside of the forearm near the elbow using a skin fluorescence spectrometer. Demographic data and health history were self-reported, and an annual standardized examination measured clinical status. Linear regression models were constructed to identify significant clinical and technical factors associated with SIF, and the final models only used factors that were significant., Results: SIF ranged from 8.7 to 54.0 arbitrary units and was log-normally distributed. Log(SIF) correlated more with mean HbA1c as the time period increased. In multivariate analyses log(SIF) was significantly associated with mean HbA1c, age,estimated glomerular filtration rate < 60mL/min/m2, smoking status, skin tone, and clinic latitude <37 N., Conclusions: SIF reflects age, mean HbA1c over time, smoking, and renal damage, which are known risk factors for diabetes complications.
- Published
- 2013
- Full Text
- View/download PDF
14. [Acute renal insufficiency in severe dehydration in infants].
- Author
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Del Rio L, Cassorla Levy E, and Villavicencio S
- Subjects
- Diagnosis, Differential, Female, Humans, Infant, Infant, Newborn, Male, Acute Kidney Injury etiology, Dehydration complications, Diarrhea, Infantile complications, Mannitol therapeutic use
- Published
- 1966
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