domingo, 10 de julio de 2011

Eportfolios faculty slideshare
Interesante material en PowerPoint donde su autor Joe Fahs nos muestra diferentes herramientas de la Web 2.0 y las redes sociales que podemos utilizar como profesores y estudiantes para crear un E-Portafolio (Portafolio Electrónico o Digital). Recomiendo su revisión ampliamente (ver más).
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the international council on medical & care compunetics

science pages
10 
July, 2011 
SUNDAY

The Taxonomy of Telemedicine

Abstract

The purpose of this article is to present a taxonomy for telemedicine. The field has markedly grown, with an increasing number of applications, a variety of technologies, and newly introduced terminology. A taxonomy would serve to bring conceptual clarity to this burgeoning set of alternatives to in-person healthcare delivery. The article starts with a brief discussion of the importance of taxonomy as an information management strategy to improve knowledge sharing, facilitate research and policy initiatives, and provide some guidance for the orderly development of telemedicine. We provide a conceptual context for the proliferation of related concepts, such as telehealth, e-health, and m-health, as well as a classification of the content of these concepts. Our main concern is to develop an explicit taxonomy of telemedicine and to demonstrate how it can be used to provide definitive information about the true effects of telemedicine in terms of cost, quality, and access. Taxonomy development and refinement is an iterative process. If this initial attempt at classification proves useful, subject matter experts could enhance the development and proliferation of telemedicine by testing, revising, and verifying this taxonomy.
10 July 2011 
Title:
The Taxonomy of Telemedicine
Author(s):
Bashshur, Rashid; Shannon, Gary; Krupinski, Elizabeth; Grigsby, Jim
Journal
Telemedicine and e-Health, Online first
(2011-06-30)
URL:
DOI:
PMID:
Keyword(s):
Citation:Bashshur R, Shannon G, Krupinski E, Grigsby J. The Taxonomy of Telemedicine. Telemed J E Health [Internet]. 2011 Jun 30;Online Ahead of Print. Available from: http://www.liebertonline.com/doi/abs/10.1089/tmj.2011.0103
In ICMCC Database
AlTelemedicine and e-Health articles (100).
Other article(s) by
Elizabeth Krupinski (1).

Discussion

5 ways telemedicine could address the healthcare crisis



505723 blood pressure 5 ways telemedicine could address the healthcare crisisPretty much everyone has an opinion about the U.S. healthcare crisis, because it affects pretty much all of us. Many people also agree that emerging information technology solutions — including those that fall into the “mHealth” category — will be key in addressing that crisis. I’m going to sidestep the political ridiculousness for this particular column.
First, a definition. The World Health Organization (WHO) defines mHealth as “the provision of health services and information via mobile technologies such as mobile phones and personal digital assistants.” The fact is, however, that these mobile technologies need the power of unified communications and other network infrastructure technologies to do their thing.
Some perspective on why mHealth is important. An April 2010 report from Juniper Research projects that by 2010 and 2014, healthcare providers (both private and public) could save up to $5.83 billion in costs worldwide by moving to mHealth technologies. Again, remember that these approaches are only as good as the infrastructure that drives them.
A March 2011 draft “position paper” from the Center for Technology and Aging suggests that mHealth and telemedicine technologies could greatly benefit older adults and the “people who support them.” If you look at the figures presented in the paper, you’ll see that the usage rate of things like mobile phones and tablets is actually pretty high among older adults. The AARP released some figures in January 2011, for example, suggesting that cell phone usage among adults more than 50 years in age was about 70 percent; smartphone usage was significantly lowers, around 7 percent of this age group. Tablet penetration is much lower, about 42 percent among this age group, according to the AARP.
There are six primary applications that the industry is watching carefully. They are:
  1. Chronic disease management: This refers to applications that help people track ongoing conditions, such as diabetes, to avoid duplicative testing and avert crises that could be avoided through the detection of early warning signs.
  2. Medication adherence: Ever forget to take your vitamins? This is a category of technologies that could help ensuring that proper dosages are maintained and also with forestalling any possible drug contraindications.
  3. Location and safety tracking: Applications typing together location technologies with monitoring systems to help provide faster action in the case of emergencies (such as a fall).
  4. Access to personal health information: The holy grail of personal health records is to create a central repository of information that is routinely updated with ALL relevant data and accessible to all caregivers involved with a particular patient.
  5. Wellness services: This refers to the services that help people track their fitness activities and dietary habits. The idea is that awareness is the first step to better wellness.
The trick for applications such as these, of course, is to make sure they are available to as many people as possible. That’s why the mobile link is so critical. But don’t underestimate that work that healthcare organizations will need to behind the scenes to make this all seem seamless.

Quit Smoking Success Rates


Quit Smoking Success Rates
‘what’s the best way to quit smoking?’



Most people are unaware of the success rates of the various methods used to quit smoking. Yet every year thousands of people make the decision to quit smoking. For many of them it will not be the first time they have tried to stop smoking. The majority will restart smoking within 1 year.
This raises a basic question: what are the quit smoking success rates of the most widely used techniques?
This is a short review of the evidence.
Statistics from studies show that the success rate of ‘going cold turkey’ is quite low – between 4% and 10%.
Hughes JR, Keely J, Naud S., "Shape of the relapse curve and long-term abstinence among untreated smokers." Addiction 2004;99:29-38 showed a 12 month success rate of less than 5%.
Doran, C.M. et al, (2006) “Smoking status of Australian general practice patients, and their quit attempts.” Addictive Behaviours 31: 758 – 766 showed an overall cessation rate for NRT with other support of just over 30%.
A review of the data in 2009 showed a 6 month abstinence rate with NRT of only 6.8%: BMJ 2009; 338:b1024
Stead LF, Perera R, Bullen C, et al; "Nicotine replacement therapy for smoking cessation." Cochrane Database Syst Rev. 2008 Jan 23;(1) also showed low long term effectiveness for NRT.
In the UK a recent review by the National Institute for Health and Clinical Excellence (NICE) of the ‘Cut Down to Quit with Nicotine Replacement Therapy’ programme showed success rates with NRT of only 6.8%! 
British Medical Journal 1983; 286(6366):595 – showed a 10% effectiveness rate for nicotine gum at 1 year.
Addictive Behaviors 1983; 8(3):253 – showed an 8% success rate for nicotine gum at 1 year.
Preventive Medicine 1995; 24(1):41 – showed a 13% success rate for nicotine patches at 1 year.
New England Journal of Medicine, 1999;340(9):685 – showed a 16% success rate for nicotine patches at 1 year.
Using NRT while pregnant exposes the unborn child to a dose of nicotine.
Using NRT patches while breastfeeding gives the baby a dose of nicotine. Breastfeeding within a hour of using nicotine gum significantly increases the amount of nicotine in breast milk.
People with a medical condition such as heart disease, an overactive thyroid gland, diabetes, severe kidney or liver disease, or stomach ulcers should exercise caution before deciding to use NRT – discuss with your doctor first.
NRT delivers a dose of nicotine, so it may cause nicotine-related side-effects such as: headaches; dizziness; a racing pulse; vivid dreams; indigestion; dry mouth; nausea; diarrhoea. Nicotine patches may cause skin irritation. Nicotine gum may cause heartburn, sore throat, or dry mouth. Nicotine inhalers may cause nasal irritation.
Bupropion is an ant-depressant drug that has been shown to reduce cravings on smoking cessation. Treatment is for a minimum of 8 weeks and a maximum of 12 weeks. Studies show efficacy of up to 25%.
According to the manufacturer’s own Zyban prescribing information leaflet, the efficacy varies, with one study producing a 1 year success rate of 23% (28% if a nicotine patch is added!), while another study produced a 6 month success rate of only 19%.
Tonnesen P, Tonstad S, Hjalmarson A, Lebargy F, Van Spiegel P I, Hider A, Sweet R, Townsend J (2003). "A multicentre, randomized, double-blind, placebo-controlled, 1-year study of bupropion SR for smoking cessation". J Intern Med 254 (2): 184–192. showed one year success rates of only 21% (11% for a very small group of patients who received placebo).
<
Jorenby D E, Hays J T, Rigotti N A, Azoulay S, Watsky E J, Williams K E, Billing C B, Gong J, Reeves K R (2006). "Efficacy of varenicline, an alpha4beta2 nicotinic acetylcholine receptor partial agonist, vs placebo or sustained-release bupropion for smoking cessation: a randomized controlled trial". JAMA 296 (1): 56–63. showed the 1 year abstinence rates for bupropion to be only 14.6% (compared to 10.3% in the placebo group). Treatment was discontinued due to side-effects in 12.6% of the bupropion group.
Doran, C.M. et al, (2006) “Smoking status of Australian general practice patients, and their quit attempts.” Addictive Behaviours 31: 758 – 766 showed an overall cessation rate for bupropion of just 21%.
Only one study has shown a higher efficacy (Hays JT, Hurt RD, Rigotti NA, et al. Sustained release bupropion for pharmacologic relapse after smoking cessation. Ann Intern Med 2001; 135:423-33., which produced a 55.1% success rate) but the patients in the study had to take bupropion continuously for 1 year (instead of 12 weeks) to achieve that level of efficacy. In other words, even taking bupropion all the time for a year, only about half of smokers remain abstinent – the other half continuing to take bupropion and continuing to smoke!
The manufacturer’s prescribing information leaflet advises that bupropion should not be prescribed (is contraindicated) to individuals with seizure disorders (e.g epilepsy or other conditions that lower the seizure threshold, such as alcohol withdrawal or benzodiazepine discontinuation), anorexia nervosa, or bulimia. It is also contraindicated in people who are also taking monoamine oxidase inhibitors (MAOIs). When switching from MAOIs to bupropion, it is important to include a washout period of about two weeks between the medications.[72] The prescribing information also recommends that caution should be exercised when treating patients with liver damage, severe kidney disease, and severe hypertension, as well as in paediatric patients, adolescents and young adults due to the increased risk of suicidal ideation. 
According to the prescribing information, the most common side-effects of Zyban are dry mouth, and insomnia. Patients have also reported stomach pains, vivid dreams, joint pain, coughing, itchiness, nausea, and sore throat.
Jorenby D E, Hays J T, Rigotti N A, Azoulay S, Watsky E J, Williams K E, Billing C B, Gong J, Reeves K R (2006). "Efficacy of varenicline, an alpha4beta2 nicotinic acetylcholine receptor partial agonist, vs placebo or sustained-release bupropion for smoking cessation: a randomized controlled trial". JAMA 296 (1): 56–63. showed a 1 year abstinence rate of 23% (14.6% for Zyban, 10.3% for placebo), with a drop-out rate due to side-effects of 10.5%.
A 2010 report by West & Shiffman suggested that varenicline produces a success rate of about 16%.
Varenicline has a range of side-effects, with nausea being the major problem. It may also cause: abdominal pain; flatulence; dyspepsia; constipation; dry mouth; rash; breathing problems; headache; increased appetite; decreased appetite; alterations to taste (dysgeusia); tiredness; insomnia; abnormal dreams or nightmares.
In 2008 the WHO stated that it does not consider e-cigarettes a legitimate therapy for smokers trying to quit because there is no scientific evidence (peer reviewed studies)that show efficacy or safety.
In a recent (December 2010) report, investigators from the University of California (Riverside) expressed concerns over safety and lack of clinical data, suggesting that the regulators (FDA) should take them off the market until there have been proper safety investigations.
A 2008 report in New Zealand (Murray Laugesen (2008). "Safety Report on the Ruyan e-cigarette Cartridge and Inhaled Aerosol". Health New Zealand Ltd. ) found traces of carcinogenic tobacco specific nitrosamines (TSNA) in tested e-cigarettes.
At the time of writing (December 2010) no e-cigarette has been licensed in the UK as a medicinal NRT product.
A two-part review by Cui Meng (Cui Meng, Advances in studies on acupuncture abstinence, Journal of Traditional Chinese Medicine, 1995, 15(4): 301–307, and Cui Meng, Advances in studies on acupuncture abstinence (continued), Journal of Traditional Chinese Medicine 1996; 16 (1): 65–69.) of a large number of clinical research papers suggests that the long term success rate (cessation at 1 year) for ear acupuncture is 30%.
An individual study in 2004 by Ausfeld-Hafter et al suggested a 41% 1 year success rate. (Ausfeld-Hafter B, Marti F, Hoffmann S. Forsch Komplementarmed Klass Naturheilkd. 2004 Feb;11(1):8-13.
Doran, C.M. et al, (2006) “Smoking status of Australian general practice patients, and their quit attempts.” Addictive Behaviours 31: 758 – 766 showed an overall cessation rate for of 53.4% for hypnotherapy.
Another review has shown a success rate of just over 66% - but this required 4 sessions of hypnosis.
Kline, M.(1970) International Journal of Clinical and Experimental Hypnosissuggested a 1 year success rate of 88%.
Crasilneck, H. B., & Hall, J. A. (1985). Clinical hypnosis: Principles and applications (2nd ed.) Orlando, FL: Grune & Stratton, quote a success rate of over 67%.
Comparison table
Method of quitting1 year success rate
Willpower aloneLess than 10%
Nicotine patches & gum alone6.8% - 16%
bupropion (Zyban)14.6% - 25%
varenicline (Champix / Chantix)16% - 23%
e-cigarettesNo published data
Acupuncture30% - 41%
Hypnosis53.4% - 88%

Analgesia obstétrica


Analgesia para trabajo de parto y el bebé: buenas noticias no son noticias
Labour analgesia and the baby: good news is no news.
Reynolds F.
St Thomas' Hospital, London, UK. felicity.reynolds@btineternet.com
Int J Obstet Anesth. 2011 Jan;20(1):38-50. Epub 2010 Dec
Abstract
When investigating different methods of maternal pain relief in labour, neonatal outcome has not always been at the forefront, or else maternal changes, such as haemodynamics, fever, length of labour, need for oxytocin or type of delivery, are taken as surrogates for neonatal outcome. It is essential to examine the actual baby and to appreciate that labour pain itself has adverse consequences for the baby. For systemic analgesia, pethidine has been most extensively studied and compared with neuraxial analgesia. It depresses fetal muscular activity, aortic blood flow, short-term heart rate variability and oxygen saturation. In the newborn it exacerbates acidosis, depresses Apgar scores, respiration, neurobehavioural score, muscle tone and suckling. Alternatives have few advantages, remifentanil being the most promising. Neuraxial analgesia is associated with better Apgar scores and variable neurobehavioural changes. Neonatal acid-base status is not only better with epidural than with systemic opioid analgesia, it is also better than with no analgesia. The effect on breast feeding has yet to be established, though it is certainly no worse than that of systemic opioid analgesia. Variations in neuraxial technique have little impact on the newborn. Widespread ignorance of the benefit to the newborn of neuraxial labour analgesia in the UK among non-anaesthetists needs to be combated

http://download.journals.elsevierhealth.com/pdfs/journals/0959-289X/PIIS0959289X10001287.pdf  
Anestesia Combinada Espinal-Epidural y sus Ventajas en Obstetricia
Dr. Luis Fernando García Gutiérrez
Director de Quirófano de CIMA Santa Engracia
Monterrey, Nuevo León. México
lgarciag@santaengracia.com
Anest Mex 2007;19:147-154.
La anestesia epidural-espinal combinada (ACEE) es una técnica regional muy aceptada para procedimientos quirúrgicos por debajo de T10 y en las pacientes obstétricas. La técnica puede reducir o eliminar los riesgos y algunas desventajas de los bloqueos subaracnoideos o peridurales cuando estos se realizan por separado. ACEE combina la rapidez, densidad y seguridad de la anestesia subaracnoidea con la flexibilidad del bloqueo epidural continuo el cual extiende la duración de la anestesia y de la analgesia postoperatoria. Se ha utilizado en todo el mundo en millones de pacientes con muy pocos problemas. El uso ACEE en el campo de la anestesia y analgesia obstétrica goza de gran popularidad. Una dosis pequeña de anestésico local añadida de un opioide en el espacio subaracnoideo produce excelente analgesia de parto, la cual puede ser complementada con dosis epidurales inyectadas a través del catéter peridural. La técnica más usada es colocar primero la aguja epidural en el espacio peridural y a través de esta aguja introducir la aguja de raquia para la punción dural y administración de los fármacos espinales, seguida de la inserción del catéter en la cavidad peridural. La ACEE es un bloqueo seguro, que se considera como una buena alternativa a la analgesia convencional epidural y se ha convertido en el procedimiento preferido para analgesia obstétrica en nuestro hospital. Este artículo revisa y discute el procedimiento de ACEE orientado en obstetricia.
Palabras clave: Bloqueo combinado epidural-espinal, analgesia obstétrica.

http://www.anestesiaenmexico.org/RAM9/RAM2007-19-3/006.pdf 
 
Eficacia analgésica de la infiltración con ropivacaína 7.5 mg/mL en la incisión Pfannestiel para cesárea
Analgesic Efficacy of Pfannenstiel Incision Infiltration with Ropivacaine 7.5 mg/mL for Caesarean Section.
Nguyen NK, Landais A, Barbaryan A, M'barek MA, Benbaghdad Y, McGee K, Lanba P.
Department of Anaesthesia and Intensive Care, Victor Dupouy Hospital, 95107 Argenteuil, France.
Anesthesiol Res Pract. 2010;2010. pii: 542375. Epub 2010 Jul 27.
Abstract
Background. Pain after Caesarean delivery is partly related to Pfannenstiel incision, which can be infiltrated with local anaesthetic solutions. Methods. A double- blind randomized control trial was designed to assess the analgesic efficacy of 7.5 mg/mL ropivacaine solution compared to control group, in two groups of one hundred and forty four parturients for each group, who underwent Caesarean section under spinal anaesthesia: group R (ropivacaine group) and group C (control group). All parturients also received spinal sufentanil (2.5 mug). Results. Ropivacaine infiltration in the Pfannenstiel incision for Caesarean delivery before wound closure leads to a reduction of 30% in the overall consumption of analgesics (348 550 mg for group R versus 504 426 mg for group C with P < .05), especially opioids in the first 24 hours, but also significantly increases the time interval until the first request for an analgesic (4 h 20 min +/- 2 h 26 for group R versus 2 h 42 +/- 1 h 30 for group C). The P values for the two groups were: P < .0001 for paracetamol, P < .0001 for ketoprofen and P for nalbuphine which was the most significant. There is no significant difference in the threshold of VAS in the two series. Conclusion. This technique can contribute towards a programme of early rehabilitation in sectioned mothers, with earlier discharge from the post-labour suite.


Perforación de duramadre con catéter epidural
Sanjoaquín , M T ; Alonso , A ; de la Gala , F ; Navia , J
R e v. Soc. Esp. Dolor 9: 189-190, 2002 

La utilización de analgesia epidural para el trabajo del parto es una técnica ampliamente extendida y segura, aunque no por ello exenta de complicaciones. Presentamos el caso de una paciente de 31 años de edad en la semana 39 de gestación, a la que se le realizó punción epidural para analgesia durante el trabajo del parto. La punción se realizó a nivel de L3-L4 bajo monitorización básica. Mediante técnica de pérdida de resistencia con suero salino se localizó el espacio epidural a 5 cm de piel sin incidencias. Posteriormente se aspiró a través de la aguja de Tuhoy sin obtener líquido ni sangre que indicara la perforación de la duramadre o la canalización de algún vaso epidural. Se administraron a través de la aguja 3 ml de bupivacaína al 0,25% sin vasoconstrictor y 15 µg de fentanilo como dosis de prueba. La paciente no refirió bloqueo motor ni sensitivo con esta dosis por lo que se completó a través de la aguja la inyección de anestésico local con otros 7 ml de bupivacaína al 0,25% sin vasoconstrictor y 35 µg de fentanilo. Se procedió entonces a la colocación del catéter epidural, dejando el mismo introducido 3 cm en espacio epidural. Se comenzó a administrar una perfusión continua de bupivacaína 0,06% y 2,5 µg.ml- 1 de fentanilo, previa aspiración por el catéter para comprobar que se encontraba en espacio epidural, a una velocidad de 14 ml.h- 1. A los 90 minutos del inicio de la perfusión la paciente refirió bloqueo motor completo de miembros inferiores y bloqueo sensitivo hasta T 10. Se suspendió la perfusión continua de anestésico local y se aspiró de nuevo a través del catéter obteniendo más de 1 ml de líquido claro. Se realizó un análisis del líquido obtenido con una tira reactiva con el fin de comprobar si contenía glucosa, siendo el resultado positivo. Posteriormente y para confirmar el resultado anterior, se llevó a cabo una bioquímica del líquido objetivándose la presencia de 56 mg.dl- 1 de glucosa y de proteínas en el mismo. Al confirmarse la presencia del catéter en espacio intradural se retiró definitivamente. No se consideró la posibilidad de realizar de nuevo una punción epidural. El bloqueo sensitivo y motor desapareció a las 2 horas de retirar el catéter epidural. El parto tuvo lugar por vía vaginal sin complicaciones. La paciente no presentó
cefalea post-punción dural

Atentamente
Dr. Benito Cortes-Blanco
Anestesiología y Medicina del Dolor

Últimos adelantos de ortopedia en cita mundial en Cuba

Últimos adelantos de ortopedia en cita mundial en Cuba

La Habana, julio 7.- Representantes de varios países se darán cita en el XXII Congreso Internacional de la Sociedad Cubana de Ortopedia y Traumatología (SCOT), que tendrá lugar del 19 al 24 de septiembre en la capital.

La cita, que incluye además la II Reunión Binacional Cubana - Mexicana de la especialidad, tratará entre otros temas, la cirugía de mínimo acceso, la artroplastia total de miembro superior (hombro y codo), fracturas del anillo pélvico y sus complicaciones y los avances en cirugía artroscópica.

El profesor Rodrigo Álvarez Cambras, presidente de la Sociedad Cubana de Ortopedia y Traumatología y del Comité Organizador, explicó a la AIN que ese método mínimamente invasivo, iniciado a principios de la década de los 70, en la isla se extiende a otras provincias con resultados notables.

Cerca del 40 por ciento de las cirugías de ortopedia se pueden realizar mediante la artroscopia, proceder de mínimo acceso que se utiliza en enfermedades de las articulaciones, como la rodilla, hombro y cadera, recalcó.

Auspiciado por las Sociedades Cubana de Ortopedia y Traumatología y la Internacional de Cirugía Ortopédica y Traumatología, el foro contará con cursos pre congreso sobre fijación externa con el sistema (RALCA), ideado por Álvarez Cambras.

También incluye la actualización acerca del tratamiento de los tumores óseos, así como una jornada postcongreso de especialidades afines a la ortopedia, del 26 al 29 de septiembre, dirigida a enfermeras, técnicos en traumatología, fisioterapeutas y otras.

Asimismo, habrá una feria comercial en la que se expondrán los instrumentales quirúrgicos y televisarán las técnicas avanzadas y novedosas, anunció Álvarez Cambras, director del Complejo Científico Ortopédico Internacional Frank País, sede del congreso.

GlobalMedia: Harvard Study backs Telemedicine Programs for Rural Hospitals « AirparkProps

GlobalMedia: Harvard Study backs Telemedicine Programs for Rural Hospitals « AirparkProps

America’s Premier Telemedicine Service |

America’s Premier Telemedicine Service |