lunes, 2 de noviembre de 2015

Marfan, embarazo, aneurisma y anestesia / Marfan, pregnancy, aneurisma and anesthesi

Noviembre 1, 2015. No. 2132

Disección aórtica en mujeres durante el embarazo o el puerperio. Informe de 11 casos en China
Aortic dissection in women during the course of pregnancy or puerperium: a report of 11 cases in central south China.
Int J Clin Exp Med. 2015 Jul 15;8(7):11607-12. eCollection 2015.
El embarazo y el crecimiento de la raíz aórtica en el síndrome de Marfanun estudio prospectivo
Pregnancy and aortic root growth in the Marfan syndrome: a prospective study
Lilian J. Meijboom, Frederiek E. Vos, Janneke Timmermans, Godfried H. Boers, Aeiko H. Zwinderman, Barbara J.M. Mulder
European Heart Journal (2005) 26, 914-920
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Disección aórtica aguda en embarazo con síndrome de Marfan
Acute aortic dissection in pregnancy with the marfan syndrome.
Korean J Thorac Cardiovasc Surg. 2014 Jun;47(3):291-3. doi: 10.5090/kjtcs.2014.47.3.291. Epub 2014 Jun 5.
Disección aórtica postparto
Postpartum aortic dissection.
Taiwan J Obstet Gynecol. 2013 Sep;52(3):318-22. doi: 10.1016/j.tjog.2013.06.003.
Síndrome de Marfan durante el embarazo. Manejo anestésico del parto en 16 casos
Marfan's syndrome during pregnancy: anesthetic management of delivery in 16 consecutive patients.
Anesth Analg. 2013 Feb;116(2):392-8. doi: 10.1213/ANE.0b013e3182768f78. Epub 2013 Jan 9.
Anestesia regional en síndrome de Marfan, no todas las ectasias durales son lo mismo. Informe de dos casos
Regional anesthesia in Marfan syndrome, not all dural ectasias are the same: a report of two cases.
Can J Anaesth. 2012 Nov;59(11):1052-7. doi: 10.1007/s12630-012-9778-5. Epub 2012 Sep 14.
Modulo CEEA Leon, Gto.      XII Congreso Virtual Mexicano de Anestesiologia

          
Anestesiología y Medicina del Dolor
52 664 6848905
vwhizar@anestesia-dolor.org
anestesia-dolor.org

Copyright © 2015

Óxido nitroso y depresión mayor / N2O and major depression

Noviembre 2, 2015. No. 2133

Combinación de óxido nitroso con isoflorano o escopolamina para depresión mayor resistente
Combination of Nitrous Oxide with Isoflurane or Scopolamine for Treatment-resistant Major Depression.
Clin Psychopharmacol Neurosci. 2015 Apr 30;13(1):118-20. doi: 10.9758/cpn.2015.13.1.118.
El óxido nitroso para tratamiento de la depresión mayor resistente: Un ensayo de prueba de concepto.
Nitrous Oxide for Treatment-Resistant Major Depression: A Proof-of-Concept Trial.
Biol Psychiatry. 2015 Jul 1;78(1):10-8. doi: 10.1016/j.biopsych.2014.11.016. Epub 2014 Dec 9.
Abstract
BACKGROUND: N-methyl-D-aspartate receptor antagonists, such as ketamine, have rapid antidepressant effects in patients with treatment-resistantdepression (TRD). We hypothesized that nitrous oxide, an inhalational general anesthetic and N-methyl-D-aspartate receptor antagonist, may also be a rapidly acting treatment for TRD. METHODS: In this blinded, placebo-controlled crossover trial, 20 patients with TRD were randomly assigned to 1-hour inhalation of 50% nitrous oxide/50% oxygen or 50% nitrogen/50% oxygen (placebo control). The primary endpoint was the change on the 21-item Hamilton Depression Rating Scale (HDRS-21) 24 hours after treatment. RESULTS: Mean duration of nitrous oxide treatment was 55.6 ± 2.5 (SD) min at a median inspiratory concentration of 44% (interquartile range, 37%-45%). In two patients, nitrous oxide treatment was briefly interrupted, and the treatment was discontinued in three patients. Depressivesymptoms improved significantly at 2 hours and 24 hours after receiving nitrous oxide compared with placebo (mean HDRS-21 difference at 2 hours, -4.8 points, 95% confidence interval [CI], -1.8 to -7.8 points, p = .002; at 24 hours, -5.5 points, 95% CI, -2.5 to -8.5 points, p < .001; comparison between nitrous oxide and placebo, p < .001). Four patients (20%) had treatment response (reduction ≥50% on HDRS-21) and three patients (15%) had a full remission (HDRS-21 ≤ 7 points) after nitrous oxide compared with one patient (5%) and none after placebo (odds ratio for response, 4.0, 95% CI, .45-35.79; OR for remission, 3.0, 95% CI, .31-28.8). No serious adverse events occurred; all adverse events were brief and of mild to moderate severity. CONCLUSIONS: This proof-of-concept trial demonstrated that nitrous oxide has rapid and marked antidepressant effects in patients with TRD.
KEYWORDS: Major depression; Nitrous oxide; Treatment-resistant depression
      XII Congreso Virtual Mexicano de Anestesiologia


          
Anestesiología y Medicina del Dolor
52 664 6848905
vwhizar@anestesia-dolor.org
anestesia-dolor.org

Copyright © 2015

viernes, 30 de octubre de 2015

Transplante de hígado/Liver transplant

Octubre 30, 2015. No. 2130Octubre, mes de lucha contra cáncer de mama.
Anestesia y Dolor

Transplante hepático para enfermedades hepáticas por alcoholismo. Lecciones aprendidas y temas no resueltos
Liver transplantation for alcoholic liver disease: Lessons learned and unresolved issues.
World J Gastroenterol. 2015 Oct 21;21(39):10994-1002. doi: 10.3748/wjg.v21.i39.10994.
Abstract
The use of liver transplantation (LT) as a treatment for alcoholic liver disease (ALD) has been highly controversial since the beginning. The ever increasing shortage of organs has accentuated the low priority given to patients suffering from ALD, which is considered a "self-inflicted" condition. However, by improving the long-term survival rates, making them similar to those from other indications, and recognizing that alcoholism is a primary disease, ALD has become one of the most common indications for LT in Europe and North America, a situation thought unfathomable thirty years ago. Unfortunately, there are still many issues with the use of this procedure for ALD. There are significant relapse rates, and the consequences of excessive drinking after LT range from asymptomatic biochemical and histological abnormalities to graft failure and death. A minimum three-month period of sobriety is required for an improvement in liver function, thus making LT unnecessary, and to demonstrate the patient's commitment to the project, even though a longer abstinence period does not guarantee lower relapse rates after LT. Recent data have shown that LT is also effective for severe alcoholic hepatitis when the patient is unresponsive to corticosteroids therapy, with low relapse rates in highly selected patients, although these results must be confirmed before LT becomes a standard procedure in this setting. Finally, LT for ALD is accompanied by an increased risk of de novo solid organ cancer, skin cancer, and lymphoproliferative disorders, which has a large impact on the survival rates.
KEYWORDS: Alcoholic hepatitis; Alcoholic liver disease; Cirrhosis; Liver transplantation; Relapse; Six-month rule; Sobriety; Solid organ cancer; Survival rates
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Modulo CEEA Leon, Gto.      XII Congreso Virtual Mexicano de Anestesiologia


          
Anestesiología y Medicina del Dolor
52 664 6848905
vwhizar@anestesia-dolor.org
anestesia-dolor.org

Copyright © 2015