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1.
Ann Thorac Surg ; 100(1): 54-8, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25886811

ABSTRACT

BACKGROUND: Vocal cord paralysis (VCP) is a serious complication associated with thoracic aortic surgery; however, there is a paucity of literature regarding the incidence and impact of VCP on postoperative outcomes. We sought to determine the incidence of VCP and its impact on clinical outcomes in patients who underwent thoracic aortic repair at our center. METHODS: A retrospective chart review was conducted on all patients who underwent thoracic aortic surgery between January 2009 and September 2012. RESULTS: A total of 259 patients underwent a thoracic aortic procedure during the study period. Vocal cord paralysis was diagnosed in 12 (5%) patients, a median of 6 [3 to 21] days after extubation. The incidence was 1%, 0%, 20%, and 25% in those undergoing an open ascending, hemiarch, total arch, or descending aortic procedure, respectively. Patients with VCP had an increased incidence of pneumonia (58% vs 17%, p = 0.003), readmission to the intensive care unit for respiratory failure (17% vs 2%, p = 0.047), and longer hospital length of stay (18 [11 to 43] days versus 9 [6 to 15] days, p = 0.002). A propensity-matched analysis confirmed a higher incidence of pneumonia (58% vs 17%, p = 0.020) and longer hospital length of stay (18 [11 to 43] vs 10 [7 to 14] days, p = 0.015) in patients suffering VCP. CONCLUSIONS: Vocal cord paralysis is a common complication in patients undergoing open surgery of the aortic arch and descending aorta, and is associated with significant morbidity. Further research may be warranted to determine if early fiberoptic examination and consideration of a vocal cord medialization procedure may mitigate the morbidity associated with VCP.


Subject(s)
Aorta, Thoracic , Aortic Diseases/surgery , Thoracic Surgical Procedures/adverse effects , Vocal Cord Paralysis/epidemiology , Vocal Cord Paralysis/etiology , Adult , Aged , Female , Humans , Incidence , Male , Middle Aged , Postoperative Complications/epidemiology , Retrospective Studies , Risk Assessment , Treatment Outcome
2.
Health Estate ; 64(8): 67-9, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20882910

ABSTRACT

With courtyards' therapeutic effects and potential positive impact on patient recovery well-documented in a number of studies, Mark Barker of Archial Architects details some successful examples of their use in healthcare and other buildings, and presents a personal view on how users can optimise their design.


Subject(s)
Hospital Design and Construction , Stress, Psychological/prevention & control , Humans , Patients/psychology
3.
Antimicrob Agents Chemother ; 48(7): 2595-8, 2004 Jul.
Article in English | MEDLINE | ID: mdl-15215114

ABSTRACT

Direct hand-to-hand contact is an important mechanism of transmission of rhinovirus infection. The rhinoviruses are inactivated at a low pH. A survey of organic acids in vitro revealed that these compounds have antirhinoviral activity that persists for at least 3 h after application to the skin. In additional studies of salicylic acid (SA) and pyroglutamic acid (PGA), the hands of volunteers were contaminated with rhinovirus at defined times after application of the acid, and then volunteers attempted to inoculate the nasal mucosa with one hand and quantitative viral cultures were done on the other hand. In one study, 3.5% SA or 1% SA with 3.5% PGA was compared with controls 15 min after application to assess the efficacy of the inactivation of virus and prevention of infection. Virus was recovered from the hands of 28 out of 31 (90%) of the volunteers in the control group compared to 4 out of 27 (15%) and 0 out of 27 in the groups administered 3.5 and 1% SA, respectively (P < 0.05). Rhinovirus infection occurred in 10 out of 31 (32%) of the controls and 2 out of 27 (7%) of volunteers in both treatment groups (P < 0.05 compared with control). In a second study, the efficacy of 4% PGA was evaluated 15 min, 1 h, and 3 h after application. Significantly fewer volunteers had positive hand cultures at all time points compared with the control group, but the proportion that developed rhinovirus infection was not significantly reduced. These results suggest the feasibility of the prevention of rhinovirus transmission by hand treatments that are virucidal on contact and have activity that persists after application.


Subject(s)
Common Cold/prevention & control , Hand/virology , Rhinovirus , Soaps/analysis , Soaps/therapeutic use , Acids , Collagen/chemistry , Common Cold/virology , Double-Blind Method , Hand Disinfection , Humans , Skin/virology
4.
J Drug Target ; 11(8-10): 539-45, 2003.
Article in English | MEDLINE | ID: mdl-15203923

ABSTRACT

Plants have recently become an attractive option for the production of recombinant proteins. Plant-based systems can be used to produce many classes of foreign proteins including candidate vaccine antigens. The selected antigen can be purified from plant material prior to delivery by the preferred route, or alternatively delivered orally in edible plant material that has been processed to give a homogeneous and stable product. Several plant species have been used to express a wide range of vaccine candidates with tobacco, potato and corn being particularly favored. Corn seed is especially well suited to various food processing technologies that generate dry homogeneous material suitable for extended storage and refrigeration-free transport and distribution. Many antigens have been expressed in corn and assessed for efficacy in trials with generally positive results. Candidate HIV vaccines are particularly good targets for plant-based oral delivery since there is a great need for an easily distributed affordable vaccine that could be administered without injection and induce strong mucosal immune responses. As a first step in evaluating plant expression technology with a relevant antigen that might easily be tested in an animal system, we expressed the SIV major surface glycoprotein gp130 (analogous to HIV gp120) in corn seed. Expression levels were achieved that are compatible with conducting oral delivery trials in animals.


Subject(s)
AIDS Vaccines , HIV Antigens/biosynthesis , Plants, Genetically Modified/metabolism , AIDS Vaccines/genetics , AIDS Vaccines/immunology , Administration, Oral , Gene Products, env/genetics , Gene Products, env/immunology , HIV Antigens/genetics , HIV Antigens/immunology , Plants, Genetically Modified/genetics , Zea mays/genetics , Zea mays/metabolism
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