ABSTRACT
The multi-copper oxidase from the hyper-thermophilic bacteria Thermus thermophilus (Tth-MCO), has been previously characterized and described as an example of a laccase with low catalytic properties, especially when it is compared with the activity of fungal laccases, but it is active at high temperatures. Structurally, Tth-MCO has a unique feature: a ß-hairpin near the T1Cu site, which is not present in any other laccases deposited at the PDB. This ß-hairpin has an expected crystallographic behavior in solvent-exposed areas of a crystallized protein: lack of electron density, high B-values and several crystalline contacts with neighboring crystallographic copies; however, its dynamical behavior in solution and its biological implications have not been described. Here, we describe four new Tth-MCO crystallographic structures, and the ß-hairpin behavior has been analyzed by molecular dynamics simulations, considering the effect of pH and temperature. The ß-hairpin new crystallographic conformations described here, together with their dynamics, were used to understand the pH-restrained laccase activity of Tth-MCO against substrates as syringaldazine. Remarkably, there are insertions in laccases from Thermus and Meiothermus genus, sharing the same position and a methionine-rich composition of the Tth-MCO ß-hairpin. This unique high methionine content of the Tth-MCO ß-hairpin is responsible to coordinate, Ag+1 and Hg+1 in oxidative conditions, but Cu+1 and Cu+2 are not coordinated in crystallographic experiments, regardless of the redox conditions; however, Ag+1 addition does not affect Tth-MCO laccase activity against syringaldazine. Here, we propose that the pH-dependent ß-hairpin dynamical behavior could explain, at least in part, the inefficient laccase activity displayed by Tth-MCO in acidic pH values.
Subject(s)
Laccase/chemistry , Laccase/metabolism , Thermus thermophilus/metabolism , Amino Acid Motifs , Bacterial Proteins/chemistry , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Crystallography, X-Ray , Hydrazones/metabolism , Hydrogen-Ion Concentration , Laccase/genetics , Methionine , Molecular Dynamics Simulation , Oxidation-Reduction , Oxidoreductases/chemistry , Oxidoreductases/metabolism , Phylogeny , Protein Conformation , TemperatureABSTRACT
OBJECTIVE: To determine tolerance, pain intensity, percentage of tests completed successfully and complications of deep sedation controlled by intensivists during gastrointestinal endoscopic procedures. DESIGN: A one-year, prospective observational study was carried out. SETTING: Department of Intensive Care intervention in the Endoscopy Unit of Hospital Universitario del Tajo (Spain). PATIENTS: Subjects over 15 years of age subjected to endoscopic procedures under deep sedation. RESULTS: A total of 868 patients were sedated during the study period, with the conduction of 1010 endoscopic procedures. The degree of tolerance was considered adequate («Very good¼/«Good¼) in 96.9% of the patients (95%CI: 95.7-98.1%), with a median score of 0 on the pain visual analog scale. A total of 988 endoscopic procedures were successfully completed (97.8%; 95%CI: 96.9-98.8%): 675 colonoscopies (97.1%) and 305 endoscopies (99.7%). Complications were recorded in 106 patients (12.2%; 95%CI: 10.0-14.5%). The most frequent being desaturation (6.1%), rhythm disturbances (5.1%) and hypotension (2.4%). CONCLUSION: Gastrointestinal endoscopic procedures under sedation controlled by intensivists are well tolerated and satisfactory for the patient, and are successfully completed in a very large percentage of cases. The procedures are associated with frequent minor complications that are resolved successfully.
Subject(s)
Critical Care , Deep Sedation , Endoscopy, Gastrointestinal , Endoscopy, Gastrointestinal/methods , Female , Humans , Male , Middle Aged , Prospective StudiesABSTRACT
Severe carbon monoxide (CO) poisoning causes fulminant deaths in common environment as well as neurological sequelae to survivors. Prevention of delayed neurological syndrome (DNS) after exposure to CO, the most important sequela, is based up to date on hyperbaric oxygen administration. Nevertheless, its use remains controversial due to the lack of evidence regarding its efficacy. The aim of this review is to report therapies under investigation for preventing or improving DNS, some of them with promising results in humans.
Subject(s)
Carbon Monoxide Poisoning/therapy , Neurotoxicity Syndromes/prevention & control , Oxygen Inhalation Therapy , Animals , Carbon Monoxide Poisoning/complications , Carbon Monoxide Poisoning/drug therapy , Humans , Neurotoxicity Syndromes/etiologySubject(s)
Chest Pain/prevention & control , Critical Illness/therapy , Nerve Block , Ventilator Weaning , Adult , Humans , Male , Middle Aged , RibsABSTRACT
OBJECTIVE: To assess the correlation between left ventricular outflow tract velocity time integral (LVOT VTI) and stroke volume index (SVI) calculated by thermodilution methods in ventilated critically ill patients. DESIGN: A prospective, descriptive, multicenter study was performed. SETTING: Five intensive care units from university hospitals. PATIENTS: Patients older than 17 years needing mechanical ventilation and invasive hemodynamic monitoring were included. INTERVENTIONS: LVOT VTI was measured by pulsatile Doppler echocardiography. Calculations of SVI were performed through a floating pulmonary artery catheter (PAC) or a Pulse index Contour Cardiac Output (PiCCO®) thermodilution methods. MAIN VARIABLES: The relation between LVOT VTI and SVI was tested by linear regression analysis. RESULTS: One hundred and fifty-six paired measurements were compared. Mean LVOT VTI was 20.83±4.86cm and mean SVI was 41.55±9.55mL/m2. Pearson correlation index for these variables was r=0.644, p<0.001; ICC was 0.52 (CI 95% 0.4-0.63). When maximum LVOT VTI was correlated with SVI, Pearson correlation index was r=0.62, p<0.001. Correlation worsened for extreme values, especially for those with higher LVOT VTI. CONCLUSIONS: LVOT VTI could be a complementary hemodynamic evaluation in selected patients, but does not eliminate the need for invasive monitoring at the present time. The weak correlation between LVOT VTI and invasive monitoring deserves additional assessment to identify the factors affecting this disagreement.
Subject(s)
Respiration, Artificial , Stroke Volume , Ventricular Function, Left , Aged , Blood Flow Velocity , Correlation of Data , Female , Humans , Male , Prospective StudiesABSTRACT
OBJECTIVES: Sedation and ventilation overnight after cardiac surgery is common practice. However, early extubation may be feasible with no increase in postoperative complications. This study examines (1) if early extubation is possible in a significant number of patients, (2) if it reduces ICU stay, and (3) if this practice increases postoperative complications. DESIGN: Prospective, controlled, randomized clinical trial. PATIENTS AND METHODS: We randomized 404 consecutive patients to early extubation (7 to 11 h postoperatively) (group A, 201 patients) or conventional extubation (between 8 and 12 AM the following day) (group B, 203 patients). Variables included type and severity of the disease, surgical risk, type of operation, operative incidences, postoperative complications, duration of mechanical ventilation, intubation and ICU stay, bleeding, reoperation, vasoactive drugs, and mortality. RESULTS: Groups were comparable. Extubation within the preestablished time was successful in 60.2% of patients in group A and 74.4% in group B. Median ICU stay was 27 h in group A and 44 h in group B (p=0.008). Discharge from ICU within the first 24 h postoperatively was 44.3% in group A and 30.5% in group B (p=0.006). There was no significant difference in complications between groups. Successfully extubated patients in group A had more reintubation and prolonged ventilation than in group B. CONCLUSIONS: (1) Sixty percent of our patients were extubated within 11 h of operation. (2) As a result, the length of stay in ICU was reduced and the percentage of patients discharged within 24 h was increased. (3) There was no increase in clinically important postoperative complications.
Subject(s)
Cardiac Surgical Procedures , Cardiopulmonary Bypass , Intubation, Intratracheal , Ventilator Weaning , APACHE , Female , Humans , Incidence , Intensive Care Units , Length of Stay/statistics & numerical data , Male , Middle Aged , Postoperative Care , Postoperative Complications/epidemiology , Prospective Studies , Risk Factors , Time Factors , Treatment Failure , Ventilator Weaning/methodsABSTRACT
The pulmonary toxicity of gold salts is an uncommon cause of life-threatening respiratory failure. Currently, patients who suffer from this do not need mechanical ventilation, and the toxicity can be difficult to diagnose when it occurs in patient with an illness producing pulmonary manifestations. We report a case of severe respiratory failure due to gold salt toxicity in a patient suffering from rheumatoid arthritis requiring mechanical ventilation. At such a time, the poor respiratory function makes some diagnostic procedures harmful. The diagnosis can be made after the exclusion of other causes of rheumatoid lung when the patient's poor respiratory status precludes invasive exploration. The clinical findings, radiological features, and results of pulmonary function tests may be enough to diagnose gold-related pneumopathy. This avoids the need for bronchoscopic examination or transfer of the patient for computed tomography. Attention must be paid to this complication because the outcome and functional prognosis are better when pulmonary involvement is gold related: in our case steroid therapy was life-saving and induced complete recovery of the lung damage.
Subject(s)
Antirheumatic Agents/adverse effects , Arthritis, Rheumatoid/drug therapy , Lung Diseases, Interstitial/chemically induced , Aged , Anti-Inflammatory Agents/therapeutic use , Bronchiolitis Obliterans/chemically induced , Diagnosis, Differential , Humans , Lung Diseases, Interstitial/diagnostic imaging , Lung Diseases, Interstitial/therapy , Male , Methylprednisolone/therapeutic use , Organogold Compounds , Positive-Pressure Respiration , Prognosis , RadiographyABSTRACT
Objective: To assess the correlation between left ventricular outflow tract velocity time integral (LVOT VTI) and stroke volume index (SVI) calculated by thermodilution methods in ventilated critically ill patients. Design: A prospective, descriptive, multicenter study was performed. Setting: Five intensive care units from university hospitals. Patients: Patients older than 17 years needing mechanical ventilation and invasive hemodynamic monitoring were included. Interventions: LVOT VTI was measured by pulsatile Doppler echocardiography. Calculations of SVI were performed through a floating pulmonary artery catheter (PAC) or a Pulse index Contour Cardiac Output (PiCCO(R)) thermodilution methods. Main variables: The relation between LVOT VTI and SVI was tested by linear regression analysis. Results: One hundred and fifty-six paired measurements were compared. Mean LVOT VTI was 20.83±4.86cm and mean SVI was 41.55±9.55mL/m2. Pearson correlation index for these variables was r=0.644, p<0.001; ICC was 0.52 (CI 95% 0.4-0.63). When maximum LVOT VTI was correlated with SVI, Pearson correlation index was r=0.62, p<0.001. Correlation worsened for extreme values, especially for those with higher LVOT VTI. Conclusions: LVOT VTI could be a complementary hemodynamic evaluation in selected patients, but does not eliminate the need for invasive monitoring at the present time. The weak correlation between LVOT VTI and invasive monitoring deserves additional assessment to identify the factors affecting this disagreement
Objetivo: Evaluar la correlación entre la integral velocidad tiempo del tracto de salida del ventrículo izquierdo (IVT TSVI) y el índice volumen sistólico (IVS) calculado por métodos de termodilución en pacientes ventilados críticamente enfermos. Diseño: Se realizó un estudio prospectivo, descriptivo y multicéntrico. Ámbito: Cinco unidades de cuidados intensivos de hospitales universitarios. Pacientes: Se incluyeron pacientes mayores de 17 años que necesitaron ventilación mecánica y monitorización hemodinámica invasiva. Intervenciones: La IVT TSVI se midió mediante Doppler pulsátil. Los cálculos de SVI se realizaron a través de un catéter de arteria pulmonar (CAP) o un método de Pulse index Contour Cardiac Output (PiCCO(R)), con métodos de termodilución. Variables principales: La relación entre IVT TSVI e IVS se evaluó mediante análisis de regresión lineal. Resultados: Se compararon 156 mediciones pareadas. La IVT TSVI media fue de 20,83±4,86cm y la media de IVS fue de 41,55±9,55ml/m2. El índice de correlación de Pearson para estas variables fue r=0,644, p<0,001; ICC fue 0,52 (IC 95%: 0,4-0,63). Cuando la IVT TSVI máxima se correlacionó con el IVS, el índice de correlación de Pearson fue r=0,62, p<0,001. La correlación empeoró para los valores extremos, especialmente para aquellos con mayor IVT TSVI. Conclusiones: La IVT TSVI podría ser una evaluación hemodinámica complementaria en pacientes seleccionados, pero no elimina la necesidad de un control invasivo en la actualidad. La débil correlación entre la IVT TSVI y la monitorización invasiva requiere estudios adicionales para identificar los factores que afectan a este desacuerdo
Subject(s)
Humans , Ventricular Function, Left/physiology , Respiration, Artificial/methods , Thermodilution/methods , Correlation of Data , Prospective Studies , Intensive Care Units/statistics & numerical data , Regression Analysis , Hemodynamic MonitoringABSTRACT
No disponible
Subject(s)
Humans , Pulmonary Infarction/diagnostic imaging , Reflex , Bronchi/diagnostic imaging , Bronchoconstriction , Pulmonary Embolism/complications , Pulmonary Embolism/diagnostic imaging , Pulmonary Ventilation , Heart Failure/diagnostic imagingABSTRACT
No disponible
Subject(s)
Humans , Male , Adult , Middle Aged , Ventilator Weaning/methods , Anesthesia/methods , Nerve Block/methods , Critical Care/methods , Intensive Care Units/statistics & numerical dataABSTRACT
OBJETIVO: Conocer la tolerancia, la intensidad del dolor, el porcentaje de pruebas completadas con éxito y las complicaciones de la sedación profunda, controlada por médicos intensivistas, para realizar procedimientos endoscópicos gastrointestinales. DISEÑO: Estudio observacional prospectivo durante un periodo de un año. Ámbito: Realizado por el Servicio de Medicina Intensiva en la Unidad de Endoscopias del Hospital Universitario del Tajo. PACIENTES: Mayores de 15 años a los que se realizó algún procedimiento endoscópico bajo sedación profunda. RESULTADOS: Durante el periodo de estudio fueron sedados 868 pacientes. Se les realizaron 1.010 procedimientos endoscópicos. El grado de tolerancia se consideró adecuado («Muy Bueno»/«Bueno») en el 96,9% (IC 95%: 95,7-98,1%) de los pacientes, con una mediana de dolor de 0 en la escala visual analógica. Un total de 988 procedimientos endoscópicos (97,8%; IC 95%: 96,9-98,8%) fueron completados con éxito, 675 colonoscopias (97,1%) y 305 gastroscopias (99,7%). Presentaron complicaciones 106 pacientes (12,2%; IC 95%: 10,0-14,5%). Las más frecuentes fueron la desaturación (6,1%), las alteraciones del ritmo (5,1%) y la hipotensión (2,4%). CONCLUSIÓN: La realización de procesos endoscópicos gastrointestinales bajo sedación profunda controlada por médicos intensivistas es bien tolerada, satisfactoria para el paciente y con un excelente porcentaje de pruebas completadas. Esta intervención se acompaña de frecuentes complicaciones, siendo todas de orden menor y resueltas con éxito
OBJECTIVE: To determine tolerance, pain intensity, percentage of tests completed successfully and complications of deep sedation controlled by intensivists during gastrointestinal endoscopic procedures. DESIGN: A one-year, prospective observational study was carried out. SETTING: Department of Intensive Care intervention in the Endoscopy Unit of Hospital Universitario del Tajo (Spain). PATIENTS: Subjects over 15 years of age subjected to endoscopic procedures under deep sedation. RESULTS: A total of 868 patients were sedated during the study period, with the conduction of 1010 endoscopic procedures. The degree of tolerance was considered adequate («Very good»/«Good») in 96.9% of the patients (95% CI: 95.7-98.1%), with a median score of 0 on the pain visual analog scale. A total of 988 endoscopic procedures were successfully completed (97.8%; 95% CI: 96.9-98.8%): 675 colonoscopies (97.1%) and 305 endoscopies (99.7%). Complications were recorded in 106 patients (12.2%; 95% CI: 10.0-14.5%). The most frequent being desaturation (6.1%), rhythm disturbances (5.1%) and hypotension (2.4%). CONCLUSION: Gastrointestinal endoscopic procedures under sedation controlled by intensivists are well tolerated and satisfactory for the patient, and are successfully completed in a very large percentage of cases. The procedures are associated with frequent minor complications that are resolved successfully
Subject(s)
Humans , Deep Sedation/methods , Endoscopy/methods , Critical Care/methods , Propofol/therapeutic use , Anesthesia/methods , Gastroscopy/methods , Colonoscopy/methods , Postoperative Complications/epidemiologySubject(s)
Humans , Angioplasty , Thrombolytic Therapy , Myocardial Infarction/therapy , Critical Care/methodsABSTRACT
No disponible
Subject(s)
Aged , Female , Male , Humans , Spinal Puncture/adverse effects , Pneumocephalus/etiology , Seizures/etiology , Pneumocephalus/diagnosisABSTRACT
Desde hace décadas el tratamiento habitual del prognatismo es la retrusión mandibular. Clásicamente nos apoyamos en la cefalometría para confirmar el diagnóstico y realizar predicciones preoperatorias que guian el plan quirúrgico y lograr una oclusión normal mediante la retrusión mandibular. Sin embargo, en algunos pacientes el estudio clínico sugiere hipoplasia del tercio medio de la cara y para su tratamiento se deben realizar avances del maxilar para mejorar la apariencia facial y la oclusión. La cirugía ortognática ha evolucionado en sus indicaciones y técnicas, y por lo tanto en sus objetivos. Inicialmente el objetivo primordial era la corrección de la oclusión, mientras que actualmente domina es la estética facial, sin olvidar la corrección oclusal. Debido a que los resultados de la expansión de los tejidos blandos son más predecibles que los de la contracción, preferimos realizar un avance maxilar con osteotomías tipo LeFort I para tener una contribución estética más previsible de los tejidos blandos. Analizamos el resultado de 16 pacientes con medidas cefalométricas de prognatismo, pero con evidencia clínica de hipoplasia en el tercio medio facial. Todos los pacientes fueron intervenidos mediante avance maxilar por osteotomías tipo LeFort I, que en algunas ocasiones se combinan con retroposición mandibular, mentoplastía u otro procedimiento sobre la mandíbula en caso de deformidad importante de la misma(AU)
By decades, the classic and traditional treatment of congenital prognathism has been the surgical mandibular retrusion. For many years we have used cephalometric values to make the diagnosis and the preoperative predictions that would give us the surgical plan for the treatment of this pathology which consistent in a mandibular retrusion to achieve normal occlusion. In some of our patients we have seen that the cephalometric analysis present signs of prognathism values even though the clinical study and the external appearance tended to look-like a hypoplasia of the facial medial third instead. Techniques and indications for ortognatig surgery have been evolutioned, and obviously the treatment goals. The primary objective was the occlusions correction, but now the most important thing is the facial esthetics, obviously not forgetting the oclusal correction. The results of the tissue expansion are more predictable than contraction outcomes, we rather to perform a maxillary advancement with LeFort I osteotomy to predict the soft-tissue changes. The present study evaluates the result of 16 patients with cephalometric confirmation of prognathism, even though the clinical study and the external appearance tended to look-like a hypoplasia of the facial medial third. All of them received surgical correction through maxillary advancement with LeFort I osteotomy, sometimes was also used mandibular retrusion, chin surgery, or another surgical procedure in the mandible in case of mandibular deformity (AU)