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2.
J Dent Res ; 98(10): 1081-1087, 2019 09.
Artículo en Inglés | MEDLINE | ID: mdl-31314998

RESUMEN

Dentists prescribe a large portion of all oral antibiotics, and these are associated with a risk of adverse drug reactions (ADRs). The aim of this study was to quantify the risk of ADRs associated with oral antibiotics commonly prescribed by dentists. NHS Digital Prescribing data and Yellow Card Drug Analysis data for 2010 to 2017 were abstracted to quantify dental antibiotic prescribing in England, and the rate and types of ADRs associated with them. During the period of study, the mean number of actively practicing dentists in England was 23,624. Amoxicillin accounted for 64.8% of dental antibiotic prescribing and had the lowest reported rate of fatal ADRs (0.1/million prescriptions) and overall ADRs (21.5/million prescriptions). Indeed, amoxicillin was respectively 6 and 3 times less likely to cause an ADR than the other penicillins, penicillin V and amoxicillin + clavulanic acid, and appears to be very safe in patients with no history of penicillin allergy. In contrast, clindamycin, which is often used in patients with penicillin allergy, had the highest rate of fatal (2.9/million prescriptions) and overall (337.3/million prescriptions) ADRs, with Clostridiodes (formerly Clostridium) difficile infections pivotal to its ADR profile. Other amoxicillin alternatives, clarithromycin and metronidazole, while significantly worse than amoxicillin, were 3 and nearly 5 times less likely to cause an ADR than clindamycin. Ranked from least to most likely to cause an ADR, antibiotics most commonly prescribed were as follows: amoxicillin < cephalosporins < erythromycin < tetracyclines < azithromycin < metronidazole < amoxicillin + clavulanic acid < clarithromycin < penicillin V < clindamycin. This study confirmed the high level of safety associated with use of amoxicillin by dentists and the significantly worse rates of fatal and nonfatal ADRs associated with other penicillins and alternatives to amoxicillin for those who are penicillin allergic. In particular, clindamycin had the highest rate of fatal and nonfatal ADRs of any of the antibiotics commonly prescribed by dentists.


Asunto(s)
Amoxicilina/efectos adversos , Antibacterianos/efectos adversos , Claritromicina/efectos adversos , Clindamicina/efectos adversos , Metronidazol/efectos adversos , Administración Oral , Sistemas de Registro de Reacción Adversa a Medicamentos , Amoxicilina/administración & dosificación , Antibacterianos/administración & dosificación , Claritromicina/administración & dosificación , Clindamicina/administración & dosificación , Odontólogos , Inglaterra , Humanos , Metronidazol/administración & dosificación , Penicilinas/administración & dosificación , Penicilinas/efectos adversos
3.
QJM ; 106(3): 237-43, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-23286921

RESUMEN

BACKGROUND: Since the introduction of the National Institute for Health and Clinical Excellence (NICE) guideline (CG064) in 2008 recommending cessation of antibiotic prophylaxis (AP) against infective endocarditis (IE), low level prescribing persists in the UK and is a potential reason why there has been no significant change in the general upward trend in cases of IE. AIM: To undertake a survey of dentists (Ds), cardiologists and cardiothoracic surgeons (C/CTSs) and infection specialists (ISs) to determine why this might be the case. DESIGN: Internet questionnaire-based survey. METHODS: A questionnaire was distributed by email to specialists via UK national societies. RESULTS: A total of 1168 responses were received. All the specialist groups are aware of the guideline (99%). Ds are broadly satisfied, whereas C/CTSs are not. Most Ds follow the NICE guidance (87%), whereas many C/CTSs (39%) do not; ISs adopt a middle course (56%). Even amongst Ds, a significant proportion believe that patients with a prosthetic heart valve (25%) or previous history of IE (38%) should receive AP. A total of 36% of Ds have prescribed AP since March 2008 and many have undertaken procedures where AP has been prescribed by someone else. The majority of respondents (65%) feel that more evidence is required, preferably in the form of a randomized controlled trial. CONCLUSION: Many patients perceived to be at high risk of IE are still receiving AP in conflict with current NICE guidance.


Asunto(s)
Profilaxis Antibiótica/estadística & datos numéricos , Actitud del Personal de Salud , Endocarditis Bacteriana/prevención & control , Guías de Práctica Clínica como Asunto , Factores de Edad , Profilaxis Antibiótica/psicología , Profilaxis Antibiótica/normas , Cardiología/estadística & datos numéricos , Odontólogos/psicología , Prescripciones de Medicamentos/estadística & datos numéricos , Endocarditis Bacteriana/epidemiología , Medicina Basada en la Evidencia/normas , Adhesión a Directriz/estadística & datos numéricos , Investigación sobre Servicios de Salud/métodos , Prótesis Valvulares Cardíacas , Humanos , Persona de Mediana Edad , Pautas de la Práctica en Odontología/estadística & datos numéricos , Pautas de la Práctica en Medicina/estadística & datos numéricos , Encuestas y Cuestionarios , Procedimientos Quirúrgicos Torácicos/estadística & datos numéricos , Reino Unido/epidemiología
4.
J Appl Physiol (1985) ; 103(3): 739-46, 2007 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-17569771

RESUMEN

Assessment of quadriceps endurance is of interest to investigators studying human disease. We hypothesized that repetitive magnetic stimulation (rMS) of the intramuscular branches of the femoral nerve could be used to induce and quantify quadriceps endurance. To test this hypothesis, we used a novel stimulating coil to compare the quadriceps endurance properties in eight normal humans and, to confirm that the technique could be used in clinical practice, in eight patients with advanced chronic obstructive pulmonary disease (COPD). To validate the method, we compared in vivo contractile properties of the quadriceps muscle with the fiber-type composition and oxidative enzyme capacity. We used a Magstim Rapid(2) magnetic nerve stimulator with the coil wrapped around the quadriceps. Stimuli were given at 30 Hz, a duty cycle of 0.4 (2 s on, 3 s off), and for 50 trains. Force generation and the surface electromyogram were measured throughout. Quadriceps twitch force, elicited by supramaximal magnetic stimulation of the femoral nerve, was measured before and after the protocol. Quadriceps muscle biopsies were analyzed for oxidative (citrate synthase, CS) and glycolytic (phosphofructokinase, PFK) enzyme activity and myosin heavy chain isoform protein expression. The time for force to fall to 70% of baseline (T(70)) was shorter in the COPD group than the control group: 55.6 +/- 26.0 vs. 121 +/- 38.7 s (P = 0.0014). Considering patients and controls together, positive correlations were observed between T(70) and the proportion of type I fibers (r = 0.68, P = 0.004) and CS-to-PFK ratio (CS/PFK) (r = 0.67, P = 0.005). We conclude that quadriceps endurance assessed using rMS is feasible in clinical studies.


Asunto(s)
Magnetismo , Fatiga Muscular/fisiología , Fuerza Muscular/fisiología , Tono Muscular/fisiología , Músculo Cuádriceps/fisiología , Anciano , Biopsia , Ejercicio Físico/fisiología , Humanos , Masculino , Persona de Mediana Edad , Enfermedad Pulmonar Obstructiva Crónica/fisiopatología , Músculo Cuádriceps/patología , Reproducibilidad de los Resultados
5.
J Sleep Res ; 15(2): 199-205, 2006 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-16704575

RESUMEN

Central Sleep Apnoea (CSA) occurs commonly in heart failure. Adaptive servo-ventilation (ASV) and deadspace (DS) have been shown in research settings to reverse CSA. The likely mechanism for this is the increase of PaCO(2) above the apnoeic threshold. However the role of increasing FiCO(2) on arousability remains unclear. To compare the effects of ASV and DS on sleep and breathing, in particular effects on Arousal Index (ArI), ten male patients with heart failure and CSA were studied during three nights with polysomnography plus measurements of PetCO(2). The order of the interventions control (C), ASV and DS was randomized. ASV and DS caused similar reductions in apnoea-hypopnoea index [(C) 30.0 +/- 6.6, (ASV) 14.0 +/- 3.8, (DS) 15.9 +/- 4.7 e h(-1); both P < 0.05]. However, DS was associated with decreased total sleep time compared with C (P < 0.02) and increased spontaneous ArI compared to C and ASV (both P < 0.01). Only DS was associated with increased DeltaPetCO(2) from resting wakefulness to eupnic sleep [(C) 2.1 +/- 0.9, (ASV) 1.3 +/- 1.0, (DS) 5.6 +/- 0.5 mmHg; P = 0.01]. ASV and DS both stabilized ventilation however DS application also increased sleep fragmentation with negative impacts on sleep architecture. We speculate that this effect is likely to be mediated by increased PetCO(2) and respiratory effort associated with DS application.


Asunto(s)
Adaptación Fisiológica/fisiología , Espacio Muerto Respiratorio/fisiología , Síndromes de la Apnea del Sueño , Apnea Central del Sueño/fisiopatología , Apnea Central del Sueño/terapia , Adulto , Insuficiencia Cardíaca/complicaciones , Insuficiencia Cardíaca/fisiopatología , Humanos , Masculino , Polisomnografía , Respiración Artificial/métodos , Apnea Central del Sueño/diagnóstico , Vigilia
6.
Respir Med ; 100(9): 1657-9, 2006 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-16488125

RESUMEN

Diaphragm paralysis may occur after traumatic phrenic nerve injury. Here we report three patients in whom right hemi-diaphragmatic paralysis developed after cardiac radiofrequency ablation. We hypothesise that local focused thermal energy at the time of the ablation may have caused direct neuronal damage by axonal coagulation necrosis. The prognosis for this type of injury may be reasonably good; two of the three patients fully recovered diaphragm function by 1 year.


Asunto(s)
Ablación por Catéter/efectos adversos , Nervio Frénico/lesiones , Ondas de Radio/efectos adversos , Parálisis Respiratoria/etiología , Adulto , Fibrilación Atrial/cirugía , Femenino , Humanos , Masculino , Persona de Mediana Edad , Complicaciones Posoperatorias/etiología , Taquicardia Sinusal/cirugía
7.
Eur Respir J ; 24(1): 137-42, 2004 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-15293616

RESUMEN

Prospective data to support the hypothesis that corticosteroids are a significant cause of muscle weakness in patients with chronic obstructive pulmonary disease (COPD) are lacking. The authors studied respiratory and quadriceps muscle function, using both volitional techniques and magnetic nerve stimulation, as well as measuring metabolic parameters during incremental cycle ergometry, in 25 stable COPD patients. The forced expiratory volume in one second was 37.6 +/- 21.4% predicted, before and after a 2-week course of o.d. prednisolone 30 mg. Quadriceps strength was also assessed in 15 control patients on two occasions. Only two patients met the British Thoracic Society definition of steroid responsiveness. There was no change either in sniff transdiaphragmatic pressure (pre: 96.8 +/- 19.7 cmH2O; post: 98.6 +/- 22.4 cmH2O) or in twitch transdiaphragmatic pressure elicited by bilateral anterolateral magnetic phrenic-nerve stimulation (pre: 16.8 +/- 9.1 cmH2O; post: 17.9 +/- 10 cmH2O). Quadriceps twitch force did not change significantly either in the steroid group (pre: 9.5 +/- 3.1 kg; post: 8.9 +/- 3.7 kg) or in the control patients (pre: 8.1 +/- 2.7 kg; post: 7.9 +/- 2.2 kg). There were no changes in either peak or isotime ventilatory and metabolic parameters during exercise. In conclusion, in stable patients with chronic obstructive pulmonary disease, a 2-week course of 30 mg prednisolone daily does not cause significant skeletal muscle dysfunction or alter metabolic parameters during exercise.


Asunto(s)
Corticoesteroides/efectos adversos , Debilidad Muscular/inducido químicamente , Enfermedad Pulmonar Obstructiva Crónica/tratamiento farmacológico , Músculos Respiratorios/efectos de los fármacos , Corticoesteroides/uso terapéutico , Anciano , Estudios de Casos y Controles , Prueba de Esfuerzo , Femenino , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Debilidad Muscular/fisiopatología , Músculo Esquelético/efectos de los fármacos , Fenómenos Fisiológicos Musculoesqueléticos/efectos de los fármacos , Probabilidad , Enfermedad Pulmonar Obstructiva Crónica/diagnóstico , Valores de Referencia , Pruebas de Función Respiratoria , Músculos Respiratorios/fisiología , Medición de Riesgo , Índice de Severidad de la Enfermedad , Reino Unido
8.
Am J Kidney Dis ; 36(5): 1041-4, 2000 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-11054363

RESUMEN

Spinal osteomyelitis is a recognized complication in dialysis patients related to hematogenous spread of infection during bacteremia-septicemia. These episodes are often associated with sepsis due to temporary dialysis access. We describe the case of an unfortunate man whose osteomyelitis was located in the posterior facet joints. Such infection is rare and in the reviewed literature is usually associated with a more favorable outcome than described here.


Asunto(s)
Vértebras Lumbares , Osteomielitis/microbiología , Diálisis Renal/efectos adversos , Infecciones Estafilocócicas , Articulación Cigapofisaria , Adulto , Resultado Fatal , Humanos , Trasplante de Riñón , Masculino , Reoperación
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