RESUMEN
BACKGROUND: Nasal septoplasty is a common surgical procedure, but a significant number of patients report equal, or some even worsened, symptom load postoperatively. Rhinologists struggle to find objective tests that adequately reflects disease burden. This study aimed to evaluate the correlation between the PNIF measurement of the most obstructed side with patient reported outcomes. METHODS: Bilateral and unilateral PNIF measurements were performed before and after topical decongestion in 528 patients scheduled for surgery due to nasal obstruction. Subjective outcomes were measured using Nasal Obstruction VAS and SNOT-22 with subdomains. Correlations between subjective and objective measurements were calculated and further explored using multivariate regression analyses. RESULTS: Significant negative correlations between PNIF and patient reported outcomes were found. Both bilateral and minimal unilateral PNIF correlations with NO-VAS were equal and stronger than correlations with SNOT-22 including subdomains concerning problems with nasal obstruction. Minimal unilateral PNIF did not show statistically significant gender difference. Topical decongestion decreased statistical correlations. CONCLUSIONS: The minimal unilateral PNIF shows a statistically significant but weak negative correlation with preoperative patient reported nasal obstruction, and values do not differ between genders. Clinical evaluation of patients presenting complaints of nasal obstruction could be supported by minimal unilateral PNIF.
Asunto(s)
Obstrucción Nasal/diagnóstico , Tabique Nasal/cirugía , Pruebas de Función Respiratoria/métodos , Costo de Enfermedad , Femenino , Humanos , Masculino , Obstrucción Nasal/cirugía , Medición de Resultados Informados por el Paciente , RinoplastiaRESUMEN
BACKGROUND: Bladder catheterisation may be inconvenient for patients, delay mobilisation and risk complications. We hypothesised that by excluding pre-operatively patients at high risk of post-operative urinary retention, the majority of patients could avoid perioperative catheterisation during low-dose spinal anaesthesia. METHODS: Patients undergoing total knee arthroplasty were assigned if fit for spinal anaesthesia and without severe symptoms of lower urinary tract obstruction, gross incontinence, mobilisation difficulties hindering micturition and > 200 ml residual urine volume. Bladder volume was monitored by ultrasound and temporary catheterisation advised if > 400 ml. RESULTS: Fifty-two patients (men 54%, age 65 ± 9 years, body mass index 31 ± 5, 30% with history of urinary tract problems) were included. Intrathecal hyperbaric bupivacaine given was 7.8 ± 1.08 mg and always 7.5 µg sufentanil providing sufficient anaesthesia in all cases. Crystalloid given during surgery was 8.5 ± 4.0 ml/kg. Voluntary micturition was reached by 46 patients (88%, confidence interval (CI) 79-97%), but six (12%, CI 3-21%) needed temporary catheterisation once (four men/two women). Larger bladder volumes were found in those catheterised than those with voluntary micturition on the pre-operative (131 ± 76 ml vs. 68 ± 57 ml, P = 0.03) and first post-operative bladder scan (445 ± 169 ml vs. 271 ± 129 ml, P = 0.004). All but two patients (96%) could be mobilised the same day. No patient suffered bladder dysfunction. CONCLUSION: Low-dose spinal anaesthesia combined with simple selection criteria allowed for early mobilisation (96%) and avoidance of bladder catheterisation in the vast majority (88%) of patients undergoing total knee arthroplasty, and the rest (12%) only needed a single temporary catheterisation.
Asunto(s)
Anestesia Raquidea/métodos , Artroplastia de Reemplazo de Rodilla , Selección de Paciente , Cateterismo Urinario , Anciano , Anestésicos Intravenosos/administración & dosificación , Anestésicos Locales/administración & dosificación , Bupivacaína/administración & dosificación , Femenino , Humanos , Masculino , Tamaño de los Órganos , Estudios Prospectivos , Sufentanilo/administración & dosificación , Ultrasonografía , Vejiga Urinaria/diagnóstico por imagen , Micción/efectos de los fármacosRESUMEN
BACKGROUND: We have consistently achieved about 90% eradication of H. pylori with liquid bismuth, metronidazole and oxytetracycline. AIM: To test eradication and adverse events of ranitidine bismuth citrate (RBC) when given with metronidazole and either oxytetracycline or spiramycin. METHODS: One hundred and eighty-three patients were randomized to one of four 10-day regimens: RBC400OM: RBC 400 mg b.d., oxytetracycline 500 mg q.d.s.; RBC400SM: RBC 400 mg b.d., spiramycin 1 g q.d.s.; RBC200OM: RBC 200 mg q.d.s., oxytetracycline 500 mg q.d.s.; RBC200SM: RBC 200 mg q.d.s., spiramycin 1 g q.d.s. Additionally, all patients received metronidazole 400 mg q.d.s. A 14C-urea breath test was performed at 8 weeks. RESULTS: Intention-to-treat eradication rates were 94%, 91%, 94% and 89% with RBC400OM, RBC400SM, RBC200OM and RBC200SM, respectively (P = 0.81). Eradication was significantly higher in ulcer patients (97%) than in those with diagnoses other than ulcer (86%) (P = 0.009). There was a strong tendency to better eradication among those who had never smoked (100%) compared with ex-smokers (93%) and smokers (89%) (P = 0.06). Fifty-three per cent experienced at least one moderate or severe adverse event, and women had more adverse events than men (P = 0.0002). CONCLUSIONS: All four regimens had comparable efficacy and adverse events. Eradication was significantly better in ulcer patients but there was a trend to better eradication in those who smoked less, used less alcohol and exercised more. Adverse events were frequent, perhaps because of the large dose of metronidazole used, but few patients stopped treatment.
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Antibacterianos/administración & dosificación , Bismuto/administración & dosificación , Helicobacter pylori/efectos de los fármacos , Metronidazol/administración & dosificación , Oxitetraciclina/administración & dosificación , Ranitidina/análogos & derivados , Espiramicina/administración & dosificación , Adulto , Anciano , Anciano de 80 o más Años , Bismuto/efectos adversos , Quimioterapia Combinada , Femenino , Humanos , Masculino , Metronidazol/efectos adversos , Persona de Mediana Edad , Oxitetraciclina/efectos adversos , Estudios Prospectivos , Ranitidina/administración & dosificación , Ranitidina/efectos adversos , Espiramicina/efectos adversosAsunto(s)
Bovinos/fisiología , Fertilidad , Periodo Posparto/fisiología , Factores de Edad , Animales , Femenino , Islandia , Leche/análisis , Ovulación , Embarazo , Progesterona/análisisAsunto(s)
Bovinos/sangre , Fertilidad , Periodo Posparto/sangre , Animales , Glucemia/análisis , Calcio/sangre , Bovinos/fisiología , Femenino , Magnesio/sangre , Periodo Posparto/fisiología , Embarazo , Urea/sangreRESUMEN
110 ewes were allocated for intrauterine insemination. One succeeded to deposite semen intra uterine in 43 of the ewes and 37 (86%) of these lambed. In the remaining 67 the semen was deposited in cervix, and of these 15 lambed (22,4%). Totally 52 (47,3%) of the inseminated ewes lambed. Similar results were obtained by one or two inseminations in the heat. Dilution 1:3 gave a significantly (p less than 0.05) higher lambing rate than dilution 1:9 when the semen was deposited in the cervix, while the results were similar for dilution 1:3 and 1:9 by intra interine deposition. A group of 49 ewes was inseminated according to the conventional method on the first day of heat and the intra uterine method on the second day. Intra uterine deposition of semen succeeded in 31 ewes and 27 (87,1%) lambed. In the 18 remaining ewes the semen was depposited in the cervix and 9 (50%) lambed. Totally 73,5% of the ewes in this group lambed.
Asunto(s)
Inseminación Artificial/veterinaria , Preservación de Semen , Ovinos , Animales , Femenino , Inseminación Artificial/métodos , Masculino , Embarazo , ÚteroRESUMEN
At the Medical Department, Telemark Central Hospital, a project has been going on for five years now to evaluate consultations in lifestyle groups in preference to individual consultations for persons with dyslipidemia. 363 persons were recruited to participate in a series of 5 group consultations at intervals of 3 months, each session to last for 2 hours. Altogether 1469 consultations were of this type. After the first session 79% said they preferred lifestyle group consultations, rather than spending their share of the allotted time on personal consultations, and after the fifth session 81%. The concept has been extended to include patients with chronic disease (asthma and chronic inflammatory bowel disease), with the principal aim of improving the patients' understanding of their disease, and showing them how to control it themselves. The project has attracted much attention, and a consultant in preventive medicine has recently been appointed to the staff. We think it important in terms of impact that the initiative to establish local expertise in preventive medicine emerged from a department that deals with emergency admissions due to lifestyle-related diseases.