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1.
Rhinology ; 56(1): 33-41, 2018 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-28942457

RESUMEN

BACKGROUND: Allergic Rhinitis and its Impact on Asthma (ARIA) and the European Union (EU) recommend a shift to guide allergic rhinitis (AR) treatment decisions from symptom severity to disease control, using a simple visual analogue scale (VAS). Using this VAS we assessed, in a real-life study in Romania, the effectiveness of MP-AzeFlu nasal spray. METHODOLOGY: In this multi-centre, prospective, non-interventional study, 253 patients (over 11 years old) with moderate-to-severe AR were prescribed MP-AzeFlu and assessed their symptoms on a VAS (0 (not at all bothersome) to 100 mm (very bothersome)) on Days 0, 1, 3, 7 and 14. The proportion of patients who achieved a defined VAS score cut-off for well-controlled (38 mm) AR were also calculated. Patients perception of disease control was assessed on Day 3. RESULTS: MP-AzeFlu use was associated with a mean (standard deviation) VAS score reduction from 78.4 (15.1) mm at baseline to 14.7 (15.1) mm on the last day. Effectiveness was consistent irrespective of disease severity, phenotype or patient age. 83.4% of patients achieved the smaller than 39 mm well-controlled VAS score cut-off by last day and 95.2% considered their symptoms to be well- or partly controlled at Day 3. CONCLUSIONS: MP-AzeFlu provided rapid, effective and sustained AR symptom control in a real-life setting in Romania, irrespective of severity, phenotype or patient age, aligning with ARIA and EU recommendations and supporting the position of MP-AzeFlu as the drug of choice for the treatment of moderate-to-severe AR.


Asunto(s)
Antialérgicos/uso terapéutico , Antiasmáticos/uso terapéutico , Fluticasona/uso terapéutico , Ftalazinas/uso terapéutico , Rinitis Alérgica/tratamiento farmacológico , Administración Intranasal , Adolescente , Adulto , Anciano , Antialérgicos/administración & dosificación , Antiasmáticos/administración & dosificación , Niño , Combinación de Medicamentos , Femenino , Fluticasona/administración & dosificación , Humanos , Masculino , Persona de Mediana Edad , Ftalazinas/administración & dosificación , Estudios Prospectivos , Rumanía , Resultado del Tratamiento
2.
Angiology ; 53(4): 429-34, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-12143948

RESUMEN

Pregnancy is associated with an increased risk of venous thromboembolism. The rate of occurrence of this complication has not been reported from this area previously. The aim of this study was to establish the incidence of venous thromboembolism in pregnancy and puerperium by using objective diagnostic methods. From January 1986 to December 1998, 39,757 deliveries were registered at King Fahad Hospital, Al Baha, and 59 of these were referred to hematology services with a clinical suspicion of venous thromboembolism. The majority (86%) of these underwent objective diagnostic methods such as ascending venogram (AV) and color Doppler imaging (CDI) of the venous system for the diagnosis of deep venous thrombosis (DVT). Pulmonary scintigraphy was performed when available and echocardiography was included towards the end of the study. Fifty-nine patients with suspicion of pregnancy-associated venous thromboembolism (PAVTE) were studied. The diagnosis was confirmed in 50 patients, who received anticoagulation therapy. DVT was diagnosed in 35 (70%) cases and pulmonary embolism in 27 (54%) cases. The cumulative incidence of PAVTE was 1.25 cases per 1,000 deliveries (95% confidence interval = 0.89-1.16). One patient died during the study period (0.025 case per 1,000 deliveries). There was a predominance of venous thromboembolism during the postpartum period (66%), and DVT occurred more frequently in the left leg (77%). The risk of pregnancy-associated venous thromboembolism is low and a resulting death rare. Proximal or whole-limb DVT occurs more frequently and there is a predilection for the left leg. The majority of events occur in the postpartum period. A hypercoagulable state probably exists and needs further evaluation.


Asunto(s)
Complicaciones Hematológicas del Embarazo/epidemiología , Trastornos Puerperales/epidemiología , Tromboembolia/epidemiología , Adulto , Femenino , Hospitales , Humanos , Incidencia , Persona de Mediana Edad , Embarazo , Estudios Prospectivos
3.
Ann Saudi Med ; 19(1): 15-9, 1999.
Artículo en Inglés | MEDLINE | ID: mdl-17337978

RESUMEN

BACKGROUND: The purpose of this study was to highlight the clinical features of spider bite envenomation, a subject which has not, to our knowledge, been previously published in Saudi Arabia. PATIENTS AND METHODS: Ten patients (8 males and 2 females) aged between 13 and 75 years (mean 36.8) were hospitalized at King Fahad Hospital, Al Baha, with the diagnosis of spider bites during the 9-year period from June 1988 to May 1997. RESULTS: One of the patients was bitten on the right hand by a brown spider, causing severe cellulitis and tissue necrosis, and requiring surgical debridement and pedicle skin flap graft. The nine other patients (90%) had bites from black spiders identified as black widow spiders. Two of the nine (22.2%) suffered only local reactions in the form of pain, erythema and swelling at the site of bite. The remaining seven (77.8%), had varying symptoms of systemic envenomation, including pulmonary edema, myocardial dysfunction with elevated creatinine kinase, electrocardiographic and echocardiographic abnormalities, progressive paresthesia, generalized body ache, etc. Therapy included analgesics, muscle relaxants, intravenous infusion of calcium gluconate and oxygen where indicated. Specific antivenin therapy was available for only four of the nine patients (44%) with black widow spider bite. Antivenin therapy still produced dramatic relief of the symptoms in the patient with pulmonary edema, even after a delay of 30 hours. CONCLUSION: Spider bite envenomation should be considered in the differential diagnosis of acute surgical abdomen and myocardial infarction.

4.
Saudi Med J ; 20(1): 56-62, 1999 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-27605274

RESUMEN

Full text is available as a scanned copy of the original print version.

5.
Saudi Med J ; 20(5): 351, 1999 May.
Artículo en Inglés | MEDLINE | ID: mdl-27631284

RESUMEN

Full text is available as a scanned copy of the original print version.

8.
Scand J Haematol ; 16(4): 295-9, 1976 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-935812

RESUMEN

The effect of salicylates on erythrocyte 2,3-diphosphoglycerate (2,3-DPG) and adenosine triphosphate (ATP) was studied in vivo in 3 groups of healthy subjects receiving acetylsalicyclic acid (18 persons), sodium salicylate (5 persons) and salicylamide (7 persons) in therapeutic dosage. No effect was found on 2,3-DPG in any of the 3 groups. ATP was significantly decreased (p less than 0.05) when acetylsalicylic acid or sodium salicylate was given.


Asunto(s)
Adenosina Trifosfato/sangre , Ácidos Difosfoglicéricos/sangre , Eritrocitos/metabolismo , Salicilatos/farmacología , Adolescente , Adulto , Ácidos Aminosalicílicos/farmacología , Aspirina/farmacología , Femenino , Humanos , Masculino , Persona de Mediana Edad , Salicilato de Sodio/farmacología
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