Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Añadir filtros








Intervalo de año
1.
New Egyptian Journal of Medicine [The]. 2007; 37 (1): 39-47
en Inglés | IMEMR | ID: emr-172355

RESUMEN

Pressure ulcers are a serious health issue causing clinical, financial, and emotional challenges. Treatment modalities that promote wound healing are therefore warranted. To assess the efficacy and safety of MEBO [Julphar Gulf Phannaceutical Industries, UAE] as compared to topical antibiotic ointment [Fucidin, Leo Pharmaceutical, Denmark] in the healing of chronic pressure ulcers. During a 4-year period [Jan 2003-Jan 2007], 45 patients of both sexes with 87 pressure ulcers seen at the Ahmadi Hospital [Kuwait] were categorized into 2 groups, those in group 1 [n=22] received MEBO while those in group 2 [n=23] received Fucidin. Age of the patients ranged between 14 and 102 years with a mean of 69, +/- 7.4 years. Patients had their ulcers prior to study entry for a mean of 10.55 months [range 2-26 months]. Data collected included demographics, nutritional status, underlying predisposing disease and co-morbidities. Ulcer surface area [SA] and healing index [HI] were calculated and compared at two-week intervals for 12 weeks. Patients in both groups had similar demographic and clinical features regarding their age, gender, underlying predisposing factor and comorbidities. Ulcer characteristics were also similar with respect to their number, site, size, duration, depth and presence or absence of sepsis. There was a significant [P<0.05] increase in HI and reduction in ulcer SA on weeks two and four respectively, that was main- tamed through 12 weeks in patients receiving MEBO as compared to those receiving Fucidin. Cumulative patient sample percentage showed that 55.8% of ulcers treated with MEBO had complete healing [HI = 1] by 12 weeks, as opposed to only 20.5% of those treated with Fucidin [P<0.001]. Moreover, none of the patients receiving MEBO had a HI of <50% by 12 weeks as compared to 27.3% of those receiving Fucidin [P<0.001]. Linear regression analysis showed that the change in ulcer size and HI can be attributed to ointment application [r2> 0.4]. No adverse effects of ointment were encountered in either group. Based on the data presented, it may be concluded that in addition to its safety, application of MEBO significantly promotes the healing of chronic pressure ulcers with significant increase in HI of any given ulcer to be expected as early as two weeks following initiation of treatment


Asunto(s)
Humanos , Masculino , Femenino , Fenetilaminas , Cicatrización de Heridas , Estudio Comparativo
2.
Medical Journal of Cairo University [The]. 2003; 71 (3): 27-32
en Inglés | IMEMR | ID: emr-63690

RESUMEN

This study sample included 215 women admitted during the latent phase of the first stage of labor and were randomized into an intervention group [n=113] who were trained during the latent phase of the first stage to use the Lamaze method for reducing pain or the control group [n=102] who received the routine care for management of pain and discomfort of both hospitals. None of the subjects in both intervention and control groups described their pain as slight or moderate pain [from 0 to 6]. The mean pain score for the intervention group was 70.41 +/- 0.77, while it was similar to the mean pain score for the control 7.06 +/- 0.74. The mean pain score for the intervention group during the second stage of labor was 9.10 +/- 0.78 compared with 8.14 +/- 0.74 for the control group


Asunto(s)
Humanos , Femenino , Dimensión del Dolor , Clínicas de Dolor , Resultado del Tratamiento , Trabajo de Parto
3.
Medical Journal of Cairo University [The]. 2003; 71 (Supp. 2): 103-109
en Inglés | IMEMR | ID: emr-63811

RESUMEN

A purposive sample of 355 women at the last month of their pregnancy was recruited from the Health Center during their antenatal visit. The sample of the study was randomly assigned into two groups: The trial group received postpartum home care and the control group received regular home care from the center. Women in both groups were interviewed using a structured interview including personal, menstrual and medical history. Their medical records were screened for medical disorders. Women in the trial group were visited nine times during the 6th postpartum weeks. At the end of postpartum period, the women satisfaction in both groups was measured. The study concluded that postpartum health care at home can satisfy the parturient women more than the routine postpartum care provided at the maternal and child health centers


Asunto(s)
Humanos , Femenino , Servicios de Atención de Salud a Domicilio , Enfermería , Satisfacción del Paciente , Atención de Enfermería , Atención Posnatal , Periodo Posparto
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA