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1.
Climacteric ; 23(sup1): S18-S23, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-33124456

RESUMO

Objective: To test whether the erbium-doped yttrium aluminum garnet (Er:YAG) SMOOTH® laser treatment efficacy on stress urinary incontinence (SUI) in hysterectomized patients is non-inferior to its efficacy in non-hysterectomized patients.Methods: In this real-world, retrospective cohort study performed in Turkey, Croatia and Italy, we enrolled a consecutive sample of 35 hysterectomized and 34 non-hysterectomized patients with SUI. We used the Er:YAG SMOOTH® laser (Fotona, Slovenia) with a wave length of 2940 nm. The primary outcome was median reduction of SUI symptoms measured by the International Consultation on Incontinence Questionnaire-Urinary Incontinence Short-Form (ICIQ-SF) with the non-inferiority margin defined as the minimum clinically important difference of ICIQ-SF (δ < 2.52 points).Results: In hysterectomized patients, the ICIQ-SF was reduced by 5 points (95% confidence interval 3-8; p < 0.001), a reduction of 45% (95% confidence interval 36-67%). After adjustment for baseline ICIQ-SF and five covariates, the reduction of symptoms in the hysterectomized group was not inferior to the reduction in the non-hysterectomized group.Conclusion: The Er:YAG SMOOTH® laser treatment seems to improve the symptoms of SUI in hysterectomized women not clinically relevantly less than in non-hysterectomized women. It seems that the beneficial effect of Er:YAG SMOOTH® laser treatment for SUI in hysterectomized women is time-limited.


Assuntos
Histerectomia , Terapia a Laser/métodos , Terapia a Laser/estatística & dados numéricos , Lasers de Estado Sólido , Incontinência Urinária por Estresse/cirurgia , Idoso , Estudos de Coortes , Croácia , Feminino , Humanos , Histerectomia/estatística & dados numéricos , Itália , Pessoa de Meia-Idade , Estudos Retrospectivos , Resultado do Tratamento , Turquia
2.
Climacteric ; 18 Suppl 1: 37-42, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26366799

RESUMO

OBJECTIVES: This is the first assessment of efficacy and safety of the Er:YAG laser in the treatment of stress urinary incontinence. The aim of this study was to assess the short-term outcome of a non-invasive laser treatment for mild-to-severe stages of this condition and to check its applicability in different body mass index and age groups. METHODS: A prospective cohort, single-center study at the Ob/Gyn Clinic, Zagreb, Croatia recruited a consecutive sample of 73 female patients suffering from stress urinary incontinence. The procedure was performed with a 2940-nm Er:YAG laser (XS Dynamis, Fotona, Slovenia) designed to achieve heating up of vaginal mucosa to around 60°C, 500-700 µm in depth. RESULTS: The score in the International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form was reduced to a median of 46% (95% confidence interval 33-67%; p < 0.001). The reduction was significantly higher in women with normal body mass index (67%) than in overweight women (25%), as well as in women younger than 39 years (100%) compared with those older than 60 years (8%) (p < 0.001). No serious adverse events were noticed. CONCLUSION: This study of Er:YAG laser therapy in women has demonstrated a clinically relevant, short-term improvement of stress urinary incontinence, with minimal adverse events of a transient nature.


Assuntos
Lasers de Estado Sólido/uso terapêutico , Incontinência Urinária por Estresse/terapia , Adulto , Fatores Etários , Índice de Massa Corporal , Estudos de Coortes , Croácia , Feminino , Humanos , Hipertermia Induzida/métodos , Pessoa de Meia-Idade , Estudos Prospectivos , Resultado do Tratamento
3.
Climacteric ; 13(6): 570-7, 2010 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-20136410

RESUMO

OBJECTIVE: Lack of adherence to therapy is a common problem in the treatment of various diseases and conditions and there are many well-documented reasons for it. This study was conducted to assess the effect of time spent on medical consultation in relation to the duration of adherence, as well as the reasons to adhere to or drop out from hormone replacement therapy (HRT). DESIGN AND METHODS: Two methods were used, self-filled questionnaires on a sample of patients and telephone interviews on a sample of doctors. The questions dealt with a number of personal and gynecological history variables. The participants were chosen using random sampling from population lists. A total of 74 participating offices recruited all postmenopausal patients, regardless of their HRT use and whether they visited the office for a specific complaint or just for a routine check-up. The doctors were interviewed regarding the average time spent with a patient, prescribing dilemmas and counselling on sexuality. RESULTS: The main finding was that the time spent on consultation and the physicians' interest in postmenopause critically influence the patients' adherence. The effective time spent with patients was in accordance with the National Health Insurance guidelines for public sector doctors, but it was twice as long for private sector doctors. CONCLUSION: This study shows that extended medical consultation promotes better compliance by lowering patient fears, while trusted authorities seem to be more convincing to patients on the benefits of HRT and therefore more effective, even if they do not take more time to talk to patients.


Assuntos
Terapia de Reposição de Estrogênios/psicologia , Cooperação do Paciente/psicologia , Pós-Menopausa , Adulto , Idoso , Aconselhamento , Medo , Feminino , Humanos , Pessoa de Meia-Idade , Papel do Médico , Qualidade de Vida , Sexualidade , Inquéritos e Questionários
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