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1.
Gynecol Obstet Fertil Senol ; 51(11-12): 493-510, 2023.
Artículo en Francés | MEDLINE | ID: mdl-37806861

RESUMEN

OBJECTIVE: To identify strategies for reducing neonatal and maternal morbidity associated with intrahepatic cholestasis pregnancy (ICP). MATERIAL AND METHODS: The quality of evidence of the literature was assessed following the GRADE methodology with questions formulated in the PICO format (Patients, Intervention, Comparison, Outcome) and outcomes defined a priori and classified according to their importance. An extensive bibliographic search was performed on PubMed, Cochrane, EMBASE and Google Scholar databases. The quality of the evidence was assessed (high, moderate, low, very low) and a (i) strong or (ii) weak recommendations or (iii) no recommendation were formulated. The recommendations were reviewed in two rounds with external reviewers (Delphi survey) to select the consensus recommendations. RESULTS: Of the 14 questions (from 12 PICO questions and one definition question outside the PICO format), there was agreement between the working group and the external reviewers on 14 (100%). The level of evidence of the literature was insufficient to provide a recommendation on two questions. ICP is defined by the occurrence of suggestive pruritus (palmoplantar, nocturnal) associated with a total bile acid level>10µmol/L or an alanine transaminase level above 2N after ruling out differential diagnoses. In the absence of suggestive symptoms of a differential diagnosis, it is recommended not to carry out additional biological or ultrasound tests. In women with CIP, ursodeoxycholic acid is recommended to reduce the intensity of maternal pruritus (Strong recommendation. Quality of the evidence moderate) and to decrease the level of total bile acids and alanine transaminases. (Strong recommendation. Quality of the evidence moderate). S-adenosyl-methionine, dexamethasone, guar gum or activated charcoal should not be used to reduce the intensity of maternal pruritus (Strong recommendation. Quality of evidence low), and there is insufficient data to recommend the use of antihistamines (No recommendation. Quality of evidence low). Rifampicin (Weak recommendation. Very low quality of evidence) or plasma exchange (Strong recommendation. Very low quality of evidence) should not be used to reduce maternal pruritus and perinatal morbidity. Serum monitoring of bile acids is recommended to reduce perinatal morbidity and mortality (stillbirth, prematurity) (Low recommendation. Quality of the evidence low). The level of evidence is insufficient to determine whether fetal heart rate or fetal ultrasound monitoring are useful to reduce perinatal morbidity (No recommendation). Birth is recommended when bile acid level is above 99µmol/L from 36 weeks gestation to reduce perinatal morbidity, in particular stillbirth. When bile acid level is above 99µmol/L is below 100µmol/L, women should be informed that induction of labor could be considered 37 and 39 weeks gestation to reduce perinatal morbidity. (Strong recommendation. Quality of evidence low). In postpartum, total bile acids and alanine transaminases level should be checked and normalized before prescribing estrogen-progestin contraception, ideally with a low estrogen dose (risk of recurrence of pruritus and cytolysis) (Low recommendation. Quality of evidence very low). CONCLUSION: Although the quality of evidence regarding ICP gestational cholestasis remains low, there is a strong consensus in France, as shown by our Delphi study, on how to manage women with ICP. The reference first-line treatment is ursodeoxycholic acid.


Asunto(s)
Colestasis Intrahepática , Complicaciones del Embarazo , Embarazo , Recién Nacido , Femenino , Humanos , Mortinato/epidemiología , Ácido Ursodesoxicólico/uso terapéutico , Obstetras , Ginecólogos , Complicaciones del Embarazo/terapia , Complicaciones del Embarazo/tratamiento farmacológico , Colestasis Intrahepática/diagnóstico , Colestasis Intrahepática/terapia , Colestasis Intrahepática/complicaciones , Ácidos y Sales Biliares , Estrógenos/uso terapéutico , Prurito/diagnóstico , Prurito/etiología , Prurito/terapia , Transaminasas/uso terapéutico , Alanina/uso terapéutico
2.
J Ren Care ; 33(1): 35-8, 2007.
Artículo en Inglés | MEDLINE | ID: mdl-17695560

RESUMEN

The palliative approach offers significant and practical care throughout the treatment of the dialysis patient until death. Varied aspects of quality of life for patients can be improved. It is possible to relieve symptoms such as sleep disorders, pain, constipation and pruritus, which, according to the present survey, are common symptoms. The treatment of dying dialysis patients or the possibility and legitimization of discontinuing treatment are complex, controversial issues with ethical and legal implications. But these issues have not yet been adequately dealt with by the nephrological community. The nurses who encounter patients daily, who constantly deal with great suffering and who lack tools to help, can lead the practice in this field within the framework of inter-disciplinary team work. In light of the obvious need for progress in this area, appropriate training courses should be considered. The implementation of the palliative approach in dialysis units could be a challenge for all of us in the coming years.


Asunto(s)
Actitud del Personal de Salud , Fallo Renal Crónico/terapia , Cuidados Paliativos , Calidad de Vida , Diálisis Renal/enfermería , Humanos , Israel , Fallo Renal Crónico/complicaciones , Fallo Renal Crónico/enfermería , Índice de Severidad de la Enfermedad
3.
EDTNA ERCA J ; 31(1): 10-2, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-16083019

RESUMEN

Peritonitis and catheter infections remain a major complication of peritoneal dialysis, accounting for much of the morbidity associated with the technique. The most common source of infection is contamination with predominantly Gram positive skin flora, Staphylococcus (S) epidermidis and S. aureus. The aims of this study were, (a) to determine the incidence of S. aureus and S. epidermidis infections in the unit, (b) to examine whether treatment of S. aureus carriers may reduce the incidence of exit site infection and (c) to examine whether improving patient education may reduce S. epidermidis peritonitis rate.


Asunto(s)
Portador Sano , Infección Hospitalaria , Control de Infecciones/métodos , Diálisis Peritoneal/efectos adversos , Infecciones Estafilocócicas , Adulto , Anciano , Anciano de 80 o más Años , Axila/microbiología , Portador Sano/diagnóstico , Portador Sano/prevención & control , Catéteres de Permanencia/efectos adversos , Protocolos Clínicos/normas , Infección Hospitalaria/diagnóstico , Infección Hospitalaria/etiología , Infección Hospitalaria/prevención & control , Ingle/microbiología , Humanos , Incidencia , Control de Infecciones/normas , Israel , Tamizaje Masivo/métodos , Tamizaje Masivo/normas , Persona de Mediana Edad , Mucosa Nasal/microbiología , Educación del Paciente como Asunto , Peritonitis/diagnóstico , Peritonitis/etiología , Peritonitis/prevención & control , Prevención Primaria/métodos , Evaluación de Programas y Proyectos de Salud , Infecciones Estafilocócicas/diagnóstico , Infecciones Estafilocócicas/etiología , Infecciones Estafilocócicas/prevención & control , Staphylococcus aureus , Staphylococcus epidermidis
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