Search Results

You are looking at 1 - 2 of 2 items for

  • Author: Anne Bachelot x
  • All content x
Clear All Modify Search
Open access

Anne Bachelot, Magaly Vialon, Amandine Baptiste, Isabelle Tejedor, Caroline Elie, Michel Polak, Philippe Touraine, and the CRMERC study group

Background

Health-related quality of life (QoL) in adult patients with congenital adrenal hyperplasia (CAH) has been variously reported. However, there is no study evaluating the impact of transition on quality of life.

Methods

Adult patients with classic or non-classic CAH diagnosed during childhood CAH, born between 1970 and 1990, were recruited from the registers of Pediatric departments belonging to the French reference center for endocrine rare disease. Primary end point was the QoL (WHOQOL-BREF).

Results

Seventy-three patients were included in the study, among them 59/73 were transferred to adult endocrinologist by their pediatricians for transition. WHOQOL-BREF scores were similar between patients with or without transition to specialist adult services, except for environment dimension score, which was slightly higher in CAH patients without transition. However, CAH patients with a regular follow-up had a better physical health, psychological health and environment score and item global QoL than the group without regular follow-up after transition.

Conclusion

Regular medical follow-up in adulthood is associated with the transition between pediatric and adult care and is associated with better QoL in adults with CAH.

Open access

Isabelle Flechtner, Magali Viaud, Dulanjalee Kariyawasam, Marie Perrissin-Fabert, Maud Bidet, Anne Bachelot, Philippe Touraine, Philippe Labrune, Pascale De Lonlay, Michel Polak, and Galactosemia Study Group Galactosemia Study Group

Classic galactosemia is a rare inborn error of galactose metabolism with a birth prevalence of about 1/30 000-60 000. Long-term complications occurring despite dietary treatment consist of premature ovarian insufficiency (POI) and neurodevelopmental impairments. We performed with the French Reference Centers for Rare Diseases a multisite collaborative questionnaire survey for classic galactosemic patients. Its primary objective was to assess their puberty, pregnancy, gonadotrop axis, and pelvic morphology by ultrasound The secondary objective was to determine predictive factors for potent pregnancy without oocyte donation. Completed questionnaires from 103 patients, 56 females (median age, 19 years [5-52 years]) and 47 males (median age, 19 years [3-45 years]), were analyzed. Among the 45 females older than 11 years old, mean age for breast development first stage was 12 years; spontaneous menarche occurred in 25 females at a mean age of 14.6 years. After puberty, 60% of females had irregular menstrual cycles and 50% experienced amenorrhea at a median age of 30 years [15;42]. All age-groups confounded, FSH was above normal range for 65% of the patients, anti-Müllerian hormone and inhibin B were below the normal range according to age, and the ovaries were small with few or no follicles detected. Among the 5 females who sought to conceive, 4 had pregnancies. Among the 47 males, 1 had cryptorchidism, all have normal testicular function and none had tried to conceive. Thus, spontaneous puberty and POI are both common in this population. Spontaneous menarche seems to be the best predictive factor for successful spontaneous pregnancy.