Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 10 de 10
Filter
1.
J Pediatr Adolesc Gynecol ; 37(3): 360-364, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38253233

ABSTRACT

STUDY OBJECTIVES: Recommendations from the Children's Oncology Group Long-Term Follow-Up (COG-LTFU) Guidelines for Survivors of Childhood, Adolescent, and Young Adult Cancer emphasize the importance of reproductive health care, yet little is known regarding adherence to these recommendations and non-fertility-related sexual and reproductive health (SRH) outcomes. METHODS: Follow-up of outcomes on the basis of the COG-LTFU guidelines was assessed in female patients who underwent fertility preservation consultation before gonadotoxic therapy between 2016 and 2022 at a single institution and were at least 6 months from treatment completion. RESULTS: We included 140 patients, with a mean time of 2.7 years from treatment completion. Eighty-six patients were 12 years old or older, of whom sexual activity was recorded in 59 (68.7%), and 12 of 31 (38.7%) sexually active patients underwent sexual function assessment. The 57 (66.3%) patients at high risk of premature ovarian insufficiency (POI) at diagnosis were more likely than minimal-risk counterparts (29, 33.7%) to have abnormal uterine bleeding (42.1% vs 17.2%, P = .03), to be diagnosed with POI (29.8% vs 0%, P = .01), and to have sexual activity recorded (77.2% vs 51.7%, P = .03). Of 17 patients with POI, 82.4% were on hormone replacement therapy, and 58.8% had undergone bone mineral density testing. CONCLUSION: This study adds to the limited literature regarding non-fertility-related SRH outcomes after gonadotoxic therapy and illustrates opportunities to improve adherence to the COG-LTFU guidelines. Increased attention to SRH guidelines may increase detection and treatment of SRH conditions, improving the health and quality of life of female cancer survivors.


Subject(s)
Fertility Preservation , Reproductive Health , Tertiary Care Centers , Humans , Female , Adolescent , Child , Young Adult , Cancer Survivors , Primary Ovarian Insufficiency/chemically induced , Hospitals, Pediatric , Adult , Sexual Health , Antineoplastic Agents/adverse effects , Neoplasms/drug therapy , Neoplasms/therapy , Neoplasms/complications , Sexual Behavior
3.
J Pediatr Adolesc Gynecol ; 36(2): 148-154, 2023 Apr.
Article in English | MEDLINE | ID: mdl-36522819

ABSTRACT

STUDY OBJECTIVE: To improve our understanding of reproductive health and sexual function in women with cloacal malformations and other anorectal malformations (ARMs) METHODS: An observational cross-sectional survey was administered to individuals assigned female at birth aged 12 to 55 with ARMs and cloacal malformations cared for at our institution. Data included age of thelarche/menarche and questions on body image, gynecologic anatomy, sexual function, and pregnancy. RESULTS: Twenty-one patients responded in the ARM group and 30 in the cloacal malformation group. There were no differences in median age of thelarche/menarche in patients with ARMs (11/12.5 years) compared with patients with cloacal malformation (11/12 years). Patients with ARMs were more likely to have native vaginal tissue than those with cloacal malformations (n = 18, 82% vs n = 12, 40%; P = .03). There were no differences between groups regarding concerns about dyspareunia and functionality of their vagina (P > .05). Forty-two percent of patients with cloacal malformations and 30% of patients with ARMs reported having been sexually active. Two patients with cloacal malformations and 2 with ARMs reported having been pregnant. Patients with cloacal malformations reported a lower quality of life score (80.4) compared with those with ARMs (87.0) (difference > 4.5). CONCLUSIONS: Patients with a cloacal malformation were less likely to have native vaginal tissue and reported a lower quality of life than those with ARMs. Despite this, patients with a cloacal malformation had similar reproductive health and sexual function compared with patients with ARMs. Our results reinforce the need for comprehensive sexual and reproductive health care for all women with ARMs.


Subject(s)
Anorectal Malformations , Pregnancy , Infant, Newborn , Animals , Female , Humans , Child , Quality of Life , Cross-Sectional Studies , Reproductive Health , Vagina/abnormalities , Cloaca/abnormalities
4.
Pediatr Blood Cancer ; 69(9): e29857, 2022 09.
Article in English | MEDLINE | ID: mdl-35732078

ABSTRACT

Fertility navigators (FNs) are important in communicating infertility risk and fertility preservation (FP) options to patients receiving gonadotoxic therapies. This retrospective study examined electronic medical records of patients with fertility consults at a large pediatric institution (2017-2019), before and after hiring a full-time FN. Of 738 patient encounters, 173 consults were performed pre-navigator and 565 post-navigator. Fertility consults for long-term follow-up cancer survivors increased most substantially: pre-navigator (n = 7) and post-navigator (n = 387). Across diagnoses, females had a larger increase in consults compared to males (χ2 [3, N = 738] = 8.17, p < .05). Findings highlight FNs' impact on counseling rates, particularly in survivorship.


Subject(s)
Cancer Survivors , Fertility Preservation , Neoplasms , Child , Female , Fertility , Fertility Preservation/psychology , Humans , Male , Neoplasms/therapy , Retrospective Studies
5.
J Pediatr Adolesc Gynecol ; 34(3): 328-333, 2021 Jun.
Article in English | MEDLINE | ID: mdl-33340647

ABSTRACT

STUDY OBJECTIVE: We investigated risk factors and common causes of tubo-ovarian abscess (TOA) in non-sexually active females in order to aid in earlier diagnosis, treatment, and improved outcomes. DESIGN: This is a retrospective observational case series of all non-sexually active females younger than age 25 years who were diagnosed with TOA. Review of the existing literature was also performed. SETTING: Academic tertiary care children's hospital. PARTICIPANTS: Ten patients meeting study inclusion criteria were identified for the study, and 33 other patients were identified in the literature. RESULTS: Average age at time of diagnosis was 14 years. Average body mass index was 24 kg/m2. Most presented with abdominal pain, often associated with fevers, nausea, vomiting, and diarrhea. Seven of 10 patients were treated surgically with pelvic washout (4 primarily and 3 after failing empiric antibiotic therapy). Most frequently, anaerobic gut flora were isolated on culture. All patients received broad-spectrum intravenous antibiotics, and were then discharged on a course of doxycycline and metronidazole or clindamycin. Three patients required additional admissions and multiple rounds of antibiotics due to persistent symptoms. The average length of stay was 3 days for patients treated with antibiotics only and 6 days for patients requiring surgical intervention. Six patients had complete resolution of symptoms and improvement on ultrasound within 2-4 weeks. The remainder were lost to follow-up. CONCLUSION: These cases, in conjunction with previous case reports, emphasize the importance of considering TOA in patients with concerning imaging or examination findings despite lack of sexual activity. Given the large proportion of cases attributable to anaerobic gut flora, treatment with antibiotics with adequate anaerobic coverage is recommended. Surgical drainage is not always necessary, but is often needed for diagnostic purposes or in patients not clinically improving with conservative measures.


Subject(s)
Abdominal Abscess/etiology , Fallopian Tube Diseases/etiology , Ovarian Diseases/etiology , Abdominal Abscess/diagnosis , Abdominal Abscess/therapy , Adolescent , Adult , Anti-Bacterial Agents/therapeutic use , Child , Combined Modality Therapy , Drainage , Fallopian Tube Diseases/diagnosis , Fallopian Tube Diseases/therapy , Female , Follow-Up Studies , Humans , Ovarian Diseases/diagnosis , Ovarian Diseases/therapy , Pelvic Inflammatory Disease/complications , Pelvic Inflammatory Disease/diagnosis , Pelvic Inflammatory Disease/therapy , Peritoneal Lavage , Retrospective Studies , Risk Factors , Treatment Outcome , Young Adult
6.
Future Oncol ; 14(29): 3059-3072, 2018 Dec.
Article in English | MEDLINE | ID: mdl-30474429

ABSTRACT

Once unimaginable, fertility management is now a nationally established part of cancer care in institutions, from academic centers to community hospitals to private practices. Over the last two decades, advances in medicine and reproductive science have made it possible for men, women and children to be connected with an oncofertility specialist or offered fertility preservation soon after a cancer diagnosis. The Oncofertility Consortium's National Physicians Cooperative is a large-scale effort to engage physicians across disciplines - oncology, urology, obstetrics and gynecology, reproductive endocrinology, and behavioral health - in clinical and research activities to enable significant progress in providing fertility preservation options to children and adults. Here, we review the structure and function of the National Physicians Cooperative and identify next steps.


Subject(s)
Fertility Preservation/methods , Fertility/physiology , Intersectoral Collaboration , Neoplasms/physiopathology , Physicians/organization & administration , Adult , Antineoplastic Agents/adverse effects , Behavioral Medicine/organization & administration , Child , Disease Progression , Endocrinology/methods , Endocrinology/organization & administration , Female , Fertility/drug effects , Gynecology/methods , Gynecology/organization & administration , Humans , Medical Oncology/methods , Medical Oncology/organization & administration , Neoplasms/complications , Neoplasms/pathology , Neoplasms/therapy , Obstetrics/methods , Obstetrics/organization & administration , Practice Guidelines as Topic , Pregnancy , Quality of Life , Reproductive Medicine/methods , Reproductive Medicine/organization & administration , United States , Urology/methods , Urology/organization & administration
7.
J Pediatr Adolesc Gynecol ; 31(4): 333-338, 2018 Aug.
Article in English | MEDLINE | ID: mdl-29653167

ABSTRACT

Adnexal torsion is an uncommon gynecologic disorder caused by the partial or complete rotation of the ovary and/or the fallopian tube on its vascular support. Delay in treatment can impact fertility adversely. The objective of this report is to provide clinical recommendations based on the latest evidence. Specifically we discuss epidemiology, clinical presentation, diagnostic approach and management of adnexal torsion in adolescents.


Subject(s)
Adnexa Uteri/pathology , Adnexal Diseases/diagnosis , Torsion Abnormality/diagnosis , Adnexal Diseases/surgery , Female , Humans , Torsion Abnormality/surgery
8.
J Pediatr Surg ; 53(4): 698-703, 2018 Apr.
Article in English | MEDLINE | ID: mdl-28797517

ABSTRACT

BACKGROUND/AIM: Patients may present with gynecologic concerns after previous posterior sagittal anorectoplasty (PSARP) for repair of an anorectal malformation (ARM). Common findings include an inadequate or shortened perineal body, as well as introital stenosis, retained vaginal septum, and remnant rectovestibular fistula. An inadequate or shortened perineal body may impact fecal continence, sexual function and recommendations regarding obstetrical mode of delivery. We describe our experience with female patients referred to our center for evaluation of their previously repaired ARM, with a specific focus on perineal body anatomy and concomitant gynecologic abnormalities. We outline our collaborative evaluation process and findings as well as subsequent repair and outcomes. MATERIAL/METHODS: A single site retrospective chart review from May 2014 to May 2016 was performed. Female patients with a history of prior ARM repair who required subsequent reoperative surgical repair with perineoplasty were included. The decision for reoperation was made collaboratively after a multidisciplinary evaluation by colorectal surgery, urology, and gynecology which included examination under anesthesia (EUA) with cystoscopy, vaginoscopy, rectal examination, and electrical stimulation of anal sphincters. The type of original malformation, indication for reoperative perineoplasty, findings leading to additional procedures performed at time of perineoplasty, postoperative complications, and the length of follow up were recorded. RESULTS: During the study period 28 patients were referred for evaluation after primary ARM repair elsewhere and 15 patients (60%) met inclusion criteria. Thirteen patients (86.6%) originally had a rectovestibular fistula with prior PSARP and 2 patients (13.4%) originally had a cloacal malformation with prior posterior sagittal anorectovaginourethroplasty. The mean age at the time of the subsequent perineoplasty was 4.6years (0.5-12). Patients had an inadequate perineal body requiring reoperative perineoplasty due to: anterior mislocation of the anus (n=11, 73.3%), prior perineal wound dehiscence with perineal body breakdown (n=2, 13.4%), acquired rectovaginal fistula (n=1, 6.6%), and posterior mislocated introitus with invasion of the perineal body (n=1, 6.6%). During the preoperative evaluation, additional gynecologic abnormalities were identified that required concomitant surgical intervention including: introital stenosis (n=4, 26.6%), retained vaginal septum (n=3, 20%) and remnant recto vestibular fistula (n=2, 13.3%). CONCLUSIONS: Patients with a previously repaired ARM may present with gynecologic concerns that require subsequent surgical intervention. The most common finding was an inadequate perineal body, but other findings included introital stenosis, retained vaginal septum and remnant recto vestibular fistula. Multidisciplinary evaluation to assess and identify abnormalities and coordinate timing and surgical approach is crucial to assure optimal patient outcomes. TYPE OF STUDY: Case series with no comparison group. LEVEL OF EVIDENCE: IV.


Subject(s)
Anorectal Malformations/surgery , Genital Diseases, Female/etiology , Plastic Surgery Procedures , Postoperative Complications , Anal Canal/pathology , Anal Canal/surgery , Child , Child, Preschool , Female , Follow-Up Studies , Genital Diseases, Female/diagnosis , Genital Diseases, Female/surgery , Humans , Infant , Perineum/pathology , Perineum/surgery , Postoperative Complications/diagnosis , Postoperative Complications/surgery , Rectovaginal Fistula/diagnosis , Rectovaginal Fistula/etiology , Rectovaginal Fistula/surgery , Retrospective Studies , Treatment Outcome , Vagina/pathology , Vagina/surgery
9.
J Pediatr Surg ; 51(11): 1864-1870, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27554917

ABSTRACT

INTRODUCTION: A significant number of internationally adopted children have congenital birth defects. As a specialist center for colorectal diagnoses, we evaluate such children with an anorectal malformation (ARM) and have found that a significant number need a reoperation. Knowledge of the common complications following ARM surgery has led us to develop treatment algorithms for patients with unknown past medical and surgical history, a situation typically encountered in the adopted population. METHODS: The results of investigations, indications, and rate of reoperation were assessed for adopted children with an ARM evaluated between 2014 and 2016. RESULTS: 56 patients (28 males) were identified. 76.8% required reoperative surgery. Mislocation of the anus outside the sphincter complex was seen in 50% of males and 39.3% of females. Anal stricture, rectal prolapse, retained vaginal septum, and a strictured vaginal introitus were also common. CONCLUSION: The reoperative surgery rate in the internationally adopted child with an ARM is high. Complete, systematic evaluation of these children is required to identify complications following initial repair. Development of mechanisms to improve the primary surgical care these children receive is needed.


Subject(s)
Abnormalities, Multiple , Adoption , Anal Canal/surgery , Anorectal Malformations/surgery , Diagnostic Imaging/methods , Digestive System Surgical Procedures/methods , Disease Management , Rectum/surgery , Anal Canal/abnormalities , Anorectal Malformations/diagnosis , Child , Child, Preschool , Female , Humans , Infant , Male , Rectum/abnormalities , Reoperation/statistics & numerical data
10.
Semin Pediatr Surg ; 24(2): 88-92, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25770370

ABSTRACT

Disorders of sexual development (DSDs) are relatively rare congenital conditions in which the development of the chromosomal, gonadal, or anatomic sex is atypical. Some conditions may not manifest until puberty or adulthood. The examination and workup of either an infant or an older patient with suspected DSD should be directed and performed systematically by a multidisciplinary team. Ideally, the team will include those with not only an interest in DSD but also experience with this group of patients. This article will briefly orient the reader to the conditions and decisions that may have been made during infancy, childhood, and adolescence and then focus on the challenges that may accompany transitioning the care of DSD patients from pediatric to adult surgeons and specialists to enable appropriate decisions and care. The actual transition will optimally involve a well-developed action plan that will take place gradually over a number of years as the person becomes educated about their condition and empowered to participate knowingly and actively in their own care.


Subject(s)
Clinical Decision-Making , Disorders of Sex Development/surgery , Patient Participation , Transition to Adult Care/standards , Adolescent , Adult , Humans
SELECTION OF CITATIONS
SEARCH DETAIL
...