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The Hastings Center, explored ethical and social issues raised by surgery aimed at making children
appear more typical. A multidisciplinary group considered medical,
psychosocial, and ethical issues associated with surgical interventions in
children born with atypical genitalia, commonly grouped as intersex.
Parents of newborns with
intersex may believe that medical evalution will reveal their infants "true
sex" and that genital surgery should proceed as soon as possible to avoid
negative psychological sequelae. However, gender identity is not perfectly
predicted by sex chromosomes or other physical parameters. Empirical evidence
challenging predictions of positive outcomes from "cosmetic" procedures were
reviewed as was diminished sexual responsiveness associated with surgical
procedures. The practice of shielding patients from details of their diagnosis
and surgical treatment is purported to precipitate disruption of relationships
with parents and health care professionals. The authors point out that guidance
documents put forth by professional societies are not based on valid clinical
investigations and that there exists substantial variability among different
specialties. The following conclusions were reached.
- A comprehensive
assessment of actual clinical practice should be undertaken.
- Current surgical procedures that normalize genital
appearance, are not alone justified. Surgery does not assure that the
individual will avoid being discriminated against.
- Appearance-altering
surgeries do not need to be performed urgently. Surgical expediency does not
necessarily outweigh the psychosocial and ethical considerations of waiting
until the patient can participate in decision-making.
- Immediately
following diagnosis families require comprehensive services, including access
to mental health professionals with intersex expertise. Psychological support
is essential.
- To reduce the
feelings of humiliation and shame, children should be informed of their
differences in an age-appropriate manner.
- Ethical practice
demands rigorous follow-up studies focusing on well-being and quality of life.
Retrospective studies should include those who have not had surgery and
prospective studies should compare the outcomes of non-surgical alternatives.
Careful study design is crucial.
- Clinicians need
more intersex education including diagnosis, the development of gender, and
sexual health.
In an accompanying
commentary, Dr. Erica Eugster juxtaposes panel recommendations against the
"real life challenges of providing compassionate and responsible care to
infants with intersex conditions and their families." Eugster draws attention
to the potential psychological risks of postponing genital surgery until the
patient is mature enough to provide informed consent. She ponders the
implications for parenting of denying the option of early surgery when the
family, demands surgery. She concludes the ultimate decision should rest with
the parents. To safeguard physical well-being of the child, Eugster reinforces
a recent recommendation that genital surgery be undertaken in centers of
excellence with intersex expertise.
Eugster welcomes the
development of multidisciplinary teams, but recognizes its rare application.
Her experience demonstrates that some families passively and/or actively reject
counseling. The full integration of counseling services with a
multidisciplinary team may temper such resistance. Regarding disclosure of
medical information to the child, Eugster welcomes the guidelines for
psychoeducational counseling but acknowledges that conflicts may be encountered
when family members wish to shield the child from diagnostic details. Eugster
enthusiastically endorses increased human sexuality education for clinicians
but recommends a targeted strategy of focused training workshops that would
serve the purpose of filling staffing gaps in multidisciplinary teams with
intersex expertise.
Frader J, Alderson P, Asch A, Aspinall C, Davis D, Dreger A, Edwards J, Feder EK, Frank A, Hedley LA, Kittay E, Marsh J, Miller PS, Mouradian W, Nelson H, Parens E. Health care professionals and intersex conditions. Arch Pediatr Adolesc Med 2004;158:426-428.
Eugster EA. Reality vs recommendations in the care of infants with intersex conditions. Arch Pediatr Adolesc Med 2004;158:428-429.
First Editor’s
Comment: These papers provide an
excellent discussion on the ethical care of patients with intersex conditions.
Both pieces underscore the value of outcome studies in guiding clinical
practice, and yet the vision of multicenter, multidisciplinary research is
largely unrealized. There are inherent limitations on research (eg randomized
clinical trial is not an option in assessing the benefits of early versus later
genital surgery). Studies examining the relative benefits of multidisciplinary
teams versus the current standard of care would be compelling and feasible. The
systemic constraints in ‘real life’ medicine represents even greater
challenges. The intense effort required in creating and maintaining
multidisciplinary teams serves as a disincentive. Creative problem solving is
needed; we will not obtain answers to the most important questions if we
restrict our inquiry to those issues that are the easiest to study.
David E. Sandberg,
PhD
Second Editor’s
Comment: The reader is encouraged
to review the article "Discordant sexual identify in some genetic males with
cloacal exstrophy assigned to female sex at birth",1 as well as the
accompanying commentaries by many experts regarding sex determination,
differentiation, and idenity.2 Altogether these articles should be
carefully considered when caring for these patients. As Eugster stated, "The
most important determinant of outcome may be an individual family's ability to
accept and unconditionally love their child." 3
Fima Lifshitz, MD
References - (linked to )
- Reiner WG, Gearhart JP. Discordant sexual identity in some genetic males with cloacal exstrophy assigned to female sex at birth.N Engl J Med 2004;350:333-341.
- Migeon CJ, Berkovitz GD, Wisniewski AB. Sex determination, differentiation, and identity. N Engl J Med 2004;350:2204-2206.
- Berenbaum SA. Management of children with intersex conditions: psychological and methodological perspectives. Growth Genetics Horm 2003:19:1-
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