Male Sexual Function after Allogeneic Hematopoietic Stem Cell Transplantation in Childhood: A Multicenter Study

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Male Sexual Function after Allogeneic Hematopoietic Stem Cell Transplantation in Childhood : A Multicenter Study. / Haavisto, Anu; Mathiesen, Sidsel; Suominen, Anu; Lähteenmäki, Päivi; Sørensen, Kaspar; Ifversen, Marianne; Juul, Anders; Mejdahl Nielsen, Malene; Müller, Klaus; Jahnukainen, Kirsi.

I: Cancers, Bind 12, Nr. 7, 1786, 04.07.2020.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Haavisto, A, Mathiesen, S, Suominen, A, Lähteenmäki, P, Sørensen, K, Ifversen, M, Juul, A, Mejdahl Nielsen, M, Müller, K & Jahnukainen, K 2020, 'Male Sexual Function after Allogeneic Hematopoietic Stem Cell Transplantation in Childhood: A Multicenter Study', Cancers, bind 12, nr. 7, 1786. https://doi.org/10.3390/cancers12071786

APA

Haavisto, A., Mathiesen, S., Suominen, A., Lähteenmäki, P., Sørensen, K., Ifversen, M., Juul, A., Mejdahl Nielsen, M., Müller, K., & Jahnukainen, K. (2020). Male Sexual Function after Allogeneic Hematopoietic Stem Cell Transplantation in Childhood: A Multicenter Study. Cancers, 12(7), [1786]. https://doi.org/10.3390/cancers12071786

Vancouver

Haavisto A, Mathiesen S, Suominen A, Lähteenmäki P, Sørensen K, Ifversen M o.a. Male Sexual Function after Allogeneic Hematopoietic Stem Cell Transplantation in Childhood: A Multicenter Study. Cancers. 2020 jul. 4;12(7). 1786. https://doi.org/10.3390/cancers12071786

Author

Haavisto, Anu ; Mathiesen, Sidsel ; Suominen, Anu ; Lähteenmäki, Päivi ; Sørensen, Kaspar ; Ifversen, Marianne ; Juul, Anders ; Mejdahl Nielsen, Malene ; Müller, Klaus ; Jahnukainen, Kirsi. / Male Sexual Function after Allogeneic Hematopoietic Stem Cell Transplantation in Childhood : A Multicenter Study. I: Cancers. 2020 ; Bind 12, Nr. 7.

Bibtex

@article{18bfb7f9ad714167b1c5d21423e514f1,
title = "Male Sexual Function after Allogeneic Hematopoietic Stem Cell Transplantation in Childhood: A Multicenter Study",
abstract = "There are many known endocrine complications after allogeneic hematopoietic stem cell transplantation (HSCT) in childhood including increased risk of biochemical hypogonadism. However, little is known about sexuality in adulthood following childhood HSCT. In this multicenter study, sexual functions and possible risk factors were assessed comprehensively in two national cohorts (Finland and Denmark) of male adult survivors of childhood HSCT. Compared to a healthy control group (n = 56), HSCT survivors (n = 97) reported less sexual fantasies, poorer orgasms, lower sexual activity with a partner and reduced satisfaction with their sex life, even in the presence of normal erectile functions and a similar frequency of autoerotic acts. Of the HSCT survivors, 35% were cohabitating/married and 66% were sexually active. Risk factors for poorer self-reported sexual functions were partner status (not cohabitating with a partner), depressive symptoms, CNS and testicular irradiation. Sexual dysfunction increased by age in the HSCT group with a pace comparable to that of the control group. However, because of the lower baseline level of sexual functions in the HSCT group, they will reach the level of clinically significant dysfunction at a younger age. Hence, male survivors of childhood HSCT should be interviewed in detail about their sexual health beyond erectile functions.",
author = "Anu Haavisto and Sidsel Mathiesen and Anu Suominen and P{\"a}ivi L{\"a}hteenm{\"a}ki and Kaspar S{\o}rensen and Marianne Ifversen and Anders Juul and {Mejdahl Nielsen}, Malene and Klaus M{\"u}ller and Kirsi Jahnukainen",
year = "2020",
month = jul,
day = "4",
doi = "10.3390/cancers12071786",
language = "English",
volume = "12",
journal = "Cancers",
issn = "2072-6694",
publisher = "M D P I AG",
number = "7",

}

RIS

TY - JOUR

T1 - Male Sexual Function after Allogeneic Hematopoietic Stem Cell Transplantation in Childhood

T2 - A Multicenter Study

AU - Haavisto, Anu

AU - Mathiesen, Sidsel

AU - Suominen, Anu

AU - Lähteenmäki, Päivi

AU - Sørensen, Kaspar

AU - Ifversen, Marianne

AU - Juul, Anders

AU - Mejdahl Nielsen, Malene

AU - Müller, Klaus

AU - Jahnukainen, Kirsi

PY - 2020/7/4

Y1 - 2020/7/4

N2 - There are many known endocrine complications after allogeneic hematopoietic stem cell transplantation (HSCT) in childhood including increased risk of biochemical hypogonadism. However, little is known about sexuality in adulthood following childhood HSCT. In this multicenter study, sexual functions and possible risk factors were assessed comprehensively in two national cohorts (Finland and Denmark) of male adult survivors of childhood HSCT. Compared to a healthy control group (n = 56), HSCT survivors (n = 97) reported less sexual fantasies, poorer orgasms, lower sexual activity with a partner and reduced satisfaction with their sex life, even in the presence of normal erectile functions and a similar frequency of autoerotic acts. Of the HSCT survivors, 35% were cohabitating/married and 66% were sexually active. Risk factors for poorer self-reported sexual functions were partner status (not cohabitating with a partner), depressive symptoms, CNS and testicular irradiation. Sexual dysfunction increased by age in the HSCT group with a pace comparable to that of the control group. However, because of the lower baseline level of sexual functions in the HSCT group, they will reach the level of clinically significant dysfunction at a younger age. Hence, male survivors of childhood HSCT should be interviewed in detail about their sexual health beyond erectile functions.

AB - There are many known endocrine complications after allogeneic hematopoietic stem cell transplantation (HSCT) in childhood including increased risk of biochemical hypogonadism. However, little is known about sexuality in adulthood following childhood HSCT. In this multicenter study, sexual functions and possible risk factors were assessed comprehensively in two national cohorts (Finland and Denmark) of male adult survivors of childhood HSCT. Compared to a healthy control group (n = 56), HSCT survivors (n = 97) reported less sexual fantasies, poorer orgasms, lower sexual activity with a partner and reduced satisfaction with their sex life, even in the presence of normal erectile functions and a similar frequency of autoerotic acts. Of the HSCT survivors, 35% were cohabitating/married and 66% were sexually active. Risk factors for poorer self-reported sexual functions were partner status (not cohabitating with a partner), depressive symptoms, CNS and testicular irradiation. Sexual dysfunction increased by age in the HSCT group with a pace comparable to that of the control group. However, because of the lower baseline level of sexual functions in the HSCT group, they will reach the level of clinically significant dysfunction at a younger age. Hence, male survivors of childhood HSCT should be interviewed in detail about their sexual health beyond erectile functions.

U2 - 10.3390/cancers12071786

DO - 10.3390/cancers12071786

M3 - Journal article

C2 - 32635426

VL - 12

JO - Cancers

JF - Cancers

SN - 2072-6694

IS - 7

M1 - 1786

ER -

ID: 251641638