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Clinical profiling of specific diagnostic subgroups of women with chronic pelvic pain.
Demetriou, Lysia; Krassowski, Michal; Abreu Mendes, Pedro; Garbutt, Kurtis; Vitonis, Allison F; Wilkins, Elizabeth; Coxon, Lydia; Arendt-Nielsen, Lars; Aziz, Qasim; Birch, Judy; Horne, Andrew W; Hoffman, Anja; Hummelshoj, Lone; Lunde, Claire E; Meijlink, Jane; Perro, Danielle; Rahmioglu, Nilufer; Terry, Kathryn L; Pogatzki-Zahn, Esther; Sieberg, Christine B; Treede, Rolf-Detlef; Becker, Christian M; Cruz, Francisco; Missmer, Stacey A; Zondervan, Krina T; Nagel, Jens; Vincent, Katy.
Afiliación
  • Demetriou L; Oxford Endometriosis Centre, Nuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom.
  • Krassowski M; Oxford Endometriosis Centre, Nuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom.
  • Abreu Mendes P; IBMC/I3S and Faculty of Medicine of Porto, Hospital S João, Porto, Portugal.
  • Garbutt K; Oxford Endometriosis Centre, Nuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom.
  • Vitonis AF; Boston Center for Endometriosis, Brigham and Women's Hospital and Boston Children's Hospital, Boston, MA, United States.
  • Wilkins E; Department of Obstetrics and Gynaecology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, United States.
  • Coxon L; Oxford Endometriosis Centre, Nuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom.
  • Arendt-Nielsen L; Oxford Endometriosis Centre, Nuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom.
  • Aziz Q; Center for Neuroplasticity and Pain (CNAP), SMI, Department of Health Science and Technology, School of Medicine, Aalborg University, Aalborg, Denmark.
  • Birch J; Department of Medical Gastroenterology, Mech-Sense, Aalborg University Hospital, Aalborg, Denmark.
  • Horne AW; Centre for Neuroscience, Surgery and Trauma, Blizard Institute, Wingate Institute of Neurogastroenterology, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
  • Hoffman A; Pelvic Pain Support Network, Poole, United Kingdom.
  • Hummelshoj L; MRC Centre for Reproductive Health, University of Edinburgh, Edinburgh, United Kingdom.
  • Lunde CE; Research & Development, Pharmaceuticals Experimental Medicine, Bayer AG, Berlin, Germany.
  • Meijlink J; Endometriosis.org, London, United Kingdom.
  • Perro D; Oxford Endometriosis Centre, Nuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom.
  • Rahmioglu N; Biobehavioral Pain Innovations Lab, Department of Psychiatry & Behavioral Sciences, Boston Children's Hospital, Boston, MA, United States.
  • Terry KL; Pain and Affective Neuroscience Center, Department of Anesthesiology, Critical Care, & Pain Medicine, Boston Children's Hospital, Boston, MA, London, United States.
  • Pogatzki-Zahn E; International Painful Bladder Foundation, Naarden, Netherlands.
  • Sieberg CB; Oxford Endometriosis Centre, Nuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom.
  • Treede RD; Oxford Endometriosis Centre, Nuffield Department of Women's and Reproductive Health, University of Oxford, Oxford, United Kingdom.
  • Becker CM; Boston Center for Endometriosis, Brigham and Women's Hospital and Boston Children's Hospital, Boston, MA, United States.
  • Cruz F; Department of Obstetrics and Gynaecology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, United States.
  • Missmer SA; Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, United States.
  • Zondervan KT; Department of Anesthesiology, Intensive Care and Pain Medicine, University Hospital Muenster, Muenster, Germany.
  • Nagel J; Biobehavioral Pain Innovations Lab, Department of Psychiatry & Behavioral Sciences, Boston Children's Hospital, Boston, MA, United States.
  • Vincent K; Pain and Affective Neuroscience Center, Department of Anesthesiology, Critical Care, & Pain Medicine, Boston Children's Hospital, Boston, MA, London, United States.
Front Reprod Health ; 5: 1140857, 2023.
Article en En | MEDLINE | ID: mdl-37325239
Introduction: Chronic pelvic pain (CPP) is a common condition affecting up to 26.6% of women, with many suffering for several years before diagnosis and/or treatment. Its clinical presentation is varied and there are frequently comorbid conditions both within and outside the pelvis. We aim to explore whether specific subgroups of women with CPP report different clinical symptoms and differing impact of pain on their quality of life (QoL). Methods: The study is part of the Translational Research in Pelvic Pain (TRiPP) project which is a cross-sectional observational cohort study. The study includes 769 female participants of reproductive age who completed an extensive set of questions derived from standardised WERF EPHect questionnaires. Within this population we defined a control group (reporting no pelvic pain, no bladder pain syndrome, and no endometriosis diagnosis, N = 230) and four pain groups: endometriosis-associated pain (EAP, N = 237), interstitial cystitis/bladder pain syndrome (BPS, N = 72), comorbid endometriosis-associated pain and BPS (EABP, N = 120), and pelvic pain only (PP, N = 127). Results: Clinical profiles of women with CPP (13-50 years old) show variability of clinical symptoms. The EAP and EABP groups scored higher than the PP group (p < 0.001) on the pain intensity scales for non-cyclical pelvic pain and higher than both the BPS and PP groups (p < 0.001) on the dysmenorrhoea scale. The EABP group also had significantly higher scores for dyspareunia (p < 0.001), even though more than 50% of sexually active participants in each pain group reported interrupting and/or avoiding sexual intercourse due to pain in the last 12 months. Scores for the QoL questionnaire (SF-36) reveal that CPP patients had significantly lower QoL across all SF-36 subscales (p < 0.001). Significant effects were also observed between the pain groups for pain interference with their work (p < 0.001) and daily lives (p < 0.001), with the EABP suffering more compared to the EAP and PP groups (p < 0.001). Discussion: Our results demonstrate the negative impact that chronic pain has on CPP patients' QoL and reveal an increased negative impact of pain on the comorbid EABP group. Furthermore, it demonstrates the importance of dyspareunia in women with CPP. Overall, our results demonstrate the need for further exploration of interventions targeting QoL more broadly and suggest that novel approaches to classifying women with CPP are needed.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Observational_studies / Risk_factors_studies Idioma: En Revista: Front Reprod Health Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Diagnostic_studies / Observational_studies / Risk_factors_studies Idioma: En Revista: Front Reprod Health Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido