Dyspareunia is associated with chronic pain in premenopausal women with sickle cell disease

References

• Laumann EO, Paik A, Rosen RC. Sexual dysfunction in the United States: prevalence and predictors. JAMA. 1999;281:537–544. doi: 10.1001/jama.281.6.537
   PubMed Web of Science ®Google Scholar
• Danielsson I, Sjoberg I, Stelund H, et al. Prevalence and incidence of prolonged and severe dyspareunia in women: results from a population study. Scand J Public Health. 2003;31:113–118. doi: 10.1080/14034940210134040
   PubMed Web of Science ®Google Scholar
• Terzi H, Terzi R, Kale A. The relationship between fibromyalgia and pressure pain threshold in patients with dyspareunia. Pain Res Manag. 2015;20:137–140. doi: 10.1155/2015/302404
   PubMed Web of Science ®Google Scholar
• Boardman LA, Stockdale CK. Sexual pain. Clin Obstet Gynecol. 2009;52:682–690. doi: 10.1097/GRF.0b013e3181bf4a7e
   PubMed Web of Science ®Google Scholar
• Ashley-Koch A, Yang Q, Olney RS. Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review. Am J Epidemiol. 2000;151:839–845. doi: 10.1093/oxfordjournals.aje.a010288
   PubMed Web of Science ®Google Scholar
• Hassell K. Sickle cell disease population estimation: application of available contemporary data to traditional methods. 35th Anniversary Convention of the National Sickle Cell Disease Program; Washington, DC; 2007.
   Google Scholar
• Rees DC, Williams TN, Gladwin MT. Sickle-cell disease. Lancet. 2010;376:2018–2031. doi: 10.1016/S0140-6736(10)61029-X
   PubMed Web of Science ®Google Scholar
• Bunn HF. Pathogenesis and treatment of sickle cell disease. N Engl J Med. 1997;337(11):762–769. doi: 10.1056/NEJM199709113371107
   PubMed Web of Science ®Google Scholar
• Smith WR, Penberthy LT, Bovbjerg VE, et al. Daily assessment of pain in adults with sickle cell disease. Ann Intern Med. 2008;148:94–101. doi: 10.7326/0003-4819-148-2-200801150-00004
   PubMed Web of Science ®Google Scholar
• Ballas SK, Lusardi M. Hospital readmission for adult acute sickle cell painful episodes: frequency, etiology, and prognostic significance. Am J Hematol. 2005;79:17–25. doi: 10.1002/ajh.20336
   PubMed Web of Science ®Google Scholar
• Brandow AM, Farley RA, Panepinto JA. Early insights into the neurobiology of pain in sickle cell disease: a systematic review of the literature. Pediatr Blood Cancer. 2015;62(9):1501–1511. doi: 10.1002/pbc.25574
   PubMed Web of Science ®Google Scholar
• Spitzer RL, Kroenke K, Williams JB. Validation and utility of a self-report version of PRIME-MD: the PHQ primary care study. JAMA. 1999;282:1737–1744. doi: 10.1001/jama.282.18.1737
   PubMed Web of Science ®Google Scholar
• Cook E, Goldman I. Empiric comparison of multivariate analytic techniques: advantages and disadvantages of recursive partitioning analysis. J Chronic Dis. 1984;37:721–731. doi: 10.1016/0021-9681(84)90041-9
   PubMedGoogle Scholar
• Tran H, Gupta M, Gupta K. Targeting novel mechanisms of pain in sickle cell disease. Blood. 2017;130(22):2377–2385. doi: 10.1182/blood-2017-05-782003
   PubMed Web of Science ®Google Scholar
• Treede RD, Meyer RA, Raja SN, et al. Peripheral and central mechanisms of cutaneous hyperalgesia. Prog Neurobiol. 1992;38:397–421. doi: 10.1016/0301-0082(92)90027-C
   PubMed Web of Science ®Google Scholar
• Brandow AM, Farley R, Panepinto JA. Neuropathic pain in patients with sickle cell disease. Pediatr Blood Cancer. 2014;61:512–517. doi: 10.1002/pbc.24838
   PubMed Web of Science ®Google Scholar
• Ezenwa MO, Molokie RE, Wang ZJ, et al. Safety and utility of quantitative sensory testing among adults with sickle cell disease: indicators of neuropathic pain? Pain Pract. 2016;16(3):282–293. doi: 10.1111/papr.12279
   PubMed Web of Science ®Google Scholar
• Brandow AM, Stucky CL, Hillery CA, et al. Patients with sickle cell disease have increased sensitivity to cold and heat. Am J Hematol. 2013;88:37–43. doi: 10.1002/ajh.23341
   PubMed Web of Science ®Google Scholar
• Sutton KS, Pukall CF, Chamberlain S. Pain ratings, sensory thresholds, and psychosocial functioning in women with provoked vestibulodynia. J Sex Marital Ther. 2009;35:262–281. doi: 10.1080/00926230902851256
   PubMed Web of Science ®Google Scholar
• Granot M. Personality traits associated with perception of noxious stimuli in women with vulvar vestibulitis syndrome. J Pain. 2005;6:168–173. doi: 10.1016/j.jpain.2004.11.010
   PubMed Web of Science ®Google Scholar
• Bohm-Starke N. Vulvar vestibulitis syndrome – pathophysiology of the vestibular mucosa. Scand J Sexol. 2001;4:227–234.
   Google Scholar
• Chadha S, Gianotten WL, Drogendijk AC, et al. Histopathologic features of vulvar vestibulitis. Int J Gynecol Pathol. 1998;17:7–11. doi: 10.1097/00004347-199801000-00002
   PubMed Web of Science ®Google Scholar
• Arnold LD, Bachmann GA, Rosen R, et al. Vulvodynia: characteristics and associations with comorbidities and quality of life. Obstet Gynecol. 2006;107:617–624. doi: 10.1097/01.AOG.0000199951.26822.27
   PubMed Web of Science ®Google Scholar
• Grover S, Mattoo SK, Pendharkar S, et al. Sexual dysfunction in patients with alcohol and opioid dependence. Indian J Psychol Med. 2014;36(4):355–365. doi: 10.4103/0253-7176.140699
   PubMedGoogle Scholar
• Öberg K, Fugl-Meyer AR, Fugl-Meyer KS. On categorization and quantification of women’s sexual dysfunctions: an epidemiological approach. Int J Impot Res. 2004;16:261–269. doi: 10.1038/sj.ijir.3901151
   PubMed Web of Science ®Google Scholar
• Jamieson DJ, Steege JF. The prevalence of dysmenorrhea, dyspareunia, pelvic pain and irritable bowel syndrome in primary care practices. Obstet Gynecol. 1996;87:55–58. doi: 10.1016/0029-7844(95)00360-6
   PubMed Web of Science ®Google Scholar
• McClish DK, Penberthy LT, Bovbjerg VE, et al. Health related quality of life in sickle cell patients: the PiSCES project. Health Qual Life Outcomes. 2005;3:50. doi: 10.1186/1477-7525-3-50
   PubMedGoogle Scholar
• Graves JK, Hodge C, Jacob E. Depression, anxiety, and quality of life in children and adolescents with sickle cell disease. Pediatr Nurs. 2016;42(3):113–119.
   PubMedGoogle Scholar
• Dampier C, LeBeau P, Rhee S, et al.;Comprehensive Sickle Cell Centers (CSCC) Clinical Trial Consortium (CTC) Site Investigators. Health-related quality of life in adults with sickle cell disease (SCD): a report from the comprehensive sickle cell centers clinical trial consortium. Am J Hematol. 2011;86(2):203–205. doi: 10.1002/ajh.21905
   PubMed Web of Science ®Google Scholar
• Barakat LP, Patterson CA, Daniel LC, et al. Quality of life among adolescents with sickle cell disease: mediation of pain by internalizing symptoms and parenting stress. Health Qual Life Outcomes. 2008;6:60. doi: 10.1186/1477-7525-6-60
   PubMed Web of Science ®Google Scholar
• Graaff AA D, D’Hooghe TM, Dunselman GA, et al. The significant effect of endometriosis on physical, mental and social wellbeing: results from an international cross-sectional survey. Hum Reprod. 2013;28(10):2677–2685. doi: 10.1093/humrep/det284
   PubMed Web of Science ®Google Scholar