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Original Research

Interrelationship between depression, anxiety, pain, and treatment adherence in hemophilia: results from a US cross-sectional survey

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Pages 1577-1587 | Published online: 20 Sep 2019

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (1)

Tom Burke, Anum Shaikh, Talaha M. Ali, Nanxin Li, Randall Curtis, Daniel-Anibal Garcia Diego, Michael Recht, Thomas Sannie, Mark Skinner & Jamie O’Hara. (2022) Association of factor expression levels with health-related quality of life and direct medical costs for people with haemophilia B. Journal of Medical Economics 25:1, pages 386-392.
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Articles from other publishers (14)

Pratima Chowdary, Francis Nissen, Tom Burke, Martynas Aizenas, Tünde Czirok, Harpal Dhillon & Jamie O'Hara. (2023) The humanistic and economic burden of problem joints for children and adults with moderate or severe haemophilia A: Analysis of the CHESS population studies. Haemophilia 29:3, pages 753-760.
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Tom Burke, Anum Shaikh, Talaha M. Ali, Nanxin Li, Barbara A. Konkle, Declan Noone, Brian O'Mahony, Steven Pipe & Jamie O'Hara. (2022) Association of factor expression levels with annual bleeding rate in people with haemophilia B. Haemophilia 29:1, pages 115-122.
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Idaira Rodriguez-Santana, Pronabesh DasMahapatra, Tom Burke, Zalmai Hakimi, José Bartelt-Hofer, Jameel Nazir & Jamie O’Hara. (2022) Health-related quality of life, direct medical and societal costs among children with moderate or severe haemophilia in Europe: multivariable models of the CHESS-PAEDs study. Orphanet Journal of Rare Diseases 17:1.
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Idaira Rodriguez-Santana, Pronabesh DasMahapatra, Tom Burke, Zalmai Hakimi, José Bartelt-Hofer, Jameel Nazir & Jamie O’Hara. (2022) Differential humanistic and economic burden of mild, moderate and severe haemophilia in european adults: a regression analysis of the CHESS II study. Orphanet Journal of Rare Diseases 17:1.
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Anum Shaikh, Gabriel Pedra, Matthew Cawson & Catherine Wiseman. (2022) Examining the impact of haemophilia treatment on health‐related quality of life. Haemophilia 28:5, pages 796-805.
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Ana María Jiménez-Cebrián, Patricia Palomo-López, Ricardo Becerro-de-Bengoa Vallejo, Marta Elena Losa-Iglesias, Emmanuel Navarro-Flores, Marta San-Antolín, César Calvo-Lobo & Daniel López-López. (2022) Impact of Depression on Patients With Hemophilia: A Retrospective Case-Control Research. Frontiers in Psychiatry 13.
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Katarina Steen Carlsson, Bent Winding, Jan Astermark, Fariba Baghaei, Elisabeth Brodin, Eva Funding, Margareta Holmström, Klaus Österholm, Sofia Bergenstråle, Emelie Andersson & Stefan Lethagen. (2022) Pain, depression and anxiety in people with haemophilia from three Nordic countries: Cross‐sectional survey data from the MIND study. Haemophilia 28:4, pages 557-567.
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Raghda Fouda, Donovan A. Argueta & Kalpna Gupta. (2022) Pain in Hemophilia: Unexplored Role of Oxidative Stress. Antioxidants 11:6, pages 1113.
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Michelle Witkop, Maria Santaella, Cynthia D Nichols, Angela Y Lambing, Kimberly Baumann, Randall G CurtisChristi Humphrey, Thomas J Humphries, Jennifer Newman, Nancy Durben, Rhonda Fritz, Kimberly Mauer, Constance B Thibodeaux, Emily Wheat & Tyler Buckner. (2022) Understanding the Pain Management Landscape Within the US Bleeding Disorder Community: A Multi-Center Survey. Pain Medicine 23:2, pages 269-279.
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Roberto Ucero‐Lozano, José Antonio López‐Pina, Alba Ortiz‐Pérez & Rubén Cuesta‐Barriuso. (2021) The relationship between chronic pain and psychosocial aspects in patients with haemophilic arthropathy. A cross‐sectional study. Haemophilia 28:1, pages 176-182.
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Tom Burke, Sohaib Asghar, Jamie O’Hara, Margaret Chuang, Eileen K. Sawyer & Nanxin Li. (2021) Clinical, humanistic, and economic burden of severe haemophilia B in adults receiving factor IX prophylaxis: findings from the CHESS II real-world burden of illness study in Europe. Orphanet Journal of Rare Diseases 16:1.
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Margaret K. Geary, Ellen Kachalsky & Aric Parnes. (2021) The actual and ideal roles of haemophilia treatment centre social workers in the United States and the barriers to ideal roles. Haemophilia 27:6.
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Michelle Witkop, George Morgan, Jamie O'Hara, Michael Recht, Tyler W. Buckner, Diane Nugent, Randall Curtis, Brian O'Mahony, Mark W. Skinner, Brendan Mulhern, Matthew Cawson, Talaha M. Ali, Eileen K. Sawyer & Nanxin Li. (2021) Patient preferences and priorities for haemophilia gene therapy in the US: A discrete choice experiment. Haemophilia 27:5, pages 769-782.
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Jamie O’Hara, Antony P. Martin, Diane Nugent, Michelle Witkop, Tyler W. Buckner, Mark W. Skinner, Brian O’Mahony, Brendan Mulhern, George Morgan, Nanxin Li & Eileen K. Sawyer. (2021) Evidence of a disability paradox in patient‐reported outcomes in haemophilia. Haemophilia 27:2, pages 245-252.
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