Factors Associated With Diagnosing Psoriatic Arthritis: A Retrospective Study in Northeast Georgia.

Q2 Social Sciences
Romina Faridizad, Brent A Flickinger, Ania Izabela Rynarzewska, Sarah Ross, Shane Robinson, Aditya Kumar Ghosh
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Abstract

Background: Approximately 15.5% of patients with psoriatic arthritis (PsA) are currently not diagnosed or experience delayed diagnosis with negative outcomes. This retrospective, cross-sectional study evaluated patients with psoriasis to determine what factors were associated with diagnosis of PsA.

Methods: A retrospective chart review was performed using electronic medical record from primary care clinics across the northeast Georgia region. The study population included patients with psoriasis evaluated in the clinic between January 1, 2017 and December 31, 2022. Patients with PsA were compared to those without PsA to assess for factors associated with the diagnosis of PsA.

Results: The probability of diagnosis of PsA increased with increasing number of clinic encounters (odds ratio [OR], 1.18; P < .05). Males (OR, 0.634; P < .001) were less likely to be diagnosed compared to females. Patients with Medicare (adjusted OR, 1.707; 95% confidence interval [CI], 1.027-2.837; P < .05) and commercial/private insurances (adjusted OR, 2.043; 95% CI, 1.28-3.258; P < .01) had a higher chance of being diagnosed in comparison to patients with Medicaid. Black patients were less likely to be diagnosed compared to White patients (OR, 0.231; P < .001). Hispanic patients were less likely to be diagnosed with PsA compared to patients who were not Hispanic (OR, 0.2; 95% CI, 0.07-0.51; P < .05).

Conclusions: The study highlighted potential factors associated with the diagnosis of PsA among patients with psoriasis. Sex, race, ethnicity, number of clinic encounters, and insurance type were all found to have associations with likelihood of receiving a PsA diagnosis. These findings were hypothesis-generating and suggest potential disparities in care, particularly for diverse populations, warranting further research.

诊断银屑病关节炎的相关因素:乔治亚州东北部的一项回顾性研究。
背景:大约15.5%的银屑病关节炎(PsA)患者目前未被诊断或经历阴性结果的延迟诊断。这项回顾性的横断面研究评估了银屑病患者,以确定哪些因素与PsA的诊断相关。方法:回顾性分析乔治亚州东北部地区初级保健诊所的电子病历。研究人群包括2017年1月1日至2022年12月31日期间在诊所评估的牛皮癣患者。将患有PsA的患者与没有PsA的患者进行比较,以评估与PsA诊断相关的因素。结果:PsA的诊断概率随着临床接触次数的增加而增加(优势比[OR], 1.18;P < 0.05)。男性(OR, 0.634;P < 0.001)被诊断的可能性低于女性。医疗保险患者(调整OR, 1.707;95%置信区间[CI], 1.027-2.837;P < 0.05)和商业/私人保险(调整OR, 2.043;95% ci, 1.28-3.258;P < 0.01)与接受医疗补助的患者相比,有更高的被诊断的机会。与白人患者相比,黑人患者被诊断的可能性更低(OR, 0.231;P < 0.001)。与非西班牙裔患者相比,西班牙裔患者被诊断为PsA的可能性更小(OR, 0.2;95% ci, 0.07-0.51;P < 0.05)。结论:该研究强调了银屑病患者PsA诊断相关的潜在因素。性别、种族、民族、就诊次数和保险类型都与接受PsA诊断的可能性有关。这些发现是假设产生的,并表明在护理方面存在潜在差异,特别是在不同人群中,值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
The Permanente journal
The Permanente journal Medicine-Medicine (all)
CiteScore
2.20
自引率
0.00%
发文量
86
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