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Transition to Adult Care in Autoinflammatory Diseases: A Cohort of 111 French Patients. 自体发炎疾病患者向成人护理的过渡:111 名法国患者的队列。
IF 2.4 4区 医学 Q2 RHEUMATOLOGY Pub Date : 2024-10-01 Epub Date: 2024-08-26 DOI: 10.1097/RHU.0000000000002132
Inès Elhani, Véronique Hentgen, Pierre Quartier, Brigitte Bader-Meunier, Isabelle Kone-Paut, Bénédicte Neven, Linda Rossi, Albert Faye, Ulrich Meinzer, Isabelle Melki, Gilles Grateau, Léa Savey, Sophie Georgin-Lavialle

Background: Transitioning from pediatric to adult care is a critical step for individuals with autoinflammatory diseases, requiring effective programs to ensure continuity of care and disease management. Despite various recommendations, the effectiveness of transition programs, particularly in monogenic autoinflammatory diseases, remains understudied.

Methods: A single-center medical records review study was conducted at the French National Reference Center for Adult Autoinflammatory Diseases in Tenon Hospital from 2017 to 2023. All patients who had consulted for the first time between the ages of 15 and 30 years and had received care for an autoinflammatory disease during childhood were included. The patients were classified according to whether they had undergone a transition, defined as either no transition, simple transition (referral letter), or joint transition (pediatrician and adult physician consultation).

Results: One hundred eleven patients (median age, 18 years) were included. Patients who consulted without transition started adult follow-up and were followed up less regularly than those who underwent the transition process ( p < 0.001 and p = 0.028). In patients with familial Mediterranean fever, the absence of a formal transition was associated with poorer disease control at baseline ( p = 0.019). The type of transition did not impact disease control during follow-up.

Conclusions: Participation in a transition program is associated with earlier and more regular follow-up in adulthood. Although transition type did not significantly impact disease control during follow-up in familial Mediterranean fever, the potential benefit of joint consultation extends beyond consultation frequency and disease outcomes, encompassing patient perspectives and self-management abilities. This study highlights the significance of collaborative transition programs in AIDs.

背景:对于患有自身炎症性疾病的患者来说,从儿科护理过渡到成人护理是至关重要的一步,需要有效的计划来确保护理和疾病管理的连续性。尽管有各种建议,但对过渡方案的有效性,尤其是单基因自身炎症性疾病的过渡方案的有效性,研究仍然不足:2017年至2023年,法国国家成人自身炎症疾病参考中心在特农医院开展了一项单中心病历回顾研究。所有首次就诊年龄在15至30岁之间、在儿童时期因自身炎症疾病接受过治疗的患者均被纳入研究范围。根据患者是否经历了转诊,将其分为无转诊、简单转诊(转诊信)或联合转诊(儿科医生和成人医生会诊):结果:共纳入 111 名患者(中位年龄为 18 岁)。未经转诊的患者开始接受成人随访,其随访频率低于经过转诊的患者(p < 0.001 和 p = 0.028)。在家族性地中海热患者中,没有正式转归与基线疾病控制较差有关(p = 0.019)。过渡类型对随访期间的疾病控制没有影响:结论:参与过渡计划与成年后更早和更定期的随访有关。虽然过渡类型对家族性地中海热患者随访期间的疾病控制没有明显影响,但联合会诊的潜在益处不仅限于会诊频率和疾病结果,还包括患者的观点和自我管理能力。这项研究强调了合作过渡计划在艾滋病中的重要性。
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引用次数: 0
Preserving Fertility in People With Rheumatic Diseases. 保护风湿病患者的生育能力。
IF 2.4 4区 医学 Q2 RHEUMATOLOGY Pub Date : 2024-10-01 DOI: 10.1097/RHU.0000000000002144
Molly Leavitt, Amanda Adeleye, Cuoghi Edens

Abstract: Rheumatology patients historically were told they "can't" or "shouldn't" become pregnant. Improved rheumatic diagnostics and treatments have led to decreased morbidity and mortality and increased quality of life resulting in an opportunity to focus on fertility and its preservation. In the same vein as rheumatic disease care, assisted reproductive technology (ART), which includes freezing of egg and sperm as well as in vitro fertilization, has made considerable strides in the recent past. ART is safe for those with rheumatic diseases and has comparable outcomes to the general public, but may take additional effort due to optimal timing, rheumatic medications, and other nuances. In a specialty that treats chronic inflammatory diagnoses using teratogens and gonadotoxins, it is important to address family building desires with patients so their goals can be met.Rheumatologists have little knowledge of ART and how it impacts or applies to their patients; however, patients want their rheumatologist to be the source of knowledge for this information (Arthritis Rheumatol. 2022;74:suppl 9). Many barriers to ART exist and will be explored, with the financial burden being paramount (Glob J Health Sci. 6;1:181-191). Future efforts to examine the future fertility of rheumatology patients in an era of biologics and "treat-to-target" are needed to better understand who would most benefit from this costly and not without risk medical treatment. Given the changing landscape of financial support for ART due to insurance mandates, rheumatologists should not modify counseling based on the anticipated ability of patients to afford care. Preservation should also be broached with patients without partners and those from the LGBTQAI+ community. In addition to expanding the education of rheumatologists regarding this topic and its incorporation into clinical care, advocacy for ART access and insurance coverage is a much-needed future direction.

摘要:风湿病患者历来被告知 "不能 "或 "不应该 "怀孕。风湿病诊断和治疗方法的改进降低了发病率和死亡率,提高了生活质量,从而使人们有机会关注生育能力及其保护。与风湿病治疗相同,辅助生殖技术(ART),包括冷冻卵子和精子以及体外受精,在最近也取得了长足的进步。辅助生殖技术对风湿病患者是安全的,其结果也与普通人相当,但由于最佳时机、风湿病药物和其他细微差别,可能需要付出更多努力。风湿免疫科医生对 ART 及其对患者的影响和应用知之甚少;然而,患者希望他们的风湿免疫科医生成为这方面知识的来源(Arthritis Rheumatol.)抗逆转录病毒疗法存在许多障碍,我们将对这些障碍进行探讨,其中最主要的障碍是经济负担(《全球健康科学》6;1:181-191)。在使用生物制剂和 "靶向治疗 "的时代,需要对风湿病患者未来的生育能力进行研究,以更好地了解谁最能从这种昂贵且不无风险的医疗中获益。由于保险规定,抗逆转录病毒疗法的经济支持不断变化,因此风湿免疫科医生不应根据患者的预期负担能力来修改咨询内容。对于没有伴侣的患者和来自 LGBTQAI+ 群体的患者,也应提出保留治疗方案的建议。除了扩大风湿免疫科医生对这一主题的教育并将其纳入临床护理外,倡导抗逆转录病毒疗法的可及性和保险覆盖面也是亟待解决的未来方向。
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引用次数: 0
Reproductive Health in RA, Lupus, and APS. RA、狼疮和 APS 的生殖健康。
IF 2.4 4区 医学 Q2 RHEUMATOLOGY Pub Date : 2024-10-01 DOI: 10.1097/RHU.0000000000002141
Dina Zucchi, Chiara Tani, Marta Mosca

Abstract: Systemic lupus erythematosus, antiphospholipid syndrome, and rheumatoid arthritis are chronic autoimmune diseases affecting women of childbearing age. These diseases may impair fertility and fecundity, as well as complicate pregnancy and the puerperium in these patients including disease flare and obstetric complications on both the maternal and fetal side. For each patient, an appropriate preconceptional counseling with risk stratification is required, including assessment of disease activity, organ involvement, serological profile, and comorbidities.In cases of pregnancy, the aims of treatment are to prevent disease activity, to treat disease activity in cases of flare, and to prevent maternal and fetal complications such as preeclampsia or fetal loss. In all patients with these diseases, close clinical monitoring during pregnancy and puerperium is mandatory. This review aims to summarize the fertility issues in patients with systemic lupus erythematosus, antiphospholipid syndrome, and rheumatoid arthritis and to provide an update on pregnancy management and outcomes in these patients.

摘要:系统性红斑狼疮、抗磷脂综合征和类风湿性关节炎是影响育龄妇女的慢性自身免疫性疾病。这些疾病可能会损害这些患者的生育能力,并使妊娠和产褥期复杂化,包括疾病复发以及母体和胎儿方面的产科并发症。对于每一位患者,都需要进行适当的孕前咨询和风险分层,包括评估疾病的活动性、受累器官、血清学特征和合并症。在妊娠的情况下,治疗的目的是预防疾病活动,在疾病复发时治疗疾病活动,以及预防母体和胎儿并发症,如子痫前期或胎儿丢失。对于所有这些疾病的患者,在妊娠期和产褥期都必须进行密切的临床监测。本综述旨在总结系统性红斑狼疮、抗磷脂综合征和类风湿性关节炎患者的生育问题,并提供有关这些患者的妊娠管理和结果的最新信息。
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引用次数: 0
Reproductive Health in the Post Roe v. Wade Era. 后罗伊诉韦德案时代的生殖健康》。
IF 2.4 4区 医学 Q2 RHEUMATOLOGY Pub Date : 2024-10-01 DOI: 10.1097/RHU.0000000000002140
Rosalind Ramsey-Goldman
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引用次数: 0
Subacute Flexion Contracture Due to Nontuberculous Mycobacterial Infection. 非结核分枝杆菌感染导致的亚急性屈曲挛缩症
IF 2.4 4区 医学 Q2 RHEUMATOLOGY Pub Date : 2024-10-01 Epub Date: 2024-08-02 DOI: 10.1097/RHU.0000000000002116
Yoshinori Taniguchi, Hirotaka Yamamoto
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引用次数: 0
Protracted Febrile Myalgia Syndrome: A Rare and Difficult Manifestation of Familial Mediterranean Fever. 持续发热性肌痛综合征:家族性地中海热罕见而棘手的表现。
IF 3.4 4区 医学 Q2 RHEUMATOLOGY Pub Date : 2024-09-14 DOI: 10.1097/rhu.0000000000002125
Eray Tunce,Kadir Ulu,Sevinç Taşar,Betül Sözeri
OBJECTIVEProtracted febrile myalgia syndrome (PFMS) is characterized by severe myalgia, fever, abdominal pain, and arthralgia/arthritis episodes lasting for several weeks in patients with familial Mediterranean fever. Treatment options include nonsteroidal anti-inflammatory drugs, corticosteroids, and anti-interleukin-1 therapy. This study aimed to share our experiences of PFMS so as to shed light on this rare and elusive condition.METHODSThis cross-sectional analysis included 17 patients diagnosed with PFMS at our pediatric rheumatology clinic between January 2018 and September 2023.RESULTSIn our clinic, 17 (1%) of 1663 familial Mediterranean fever patients presented with PFMS, and it was the initial manifestation in 10 patients (58.8%) in the cohort. Eight of the 17 patients had an M694V homozygous mutation in the MEFV gene. A magnetic resonance imaging showed myositis and fasciitis in just 1 patient, and myositis alone was evident in 5 others. Symptoms improved in 2 patients with nonsteroidal anti-inflammatory drugs, whereas prednisolone improved symptoms in 12 patients and anakinra was required in 3 patients. Patients who received anakinra had another severe attack and required long-term anakinra or canakinumab.CONCLUSIONSSyndrome for PFMS is difficult to recognize as it can sometimes be the first manifestation of familial Mediterranean fever. The syndrome is not accompanied by fever in some patients, even though the word febrile is part of its name. Most patients respond dramatically to nonsteroidal anti-inflammatory drugs or corticosteroids. In some patients with PFMS, long-term anakinra or canakinumab treatment may be more useful in preventing severe attacks of PFMS than short-term (5 to 7 days) anakinra treatment.
目的:持续发热性肌痛综合征(PFMS)的特征是家族性地中海热患者出现持续数周的严重肌痛、发热、腹痛和关节痛/关节炎发作。治疗方法包括非甾体抗炎药、皮质类固醇激素和抗白细胞介素-1疗法。本研究旨在分享我们在 PFMS 方面的经验,以揭示这种罕见而难以捉摸的疾病。方法本横断面分析纳入了 2018 年 1 月至 2023 年 9 月期间在我们的儿科风湿病诊所确诊为 PFMS 的 17 例患者。结果在我们的诊所,1663 例家族性地中海热患者中有 17 例(1%)表现为 PFMS,其中 10 例患者(58.8%)的初始表现为 PFMS。在这17名患者中,有8名患者的MEFV基因发生了M694V同源突变。磁共振成像显示,仅有1名患者出现肌炎和筋膜炎,另外5名患者仅出现肌炎。2名患者服用非甾体抗炎药后症状有所改善,12名患者服用泼尼松龙后症状有所改善,3名患者需要服用阿那金拉。结论PFMS综合征很难识别,因为它有时可能是家族性地中海热的首发表现。尽管发热是该综合征名称的一部分,但有些患者并不伴有发热。大多数患者对非甾体类抗炎药或皮质类固醇反应明显。对于某些 PFMS 患者,长期服用 anakinra 或 canakinumab 比短期(5 到 7 天)服用 anakinra 更能预防 PFMS 的严重发作。
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引用次数: 0
IRF5 Variants Are Risk Factors for Systemic Lupus Erythematosus in 2 Mexican Populations. IRF5 变异是两个墨西哥人群患系统性红斑狼疮的风险因素。
IF 3.4 4区 医学 Q2 RHEUMATOLOGY Pub Date : 2024-09-14 DOI: 10.1097/rhu.0000000000002121
Isaac A López-Briceño,Julian Ramírez-Bello,Isela Montúfar-Robles,Rosa Elda Barbosa-Cobos,Angélica V Ángulo-Ramírez,Guillermo Valencia-Pacheco
INTRODUCTIONInterferon regulatory factor 5 (IRF5) is one of the pivotal genes implicated in systemic lupus erythematosus (SLE) among diverse ethnic groups, including Europeans, Asians, Hispanics, and Africans. Notably, its significance appears particularly pronounced among Hispanic populations. Previous studies have identified several single-nucleotide variants within IRF5, such as rs2004640G/T, rs2070197T/C, and rs10954213G/A, as associated with susceptibility to SLE among patients from Mexico City. However, the population of Yucatan, located in the Southeast of Mexico and characterized by a greater Amerindian genetic component, remains largely unexplored in this regard.OBJECTIVESOur study aimed to replicate the observed association between IRF5 variants and susceptibility to SLE among patients from Central Mexico and Yucatan. Furthermore, we investigated the impact of IRF5 rs59110799G/T, a variant that has not been previously studied in SLE individuals.METHODOur study included 204 SLE patients and 160 controls from Central Mexico, as well as 184 SLE patients and 184 controls from Yucatan. All participants were females 18 years and older. We employed a TaqMan assay to detect the presence of the following single-nucleotide variants: rs2004640G/T, rs2070197T/C, rs10954213G/A, and rs59110799G/T. Furthermore, we utilized 2 distinct web tools and databases to predict the potential functional implications of IRF5 variants.RESULTSIn SLE patients from Central Mexico, several IRF5 alleles showed significant associations with the disease following adjustment by the Bonferroni test: the rs2070197C allele (odds ratio [OR], 2.08), the rs10954213A allele (OR, 1.59), and the rs59110799G allele (OR, 1.71). Conversely, among patients from Yucatan, the following alleles showed associations: rs2004640T (OR, 1.51), rs2070197C (OR, 1.62), rs10954213A (OR, 1.67), and rs59110799G (OR, 1.44).CONCLUSIONOur findings highlight genetic variations between Mexican populations and emphasize the role of IRF5 as a risk factor in SLE patients from both Central Mexico and Yucatan.
简介干扰素调节因子 5(IRF5)是与欧洲人、亚洲人、西班牙裔人和非洲人等不同种族群体中的系统性红斑狼疮(SLE)有关的关键基因之一。值得注意的是,它在西班牙裔人群中的重要性似乎尤为明显。先前的研究发现,IRF5 中的几个单核苷酸变异,如 rs2004640G/T、rs2070197T/C 和 rs10954213G/A 与墨西哥城患者的系统性红斑狼疮易感性有关。我们的研究旨在复制在墨西哥中部和尤卡坦患者中观察到的 IRF5 变体与系统性红斑狼疮易感性之间的关联。此外,我们还调查了IRF5 rs59110799G/T的影响,该变异以前从未在系统性红斑狼疮患者中进行过研究。方法我们的研究包括来自墨西哥中部的204名系统性红斑狼疮患者和160名对照者,以及来自尤卡坦半岛的184名系统性红斑狼疮患者和184名对照者。所有参与者均为 18 岁及以上的女性。我们采用 TaqMan 分析法检测以下单核苷酸变异的存在:rs2004640G/T、rs2070197T/C、rs10954213G/A 和 rs59110799G/T。结果在墨西哥中部的系统性红斑狼疮患者中,经 Bonferroni 检验调整后,几个 IRF5 等位基因显示与疾病有显著关联:rs2070197C 等位基因(比值比 [OR],2.08)、rs10954213A 等位基因(OR,1.59)和 rs59110799G 等位基因(OR,1.71)。相反,在尤卡坦患者中,以下等位基因显示出相关性:rs2004640T(OR,1.51)、rs2070197C(OR,1.62)、rs10954213A(OR,1.67)和 rs59110799G(OR,1.44)。
{"title":"IRF5 Variants Are Risk Factors for Systemic Lupus Erythematosus in 2 Mexican Populations.","authors":"Isaac A López-Briceño,Julian Ramírez-Bello,Isela Montúfar-Robles,Rosa Elda Barbosa-Cobos,Angélica V Ángulo-Ramírez,Guillermo Valencia-Pacheco","doi":"10.1097/rhu.0000000000002121","DOIUrl":"https://doi.org/10.1097/rhu.0000000000002121","url":null,"abstract":"INTRODUCTIONInterferon regulatory factor 5 (IRF5) is one of the pivotal genes implicated in systemic lupus erythematosus (SLE) among diverse ethnic groups, including Europeans, Asians, Hispanics, and Africans. Notably, its significance appears particularly pronounced among Hispanic populations. Previous studies have identified several single-nucleotide variants within IRF5, such as rs2004640G/T, rs2070197T/C, and rs10954213G/A, as associated with susceptibility to SLE among patients from Mexico City. However, the population of Yucatan, located in the Southeast of Mexico and characterized by a greater Amerindian genetic component, remains largely unexplored in this regard.OBJECTIVESOur study aimed to replicate the observed association between IRF5 variants and susceptibility to SLE among patients from Central Mexico and Yucatan. Furthermore, we investigated the impact of IRF5 rs59110799G/T, a variant that has not been previously studied in SLE individuals.METHODOur study included 204 SLE patients and 160 controls from Central Mexico, as well as 184 SLE patients and 184 controls from Yucatan. All participants were females 18 years and older. We employed a TaqMan assay to detect the presence of the following single-nucleotide variants: rs2004640G/T, rs2070197T/C, rs10954213G/A, and rs59110799G/T. Furthermore, we utilized 2 distinct web tools and databases to predict the potential functional implications of IRF5 variants.RESULTSIn SLE patients from Central Mexico, several IRF5 alleles showed significant associations with the disease following adjustment by the Bonferroni test: the rs2070197C allele (odds ratio [OR], 2.08), the rs10954213A allele (OR, 1.59), and the rs59110799G allele (OR, 1.71). Conversely, among patients from Yucatan, the following alleles showed associations: rs2004640T (OR, 1.51), rs2070197C (OR, 1.62), rs10954213A (OR, 1.67), and rs59110799G (OR, 1.44).CONCLUSIONOur findings highlight genetic variations between Mexican populations and emphasize the role of IRF5 as a risk factor in SLE patients from both Central Mexico and Yucatan.","PeriodicalId":14745,"journal":{"name":"JCR: Journal of Clinical Rheumatology","volume":"3 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142259976","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development and Validation of Nosocomial Bacterial Infection Prediction Models for Patients With Systemic Lupus Erythematosus. 开发并验证系统性红斑狼疮患者的非社会性细菌感染预测模型
IF 3.4 4区 医学 Q2 RHEUMATOLOGY Pub Date : 2024-09-12 DOI: 10.1097/rhu.0000000000002120
Mauricio Restrepo Escobar,Fabián Jaimes Barragán,Gloria María Vásquez Duque,Daniel Camilo Aguirre Acevedo,Édgar Alfonso Peñaranda Parada,Johana Prieto-Alvarado,Miguel Antonio Mesa-Navas,Estefanía Calle-Botero,Álvaro Arbeláez-Cortés,Carlos Jaime Velásquez-Franco,Óscar Vergara-Serpa,David Julián Del-Castillo-Gil,Camilo Andrés Gordillo-González,Luis Carlos Guzmán-Naranjo,Paula Andrea Granda-Carvajal,Daniel Jaramillo-Arroyave,Carlos Horacio Muñoz-Vahos,Mariana Vélez-Marín,Johanna Hernández-Zapata,Ruth Eraso-Garnica,Adriana Lucía Vanegas-García,Luis Alonso González-Naranjo
BACKGROUNDHospital-acquired bacterial infections are associated with high morbidity and mortality rates in patients with systemic lupus erythematosus (SLE). This study aimed to develop and validate predictive models for the risk of hospital-acquired bacterial infections in patients with SLE.METHODSA historical cohort study was designed for development, and another bidirectional cohort study was used for external validation. The risk of bacterial infection was assessed upon admission and after 5 days of hospitalization. Predictor selection employed the least absolute shrinkage and selection operator (LASSO) techniques. Multiple imputations were used to handle missing data. Logistic regression models were applied, and the properties of discrimination, calibration, and decision curve analysis were evaluated.RESULTSThe development cohort comprised 1686 patients and 237 events (14.1%) from 3 tertiary hospitals. The external validation cohort included 531 patients and 84 infection outcomes (15.8%) from 10 hospital centers in Colombia (secondary and tertiary level). The models applied at admission and after 120 hours of stay exhibited good discrimination (AUC > 0.74). External validation demonstrated good performance among patients from the same tertiary institutions where the models were developed. However, geographic validation at other institutions has been suboptimal.CONCLUSIONSTwo predictive models for nosocomial bacterial infections in patients with SLE are presented. All infection prevention recommendations should be maximized in patients at moderate/high risk. Further validation studies in diverse contexts, as well as clinical impact trials, are necessary before potential applications in research and clinical care.
背景医院获得性细菌感染与系统性红斑狼疮(SLE)患者的高发病率和高死亡率有关。本研究旨在开发和验证系统性红斑狼疮患者医院获得性细菌感染风险的预测模型。方法设计了一个历史队列研究用于开发,另一个双向队列研究用于外部验证。细菌感染风险在入院时和住院 5 天后进行评估。预测因子的选择采用了最小绝对收缩和选择算子(LASSO)技术。多重推定用于处理缺失数据。结果开发队列包括来自 3 家三级医院的 1686 名患者和 237 个事件(14.1%)。外部验证队列包括来自哥伦比亚 10 家医院中心(二级和三级医院)的 531 名患者和 84 个感染结果(15.8%)。入院时和住院 120 小时后应用的模型显示出良好的区分度(AUC > 0.74)。外部验证表明,在开发模型的同一家三级医院的患者中表现良好。结论:本文介绍了两种针对系统性红斑狼疮患者院内细菌感染的预测模型。所有预防感染的建议都应尽量适用于中度/高度风险患者。在可能应用于研究和临床护理之前,有必要在不同情况下进行进一步的验证研究以及临床影响试验。
{"title":"Development and Validation of Nosocomial Bacterial Infection Prediction Models for Patients With Systemic Lupus Erythematosus.","authors":"Mauricio Restrepo Escobar,Fabián Jaimes Barragán,Gloria María Vásquez Duque,Daniel Camilo Aguirre Acevedo,Édgar Alfonso Peñaranda Parada,Johana Prieto-Alvarado,Miguel Antonio Mesa-Navas,Estefanía Calle-Botero,Álvaro Arbeláez-Cortés,Carlos Jaime Velásquez-Franco,Óscar Vergara-Serpa,David Julián Del-Castillo-Gil,Camilo Andrés Gordillo-González,Luis Carlos Guzmán-Naranjo,Paula Andrea Granda-Carvajal,Daniel Jaramillo-Arroyave,Carlos Horacio Muñoz-Vahos,Mariana Vélez-Marín,Johanna Hernández-Zapata,Ruth Eraso-Garnica,Adriana Lucía Vanegas-García,Luis Alonso González-Naranjo","doi":"10.1097/rhu.0000000000002120","DOIUrl":"https://doi.org/10.1097/rhu.0000000000002120","url":null,"abstract":"BACKGROUNDHospital-acquired bacterial infections are associated with high morbidity and mortality rates in patients with systemic lupus erythematosus (SLE). This study aimed to develop and validate predictive models for the risk of hospital-acquired bacterial infections in patients with SLE.METHODSA historical cohort study was designed for development, and another bidirectional cohort study was used for external validation. The risk of bacterial infection was assessed upon admission and after 5 days of hospitalization. Predictor selection employed the least absolute shrinkage and selection operator (LASSO) techniques. Multiple imputations were used to handle missing data. Logistic regression models were applied, and the properties of discrimination, calibration, and decision curve analysis were evaluated.RESULTSThe development cohort comprised 1686 patients and 237 events (14.1%) from 3 tertiary hospitals. The external validation cohort included 531 patients and 84 infection outcomes (15.8%) from 10 hospital centers in Colombia (secondary and tertiary level). The models applied at admission and after 120 hours of stay exhibited good discrimination (AUC > 0.74). External validation demonstrated good performance among patients from the same tertiary institutions where the models were developed. However, geographic validation at other institutions has been suboptimal.CONCLUSIONSTwo predictive models for nosocomial bacterial infections in patients with SLE are presented. All infection prevention recommendations should be maximized in patients at moderate/high risk. Further validation studies in diverse contexts, as well as clinical impact trials, are necessary before potential applications in research and clinical care.","PeriodicalId":14745,"journal":{"name":"JCR: Journal of Clinical Rheumatology","volume":"84 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142259978","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Rituximab as Treatment for Lupus Nephritis: Data From the Peruvian ALMENARA Lupus Cohort. 利妥昔单抗治疗狼疮性肾炎:来自秘鲁 ALMENARA 狼疮队列的数据。
IF 2.4 4区 医学 Q2 RHEUMATOLOGY Pub Date : 2024-09-01 Epub Date: 2024-07-03 DOI: 10.1097/RHU.0000000000002112
Victor R Pimentel-Quiroz, Cristina Reátegui-Sokolova, Rocío V Gamboa-Cárdenas, Claudia Elera-Fitzcarrald, Zoila Rodríguez-Bellido, César A Pastor-Asurza, Risto Perich-Campos, Graciela S Alarcón, Manuel F Ugarte-Gil

Objective: The aim of this study was to evaluate the response to rituximab (RTX) as treatment for lupus nephritis (LN) in a Latin American Lupus cohort.

Methods: The medical records from LN patients from a single-center cohort spanning between January 2012 and December 2020 were reviewed. Demographic factors (age at diagnosis and baseline, gender), disease duration, previous and concomitant treatments, serum creatinine, and 24-hour proteinuria (24-HP) levels at baseline, and 6th and 12th months were obtained. Complete response (CR) or responder status was defined according to the LUNAR, AURORA-1, and BLISS-LN trials.

Results: Thirty-six patients received RTX as induction treatment; 32 (88.9%) were women. Their age at baseline and disease duration were 32.6 (11.7) and 7.6 (6.5) years, respectively. The time between renal biopsy and RTX use was 2.64 (4.41) years. At baseline, serum creatinine and 24-HP levels were 1.5 (1.5) mg/dL and 3.4 (2.8) g, respectively. At months 6 and 12, serum creatinine levels were 1.6 (1.6) and 1.6 (1.5) mg/dL, and 24-HP were 2.2 (2.2) and 1.6 (1.5) g, respectively. According to LUNAR and AURORA-1 criteria, CR at 6th and 12th months were 6/34 (17.6%) and 8/30 (26.7%) and 6/34 (17.6%) and 7/31 (22.6%) patients, respectively. According to BLISS-LN criteria, responders at 6th and 12th months were 9/34 (26.5%) and 10/31 (32.3%) patients, respectively.

Conclusions: CR and responder status were reached in less than one third of LN patients treated with RTX, regardless of the criteria used to define them. However, serum creatinine levels did not increase, and there was a decrease in proteinuria levels during the follow-up.

研究目的本研究旨在评估拉丁美洲狼疮队列中狼疮肾炎(LN)患者对利妥昔单抗(RTX)治疗的反应:方法:研究人员回顾了2012年1月至2020年12月期间一个单中心队列中狼疮肾炎患者的医疗记录。研究人员收集了基线、第 6 个月和第 12 个月的人口统计学因素(诊断时和基线年龄、性别)、病程、既往治疗和伴随治疗、血清肌酐和 24 小时蛋白尿 (24-HP) 水平。完全应答(CR)或应答者状态根据LUNAR、AURORA-1和BLISS-LN试验进行定义:36名患者接受了RTX诱导治疗,其中32人(88.9%)为女性。她们的基线年龄和病程分别为32.6(11.7)岁和7.6(6.5)岁。肾活检与使用 RTX 之间的间隔时间为 2.64(4.41)年。基线时,血清肌酐和 24-HP 水平分别为 1.5 (1.5) mg/dL 和 3.4 (2.8) g。第 6 个月和第 12 个月时,血清肌酐水平分别为 1.6 (1.6) mg/dL 和 1.6 (1.5) mg/dL,24-HP 分别为 2.2 (2.2) g 和 1.6 (1.5) g。根据 LUNAR 和 AURORA-1 标准,第 6 个月和第 12 个月 CR 患者分别为 6/34 (17.6%) 和 8/30 (26.7%),以及 6/34 (17.6%) 和 7/31 (22.6%)。根据BLISS-LN标准,第6个月和第12个月的应答者分别为9/34(26.5%)和10/31(32.3%)例:结论:在接受 RTX 治疗的 LN 患者中,只有不到三分之一的患者达到 CR 和应答状态,无论采用何种标准对其进行定义。然而,在随访期间,血清肌酐水平并未升高,蛋白尿水平也有所下降。
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引用次数: 0
Contemporary Patterns of Financial Toxicity Among Patients With Rheumatologic Disease in the United States. 美国风湿病患者财务毒性的当代模式。
IF 2.4 4区 医学 Q2 RHEUMATOLOGY Pub Date : 2024-09-01 Epub Date: 2024-07-08 DOI: 10.1097/RHU.0000000000002110
Troy B Amen, Edward Christopher Dee, Bhav Jain, Stephen Batter, Urvish Jain, Simar S Bajaj, Nathan H Varady, Lauren J Amen, Susan M Goodman

Background/objective: Rheumatologic diseases encompass a group of disabling conditions that often require expensive clinical treatments and limit an individual's ability to work and maintain a steady income. The purpose of this study was to evaluate contemporary patterns of financial toxicity among patients with rheumatologic disease and assess for any associated demographic factors.

Methods: The cross-sectional National Health Interview Survey was queried from 2013 to 2018 for patients with rheumatologic disease. Patient demographics and self-reported financial metrics were collected or calculated including financial hardship from medical bills, financial distress, food insecurity, and cost-related medication (CRM) nonadherence. Multivariable logistic regressions were used to assess for factors associated with increased financial hardship.

Results: During the study period, 20.2% of 41,502 patients with rheumatologic disease faced some degree of financial hardship due to medical bills, 55.0% of whom could not pay those bills. Rheumatologic disease was associated with higher odds of financial hardship from medical bills (adjusted odds ratio, 1.29; 95% confidence interval, 1.22-1.36; p < 0.001) with similar trends for patients suffering from financial distress, food insecurity, and CRM nonadherence (p < 0.001 for all). Financial hardship among patients with rheumatologic disease was associated with being younger, male, Black, and uninsured ( p < 0.001 for all).

Conclusion: In this nationally representative study, we found that a substantial proportion of adults with rheumatologic disease in the United States struggled with paying their medical bills and suffered from food insecurity and CRM nonadherence. National health care efforts and guided public policy should be pursued to help ease the burden of financial hardship for these patients.

背景/目的:风湿病是一组致残性疾病,通常需要昂贵的临床治疗,并限制了个人工作和维持稳定收入的能力。本研究的目的是评估风湿病患者财务毒性的当代模式,并评估与之相关的人口统计学因素:从 2013 年到 2018 年,对风湿病患者进行了横断面国家健康访谈调查。收集或计算了患者的人口统计学特征和自我报告的财务指标,包括医疗账单造成的经济困难、经济窘迫、食品不安全和与费用相关的药物治疗(CRM)不依从性。多变量逻辑回归用于评估与经济困难加剧相关的因素:在研究期间,41502 名风湿病患者中有 20.2% 因医疗费用而面临一定程度的经济困难,其中 55.0% 无法支付这些费用。风湿病患者因医疗费用而陷入经济困境的几率较高(调整后的几率比为 1.29;95% 置信区间为 1.22-1.36;P <0.001),而经济窘迫、粮食不安全和不遵守 CRM 的患者也有类似的趋势(P <0.001)。风湿病患者的经济困难与年轻、男性、黑人和无保险有关(所有因素的 p < 0.001):在这项具有全国代表性的研究中,我们发现美国有相当一部分成年风湿病患者在支付医疗费用方面举步维艰,并面临粮食不安全和 CRM 不达标的问题。应通过国家医疗保健努力和有指导性的公共政策来帮助减轻这些患者的经济负担。
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JCR: Journal of Clinical Rheumatology
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