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1.
Leora I. Horwitz; Tanayott Thaweethai; Shari B. Brosnahan; Mine S. Cicek; Megan L. Fitzgerald; Jason D. Goldman; Rachel Hess; S. L. Hodder; Vanessa L. Jacoby; Michael R. Jordan; Jerry A. Krishnan; Adeyinka O. Laiyemo; Torri D. Metz; Lauren Nichols; Rachel E. Patzer; Anisha Sekar; Nora G. Singer; Lauren E. Stiles; Barbara S. Taylor; Shifa Ahmed; Heather A. Algren; Khamal Anglin; Lisa Aponte-Soto; Hassan Ashktorab; Ingrid V. Bassett; Brahmchetna Bedi; Nahid Bhadelia; Christian Bime; Marie-Abele C. Bind; Lora J. Black; Andra L. Blomkalns; Hassan Brim; Mario Castro; James Chan; Alexander W. Charney; Benjamin K. Chen; Li Qing Chen; Peter Chen; David Chestek; Lori B. Chibnik; Dominic C. Chow; Helen Y. Chu; Rebecca G. Clifton; Shelby Collins; Maged M. Costantine; Sushma K. Cribbs; Steven G. Deeks; John D. Dickinson; Sarah E. Donohue; Matthew S. Durstenfeld; Ivette F. Emery; Kristine M. Erlandson; Julio C. Facelli; Rachael Farah-Abraham; Aloke V. Finn; Melinda S. Fischer; Valerie J. Flaherman; Judes Fleurimont; Vivian Fonseca; Emily J. Gallagher; Jennifer C. Gander; Maria Laura Gennaro; Kelly S. Gibson; Minjoung Go; Steven N. Goodman; Joey P. Granger; Frank L. Greenway; John W. Hafner; Jenny E. Han; Michelle S. Harkins; Kristine S.P. Hauser; James R. Heath; Carla R. Hernandez; On Ho; Matthew K. Hoffman; Susan E. Hoover; Carol R. Horowitz; Harvey Hsu; Priscilla Y. Hsue; Brenna L. Hughes; Prasanna Jagannathan; Judith A. James; Janice John; Sarah Jolley; S. E. Judd; Joy J. Juskowich; Diane G. Kanjilal; Elizabeth W. Karlson; Stuart D. Katz; J. Daniel Kelly; Sara W. Kelly; Arthur Y. Kim; John P. Kirwan; Kenneth S. Knox; Andre Kumar; Michelle F. Lamendola-Essel; Margaret Lanca; Joyce K. Lee-lannotti; R. Craig Lefebvre; Bruce D. Levy; Janet Y. Lin; Brian P. Logarbo Jr.; Jennifer K. Logue; Michele T. Longo; Carlos A. Luciano; Karen Lutrick; Shahdi K. Malakooti; Gail Mallett; Gabrielle Maranga; Jai G. Marathe; Vincent C. Marconi; Gailen D. Marshall; Christopher F. Martin; Jeffrey N. Martin; Heidi T. May; Grace A. McComsey; Dylan McDonald; Hector Mendez-Figueroa; Lucio Miele; Murray A. Mittleman; Sindhu Mohandas; Christian Mouchati; Janet M. Mullington; Girish N Nadkarni; Erica R. Nahin; Robert B. Neuman; Lisa T. Newman; Amber Nguyen; Janko Z. Nikolich; Igho Ofotokun; Princess U. Ogbogu; Anna Palatnik; Kristy T.S. Palomares; Tanyalak Parimon; Samuel Parry; Sairam Parthasarathy; Thomas F. Patterson; Ann Pearman; Michael J. Peluso; Priscilla Pemu; Christian M. Pettker; Beth A. Plunkett; Kristen Pogreba-Brown; Athena Poppas; J. Zachary Porterfield; John G. Quigley; Davin K. Quinn; Hengameh Raissy; Candida J. Rebello; Uma M. Reddy; Rebecca Reece; Harrison T. Reeder; Franz P. Rischard; Johana M. Rosas; Clifford J. Rosen; Nadine G. Rouphae; Dwight J. Rouse; Adam M. Ruff; Christina Saint Jean; Grecio J. Sandoval; Jorge L. Santana; Shannon M. Schlater; Frank C. Sciurba; Caitlin Selvaggi; Sudha Seshadri; Howard D. Sesso; Dimpy P. Shah; Eyal Shemesh; Zaki A. Sherif; Daniel J. Shinnick; Hyagriv N. Simhan; Upinder Singh; Amber Sowles; Vignesh Subbian; Jun Sun; Mehul S. Suthar; Larissa J. Teunis; John M. Thorp Jr.; Amberly Ticotsky; Alan T. N. Tita; Robin Tragus; Katherine R. Tuttle; Alfredo E. Urdaneta; P. J. Utz; Timothy M. VanWagoner; Andrew Vasey; Suzanne D. Vernon; Crystal Vidal; Tiffany Walker; Honorine D. Ward; David E. Warren; Ryan M. Weeks; Steven J. Weiner; Jordan C. Weyer; Jennifer L. Wheeler; Sidney W. Whiteheart; Zanthia Wiley; Natasha J. Williams; Juan P. Wisnivesky; John C. Wood; Lynn M. Yee; Natalie M. Young; Sokratis N. Zisis; Andrea S. Foulkes; - Recover Initiative.
medrxiv; 2023.
Preprint en Inglés | medRxiv | ID: ppzbmed-10.1101.2023.05.26.23290475

RESUMEN

Importance: SARS-CoV-2 infection can result in ongoing, relapsing, or new symptoms or other health effects after the acute phase of infection; termed post-acute sequelae of SARS-CoV-2 infection (PASC), or long COVID. The characteristics, prevalence, trajectory and mechanisms of PASC are ill-defined. The objectives of the Researching COVID to Enhance Recovery (RECOVER) Multi-site Observational Study of PASC in Adults (RECOVER-Adult) are to: (1) characterize PASC prevalence; (2) characterize the symptoms, organ dysfunction, natural history, and distinct phenotypes of PASC; (3) identify demographic, social and clinical risk factors for PASC onset and recovery; and (4) define the biological mechanisms underlying PASC pathogenesis. Methods: RECOVER-Adult is a combined prospective/retrospective cohort currently planned to enroll 14,880 adults aged [≥]18 years. Eligible participants either must meet WHO criteria for suspected, probable, or confirmed infection; or must have evidence of no prior infection. Recruitment occurs at 86 sites in 33 U.S. states, Washington, DC and Puerto Rico, via facility- and community-based outreach. Participants complete quarterly questionnaires about symptoms, social determinants, vaccination status, and interim SARS-CoV-2 infections. In addition, participants contribute biospecimens and undergo physical and laboratory examinations at approximately 0, 90 and 180 days from infection or negative test date, and yearly thereafter. Some participants undergo additional testing based on specific criteria or random sampling. Patient representatives provide input on all study processes. The primary study outcome is onset of PASC, measured by signs and symptoms. A paradigm for identifying PASC cases will be defined and updated using supervised and unsupervised learning approaches with cross-validation. Logistic regression and proportional hazards regression will be conducted to investigate associations between risk factors, onset, and resolution of PASC symptoms. Discussion: RECOVER-Adult is the first national, prospective, longitudinal cohort of PASC among US adults. Results of this study are intended to inform public health, spur clinical trials, and expand treatment options.


Asunto(s)
COVID-19 , Síndrome Respiratorio Agudo Grave
2.
Rachel Gross; Tanayott Thaweethai; Erika B. Rosenzweig; James Chan; Lori B. Chibnik; Mine S. Cicek; Amy J. Elliott; Valerie J. Flaherman; Andrea S. Foulkes; Margot Gage Witvliet; Richard Gallagher; Maria Laura Gennaro; Terry L. Jernigan; Elizabeth W. Karlson; Stuart D. Katz; Patricia A. Kinser; Lawrence C. Kleinman; Michelle F. Lamendola-Essel; Joshua D. Milner; Sindhu Mohandas; Praveen C. Mudumbi; Jane W. Newburger; Kyung E. Rhee; Amy L. Salisbury; Jessica N. Snowden; Cheryl R. Stein; Melissa S. Stockwell; Kelan G. Tantisira; Moriah E. Thomason; Dongngan T. Truong; David Warburton; John C. Wood; Shifa Ahmed; Almary Akerlundh; Akram N. Alshawabkeh; Brett R. Anderson; Judy L. Aschner; Andrew M. Atz; Robin L. Aupperle; Fiona C. Baker; Venkataraman Balaraman; Dithi Banerjee; Deanna M. Barch; Arielle Baskin-Sommers; Sultana Bhuiyan; Marie-Abele C. Bind; Amanda L. Bogie; Natalie C. Buchbinder; Elliott Bueler; Hülya Bükülmez; B.J. Casey; Linda Chang; Duncan B. Clark; Rebecca G. Clifton; Katharine N. Clouser; Lesley Cottrell; Kelly Cowan; Viren D'sa; Mirella Dapretto; Soham Dasgupta; Walter Dehority; Kirsten B. Dummer; Matthew D. Elias; Shari Esquenazi-Karonika; Danielle N. Evans; E. Vincent S. Faustino; Alexander G. Fiks; Daniel Forsha; John J. Foxe; Naomi P. Friedman; Greta Fry; Sunanda Gaur; Dylan G. Gee; Kevin M. Gray; Ashraf S. Harahsheh; Andrew C. Heath; Mary M. Heitzeg; Christina M. Hester; Sophia Hill; Laura Hobart-Porter; Travis K.F. Hong; Carol R. Horowitz; Daniel S. Hsia; Matthew Huentelman; Kathy D. Hummel; William G. Iacono; Katherine Irby; Joanna Jacobus; Vanessa L. Jacoby; Pei-Ni Jone; David C. Kaelber; Tyler J. Kasmarcak; Matthew J. Kluko; Jessica S. Kosut; Angela R. Laird; Jeremy Landeo-Gutierrez; Sean M. Lang; Christine L. Larson; Peter Paul C. Lim; Krista M. Lisdahl; Brian W. McCrindle; Russell J. McCulloh; Alan L. Mendelsohn; Torri D. Metz; Lerraughn M. Morgan; Eva M. Müller-Oehring; Erica R. Nahin; Michael C. Neale; Manette Ness-Cochinwala; Sheila M. Nolan; Carlos R. Oliveira; Matthew E. Oster; Ronald M. Payne; Hengameh Raissy; Isabelle G. Randall; Suchitra Rao; Harrison T. Reeder; Johana M. Rosas; Mark W. Russell; Arash A. Sabati; Yamuna Sanil; Alice I. Sato; Michael S. Schechter; Rangaraj Selvarangan; Divya Shakti; Kavita Sharma; Lindsay M. Squeglia; Michelle D. Stevenson; Jacqueline Szmuszkovicz; Maria M. Talavera-Barber; Ronald J. Teufel; Deepika Thacker; Mmekom M. Udosen; Megan R. Warner; Sara E. Watson; Alan Werzberger; Jordan C. Weyer; Marion J. Wood; H. Shonna Yin; William T. Zempsky; Emily Zimmerman; Benard P. Dreyer; - RECOVER Initiative.
medrxiv; 2023.
Preprint en Inglés | medRxiv | ID: ppzbmed-10.1101.2023.04.27.23289228

RESUMEN

Importance: The prevalence, pathophysiology, and long-term outcomes of COVID-19 (post-acute sequelae of SARS-CoV-2 [PASC] or "Long COVID") in children and young adults remain unknown. Studies must address the urgent need to define PASC, its mechanisms, and potential treatment targets in children and young adults. Observations: We describe the protocol for the Pediatric Observational Cohort Study of the NIHs REsearching COVID to Enhance Recovery (RECOVER) Initiative. RECOVER-Pediatrics is an observational meta-cohort study of caregiver-child pairs (birth through 17 years) and young adults (18 through 25 years), recruited from more than 100 sites across the US. This report focuses on two of five cohorts that comprise RECOVER-Pediatrics: 1) a de novo RECOVER prospective cohort of children and young adults with and without previous or current infection; and 2) an extant cohort derived from the Adolescent Brain Cognitive Development (ABCD) study (n=10,000). The de novo cohort incorporates three tiers of data collection: 1) remote baseline assessments (Tier 1, n=6000); 2) longitudinal follow-up for up to 4 years (Tier 2, n=6000); and 3) a subset of participants, primarily the most severely affected by PASC, who will undergo deep phenotyping to explore PASC pathophysiology (Tier 3, n=600). Youth enrolled in the ABCD study participate in Tier 1. The pediatric protocol was developed as a collaborative partnership of investigators, patients, researchers, clinicians, community partners, and federal partners, intentionally promoting inclusivity and diversity. The protocol is adaptive to facilitate responses to emerging science. Conclusions and Relevance: RECOVER-Pediatrics seeks to characterize the clinical course, underlying mechanisms, and long-term effects of PASC from birth through 25 years old. RECOVER-Pediatrics is designed to elucidate the epidemiology, four-year clinical course, and sociodemographic correlates of pediatric PASC. The data and biosamples will allow examination of mechanistic hypotheses and biomarkers, thus providing insights into potential therapeutic interventions.


Asunto(s)
COVID-19 , Trastornos del Conocimiento
3.
medrxiv; 2022.
Preprint en Inglés | medRxiv | ID: ppzbmed-10.1101.2022.02.07.21268280

RESUMEN

Multisystem inflammatory syndrome in children (MIS-C) is a novel disease identified during the COVID-19 pandemic characterized by systemic inflammation following SARS-CoV-2 infection. Delays in diagnosing MIS-C may lead to more severe disease with cardiac dysfunction or death. Most pediatric patients recover fully with anti-inflammatory treatments, but early detection of MIS-C remains a challenge given its clinical similarities to Kawasaki disease (KD) and other acute childhood illnesses. We present KIDMATCH (KawasakI Disease vs Multisystem InflAmmaTory syndrome in CHildren), a deep learning algorithm for screening patients for MIS-C, KD, or other febrile illness. KIDMATCH incorporates a conformal prediction framework to tag patients with erroneous data or distribution shifts, enhancing the model generalizability and confidence by flagging unfamiliar cases as indeterminate instead of making spurious predictions. Using routinely collected clinical and laboratory data, KIDMATCH achieved a high area under the curve [0.95-0.98]. Additional external validation of this model on MIS-C patients from 16 hospitals across the United States achieved a positive detection rate of over 90%. Our algorithm has the potential to aid frontline clinicians with distinguishing between MIS-C, KD, and similar febrile illnesses in a timely manner to allow prompt treatment and prevent severe complications.


Asunto(s)
Síndromes Periódicos Asociados a Criopirina , Síndrome Mucocutáneo Linfonodular , Fiebre , Discapacidades para el Aprendizaje , Muerte , COVID-19 , Cardiopatías , Inflamación
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