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Dive into the research topics where Paula Aristizabal is active.

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Featured researches published by Paula Aristizabal.


Pediatric Blood & Cancer | 2015

Participation in pediatric oncology research protocols: Racial/ethnic, language and age-based disparities

Paula Aristizabal; Jenelle Singer; Renee Cooper; Kristen J. Wells; Jesse Nodora; Mehrzad Milburn; Sheila Gahagan; Deborah Schiff; Maria Elena Martinez

Survival rates in pediatric oncology have improved dramatically, in part due to high patient participation in clinical trials. Although racial/ethnic inequalities in clinical trial participation have been reported in adults, pediatric data and studies comparing participation rates by socio‐demographic characteristics are scarce. The goal of this study was to assess differences in research protocol participation for childhood cancer by age, sex, race/ethnicity, parental language, cancer type, and insurance status.


Hepatology | 2015

Temporal dynamics of inflammatory cytokines/chemokines during sofosbuvir and ribavirin therapy for genotype 2 and 3 hepatitis C infection

Aaron F. Carlin; Paula Aristizabal; Qinghua Song; Huan Wang; Matthew Paulson; Luisa M. Stamm; Robert T. Schooley; David L. Wyles

The analysis of inflammatory cytokines and chemokines produced during hepatitis C virus (HCV) infection has advanced our understanding of viral‐host interactions and identified predictors of treatment response. Administration of interferons (IFNs) made it difficult to interpret biomarkers of immune activation during treatment. Direct‐acting antiviral (DAA) regimens without IFN are now being used to treat HCV with excellent efficacy. To gain insight into HCV‐host interactions occurring before, during, and after HCV treatment, we performed a case‐control study that measured serial plasma levels of IFN‐γ‐inducible protein 10 (IP‐10), monocyte chemoattractant protein 1 (MCP‐1), macrophage inflammatory protein 1 beta (MIP‐1β), and interleukin‐18 (IL‐18) in 131 patients with chronic HCV treated with sofosbuvir (SOF) plus ribavirin (RBV). A linear regression analysis using baseline factors identified strong positive associations between elevated alanine aminotransferase and pretreatment IP‐10 and between the presence of cirrhosis and elevated pretreatment IL‐18. Mean IP‐10, MCP‐1, MIP‐1β, and IL‐18 levels all decline on therapy, but display different dynamics late in treatment and after cessation of therapy. On treatment, IP‐10 and MIP‐1β levels were significantly higher in individuals who achieved sustained virological response (SVR). Logistic regression analyses examining treatment response in all patients demonstrated significant associations between higher baseline MIP‐1β levels and smaller decreases in MIP‐1β early in treatment and SVR. Higher early MIP‐1β levels were also significantly associated with SVR in subsets of patients with cirrhosis and individuals with genotype 3 (GT3) infection, two factors associated with decreased responsiveness to treatment. Conclusion: Changes in IP‐10 levels mirror HCV RNA, suggesting that IP‐10 is an indicator of innate immune viral recognition. MIP‐1β levels remain elevated in GT2/3 patients who achieved SVR, suggesting differential immune activation in those who respond to SOF/RBV therapy and a potential role in predicting treatment responses. (Hepatology 2015;62:1047‐1058)


American Journal of Infection Control | 2016

The Centers for Disease Control and Prevention definition of mucosal barrier injury-associated bloodstream infection improves accurate detection of preventable bacteremia rates at a pediatric cancer center in a low- to middle-income country

Dara Torres; Miriam L. González; Adriana Loera; Marco Aguilera; George Relyea; Paula Aristizabal; Miguela Caniza

BACKGROUND The US National Healthcare Safety Network has provided a definition of mucosal barrier injury-associated, laboratory-confirmed bloodstream infection (MBI-LCBI) to improve infection surveillance. To date there is little information about its influence in pediatric oncology centers in low- to middle-income countries. OBJECTIVES To determine the influence of the definition on the rate of central line-associated bloodstream infection (CLABSI) and compare the clinical characteristics of MBI versus non-MBI LCBI cases. METHODS We retrospectively applied the National Healthcare Safety Network definition to all CLABSIs recorded at a pediatric oncology center in Tijuana, Mexico, from January 2011 through December 2014. CLABSI events were reclassified according to the MBI-LCBI definition. Clinical characteristics and outcomes of MBI and non-MBI CLABSIs were compared. RESULTS Of 55 CLABSI events, 44% (24 out of 55) qualified as MBI-LCBIs; all were MBI-LCBI subcategory 1 (intestinal flora pathogens). After the number of MBI-LCBI cases was removed from the numerator, the CLABSI rate during the study period decreased from 5.72-3.22 infections per 1,000 central line days. Patients with MBI-LCBI were significantly younger than non-MBI-LCBI patients (P = .029) and had a significantly greater frequency of neutropenia (100% vs 39%; P = .001) and chemotherapy exposure (87% vs 58%; P = .020) and significantly longer median hospitalization (34 vs 23 days; P = .008). CONCLUSION A substantial proportion of CLABSI events at our pediatric cancer center met the MBI-LCBI criteria. Our results support separate monitoring and reporting of MBI and non-MBI-LCBIs in low- to middle-income countries to allow accurate detection and tracking of preventable (non-MBI) bloodstream infections.


World journal of clinical oncology | 2016

Factors associated with cervical cancer screening in a safety net population

Meredith A. Heberer; Ian K. Komenaka; Jesse S. Nodora; Chiu Hsieh Hsu; Sonal G. Gandhi; Lauren E. Welch; Marcia E. Bouton; Paula Aristizabal; Barry D. Weiss; Maria Elena Martinez

AIM To identify factors associated with Papanicolaou-smear (Pap-smear) cervical cancer screening rates in a safety net population. METHODS From January 2012 to May 2013, the use of Pap-smear was determined for all patients seen at the breast clinic in a safety net hospital. Health literacy assessment was performed using the validated Newest Vital Sign. The records of patients were reviewed to determine if they had undergone Pap-smears for cervical cancer screening. Sociodemographic information was collected included age, education, monthly income, race/ethnicity, employment, insurance status, and primary care provider of the patient. Logistic regression analysis was then performed to determine factors associated with utilization of Pap-smears. Crude and adjusted odds ratios derived from multivariate logistic regression models were calculated as well as the associated 95%CIs and P-values. RESULTS Overall, 39% had Pap-smears in the prior 15 mo, 1377 consecutive women were seen during the study period and their records were reviewed. Significantly more patients with adequate health literacy underwent Pap-smears as compared to those with limited health literacy (59% vs 34%, P < 0.0001). In multivariate analysis, patients with adequate health literacy, younger patients, and those with later age of first live birth were more likely to undergo Pap-smears. Patients whose primary care providers were gynecologists were also significantly more likely to have Pap-smears compared to other specialties (P < 0.0001). Patients younger than 21 years or older than 65 years underwent screening less frequently (11% and 11%, respectively) than those 21-64 years (41%, P < 0.0001). Race, ethnicity, language, and insurance status were not associated with Pap-smear screening rates. CONCLUSION Patient health literacy and primary care physician were associated with Pap-smear utilization. Development of interventions to target low health literacy populations could improve cervical cancer screening.


Frontiers in Public Health | 2015

Improving Pediatric Cancer Care Disparities Across the United States–Mexico Border: Lessons Learned from a Transcultural Partnership between San Diego and Tijuana

Paula Aristizabal; Spencer Fuller; Rebeca Rivera; David H. Beyda; Raul C. Ribeiro; William Roberts

In 2007, the 5-year survival rate for children with acute leukemia in Baja California, Mexico was estimated at 10% (vs. 88% in the United States). In response, stakeholders at St. Jude Children’s Research Hospital, Rady Children’s Hospital San Diego, and the Hospital General de Tijuana (HGT) implemented a transcultural partnership to establish a pediatric oncology program. The aim was to improve clinical outcomes and overall survival for children in Baja California. An initial needs assessment evaluation was performed and a culturally sensitive, comprehensive, 5-year plan was designed and implemented. After six years, healthcare system accomplishments include the establishment of a fully functional pediatric oncology unit with 60 new healthcare providers (vs. five in 2007). Patient outcome improvements include a rise in 5-year survival for leukemia from 10 to 43%, a rise in new cases diagnosed per year from 21 to 70, a reduction in the treatment abandonment rate from 10% to 2%, and a 45% decrease in the infection rate. More than 600 patients have benefited from this program. Knowledge sharing has taken place between teams at the HGT and Rady Children’s Hospital San Diego. Further, one of the most significant outcomes is that the HGT has transitioned into a regional referral center and now mentors other hospitals in Mexico. Our results show that collaborative initiatives that implement long-term partnerships along the United States–Mexico border can effectively build local capacity and reduce the survival gap between children with cancer in the two nations. Long-term collaborative partnerships should be encouraged across other disciplines in medicine to further reduce health disparities across the United States–Mexico border.


Journal of Pediatric Hematology Oncology | 2017

Medulloblastoma With Extensive Nodularity: Tailored Therapy in a Low-resource Setting.

Paula Aristizabal; Luke Burns; Rebeca Rivera-Gomez; Michael L. Levy; William Roberts; John R. Crawford

Treatment for medulloblastoma carries significant risks, particularly in resource-constrained settings. We report a case of a Mexican infant with desmoplastic/nodular medulloblastoma. Given the nature of her tumor, we developed a tailored regimen following subtotal resection to avoid both radiation therapy and the high-dose cisplatin therapy offered at most centers in the United States. The patient is in remission 4 years after the initial diagnosis. This case suggests an alternative treatment plan for this particular tumor variant that accommodates the limited resources of many centers around the world and avoids the risks associated with radiation therapy at a young age.


Pediatric Neurology | 2015

Preoperative Presentation of a Variant of Cerebellar Mutism Syndrome in a Young Boy With Juvenile Pilocytic Astrocytoma

Dillon Y. Chen; Paula Aristizabal; John R. Crawford

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Pediatric Hematology and Oncology | 2018

An overview of disparities in childhood cancer: Report on the Inaugural Symposium on Childhood Cancer Health Disparities, Houston, Texas, 2016

Michael E. Scheurer; Philip J. Lupo; Joachim Schüz; Logan G. Spector; Joseph L. Wiemels; Richard Aplenc; M. Monica Gramatges; Joshua D. Schiffman; Maria S. Pombo-de-Oliveira; Jun Yang; Julia E. Heck; Catherine Metayer; Manuela A. Orjuela-Grimm; Kira Bona; Paula Aristizabal; Mary T. Austin; Karen R. Rabin; Heidi V. Russell; David G. Poplack

e see front matter 2015 Elsevier Inc. All rights reserved. http://dx.doi.org/10.1016/j.pediatrneurol.2015.06.001 with subacute hydrocephalus; an urgent ventriculoperitoneal shunt placement did not relieve his symptoms. His examination revealed bilateral papilledema and delayed visual fixation flaccid hypotonia of bilateral upper and lower extremities, and a positive Babinski sign. Contrast-enhanced magnetic resonance imaging showed a large primarily cystic peripherally enhancing mass in the posterior fossa with


Pediatric Blood & Cancer | 2017

Addressing regional disparities in pediatric oncology: Results of a collaborative initiative across the Mexican-North American border.

Paula Aristizabal; Spencer Fuller; Rebeca Rivera-Gomez; Mario Ornelas; Laura Nuno; Carlos Rodriguez-Galindo; Raul C. Ribeiro; William Roberts

ABSTRACT The Inaugural Symposium on Childhood Cancer Health Disparities was held in Houston, Texas, on November 2, 2016. The symposium was attended by 109 scientists and clinicians from diverse disciplinary backgrounds with interests in pediatric cancer disparities and focused on reviewing our current knowledge of disparities in cancer risk and outcomes for select childhood cancers. Following a full day of topical sessions, everyone participated in a brainstorming session to develop a working strategy for the continued expansion of research in this area. This meeting was designed to serve as a springboard for examination of childhood cancer disparities from a more unified and systematic approach and to enhance awareness of this area of need.


Cancer Epidemiology, Biomarkers & Prevention | 2015

Abstract B33: Who am I? Improving quality of data collection for race/ethnicity and language

Paula Aristizabal; Foyinsola Ani; Erica Del Muro; Teresa Cassidy; William Roberts; Erin Stucky-Fisher; Maria Elena Martinez

Cancer is emerging as a major cause of childhood mortality in low‐ and middle‐income countries. In Mexico, cancer is the number one cause of death in children aged 5–14. Until recently, many children with cancer from Baja California, Mexico, went untreated. We reasoned that an initiative inspired by the St. Jude Childrens Research Hospital (SJCRH) “twinning” model could successfully be applied to the San Diego–Tijuana border region. In 2008, a twinning project was initiated by Rady Childrens Hospital, SJCRH, and the General Hospital Tijuana (GHT). Our aim was to establish a pediatric oncology unit in a culturally sensitive manner, adapted to the local healthcare system.

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Raul C. Ribeiro

St. Jude Children's Research Hospital

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Rebeca Rivera-Gomez

Autonomous University of Baja California

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Deborah Schiff

University of California

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Erica Del Muro

Boston Children's Hospital

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Foyinsola Ani

San Diego State University

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