Jorge Armando Egurrola-Pedraza

Dr. Jorge Armando Egurrola-Pedraza

orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2017 in International Journal of Infectious Diseases
Verified
Journal Article
Open access
MCMabel Carabali
Mabel Carabali
JLJacqueline Kyungah Lim
Jacqueline Kyungah Lim
DVDiana Carolina Velez
Diana Carolina Velez
ATAndrea Trujillo
Andrea Trujillo
JEJorge Armando Egurrola-Pedraza
Jorge Armando Egurrola-Pedraza
JOJorge E. Osorio
Jorge E. Osorio
Dengue is an important public health problem worldwide. A vaccine has recently been licensed in some countries of Latin America and Asia. Recommendations for dengue vaccine introduction include endemicity and a high serological prevalence of dengue in the territories considering its introduction. A community-based survey was conducted to estimate dengue seroprevalence and age-specific seroconversion rates in a community in Medellin, Colombia, using a dengue serological test (IgG indirect ELISA). Residents were selected at random and were first screened for dengue infection; they were then followed over 2.5 years. A total of 3684 individuals aged between 1 and 65 years participated in at least one survey. The overall dengue seroprevalence was 61%, and only 3.3% of seropositive subjects self-reported a past history of dengue. Among dengue virus (DENV)-naïve subjects with more than two visits (n=1002), the overall seroconversion rate was 8.7% (95% confidence interval 7.3-10.4) per 1000 person-months, over the study period. Overall, the mean age of DENV prevalent subjects was significantly higher than the mean age of seroconverted subjects. Specifically, DENV seropositivity over 70% was observed in participants over 21 years old. Serotype-specific plaque-reduction neutralization tests (PRNT) revealed that all four dengue serotypes were circulating, with DENV4 being most prevalent. These laboratory-based findings could inform dengue vaccine decisions, as they provide age-specific seroprevalence and seroconversion data, evidencing permanent and ongoing dengue transmission in the study area. This study provides evidence for the existing rates of secondary and heterotypic responses, presenting a challenge that must be addressed adequately by the new vaccine candidates.

1 November 2020 in JCO Global Oncology
Verified
Journal Article
Open access
AAAdriana Alméciga
Adriana Alméciga
JRJuliana Rodriguez
Juliana Rodriguez
JBJulián Beltrán
Julián Beltrán
JSJames Sáenz
James Sáenz
AMAbel Merchán
Abel Merchán
RPRené Pareja
René Pareja
PURPOSE: Locally advanced cervical cancer may present with uncontrollable vaginal bleeding in up to 70% of cases. Pelvic vessel embolization has been used as an urgent maneuver for achieving fast hemostatic control. This report describes outcomes of selective pelvic vessel embolization in patients with severe bleeding due to a locally advanced cervical cancer. METHODS: In this retrospective study, technical aspects, clinical variables, and bleeding-related morbidity were described. The frequency of recurrent disease and the vital status at 1 year of follow-up were determined. Analysis was performed with statistical software R, version 3.6.2. The setting was Instituto Nacional de Cancerología- Bogotá, Colombia, between January 2009 and July 2017. RESULTS: A total of 47 patients were included. Median age was 44 years (range, 26-70 years). The pre-embolization median hemoglobin level was 7.9 g/dL (range, 5.0-11.3 g/dL). Blood transfusions were administered to 41 women (87.2%). Bleeding control was achieved in 95.7% of cases in the first 24 hours after the embolization. There were no major complications. In 17 cases (36.2%), minor complications were reported; the most common was pelvic pain. In 17.1% of cases, a second embolization was required. After 12 months of follow-up, 27.7% of patients were alive without disease, 44.7% were alive with disease, and 25.5% of them have died of cervical cancer progression. CONCLUSION: Selective pelvic vessel embolization is a useful alternative in patients with locally advanced cervical cancer and life-threatening bleeding. Its impact on recurrent disease and death due to oncologic cause is not clear.

2 July 2020 in BMC Infectious Diseases
Verified
Journal Article
Open access
PDF file
JLJacqueline Kyungah Lim
Jacqueline Kyungah Lim
MCMabel Carabali
Mabel Carabali
ECErwin Camacho
Erwin Camacho
DVDiana Carolina Velez
Diana Carolina Velez
ATAndrea Trujillo
Andrea Trujillo
JOJorge E. Osorio
Jorge E. Osorio
Background: Dengue fever is a major public health problem in Colombia. A fever surveillance study was conducted for evaluation of the clinical, epidemiological, and molecular patterns of dengue, prior to Chikungunya and Zika epidemics. Methods: In November 2011–February 2014, a passive facility-based surveillance was implemented in Santa Cruz Hospital, Medellin, and enrolled eligible febrile patients between 1 and 65 years-of-age. Acute and convalescent blood samples were collected 10–21 days apart and tested for dengue using IgM/IgG ELISA. RNA was extracted for serotyping using RT-PCR on acute samples and genotyping was performed by sequencing. Results: Among 537 febrile patients enrolled during the study period, 29% (n = 155) were identified to be dengue-positive. Only 7% of dengue cases were hospitalized, but dengue-positive patients were 2.6 times more likely to be hospitalized, compared to non-dengue cases, based on a logistic regression. From those tested with RT-PCR (n = 173), 17 were dengue-confirmed based on PCR and/or virus isolation showing mostly DENV-3 (n = 9) and DENV-4 (n = 7) with 1 DENV-1. Genotyping results showed that: DENV-1 isolate belongs to the genotype V or American/African genotype; DENV-3 isolates belong to genotype III; and DENV-4 isolates belong to the II genotype and specifically to the IIb sub-genotype or linage. Conclusions: Our surveillance documented considerable dengue burden in Santa Cruz comuna during non-epidemic years, and genetic diversity of circulating DENV isolates, captured prior to Chikungunya epidemic in 2014 and Zika epidemic in 2015. Our study findings underscore the need for continued surveillance and monitoring of dengue and other arboviruses and serve as epidemiological and molecular evidence base for future studies to assess changes in DENV transmission in Medellin, given emerging and re-emerging arboviral diseases in the region.

1 January 2018 in Cadernos de Saude Publica
Verified
Journal Article
Open access
PDF file
JEJorge Armando Egurrola-Pedraza
Jorge Armando Egurrola-Pedraza
LGLuis Rodolfo Gómez-Wolff
Luis Rodolfo Gómez-Wolff
COCarlos Andrés Ossa-Gómez
Carlos Andrés Ossa-Gómez
VSViviana Sánchez-Jiménez
Viviana Sánchez-Jiménez
FHFernando Herazo-Maya
Fernando Herazo-Maya
HGHéctor Iván García-García
Héctor Iván García-García
El objetivo fue estimar el efecto del aseguramiento en salud sobre la supervivencia global y libre de enfermedad en pacientes con cáncer de mama. La muestra se compuso de mujeres operadas en el Instituto de Cancerología, Medellín, Colombia, con datos del registro institucional. Las variables se compararon entre régimen subsidiado y contributivo com chi cuadrado test (χ2) o test t de Student, método de Kaplan-Meier y prueba de rangos logarítmicos (log-rank test). La variable de interés se ajustó con una regresión de Cox. Se incluyeron 2.732 pacientes con mediana de seguimiento de 36 meses. Del régimen contributivo murieron el 10% y del régimen subsidiado murieron 23%. Hubo diferencias en tiempos de acceso a tratamiento (régimen contributivo: 52 vs. régimen subsidiado: 112 días, p < 0,05). Supervivencia libre de enfermedad y supervivencia global fueron mejores en régimen contributivo que en régimen subsidiado (p < 0,05); supervivencia global depende de variables del tumor y del tratamiento. Supervivencia global y supervivencia libre de enfermedad y tiempos de acceso para atención y diagnóstico en etapa temprana fueron mejores en régimen contributivo que en régimen subsidiado.

15 September 2014 in Acta Biológica Colombiana
Verified
Journal Article
Open access
EBEduar Elías Bejarano
Eduar Elías Bejarano
SUSandra I. Uribe-Soto
Sandra I. Uribe-Soto
APAlveiro Pérez-Doria
Alveiro Pérez-Doria
JEJorge Armando Egurrola-Pedraza
Jorge Armando Egurrola-Pedraza
JDJuan Carlos Dib
Juan Carlos Dib
CPCharles Poter
Charles Poter

9 February 2023 in Journal of Investigative Medicine
Verified
Journal Article
Closed access
MLMauricio Luján
Mauricio Luján
MLMauricio Lema
Mauricio Lema
BPBeatriz Preciado
Beatriz Preciado
CLCamila Lema
Camila Lema
JEJorge Armando Egurrola-Pedraza
Jorge Armando Egurrola-Pedraza
DMDiego Morán
Diego Morán
Nivolumab is a human programmed death receptor-1 blocking antibody, used as treatment option in patients with advanced non-small-cell lung cancer (NSCLC). We assessed the nivolumab efficacy in terms of survival and response to treatment as second-line (2L) or third-line (3L) therapy in patients with advanced NSCLC. This is a multicentric observational study. Data of patients with advanced NSCLC who received nivolumab as 2L or 3L treatment were analyzed retrospectively. Information regarding patient demographics and clinical backgrounds, treatment patterns from diagnosis to post-nivolumab treatment, effectiveness, and safety of nivolumab treatment were collected. The outcomes evaluated were overall survival (OS), progression-free survival (PFS), and objective response rate (ORR) to treatment. OS and PFS were estimated with the Kaplan–Meier method and the differences were evaluated through the log-rank test. Data of 178 patients were included. The median follow-up was 26.8 months (interquartile range (IQR): 20.3–40.4). Nivolumab was commonly used as a 2L treatment (77.5%). The outcomes in this setting (2L) were as follows: ORR was 21.0%, and the median PFS and OS were 5.5 months (95% confidence interval (CI): 4.5–6.5) and 12.4 months (95% CI: 10.8–14.0), respectively. In 3L, the ORR with nivolumab was 15.0%, the median PFS and OS were 4.1 months (95% CI: 3.1–5.1) and 10.1 months (95% CI: 9.4–10.6), respectively. Three patients (1.7%) required discontinuation due to toxicity. Nivolumab effectiveness and safety in this scenario was consistent with that reported by previous trials and other real-world data.