Resultados perinatales en gestantes diabéticas en instituciones prestadoras de servicios en salud de la ciudad de Bogotá
Objetivo: Evaluar los desenlaces perinatales en gestantes con diabetes gestacional (DG) según el tipo de tratamiento recibido (dieta, metformina o insulina) en cuatro instituciones de salud de Bogotá, Colombia. Materiales y métodos: Estudio de cohortes prospectivo. Se incluyeron gestantes con DG dia...
- Autores:
-
Fuentes Obando, Lina Paola
- Tipo de recurso:
- https://purl.org/coar/resource_type/c_7a1f
- Fecha de publicación:
- 2025
- Institución:
- Universidad El Bosque
- Repositorio:
- Repositorio U. El Bosque
- Idioma:
- spa
- OAI Identifier:
- oai:repositorio.unbosque.edu.co:20.500.12495/15615
- Acceso en línea:
- https://hdl.handle.net/20.500.12495/15615
- Palabra clave:
- Diabetes
Gestacional
Insulina
Metformina
Dieta
Gestational
Diabetes
Diet
Metformin
Insulin
WQ 200
- Rights
- closedAccess
- License
- Acceso cerrado
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Resultados perinatales en gestantes diabéticas en instituciones prestadoras de servicios en salud de la ciudad de Bogotá |
| dc.title.translated.none.fl_str_mv |
Perinatal Outcomes in Diabetic Pregnant Women in Health Care Institutions in Bogotá |
| title |
Resultados perinatales en gestantes diabéticas en instituciones prestadoras de servicios en salud de la ciudad de Bogotá |
| spellingShingle |
Resultados perinatales en gestantes diabéticas en instituciones prestadoras de servicios en salud de la ciudad de Bogotá Diabetes Gestacional Insulina Metformina Dieta Gestational Diabetes Diet Metformin Insulin WQ 200 |
| title_short |
Resultados perinatales en gestantes diabéticas en instituciones prestadoras de servicios en salud de la ciudad de Bogotá |
| title_full |
Resultados perinatales en gestantes diabéticas en instituciones prestadoras de servicios en salud de la ciudad de Bogotá |
| title_fullStr |
Resultados perinatales en gestantes diabéticas en instituciones prestadoras de servicios en salud de la ciudad de Bogotá |
| title_full_unstemmed |
Resultados perinatales en gestantes diabéticas en instituciones prestadoras de servicios en salud de la ciudad de Bogotá |
| title_sort |
Resultados perinatales en gestantes diabéticas en instituciones prestadoras de servicios en salud de la ciudad de Bogotá |
| dc.creator.fl_str_mv |
Fuentes Obando, Lina Paola |
| dc.contributor.advisor.none.fl_str_mv |
Romero Infante , Ximena Carolina Sarmiento , Diana Piedad Uriel Calvo, María Montserrat Gómez Cruz , Melissa De la Hoz-Valle , José Antonio Bastidas, Karina Bonilla, Leonardo Sánchez, Sandra Beltrán, Sandra Sarmiento, Andrés Barón , Germán Reyes Skinner, Carolina Gonzalez, Ricardo Reyes , Guillermo |
| dc.contributor.author.none.fl_str_mv |
Fuentes Obando, Lina Paola |
| dc.subject.none.fl_str_mv |
Diabetes Gestacional Insulina Metformina Dieta |
| topic |
Diabetes Gestacional Insulina Metformina Dieta Gestational Diabetes Diet Metformin Insulin WQ 200 |
| dc.subject.keywords.none.fl_str_mv |
Gestational Diabetes Diet Metformin Insulin |
| dc.subject.nlm.none.fl_str_mv |
WQ 200 |
| description |
Objetivo: Evaluar los desenlaces perinatales en gestantes con diabetes gestacional (DG) según el tipo de tratamiento recibido (dieta, metformina o insulina) en cuatro instituciones de salud de Bogotá, Colombia. Materiales y métodos: Estudio de cohortes prospectivo. Se incluyeron gestantes con DG diagnosticada según los criterios de la Asociación Internacional de Grupos de Estudio sobre Diabetes y Embarazo (IADPSG) y Carpenter y Coustan. Se recolectaron variables sociodemográficas, obstétricas y desenlaces materno-perinatales. Se aplicaron pruebas de Chi-cuadrado, test exacto de Fisher y Kruskal-Wallis. Se construyó un modelo de regresión logística multivariado para identificar predictores de desenlaces perinatales adversos (p < 0,05). Resultados: Se analizaron 385 gestantes, 92.7% completó el seguimiento. Al ingreso, 42.9% recibió dieta, 27.5% metformina y 29.6% insulina. El control metabólico adecuado fue más frecuente con insulina (90.0%; p = 0.018). Se observó mayor frecuencia de ingreso a UCIN (41.4%) y SDRA (25.9%) en el grupo insulina. En el modelo ajustado, aumentaron el riesgo de desenlaces adversos: insulina (OR: 14.86) , metformina (OR: 5.11), preeclampsia (OR: 2.34), fetopatía diabética (OR: 3.78) y menor peso fetal (OR: 0.99). El tratamiento instaurado al parto fue protector (metformina OR: 0.18; insulina OR: 0.11). AUC: 0.783; sensibilidad: 64.8%; especificidad: 75.5%. Conclusiones: La frecuencia de desenlaces maternos y perinatales en mujeres con DG varió según la estrategia terapéutica. La insulina se asoció con mejor control glucémico pero mayor riesgo perinatal. La preeclampsia, signos ecográficos de fetopatía diabética, menor peso fetal al nacer y la instauración temprana de tratamiento farmacológico fueron predictores de desenlace perinatal adverso. |
| publishDate |
2025 |
| dc.date.accessioned.none.fl_str_mv |
2025-07-31T20:18:03Z |
| dc.date.available.none.fl_str_mv |
2025-07-31T20:18:03Z |
| dc.date.issued.none.fl_str_mv |
2025-07 |
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http://purl.org/coar/resource_type/c_7a1f |
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Tesis/Trabajo de grado - Monografía - Especialización |
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https://purl.org/coar/resource_type/c_7a1f |
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info:eu-repo/semantics/bachelorThesis |
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https://hdl.handle.net/20.500.12495/15615 |
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instname:Universidad El Bosque |
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London: National Institute for Health and Care Excellence (NICE); 2020 Dec 16. (NICE Guideline, No. 3.) Disponible en: https://www.ncbi.nlm.nih.gov/books/NBK555331/ 49. Sweeting A, Hannah W, Backman H, Catalano P, Feghali M, Herman WH, et al. Epidemiology and management of gestational diabetes. Lancet [Internet]. 2024;404(10448):175–92. Disponible en: http://dx.doi.org/10.1016/S0140- 6736(24)00825-0 50. Bethune M, Bell R. Evaluation of the measurement of the fetal fat layer, interventricular septum and abdominal circumference percentile in the prediction of macrosomia in pregnancies affected by gestational diabetes: Prediction of macrosomia in gestational diabetes. Ultrasound Obstet Gynecol [Internet]. 2003;22(6):586–90. Disponible en: http://dx.doi.org/10.1002/uog.885 51. Declaración de Helsinki de la AMM – Principios éticos para las investigaciones médicas con participantes humanos [Internet]. Wma.net. [citado el 11 de junio de 2025]. Disponible en: https://www.wma.net/es/policies-post/declaracion-de- helsinki-de-la-amm-principios-eticos-para-las-investigaciones-medicas-en-seres- humanos/ 52. Ley 1581 de 2012 - Gestor Normativo [Internet]. Gov.co. [citado el 11 de junio de 2025]. Disponible en: https://www.funcionpublica.gov.co/eva/gestornormativo/norma.php?i=49981 53. Ovesen PG, Jensen DM, Damm P, Rasmussen S, Kesmodel US. Maternal and neonatal outcomes in pregnancies complicated by gestational diabetes. a nation-wide study. J Matern Fetal Neonatal Med [Internet]. 2015;28(14):1720–4. Disponible en: http://dx.doi.org/10.3109/14767058.2014.966677 54. Ye W, Luo C, Huang J, Li C, Liu Z, Liu F. Gestational diabetes mellitus and adverse pregnancy outcomes: systematic review and meta-analysis. BMJ [Internet]. 2022;377:e067946. Disponible en: http://dx.doi.org/10.1136/bmj-2021-067946 55. Koren R, Hochman Y, Koren S, Ziv-Baran T, Wiener Y. Insulin treatment of patients with gestational diabetes: does dosage play a role? J Matern Fetal Neonatal Med [Internet]. 2022;35(5):914–20. Disponible en: http://dx.doi.org/10.1080/14767058.2020.1733523 56. Kong L, Nilsson IAK, Gissler M, Lavebratt C. Associations of maternal diabetes and body mass index with offspring birth weight and prematurity. JAMA Pediatr [Internet]. 2019;173(4):371–8. Disponible en: http://dx.doi.org/10.1001/jamapediatrics.2018.5541 57. Hedderson MM, Ferrara A, Sacks DA. Gestational diabetes mellitus and lesser degrees of pregnancy hyperglycemia: association with increased risk of spontaneous preterm birth. Obstet Gynecol [Internet]. 2003;102(4):850–6. Disponible en: http://dx.doi.org/10.1016/s0029-7844(03)00661-6 58. Suksai M, Geater A, Amornchat P, Suntharasaj T, Suwanrath C, Pruksanusak N. Preeclampsia and timing of delivery: Disease severity, maternal and perinatal outcomes. Pregnancy Hypertens [Internet]. 2024;37(101151):101151. Disponible en: http://dx.doi.org/10.1016/j.preghy.2024.101151 59. Madden JV, Flatley CJ, Kumar S. Term small-for-gestational-age infants from low risk women are at significantly greater risk of adverse neonatal outcomes. Am J Obstet Gynecol [Internet]. 2018;218(5):525.e1-525.e9. Disponible en: http://dx.doi.org/10.1016/j.ajog.2018.02.008 60. Tarry-Adkins JL, Ozanne SE, Aiken CE. Impact of metformin treatment during pregnancy on maternal outcomes: a systematic review/meta-analysis. Sci Rep [Internet]. 2021;11(1):9240. Disponible en: http://dx.doi.org/10.1038/s41598-021- 88650-5 |
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Romero Infante , Ximena CarolinaSarmiento , Diana PiedadUriel Calvo, María MontserratGómez Cruz , MelissaDe la Hoz-Valle , José AntonioBastidas, KarinaBonilla, LeonardoSánchez, SandraBeltrán, SandraSarmiento, AndrésBarón , GermánReyes Skinner, CarolinaGonzalez, RicardoReyes , GuillermoFuentes Obando, Lina Paola2025-07-31T20:18:03Z2025-07-31T20:18:03Z2025-07https://hdl.handle.net/20.500.12495/15615instname:Universidad El Bosquereponame:Repositorio Institucional Universidad El Bosquerepourl:https://repositorio.unbosque.edu.coObjetivo: Evaluar los desenlaces perinatales en gestantes con diabetes gestacional (DG) según el tipo de tratamiento recibido (dieta, metformina o insulina) en cuatro instituciones de salud de Bogotá, Colombia. Materiales y métodos: Estudio de cohortes prospectivo. Se incluyeron gestantes con DG diagnosticada según los criterios de la Asociación Internacional de Grupos de Estudio sobre Diabetes y Embarazo (IADPSG) y Carpenter y Coustan. Se recolectaron variables sociodemográficas, obstétricas y desenlaces materno-perinatales. Se aplicaron pruebas de Chi-cuadrado, test exacto de Fisher y Kruskal-Wallis. Se construyó un modelo de regresión logística multivariado para identificar predictores de desenlaces perinatales adversos (p < 0,05). Resultados: Se analizaron 385 gestantes, 92.7% completó el seguimiento. Al ingreso, 42.9% recibió dieta, 27.5% metformina y 29.6% insulina. El control metabólico adecuado fue más frecuente con insulina (90.0%; p = 0.018). Se observó mayor frecuencia de ingreso a UCIN (41.4%) y SDRA (25.9%) en el grupo insulina. En el modelo ajustado, aumentaron el riesgo de desenlaces adversos: insulina (OR: 14.86) , metformina (OR: 5.11), preeclampsia (OR: 2.34), fetopatía diabética (OR: 3.78) y menor peso fetal (OR: 0.99). El tratamiento instaurado al parto fue protector (metformina OR: 0.18; insulina OR: 0.11). AUC: 0.783; sensibilidad: 64.8%; especificidad: 75.5%. Conclusiones: La frecuencia de desenlaces maternos y perinatales en mujeres con DG varió según la estrategia terapéutica. La insulina se asoció con mejor control glucémico pero mayor riesgo perinatal. La preeclampsia, signos ecográficos de fetopatía diabética, menor peso fetal al nacer y la instauración temprana de tratamiento farmacológico fueron predictores de desenlace perinatal adverso.Hospital Universitario Clínica San RafaelCentro Policlínico del OlayaObgyn – Centro Diagnóstico Para La MujerSubred Sur Occidente de KennedyEspecialista en Medicina Materno-FetalEspecializaciónObjective: To evaluate perinatal outcomes in pregnant women with gestational diabetes (GD) according to the type of treatment received (diet, metformin, or insulin) in four healthcare institutions in Bogotá, Colombia. Materials and methods: Prospective cohort study. Pregnant women with GD were included based on the diagnostic criteria of the International Association of Diabetes and Pregnancy Study Groups (IADPSG) and Carpenter and Coustan. Sociodemographic, obstetric, and maternal-perinatal outcome variables were collected. Statistical analyses included Chi-square test, Fisher's exact test, and Kruskal-Wallis test. A multivariable logistic regression model was constructed to identify predictors of adverse perinatal outcomes (p < 0.05). Results: A total of 385 pregnant women were analyzed; 92.7% completed follow-up. At inclusion, 42.9% received dietary management, 27.5% metformin, and 29.6% insulin. Adequate metabolic control was more frequent in the insulin group (90.0%; p = 0.018). Admission to NICU (41.4%) and neonatal respiratory distress syndrome (NRDS, 25.9%) were more frequent in the insulin group. In the adjusted model, the following were associated with increased risk of adverse outcomes: insulin (OR: 14.86), metformin (OR: 5.11), preeclampsia (OR: 2.34), sonographic signs of diabetic fetopathy (OR: 3.78), and lower birthweight (OR: 0.99). Pharmacological treatment initiated at delivery was protective (metformin OR: 0.18; insulin OR: 0.11). AUC: 0.783; sensitivity: 64.8%; specificity: 75.5%. Conclusions: The frequency of maternal and perinatal outcomes in women with GD varied by treatment strategy. Insulin was associated with better glycemic control but higher perinatal risk. 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