Evidence map›Paper›PMID 37433316›Full record

ArticleThe Lancet. Oncology2023

Effect of paediatric early warning systems (PEWS) implementation on clinical deterioration event mortality among children with cancer in resource-limited hospitals in Latin America: a prospective, multicentre cohort study.

Asya Agulnik, Hilmarie Muniz-Talavera, Linh T D Pham, Yichen Chen, Angela K Carrillo, Adolfo Cárdenas-Aguirre, Alejandra Gonzalez Ruiz, Marcela Garza, Tania Maria Conde Morelos Zaragoza, Dora Judith Soberanis Vasquez and 39 more

Abstract readMulticenter Study
In one paragraph

Article in The Lancet. Oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 3 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

49 authors.

Asya AgulnikSt Jude Children's Research Hospital, Memphis, TN, USA. Electronic address: asya.agulnik@stjude.org.
Hilmarie Muniz-TalaveraSt Jude Children's Research Hospital, Memphis, TN, USA.
Linh T D PhamSt Jude Children's Research Hospital, Memphis, TN, USA.
Yichen ChenSt Jude Children's Research Hospital, Memphis, TN, USA.
Angela K CarrilloSt Jude Children's Research Hospital, Memphis, TN, USA.
Adolfo Cárdenas-AguirreSt Jude Children's Research Hospital, Memphis, TN, USA.
Alejandra Gonzalez RuizSt Jude Children's Research Hospital, Memphis, TN, USA.
Marcela GarzaSt Jude Children's Research Hospital, Memphis, TN, USA.
Tania Maria Conde Morelos ZaragozaCasa de la Amistad, México City, México.
Dora Judith Soberanis VasquezUnidad Nacional de Oncología Pediátrica, Guatemala City, Guatemala.
Alejandra Méndez-AceitunoUnidad Nacional de Oncología Pediátrica, Guatemala City, Guatemala.
Carlos Acuña-AguirreHospital Dr. Luis Calvo Mackenna, Santiago, Chile.
Yvania Alfonso-CarrerasHospital Saint Damien, Port-Au-Prince, Haiti.
Shillel Yahamy Alvarez ArellanoBenemérito Hospital General con Especialidades "Juan María de Salvatierra", La Paz, México.
Leticia Aradi Andrade SarmientoCentro Médico Nacional Siglo XXI, México City, México.
Rosario BatistaHospital Jose Domingo De Obaldia, Chiriquí, Panama.
Erika Esther Blasco ArriagaSOLCA Guayaquil, Guayaquil, Ecuador.
Patricia CalderonHospital Infantil de Nicaragua, Managua, Nicaragua.
Mayra Chavez RiosHospital del Niño Poblano, Puebla, México.
María Eugenia CostaHospital del Niños de la Santísima Trinidad de Córdoba, Cordoba, Argentina.
Rosdali Díaz-CoronadoInstituto Nacional de Enfermedades Neoplásicas, Lima, Peru.
Ever Amilcar Fing SotoHospital General de Celaya, Celaya, Mexico.
Wendy Cristhyna Gómez GarcíaHospital Infantil Dr. Robert Reid Cabral, Santo Domingo, Dominican Republic.
Martha Herrera AlmanzaHospital Infantil de Especialidades de Chihuahua, Chihuahua, Mexico.
Maria Susana Juarez TobíasHospital Central Dr. Ignacio Morones Prieto, San Luis Potosí, Mexico.
Esmeralda Mercedes León LópezHospital Guillermo Almenara Irigoyen, Lima, Peru.
Norma Araceli López FacundoInstituto de Seguridad Social del Estado de México y Municipios Hospital Materno Infantil, Toluca, Mexico.
Ruth Angelica Martinez SoriaHospital General de Tijuana, Tijuana, Mexico.
Kenia MillerHospital del Niño "Jose Renan Esquivel", Panama, Panama.
Scheybi Teresa Miralda MéndezHospital Escuela, Tegucigalpa, Honduras.
Lupe Nataly Mora RoblesInstituto del Cáncer SOLCA Cuenca, Cuenca, Ecuador.
Natalia Del Carmen Negroe OcampoHospital General Agustin O'Horan, Mérida, Mexico.
Berenice Noriega AcuñaHospital de Especialidades Pediátricas, Tuxtla Gutierrez, Mexico.
Alejandra Osuna GarciaHospital Pediátrico de Sinaloa, Culiacán, Mexico.
Carlos M Pérez AlvaradoCentro Estatal de Cancerología Dr Miguel Dorantes Mesa, Xalapa, Mexico.
Clara Krystal Pérez FerminHospital Infantil Regional Universitario Dr. Arturo Grullón, Santiago, Dominican Republic.
Estuardo Enrique Pineda UrquillaHospital Nacional de Niños Benjamín Bloom, San Salvador, El Salvador.
Carlos Andrés Portilla FigueroaCentro Médico Imbanaco, Cali, Colombia.
Ligia Estefanía Ríos LopezHospital Nacional Edgardo Rebagliati Martins, Lima, Peru.
Jocelyn Rivera MijaresHospital Infantil Teletón de Oncología, Querétaro, Mexico.
Verónica Soto ChávezHospital Civil de Guadalajara, Guadalajara, Mexico.
Jorge Iván Suarez SotoHospital del Niño. Sistema integral para el Desarrollo de la Familia (DIF), Pachuca, Mexico.
Juliana Teixeira CostaHospital Martagão Gesteira, Salvador, Bahía, Brazil.
Isidoro Tejocote RomeroInstitutio Materno Infantil del Estado de México-IMIEM, Toluca, Mexico.
Erika Elena Villanueva HoyosHospital Oncológico Solca Núcleo de Quito, Quito, Ecuador.
Marielba Villegas PachecoCentro Estatal de Oncología, Campeche, Mexico.
Meenakshi DevidasSt Jude Children's Research Hospital, Memphis, TN, USA.
Carlos Rodriguez-GalindoSt Jude Children's Research Hospital, Memphis, TN, USA.
EVAT Study Group

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
NCI NIH HHS P30 CA021765
6 · The paper itself

Abstract

backgroundPaediatric early warning systems (PEWS) aid in the early identification of clinical deterioration events in children admitted to hospital. We aimed to investigate the effect of PEWS implementation on mortality due to clinical deterioration in children with cancer in 32 resource-limited hospitals across Latin America.

methodsProyecto Escala de Valoración de Alerta Temprana (Proyecto EVAT) is a quality improvement collaborative to implement PEWS in hospitals providing childhood cancer care. In this prospective, multicentre cohort study, centres joining Proyecto EVAT and completing PEWS implementation between April 1, 2017, and May 31, 2021, prospectively tracked clinical deterioration events and monthly inpatient-days in children admitted to hospital with cancer. De-identified registry data reported between April 17, 2017, and Nov 30, 2021, from all hospitals were included in analyses; children with limitations on escalation of care were excluded. The primary outcome was clinical deterioration event mortality. Incidence rate ratios (IRRs) were used to compare clinical deterioration event mortality before and after PEWS implementation; multivariable analyses assessed the correlation between clinical deterioration event mortality and centre characteristics.

findingsBetween April 1, 2017, and May 31, 2021, 32 paediatric oncology centres from 11 countries in Latin America successfully implemented PEWS through Proyecto EVAT; these centres documented 2020 clinical deterioration events in 1651 patients over 556 400 inpatient-days. Overall clinical deterioration event mortality was 32·9% (664 of 2020 events). The median age of patients with clinical deterioration events was 8·5 years (IQR 3·9-13·2), and 1095 (54·2%) of 2020 clinical deterioration events were reported in male patients; data on race or ethnicity were not collected. Data were reported per centre for a median of 12 months (IQR 10-13) before PEWS implementation and 18 months (16-18) after PEWS implementation. The mortality rate due to a clinical deterioration event was 1·33 events per 1000 patient-days before PEWS implementation and 1·09 events per 1000 patient-days after PEWS implementation (IRR 0·82 [95% CI 0·69-0·97]; p=0·021). In the multivariable analysis of centre characteristics, higher clinical deterioration event mortality rates before PEWS implementation (IRR 1·32 [95% CI 1·22-1·43]; p<0·0001), being a teaching hospital (1·18 [1·09-1·27]; p<0·0001), not having a separate paediatric haematology-oncology unit (1·38 [1·21-1·57]; p<0·0001), and having fewer PEWS omissions (0·95 [0·92-0·99]; p=0·0091) were associated with a greater reduction in clinical deterioration event mortality after PEWS implementation; no association was found with country income level (IRR 0·86 [95% CI 0·68-1·09]; p=0·22) or clinical deterioration event rates before PEWS implementation (1·04 [0·97-1·12]; p=0·29).

interpretationPEWS implementation was associated with reduced clinical deterioration event mortality in paediatric patients with cancer across 32 resource-limited hospitals in Latin America. These data support the use of PEWS as an effective evidence-based intervention to reduce disparities in global survival for children with cancer.

fundingAmerican Lebanese Syrian Associated Charities, US National Institutes of Health, and Conquer Cancer Foundation. TRANSLATIONS: For the Spanish and Portuguese translations of the abstract see Supplementary Materials section.

Indexed as

Clinical DeteriorationNeoplasmsAdolescentChildChild, PreschoolCohort StudiesHospitalsHumansLatin AmericaMaleProspective Studies

Identifiers

PMID37433316
PMCPMC10727097

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