Evidence map›Paper›PMID 39475844›Full record

ArticlePLOS digital health2024

A novel digital health approach to improving global pediatric sepsis care in Bangladesh using wearable technology and machine learning.

Stephanie C Garbern, Gazi Md Salahuddin Mamun, Shamsun Nahar Shaima, Nicole Hakim, Stephan Wegerich, Srilakshmi Alla, Monira Sarmin, Farzana Afroze, Jadranka Sekaric, Alicia Genisca and 7 more

Abstract read
In one paragraph

Article in PLOS digital health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–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

16 citing papers in PubMed.

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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

17 authors.

Stephanie C GarbernDepartment of Emergency Medicine, Warren Alpert Medical School, Brown University, Providence, Rhode Island, United States of America.ORCID https://orcid.org/0000-0002-0919-2841
Gazi Md Salahuddin MamunInternational Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
Shamsun Nahar ShaimaInternational Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
Nicole HakimPhysIQ, Inc. Chicago, Illinois, United States of America.
Stephan WegerichPhysIQ, Inc. Chicago, Illinois, United States of America.
Srilakshmi AllaPhysIQ, Inc. Chicago, Illinois, United States of America.
Monira SarminInternational Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
Farzana AfrozeInternational Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
Jadranka SekaricPhysIQ, Inc. Chicago, Illinois, United States of America.
Alicia GeniscaDepartment of Emergency Medicine, Warren Alpert Medical School, Brown University, Providence, Rhode Island, United States of America.
Nidhi KadakiaDepartment of Emergency Medicine, Warren Alpert Medical School, Brown University, Providence, Rhode Island, United States of America.
Kikuyo ShawBrown University, Providence, Rhode Island, United States of America.
Abu Sayem Mirza Md Hasibur RahmanInternational Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
Monique GaineyDepartment of Emergency Medicine, Warren Alpert Medical School, Brown University, Providence, Rhode Island, United States of America.ORCID https://orcid.org/0000-0002-2860-9104
Tahmeed AhmedInternational Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
Mohammod Jobayer ChistiInternational Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.
Adam C LevineDepartment of Emergency Medicine, Warren Alpert Medical School, Brown University, Providence, Rhode Island, United States of America.ORCID https://orcid.org/0000-0003-3982-3824

Funding

Supplement to Development of a Mobile Health Personalized Physiologic Analytics Tool for Pediatric Patients with SepsisR33TW012211 · FIC · RHODE ISLAND HOSPITAL · PI GARBERN, STEPHANIE CHOW, LEVINE, ADAM CARL · 2023 to 2025
$1.1M
Development of a Mobile Health Personalized Physiologic Analytics Tool for Pediatric Patients with SepsisR21TW012211 · FIC · RHODE ISLAND HOSPITAL · PI LEVINE, ADAM CARL · 2021 to 2022
$456k
FIC NIH HHS R21 TW012211FIC NIH HHS R33 TW012211
6 · The paper itself

Abstract

Sepsis is the leading cause of child death globally with low- and middle-income countries (LMICs) bearing a disproportionate burden of pediatric sepsis deaths. Limited diagnostic and critical care capacity and health worker shortages contribute to delayed recognition of advanced sepsis (severe sepsis, septic shock, and/or multiple organ dysfunction) in LMICs. The aims of this study were to 1) assess the feasibility of a wearable device for physiologic monitoring of septic children in a LMIC setting and 2) develop machine learning models that utilize readily available wearable and clinical data to predict advanced sepsis in children. This was a prospective observational study of children with sepsis admitted to an intensive care unit in Dhaka, Bangladesh. A wireless, wearable device linked to a smartphone was used to collect continuous recordings of physiologic data for the duration of each patient's admission. The correlation between wearable device-collected vital signs (heart rate [HR], respiratory rate [RR], temperature [T]) and manually collected vital signs was assessed using Pearson's correlation coefficients and agreement was assessed using Bland-Altman plots. Clinical and laboratory data were used to calculate twice daily pediatric Sequential Organ Failure Assessment (pSOFA) scores. Ridge regression was used to develop three candidate models for advanced sepsis (pSOFA > 8) using combinations of clinical and wearable device data. In addition, the lead time between the models' detection of advanced sepsis and physicians' documentation was compared. 100 children were enrolled of whom 41% were female with a mean age of 15.4 (SD 29.6) months. In-hospital mortality rate was 24%. Patients were monitored for an average of 2.2 days, with > 99% data capture from the wearable device during this period. Pearson's r was 0.93 and 0.94 for HR and RR, respectively) with r = 0.72 for core T). Mean difference (limits of agreement) was 0.04 (-14.26, 14.34) for HR, 0.29 (-5.91, 6.48) for RR, and -0.0004 (-1.48, 1.47) for core T. Model B, which included two manually measured variables (mean arterial pressure and SpO2:FiO2) and wearable device data had excellent discrimination, with an area under the Receiver-Operating Curve (AUC) of 0.86. Model C, which consisted of only wearable device features, also performed well, with an AUC of 0.78. Model B was able to predict the development of advanced sepsis more than 2.5 hours earlier compared to clinical documentation. A wireless, wearable device was feasible for continuous, remote physiologic monitoring among children with sepsis in a LMIC setting. Additionally, machine-learning models using wearable device data could discriminate cases of advanced sepsis without any laboratory tests and minimal or no clinician inputs. Future research will develop this technology into a smartphone-based system which can serve as both a low-cost telemetry monitor and an early warning clinical alert system, providing the potential for high-quality critical care capacity for pediatric sepsis in resource-limited settings.

Identifiers

PMID39475844
PMCPMC11524492

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.