Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
2,042
datasets available to search
ShareScore release 0.9.0
Dataset results
2,042 results for “Preterm”
Data from: Longer duration of deferred cord clamping improves preterm survival without major morbidities
Open the record for dataset details and reuse information.
Preterm Birth Initiative-Rwanda antenatal care and postnatal care providers survey
Open the record for dataset details and reuse information.
Data from: Impact of a pre-feeding oral stimulation program on first feed attempt in preterm infants: Double-blind controlled clinical trial
<p><b>Objective: </b>To evaluate the effect of an oral stimulation program in preterm on the performance in the first oral feeding, oral feeding skills and transition time from tube to total oral intake.</p> <p><b>Study Designer: </b>Double-blind randomized clinical trial including very preterm newborns. Congenital malformations, intracranial hemorrhage grade III or IV, bronchopulmonary dysplasia, and necrotizing enterocolitis were excluded. Intervention group (GI) received an oral stimulation program of tactile extra-, peri-, and intraoral tactile manipulation once a day for 15 minutes, during a 10-day period. Control group (GII) received sham procedure with same duration of time. Feeding ability was assessed by a speech-language pathologist blinded to group assignment. The classification of infants' oral performance was determined by Oral Feeding Skills (OFS). Neonates were monitored until hospital discharge.</p> <p><b>Results: </b>Seventy-four (37 in each group) were randomized. Mean gestational ages and birth weights were 30±1.4 and 30±1.5 weeks, and 1,452±330g and 1,457±353g for intervention and control groups, respectively. Mean proficiency (PRO), transfer rate (RT), and overall transfer (OT) were 41.5%±18.3 and 19.9%±11.6 (p<0.001), 2.3 mL/min and 1.1 mL/min (p<0.001), 57.2%±19.7 and 35.0%±15.7 (p<0.001) in intervention and control groups, respectively. Median transition time from tube to oral feeding was 4 (3-11) and 8 days in intervention and control groups, respectively (p=0.003). Intake of breast milk was found to reduce transition time from tube feeds to exclusive oral feeding (p<0.001, HR 1.01, 95%CI 1.005-1.019), but the impact of the study intervention remained significant (p=0.007, HR 1.97, 95%CI 1.2-3.2).</p> <p><b>Conclusion: </b>Infants who were breast-fed and an oral stimulation program proved beneficial in reducing transition time from tube feeding to oral feeding.</p> <p>ClinicalTrials.gov number NCT03025815</p>
Rates of rehospitalisation in the first two years among preterm infants discharged from the NICU of a tertiary children hospital in Vietnam – A follow-up study
<p><b>Objectives</b> To describe the characteristics of rehospitalisation in Vietnamese preterm infants, and to examine the time-to-first-readmission between two gestational age (GA) groups (extremely/very preterm, EVP, versus moderate/late preterm, MLP). Further, to compare rehospitalisation rates according to GA and corrected age (CA), and to examine the association between potential risk factors and rehospitalisation rates.</p> <p><b>Design and Setting</b> Cohort study to follow up preterm infants discharged from a neonatal intensive care unit (NICU) of a tertiary children's hospital in Vietnam.</p> <p><b>Participants</b> All preterm newborns admitted to the NICU from July 2013 to September 2014. </p> <p><b>Main outcomes</b> Rates, durations and causes of hospital admission during the first two years. </p> <p><b>Results</b> Of 294 preterm infants admitted to NICU (all out-born, GA ranged from 26 to 36 weeks), 255 were discharged alive, and 211 (83%) NICU graduates were followed up at least once during the first two years CA, of whom 56% was hospital readmitted. Median (interquartile range) of hospital stay was 7 (6 to 10) days. Respiratory diseases were the major cause (70%). Compared with MLP infants, EVP infants had a higher risk of first rehospitalisation within the first 6 months of age (p = 0.01). However, the difference in risk declined thereafter and was similar from 20 months of age. There was an interaction in rehospitalisation rates between GA and CA. Longer duration of neonatal respiratory support and having older sibling were associated with higher rehospitalisation rates. Lower rates of rehospitalisation were seen in infants with higher cognitive and motor scores (not statistically significant in cognitive scores).</p> <p><b>Conclusions</b> Hospital readmission of Vietnamese preterm infants discharged from NICU was frequent during their first two years, mainly due to respiratory diseases. Scale-up of follow-up programmes for preterm infants are needed in LMICs and attempts to prevent respiratory diseases should be considered.</p>
Single Cell Preterm Dataset
<div> <p>The dataset is a CyTOF preterm women dataset, which collected 42 thousand cells across 36 dimensions from 42 samples\cite{peterson2021single}. The patients ranged from 17 preterm women and 25 term women, which is defined as the predicted label. The covariate of the preterm dataset includes gestational age, history of miscarriage, and the record of preeclampsia. </p> <p>Here is the file structure that fits in CytoCo-set input format (symbol "X(____)X" defined as file name describe):</p> <p>data folder</p> <ul> <li>csv_info.csv</li> <li>filenames_X(trials_number)X.json</li> <li>preterm_csv <ul> <li>all <ul> <li>X(sample_file_name)X.csv</li> <li>test_labels_X(trials_number)X.csv</li> <li>train_labels_X(trials_number)X.csv</li> </ul> </li> <li>marker.csv</li> </ul> </li> <li>tripletlists_X(covariate)X_X(trials_number)X <ul> <li>X(covariate)X_tripletlist_subpick_test_rffX(medianpooling_or_maxpooling)X_sameX(same_threhold_percange)X_diffX(diff_threhold_percange)X.txt</li> <li>X(covariate)X_tripletlist_subpick_trainval_rffX(medianpooling_or_maxpooling)X_sameX(same_threhold_percange)X_diffX(diff_threhold_percange)X.txt</li> </ul> </li> </ul> <p> </p> <p>The dataset uploaded all the sample's raw features data (csv file in "all" file) and some file examples. csv_info.csv records all sample's true labels and covariates.</p> <p> </p> </div>
Supplemental File 9: Forest Plots of pairwise comparisons of NRS modes as primary support in preterm neonates for Treatment Failure
Open the record for dataset details and reuse information.
Preterm birth is not associated with asymptomatic/mild SARS-CoV-2 infection per se: pre-pregnancy state is what matters
<p><span><span><span><span><span><span><span><span><span><span><span>Evidence for the real impact of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection on preterm birth is unclear, as available series report composite pregnancy outcomes and/or do not stratify patients according to disease severity.The purpose of the research was to determine the real impact of asymptomatic/mild SARS-CoV-2 infection on preterm birth not due to maternal respiratory failure. </span></span></span></span></span></span></span></span></span></span></span></p> <p><span><span><span><span><span><span><span><span><span><span><span>This case-control study involved women admitted to a hospital for delivery between 20 September 2020 and 9 January 2021 in northern Italy. The cumulative incidence of Coronavirus disease-19 was compared between preterm birth (case group, n = 102) and full-term delivery (control group, n = 127). Only women with spontaneous or medically-indicated preterm birth because of placental vascular malperfusion (pregnancy-related hypertension and its complications) were included. Current or past SARS-CoV-2 infection was determined by nasopharyngeal swab testing and detection of IgM/IgG antibodies in blood samples. </span></span></span></span></span></span></span></span></span></span></span><span><span><span><span><span><span><span><span><span><span><span>A significant difference in the cumulative incidence of Coronavirus disease-19 between the case (21/102, 20.5%) and the control group (32/127, 25.1%) (<i>P</i>= 0.50) was not observed, although the case group was burdened by a higher prevalence of three known risk factors (body mass index > 24.9, asthma, chronic hypertension) for severe Coronavirus disease-19. Logistic regression analysis showed that asymptomatic/mild SARS-CoV-2 infection was not an independent predictor of spontaneous and medically-indicated preterm birth due to pregnancy-related hypertension and its complications (0.77; 95% confidence interval, 0.41-1.43). </span></span></span></span></span></span></span></span></span></span></span></p> <p><span><span><span><span><span><span><span><span><span><span><span>Pregnant patients without comorbidities need to be reassured that asymptomatic/mild SARS-CoV-2 infection does not increase the risk of preterm delivery. Preterm birth and severeCoronavirus disease-19 share common risk factors (i.e., body mass index > 24.9, asthma, chronic hypertension), which may explain the high rate of indicated preterm birth due to maternal conditions reported in the literature. </span></span></span></span></span></span></span></span></span></span></span></p>
Effects of an Information-Based Discharge Service on Preterm Infants, Parents, and Hospitals
ClinicalTrials.gov study NCT06613386. IPD Sharing: NO. Countries: 0. Publications: 10.
Relationship Between EIT and Respiratory Status in Very Preterm Infants
ClinicalTrials.gov study NCT06609135. IPD Sharing: YES. Countries: 1. Publications: 0.
Vaginal Compared With Intramuscular Progesterone for Prevention of Preterm Birth in High Risk Pregnant Women
ClinicalTrials.gov study NCT02304237. IPD Sharing: Not stated. Countries: 0. Publications: 1.
Effect of Early L-Carnitine Supplementation on Neurodevelopmental Outcomes in Very Preterm Infants
ClinicalTrials.gov study NCT01783041. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Mothers' Own Milk Optimization for Preterm Infants Project (MoMO PIP) Pilot Study
ClinicalTrials.gov study NCT04629534. IPD Sharing: NO. Countries: 1. Publications: 0.
Oral Nystatin Prophylaxis to Prevent Systemic Fungal Infection in Very Low Birth Weight Preterm Infants
ClinicalTrials.gov study NCT03390374. IPD Sharing: Not stated. Countries: 0. Publications: 1.
MINImising Total Radiation EXposure in Preterm Infants
ClinicalTrials.gov study NCT06975189. IPD Sharing: YES. Countries: 0. Publications: 0.
Efficacy and Safety of Aspirin and Lansoprazole for Prevention of Preterm Birth in High-Risk Pregnant Women: A Biomarker-Enriched Trial
ClinicalTrials.gov study NCT07337655. IPD Sharing: YES. Countries: 1. Publications: 0.
Trial To Assess The Safety And Tolerability Of Lucinactant For Inhalation In Preterm Neonates 26 to 28 Weeks PMA
ClinicalTrials.gov study NCT02528318. IPD Sharing: NO. Countries: 4. Publications: 0.
Reducing Preterm Births in Underserved Pregnant Women
ClinicalTrials.gov study NCT01344616. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Early Weaning of Preterm Newborn From Incubator to Cot at 1400 Grams
ClinicalTrials.gov study NCT04351425. IPD Sharing: NO. Countries: 0. Publications: 18.
Nasal High Frequency Ventilation in Preterm Infants: A Pilot Study
ClinicalTrials.gov study NCT00296231. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Effectiveness and Safety of Fast Enteral Feeding in Preterm Infants Between 1000 and 2000 Grams of Birth Weight
ClinicalTrials.gov study NCT02998489. IPD Sharing: NO. Countries: 0. Publications: 2.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.