| Literature DB >> 33196698 |
Pablo Duran1, Janine A Sommer2, Paula Otero2, Mariana Daus2, Sonia Benitez2, Suzanne Serruya1, Luis Andres De Francisco3.
Abstract
OBJECTIVES: To identify scientific evidence on the use and results of information and communication technologies for the improvement of neonatal health in general or specific health problems or interventions, and to describe the type of intervention and its results.Entities:
Keywords: Information technology; eHealth strategies; evidence-based medicine; infant health; perinatal care; telemedicine
Year: 2020 PMID: 33196698 PMCID: PMC7655061 DOI: 10.26633/RPSP.2020.123
Source DB: PubMed Journal: Rev Panam Salud Publica ISSN: 1020-4989
FIGURE 1.Article search and selection process
Characteristics of the 10 studies included in the review (population, design, study/intervention, results and limitations)
Study | Design | Population | Study intervention | Results | Limitations |
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Observational study | Regularly scheduled diagnostic examinations by an ophthalmologist compared with digital imaging by non-physician staff using a wide-field digital camera. | 1257 infants (mean BW 864g, mean gestational age 27 weeks) underwent a median of 3 sessions of examinations and imaging. | • Difficulty of comparing image grading results to a criterion standard with known inherent variability. | ||
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| Ophthalmologists documented whether an eye met criteria for RW-ROP, i.e. zone I ROP, stage 3 ROP, or plus disease. | Diagnostic examination identified RW-ROP in 18.2% of eyes (19.4% of infants). | • Limited enrollment to infants at high risk i.e. <1251g BW, and may not be generalizable to all infants eligible for ROP examinations |
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| A standard 6-image set per eye was sent to a central server and graded by two trained, masked, non-physician readers. | Remote grading of images of an eye at a single session had sensitivity of 81.9% (95% confidence interval (CI): 77.4–85.6%) and specificity of 90.1% (95% CI: 87.9–91.8%). | • Was not designed to assess the time to reporting results to the clinical center or to provide rapid feedback requesting additional images when image quality was poor |
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| A Reading Supervisor adjudicated disagreements. | When both eyes are considered for the presence of RW-ROP, as would routinely be done in a screening, the sensitivity was 90.0% (95% CI 85.4–93.5%) with specificity of 87.0% (95% CI 84.0–89.5%), negative predictive value 97.3% and positive predictive value 62.5% at the observed RW-ROP rate of 19.4%. | • The availability of ROP specialists, licensing and liability issues must be dealt with, as well as establishing a consistent and reliable reading center. Procedures to address poor image quality are needed |
RCT | An Internet-based telemedicine system was used to also allow interactive telephone voice communication between patients and providers and to provide automatic reminders to transmit data. | There were no significant differences between the two groups (telemedicine vs. controls) in regard to maternal blood glucose values or infant birth weight. | • Short period of the intervention (2 months) | ||
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| Women with GDM were randomized to the telemedicine group (n = 40) or to the control group (n = 40) and were asked to control their blood glucose levels four times a day. | Adding telephone access and reminders increased transmission rates of data in the intervention group compared with the intervention group in our previous study (35.6±32.3 sets of data vs.17.4±16.9 sets of data; P<0.01) |
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| The women in the intervention group transmitted these values through the telemedicine system, while the women in the control group maintained paper registration journals, which were reviewed at prenatal visits. | No significant differences between the two groups with regard to birth weight on univariate or multivariate analysis (after controlling for gender, parity, prepregnancy BMI, and treatment), gestational age at delivery, 1- and 5-min Apgar scores, and rates of large for gestational age. | • Relatively small sample size |
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| The primary outcomes were the weight of the newborn and the control of maternal glucose. The data collection included blood glucose records, transmission rates for the intervention group and review of charts. | Eleven newborns required admission to the neonatal intensive care unit, but there were no perinatal/neonatal deaths. | • The neonates from the intervention group were born 0.7 week later than control group |
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| The primary end points in this trial were maternal glucose control and infant birth weight. | Women using the Internet sent in significantly more transmissions than did women using the phone/IVR system (42.8 – 32.4 vs. 10.9 – 16.3 data sets; P = 0.007). | • One could postulate that these differences in neonatal outcomes may have reached statistical significance with a larger sample size |
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| Secondary end points included pregnancy outcomes (mode of delivery, gestational age at de- livery, neonatal intensive care unit admission, Apgar scores, and rates of large for gestational age, and other neonatal morbidities) and system use. | In summary, our enhanced telemedicine monitoring system increased contact between women with GDM and their healthcare providers but did not impact upon pregnancy outcomes. |
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RCT | 1598 post partum women with Internet access attending eight ‘Attention to Sexual and Reproductive Health units at Primary Health Care centres | At each of the eight units, 100 women were randomly assigned to the intervention group and 100 to the control group. Women in the intervention group could consult midwives by videoconference or telephone and could also receive standard care. Women in the control group received standard care from midwives at their health centres or at home. | 1401 women studied; 683 in intervention and 718 in control group. Two hundred and seventy-six women (40.4%) used videoconferencing or telephone in the intervention group. | • Differences in the competencies of the midwives in the two countries | |
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| Main outcome variables: number and type of visits, reasons for consultation, type of infant’s feeding at six weeks and mothers’ satisfaction with the care provided. Additionally, sociodemographic and obstetric characteristics, number of visits, number of visits involving online consultation and technology used. | Mean total visits, virtual and face-to-face, was higher in intervention group than in controls (2.74 versus 1.22). Women in the intervention group made fewer visits to the health centre (mean=1) than CG women (mean=1.17). Both differences were statistically significant (p<0.001 and p=0.002 respectively). | • The information on the visits made by women to emergency services in hospitals and to pediatric outpatient clinics at health centres was only collected via direct self-reports |
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| Prevalence of breastfeeding was similar in the two groups (intervention 64.5%, and control 65.4%). Mean overall satisfaction of women with midwife care was very high in both groups (intervention 4.77/5, control 4.76/5). | • The videoconferencing is only available for Internet users. |
RCT | Parents in the intervention arm received standard notification – an appointment card at the previous appointment– plus reminder text messages 7 days before their child’s immunizations which were due at 2, 4 and 6-months of age. Text messages were sent using a computer-based software program that connected to a cellular phone to send text messages. Parents in the control arm received standard notification of immunizations due only. Each participant was enrolled for seven months. | There were no significant differences in immunization rates between groups at 7 months of age. | • The text messaging service provider was accurate with the dates of the text messages for almost of the time | ||
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| Text messages immunization reminders sent 4 weeks prior and 2 weeks prior to the due date for the infant’s 2, 4, and 6 month vaccinations. Main outcomes were barriers and immunization rates between groups | Overall immunization compliance at all measurement intervals was low, and as the infants got older, there was a decrease in immunization compliance rates. A higher percentage of experimental (58.8%) than control (34.8%) were not UTD at 7 months. | • More parents in the intervention group did not complete the study • There was loss of follow-up of 39% of the experimental group compared to a loss of 10% of the control • Small size of the sample |
Pilot RCT | Text message immunization reminders prior to immunization due dates. | Greater numbers of intervention children received immunizations and were “on time” using per protocol analysis; though not statistically significance. However, post-intervention interviews (N=18) indicated strong support for TRICKs; 83% found the text message reminders very helpful and 17% somewhat helpful. | • Small size of the sample | ||
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| Participants received a $20 gift card at the time of enrollment. Parents in the intervention group also received a $20 gift card for completing the post-intervention interview. | • Loss of phone service at 7 months for 40% of intervention parents | |
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| Outcomes: rate of immunizations, and rate of immunizations on time. |
| • Problematic text messaging software |
RCT | Each subject participated in three standardized simulated neonatal resuscitation scenarios (A, B, C) presented in random order. Primary outcomes included percent adherence to the NRP algorithm in providing Positive Pressure Ventilation (PPV) and Chest Compression (CC) when clinically indicated, and the frequency of fraction of inspired oxygen (FiO2) adjustments. | Sixty-five healthcare professionals were recruited and randomized to the control or intervention group. Positive pressure ventilation was performed correctly 55-80% of the time in the control group vs. 94-95% in the intervention group across all three scenarios (p<0.0001). Chest compressions were performed correctly 71-81% of the time in the control group vs. 82-93% in the intervention group in the two scenarios in which they were indicated (p<0.0001). FiO2 was addressed three times more frequently in the intervention group compared to the control group (p<0.001) | • Pilot study; Subjects did not serve as their own controls • The focus of this study was limited to decision-making, and did not include evaluation of other cognitive, technical or behavior skills • This study was performed in a highly standardized simulated delivery room environment, not on real ambient | ||
Cluster-randomized clinical trial in 5 rural districts of Ethiopia | Health care workers in intervention facilities received a smartphone with a Safe Delivery App (SDA). The SDA is a training tool in emergency obstetric and neonatal care that uses visual guidance in animated videos with clinical instructions for management. The SDA conveys knowledge and skills on neonatal resuscitation. Study to estimate the effect of the safe delivery app on perinatal mortality and the neonatal resuscitation skills and knowledge of health care workers in Ethiopia. The primary outcome was perinatal death, which was de- fined as a composite of a stillbirth or an early neonatal death. | Use of the SDA was associated with a nonsignificant lower perinatal mortality of 14 per 1000 births in intervention clusters compared with 23 per 1000 births in control clusters (odds ratio, 0.76; 95% CI, 0.32-1.81). The skill scores of intervention health care workers increased significantly compared with those of controls at 6 months (mean difference, 6.04; 95% CI, 4.26-7.82) and 12 months (mean difference, 8.79; 95% CI, 7.14-10.45) from baseline, corresponding to 80% and 107%, respectively, above the control level. Knowledge scores also significantly improved in the intervention compared with the control group at 6 months (mean difference, 1.67; 95% CI, 1.02-2.32) and at 12 months (mean difference, 1.54; 95% CI, 0.98-2.09), corresponding to 39% and 38%, respectively, above the control level. | • The findings are limited by the study location and population • Blinding of intervention and control clusters was impossible owing to the nature of the intervention, which increased the risk for a selection or information bias | ||
RCT | Twenty-four primary healthcare facilities in six districts in Zanzibar were allocated by simple randomisation to either mobile phone intervention (n = 12) or standard care (n = 12). The intervention consisted of a short messaging service (SMS) and mobile phone voucher component. | The mobile phone intervention was associated with an increase in skilled delivery attendance: 60% of the women in the intervention group versus 47% in the control group delivered with skilled attendance. The intervention produced a significant increase in skilled delivery attendance amongst urban women (odds ratio, 5.73; 95% confidence interval, 1.51-21.81), but did not reach rural women. | • The intervention not reach rural women, who are the poorest and most vulnerable to obstetric emergencies • As geographical distances, poverty, quality of care and sociocultural factors, influence the receptiveness of the mobile phone interventions | ||
RCT | In-service staff nurses were randomized to receive training by tele-education instruction (TI n=26) or classroom teaching (CT n=22) method from two neonatology instructors using a standardized teaching module on neonatal resuscitation. Gain in knowledge and skill scores of neonatal resuscitation were measured using objective assessment methods. | Age, educational qualification and professional experience of the participants in two groups were comparable. | • Technology limitations like interruptions during the lectures inability to transmit images of the instructors and their presentation at the same time and occasional delay in the focusing of the camera | ||
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| Pre-training mean knowledge scores were higher in TI group (8.3±1.7 vs 6.6±1.4, P ¼ 0.004). | • The sample of nurses may not represent in a true sense all nurses in remote places |
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| Skill scores were comparable in the two groups (11.7±3 vs 10.3±2.9, P = 0.13). Training resulted in a significant and comparable gain in knowledge scores (4.2±2.2 vs 5.3±1.7; P =0.06) and skills scores (4.5±3.3 vs 5.0±3.1, P =0.62) in both the groups. |
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| The post-training knowledge scores (TI: 12.5±1.7 vs CT: 12.0±1.7, P = 0.37) and the post-training skill scores (TI: 16.0±0.5 vs CT: 15.6±2.5, P = 0.55) were comparable in the two groups. Post-training scores, adjusted for baseline knowledge scores, were statistically higher in the in-person group compared with the telemedicine group (knowledge: 12.46±0.03 vs 12.16±0.01, P < 0.00; skills: 15.6±2.5 vs 16.0±2.8, P < 0.00). The quantum of lower scores in the telemedicine group was only 2% for knowledge and 6% for skills. This difference was felt to be of only marginal importance. Satisfaction scores among trainees and instructors were comparable in the two groups. |
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RCT | All participants were beneficiaries of a nursing quality improvement campaign in infant safe sleep practices (intervention) or breastfeeding (control), and then received a 60-day mobile health program, in which mothers received frequent emails or text messages containing short videos with educational content about infant safe sleep practices (intervention) or breastfeeding (control) and queries about infant care practices | 1263 mothers in the adjusted analyses, receiving the safe sleep mobile health intervention had higher prevalence of placing their infants supine compared with mothers receiving the control mobile health intervention (89.1% vs 80.2%, respectively; adjusted risk difference, 8.9% [95% CI, 5.3%–11.7%]), room sharing without bed sharing (82.8% vs 70.4%; adjusted risk difference, 12.4% [95% CI, 9.3%–15.1%]), no soft bedding use (79.4% vs 67.6%; adjusted risk difference, 11.8% [95% CI, 8.1%–15.2%]), and any pacifier use (68.5% vs 59.8%; adjusted risk difference, 8.7% [95% CI, 3.9%–13.1%]). | • There was a lost to follow-up rate of 21% | ||
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| The independent effect of the nursing quality improvement intervention was not significant for all outcomes. Interactions between the 2 interventions were only significant for the supine sleep position. | • Enrollment was limited to English speakers • The large majority of responses (72.6%) occurred when infants were aged 8 to 12 weeks • This study not evaluates adverse events • This study did not measure clinical outcomes (ie, rates of sudden unexpected infant death) • This trial has limitations inherent in self-reporting |