| Literature DB >> 31552212 |
Noel Britton1, Michael A Miller2, Sami Safadi3, Ariel Siegel3, Andrea R Levine1,3, Michael T McCurdy3.
Abstract
Background: Telemedicine, or healthcare delivery from a distance, has evolved over the past 50 years and helped alter health care delivery to patients around the globe. Its integration into numerous domains has permitted high quality care that transcends obstacles of geographic distance, lack of access to health care providers, and cost. Ultrasound is an effective diagnostic tool and its application within telemedicine ("tele-ultrasound") has advanced substantially in recent years, particularly in high-income settings. However, the utility of tele-ultrasound in resource-limited settings is less firmly established. Objective: To determine whether remote tele-ultrasound is a feasible, accurate, and care-altering imaging tool in resource-limited settings. Data Sources: PubMed, MEDLINE, and Embase. Study Eligibility Criteria: Twelve original articles met the following eligibility criteria: full manuscript available, written in English, including a direct patient-care intervention, performed in a resource-limited setting, images sent to a remote expert reader for interpretation and feedback, contained objective data on the impact of tele-ultrasound. Study Appraisal and SynthesisEntities:
Keywords: LMIC; eHealth; global health; resource-limited; tele-radiology; tele-ultrasound; telemedicine; ultrasound
Year: 2019 PMID: 31552212 PMCID: PMC6738135 DOI: 10.3389/fpubh.2019.00244
Source DB: PubMed Journal: Front Public Health ISSN: 2296-2565
Assessment of bias in individual papers.
| Adambounou et al. ( | (1) Bias in selection of participants into the study | (1) No information | (1) Details of participant selection including inclusion and exclusion criteria are not provided for participants undergoing US or for participants performing US |
| (2) Bias in measurement of outcomes | (2) Serious | (2) Image quality and diagnoses were assessed by a single expert radiologist; Standard scoring mechanism for image quality was not utilized | |
| Adambounou et al. ( | (1) Bias in selection of participants into the study | (1) No information | (1) Details of selection for non-physician participants performing US are not provided: “With inexperienced ultrasound operators at CHR Tsévie (e.g., radio operators, nurses, midwives), 10 delayed-time diagnostic tele-ultrasound cases were performed with the virtual navigation program ECHO-CNES.”; Details of selection for participants undergoing US are lacking in precision: “Patients gave full informed consent. These patients were either recruited upon emergency admission to hospital or were already hospitalized at CHR Tsévie.” |
| (2) Bias in measurement of outcomes | (2) Moderate | (2) A description of how image quality was standardized and assessed by experts is not provided: “The quality of the images tele-transmitted were appreciated by three expert radiologists (University hospital radiologist), the appreciation retained for the quality of the transmitted images for every bandwidth was that of at least two of the three expert radiologists.” | |
| (3) Bias in classifications of interventions | (3) Serious | (3) US were performed by both experienced physicians and inexperienced ultrasound operators. Comparing image quality between these two different groups of ultrasound operators compromises the internal validity of the study: “With inexperienced ultrasound operators at CHR Tsévie (e.g., radio operators, nurses, midwives), 10 delayed-time diagnostic tele-ultrasound cases were performed with the virtual navigation program ECHO-CNES.” | |
| Bagayoko et al. ( | (1) Bias in selection of participants into the study | (1) No information | (1) Details of selection for non-physician/non-midwife participants performing US are not provided: “For the shifting of these tasks in ultrasound imaging and cardiology, a 3 week training of health care professionals was held in Bamako in order to develop basic technical skills.”; Details of selection of study sites are not provided: “Our study was conducted in district hospitals in Bank- ass, Dioila, Kolokani, and Djenne, in rural Mali.”; Details of eligibility criteria for participants undergoing ultrasound are not provided: “Between March 2012 and March 2013, study participants presenting to the one of the four district hospitals with an obstetrical or cardiac problem were invited to participate and were enrolled prospectively to the study.” |
| (2) Bias in measurement of outcomes | (2) Serious | (2) Data regarding the impact on care were collected using an unvalidated questionnaire. It is unclear if more than one physician validated these questionnaire results: “The medical evaluation questionnaires were completed by physicians after the consultation with the patient.” | |
| (3) Bias in classifications of interventions | (3) Critical | (3) Data regarding the use of EKG and US were presented together as one intervention rather than being separated out from each other. As these two interventions are very different, this aggregation could create a critical lack of internal validity. | |
| (4) Bias due to confounding | (4) Moderate | (4) Clinical sites were chosen to serve as study sites or control sites for outcomes regarding impact on attendance in health centers. No information was provided about the allocation of clinics to either study site or control. No information was provided about the demographic characteristics of the clinics to allow for comparison. The possibility for significant confounding factors to bias results between clinical sites exists. | |
| (5) Bias due to missing data | (5) Moderate | (5) There were a significant number of missing data regarding impact on care: “The sample consisted of 215 participants for the first indicator, 103 for the second, and 211 for the last.” | |
| Bhavnani et al. ( | (1) Bias due to participant selection | (1) Moderate | (1) Details of selection for physician participants are not provided: “Five cardiologists and 12 sonographers from 12 academic medical centers across the United States, 15 cardiologists and cardiothoracic surgeons from SSSIHMS, and 30 cardiologists from across India participated in the study.” |
| (2) Bias due to confounding | (2) Low | (2) Details of the randomization of clinical sites to mHealth or standard-care are not provided: “Study subjects were evaluated in either 1 of 10 (5 mHealth, or 5 standard care) clinical sites all located at SSSIHMS.” | |
| (3) Bias due to missing data | (3) Low | (3) There was minimal missing data at 12-month follow up (mHealth: 7%, standard-care: 8%). However, the rates of those lost to follow up were nearly identical in each intervention group. | |
| (4) Bias due to measurement of outcomes | (4) Low | (4) All testing was performed according to standardized and validated protocols diminishing bias. mHealth devices were subject to daily quality control testing. Results of testing were interpreted by a single physician; however surgical decision making was performed by blinded physicians. Additionally, all results were adjudicated by the primary investigators.: “The primary investigators at SSSIHMS adjudicated all clinical endpoints and determined the necessity for percutaneous or surgical treatment … Subsequently, operating interventional cardiologists and surgeons (different than those performing the initial assessment) were blinded to a study subject's group allocation; however, they reviewed the findings on TTE for diagnostic accuracy at the time of planned percutaneous intervention or surgical procedures.” | |
| Epstein et al. ( | (1) Bias due to participant selection | (1) No information | (1) Details of participant selection including inclusion and exclusion criteria are not provided for participants undergoing US. The potential for selecting participants with more acute illness is very possible: “Over a 14-day period, 23 of the 75 (30%) acutely ill patients received, by clinical indication, augmented physical examination using pocket size ultrasound machine.” |
| (2) Bias in measurement of outcomes | (2) Serious | (2) The initial diagnosis and POCUS were performed by a physician in training and were then confirmed by a single experienced physician: “The studies were performed over a period of 14 days by an internal medicine resident, who was providing volunteer medical care as part of the Israeli Medicine on the Equator project. All studies were conducted for clinical indications … all the studies were reviewed by experienced radiologists and cardiologists, who were all in agreement with the treating physician.” | |
| Martinov et al. ( | (1) Bias due to participant selection | (1) No information | (1) Details of participant selection including inclusion and exclusion criteria are not provided for participants undergoing US. |
| (2) Bias in measurement of outcomes | (2) Moderate | (2) The still images were reviewed by 5 experienced clinicians; however, the video footage was reviewed by a separate single reviewer only: “An image database was created by 50 transmitted images. Five experienced clinicians from Children's Hospital in Novi Sad, Serbia assessed the quality of transmitted saved images by grading them from 1 to 5, where 1 was lowest and 5 was the highest grade. Reviewers graded transmitted images that were offered in uniform form. Grading was based on the presence or absence of anatomic landmarks (points and lines) used for morphologic classification of sonographic images according to Graf … Another reviewer graded transmitted real time video stream of DDH examination. Grading was based on diagnostic usefulness to confirm or exclude the DDH: can establish the diagnosis, need to repeat the examination, can't establish the diagnosis.” | |
| (3) Bias due to confounding | (3) Moderate | (3) All participants had normal US results. The results in the study may be biased by the exclusion of participants with abnormal US results: “Ultrasound examination of both hips revealed normal findings in all 25 examined babies.” | |
| Nascimento et al. ( | (1) Bias in measurement of outcomes | (1) Serious | (1) “…Because follow-up confirmatory echocardiograms were not considered, prevalence estimates may be biased upward, especially for handheld devices.” |
| (2) Bias due to confounding | (2) Moderate | (2) Prevalence findings may be impacted by the differing demographic factors and other confounders between the different school groups: “…despite the multiple engagement strategies applied by the PROVAR study (markedly, the multiple educational strategies), student participation in public schools remained marginal, which may bias prevalence estimates … all consented children were consecutively included, without stratified sampling procedures, increasing the risk of bias associated with differences between groups (e.g., higher median age in private schools).” | |
| Ross et al. ( | (1) Bias due to confounding | (1) Moderate | (1) Historical control data was obtained from the period prior to the introduction of the US (June 2010). The validity of the historical control was assessed and Kruskal Wallis was used to determine if the data was consistent over time prior to June 2010 and after June 2012. Because there were no inconsistencies pre ultrasound and post ultrasound, confounding was believed not to have occurred and contributed to the # of deliveries or antenatal care visits. Additionally, # of delivers were obtained from a nearby government facility for the 2 years prior to and the 2 years following June 2010. The number of deliveries at this facility did not change prior to or after June 2010, further supporting the assumption that no confounding event occurred that affected the # of deliveries at the time ultrasound was introduced (June 2010) |
| Sekar and Vilvanathan ( | (1) Bias in selection of the participants into the study | (1) No information | (1) No information was provided on how the clinicians determined “suspected congenital heart disease” in the patients they enrolled |
| (2) Bias in measurement of outcome | (2) No information | (2) No information is provided about the pediatric cardiologist and whether a single cardiologist interpreted the images or if multiple cardiologists confirmed the findings | |
| Sutherland et al. ( | (1) Bias due to missing data | (1) Critical | (1) The authors initially included 6 ultrasound interpreters for the intervention group. However, 3 were |
| Vinals et al. ( | (1) Bias in selection of the participants into the study | (1) No information | (1) Two clinicians were chosen to participate in the study and were invited by email without clear indication how they were chosen |
| (2) Bias in measurement of outcome | (2) Moderate | (2) Standardized image checklist was used but is not easily available in this publication or the reference publication and quality assessment is determined by a non-validated tool | |
| Vinayak et al. ( | (1) Bias in selection of the participants into the study | (1) No information | (1) Midwife participants volunteered to participate in the study which suggests a degree of interest and motivation and threatens external validity |
| (2) Bias in measurement of outcome | (2) Moderate | (2) Standardized assessment tool was used by expert radiologists but not validated |
Figure 1Search results: PRISMA diagram.
ROBINS-I risk categories.
| Low | The study is comparable to a well-performed randomized trial with regard to this domain |
| Moderate | The study is sound for a non-randomized trial with regard to this domain but cannot be considered comparable to a well-performed randomized trial |
| Serious | The study has some important problems with regards to this domain |
| Critical | The bias in this domain is too problematic to provide any useful evidence on the effects of the intervention from this study |
| No information | No information on which to base a judgement about risk of bias for this domain |
Study data for obstetrics-related papers.
| Bagayoko et al. ( | Mali | 215 | Not specified | Midwifes and general physicians | 3-week training | Not specified | No | Not specified | Laptops and low-bandwidth internet connections | (1) US helpful in diagnosis, frequently resulted in changed diagnosis and management; |
| Vinals et al. ( | Chile | 50 | Asynchronous | Obstetricians | Not specified | Fetal echocardiography expert in Chile | No | STIC (Voluson 730 Expert series US scanner) | Broadband connection. Data received/stored in an external hard disk via USB connection | (1) Operators were successfully able to acquire images; |
| Vinayak et al. ( | Kenya | 271 | Asynchronous | Midwives | 4-week training | 2 radiologists with OB experience | No | Philips VISIQ tablet portable US | Mobile phone network and modem weblink | (1) Accuracy of images and measurements was 99.63%; |
| Ross et al. ( | Uganda | Unclear | Asynchronous | Midwives | 3-day training | Referral hospital in Uganda | No | Not specified | Images compressed locally then transmitted via cellphone modem to remote server | (1) Increased number of attended deliveries after US implemented; |
Study data for non-obstetrics and non-cardiology-related papers.
| Adambounou et al. ( | Togo | 50 | Both | Either physician or lay person using virtual navigation program | Unclear | Radiologists in France | Partial | GE Logiq 200 | IP camera and remote access software | Adequate quality image transfer; satisfactory tele-diagnosis; low bandwidth requirement |
| Adambounou et al. ( | Togo | 22 | Real-time | Physicians and technicians | Unclear | Radiologists in France | Yes | GE Logiq 200 | video camera, internet, custom software for 3D reconstruction | Satisfactory diagnostic utility; good image quality; tele-mentored US possible |
| Epstein et al. ( | Uganda | 23 | Real-time | Internal medicine resident | 5 days | Radiologists and cardiologists in Israel | Yes | GE VScan | Commercially available video-chat software on cellular phones | Positive findings in 70% of cases; tele-US changed management 87% of cases |
| Sutherland et al. ( | Veron, Dominican Republic | 105 | Asynchronous | Physician | 2 months | 6 volunteer radiologists in USA | No | Sonosite Titan | jpeg images sent by email and reports returned by email | Greater follow-up appointment attendance and shorter time to report in telemedicine group |
| Martinov et al. ( | Zrenjanin, Serbia | 25 | Real-time | Sonographer | No additional training | Two sets of expert radiologists in USA and Serbia | No | Sonosite 180 | Low bandwidth internet, commercially available software, video camera | Tele-diagnosis established from 62% of still images, 92% of videos; repeat scan needed in 8% of videos |
Study data for cardiology-related papers.
| Bhavnani et al. ( | Bangalore, India | 139 | Asynchronous | Physicians | Yes, length not specified | Global consortium of 75 cardiologists | No | GE VScan | Cloud based system with broadband internet | Decreased time to referral for valvular interventions; lower probability of hospitalization or death |
| Sekar and Vilvanathan ( | Aragonda, India | 102 | Real-time | Echo tech | Unknown | Pediatric cardiologist | Yes | Not specified | Very Small Aperture Terminal Satellite bandwidth; videoconferencing; satellite dish, high resolution camera, s-video cable, computer with webcam, monitor screen | Images were high quality; pathology ruled out in 49% of children; 51% were diagnosed with cardiac detect, and 29% referred for cardiac surgery |
| Nascimento et al. ( | Minas Gerais, Brazil | 12,048 | Asynchronous | Nurse coordinators, biochemical & imaging technicians | 12 weeks | Cardiologists | No | GE VIVID Q VScan | Dropbox© Cloud storage and downloaded for interpretation by dedicated VSCAN Gateway software | RHD overall prevalence was 4.0%; 29,695 children received educational curriculum |