WASHINGTON (March 17, 2026) –Today the Environmental Protection Agency (EPA) announced a solicitation of comments on advanced recycling technologies under the Clean Air Act. The following statement is attributable to Ross Eisenberg, president of America’s Plastic Makers:
“America’s Plastic Makers applaud EPA for seeking comment on clarifying that pyrolysis technologies used for advanced recycling are not forms of incineration under the Clean Air Act. These advanced recycling technologies convert used plastic into valuable feedstocks to make new products, rather than combusting the plastic for energy purposes or landfilling it.”
“This is a key step toward improving recycling and spurring innovation in the United States while retaining strong environmental standards. By using heat in no or low-oxygen environments, pyrolysis can convert used plastics that are difficult to recycle back into their molecular building blocks to make new products.
“Today’s solicitation of comment helps address the current state of regulatory uncertainty that has been a headwind to scaling advanced recycling technologies. Expanding and modernizing America’s recycling infrastructure can help strengthen American manufacturing, create jobs and bolster international competitiveness.”
“America’s Plastic Makers look forward to providing comments to the EPA during the rulemaking process.”
High volumes of emergency department (ED) visits and unplanned hospital readmissions following discharge have significant implications for patient outcomes, health care costs, and overall system efficiency. Readmissions within 30 days, which are often considered unplanned and avoidable, are linked to poor patient satisfaction [], increased mortality risk [], and substantial financial burden, accounting for over US $2.3 billion annually in Canada []. While not all ED visits and readmissions can be prevented, strengthening postdischarge follow-up and care coordination can help reduce these rates and improve patient experience.
The postdischarge period is a particularly vulnerable time for patients as they transition from hospital to home and assume responsibility for their own care. Patients often leave the hospital with new medications, recommended lifestyle changes, or with ongoing care needs, but many may not fully understand their discharge instructions []. Limited awareness of their symptoms, difficulty accessing follow-up care, and a lack of support at home can further increase their risk of complications []. Without proper guidance and resources, patients are more likely to experience preventable adverse events, leading to ED visits or hospital readmissions []. Proactive care coordination during this transition period has the potential to reduce hospital utilization, including ED [] and hospital readmission rates [,]. One promising intervention is postdischarge telephone calls.
Telephone Calls as Digital Health Interventions
While digital health is often associated with apps, wearables, and video consultations, it is important to recognize that telephone-based care is a legitimate and impactful digital health tool, particularly in real-world contexts where access and equity are paramount. Digital health can be broadly defined as the delivery of care at a distance, the digital storage and sharing of health information, and the use of health-related data to improve services and systems. This broad definition allows inclusion of “low-tech” modalities, such as telephone or SMS text messaging–based interventions, alongside more “high-tech” solutions like app-based programs or algorithm-driven self-management tools [].
Telephones are widely accessible and require no broadband internet, which makes them particularly valuable for reaching populations who may be marginalized by more complex digital platforms (eg, older adults, those with lower incomes, and those with limited English proficiency) []. Unlike video visits and other forms of digital care which demand stable internet and technical know-how [], telephone calls lower the barrier to entry, enabling broader participation in virtual care [].
From an equity standpoint, telephone-based care helps mitigate the digital divide [,]. Research has shown that disparities in mobile phone ownership are significantly less pronounced than those in internet access or smartphone usage []. This positions telephone calls as a uniquely inclusive tool in digital health strategies.
Postdischarge Calls
Postdischarge calls aim to bridge information gaps, enhance adherence to care plans, and offer emotional support to patients during their transition from hospital to home []. Although postdischarge calls have been implemented across various patient populations [], the evidence supporting their effectiveness remains mixed. Studies have found that postdischarge calls are feasible [], can improve patients’ experience [], and may improve follow-up with primary care providers []. However, findings on their effectiveness in reducing ED visits and hospital readmissions are inconclusive, partly due to methodological limitations such as small sample size or variability in intervention protocols []. Despite these mixed results, the potential for postdischarge calls as part of a comprehensive care intervention continues to be explored, with some studies suggesting their effectiveness in reducing readmissions [-].
This study aimed to evaluate the effectiveness of nurse-led postdischarge telephone calls provided by Fraser Health Virtual Care (FHVC) for high-risk patients. Specifically, we examined the impact of a telephone call made 48 hours after hospital discharge on ED visits and hospital readmission within 7 and 30 days following the call. By assessing this intervention, we aim to provide further insight into the role of structured postdischarge follow-up calls in reducing hospital service use and improving patient outcomes.
FHVC Service
Fraser Health is 1 of 5 health authorities in British Columbia, Canada, and provides care to more than 2 million people across 20 diverse communities through 12 acute care hospitals, outpatient and surgery centers, and various community care sites [].
In response to the COVID-19 pandemic and the growing need for digitally enabled care, Fraser Health launched FHVC in April 2020, a nurse-led virtual health service that delivers clinical assessment and navigation support through telephone, video, and secure web chat. FHVC services include general health advice and information, personalized clinical assessments, and referrals to appropriate Fraser Health programs and services [].
FHVC is integrated within the health authority’s digital infrastructure: clinicians document each encounter directly into the electronic health record (EHR), access real-time clinical data, and coordinate follow-up or referrals electronically. The service also supports medical interpreter access, ensuring linguistic inclusivity and equitable reach across the region.
In March 2021, FHVC expanded to include proactive postdischarge outreach calls to patients within 48 hours of hospital discharge. This initiative was introduced as part of a regional digital quality improvement strategy to strengthen care transitions and reduce avoidable ED visits and readmissions. Calls are initiated automatically from daily EHR-generated discharge lists, and nurses follow a standardized digital protocol addressing symptoms, medications, follow-up appointments, and home supports.
This postdischarge component represents a digitally enabled care coordination model that leverages FHVC’s integrated data systems, digital workflows, and virtual communication tools. Unlike usual care, which relies on patients or community providers to initiate follow-up, FHVC’s model provides proactive, system-triggered outreach, a scalable approach to virtual care that blends clinical expertise with health-system data infrastructure.
Methods
Study Design
This study was a multicenter, pragmatic quasi-randomized trial conducted across all 12 acute care hospitals in the Fraser Health region (British Columbia, Canada) from May 16, 2022, to September 21, 2022. The trial evaluated the effect of a routine, operationally delivered, postdischarge follow-up phone call on ED visits and hospital readmissions among high-risk patients. The design was pragmatic in nature, embedded within routine care delivery and implemented by the existing FHVC nursing staff, to reflect real-world practice conditions. The trial was retrospectively registered with the ISRCTN registry (registration submission date: September 3, 2025).
The primary objective was to determine the impact of a 1-time follow-up phone call 48 hours after hospital discharge on 30-day ED visits for participants at high risk of readmission. Secondary objectives were to assess 7-day ED visits, 7- and 30-day readmissions, and participant experiences with the service. This trial is reported in accordance with the CONSORT guidelines ().
Participants and Setting
Participants were adults (≥18 y) discharged from any of Fraser Health’s 12 acute care hospitals. The inclusion and exclusion criteria reflected routine FHVC operational parameters, designed to identify typical patients most likely to benefit from postdischarge follow-up.
Eligibility was informed by the LACE index [,,], a validated measure of 30-day readmission risk incorporating Length of stay (LOS), Acuity of admission, Comorbidities, and Emergency department use. Participants were eligible if they had a LACE score ≥10, or a score <9, and were aged 45 years or older. These thresholds were derived from internal data showing an elevated risk of unplanned readmission.
Exclusion criteria included patients discharged from psychiatric units, to hospice or community nursing programs (where follow-up is routine), those who received additional postdischarge support, or were readmitted or deceased prior to follow-up.
Intervention
The intervention was a one-time, proactive follow-up call from an FHVC registered nurse approximately 48 hours after discharge. The intervention required no additional infrastructure, using existing FHVC systems, staff, and workflows. Nurses used automated discharge lists generated daily from the EHR to identify eligible participants.
During the calls, nurses followed a semistructured clinical assessment tool covering as follows:
Understanding of discharge diagnosis and instructions,
Medication adherence and reconciliation,
Symptoms or concerns postdischarge, and
Follow-up appointments and home supports
Calls were tailored to each patient’s discharge plan and medical record. If issues were identified, nurses provided clarification, reinforced education, or facilitated referrals to community or primary care services. Interpreter services were available when required. Nurses used an assessment form to track this information as shown in Appendix S2 in .
The intervention reflected usual care processes augmented by proactive outreach and was intentionally flexible to accommodate real-world nursing workflow and patient needs.
Comparator (Usual Care)
Participants in the control group received standard care only, which typically includes written discharge instructions and follow-up arranged by hospital units or primary care providers at their discretion. No proactive FHVC calls were made to these participants.
Recruitment and Allocation
Eligible participants were identified through the use of a custom iTracker report that automatically retrieved electronic medical record (EMR) discharge data across Fraser Health hospitals. Each morning, a research assistant applied the eligibility criteria and randomly selected up to 70 participants (using Microsoft Excel’s RAND function) for the intervention group, based on daily nurse capacity. The remaining eligible participants were assigned to the control group.
Because the assignment depended on operational capacity, the allocation was quasi-random and not concealed. On days when the total number of eligible discharges was fewer than 70, all available participants were assigned to the intervention group to maintain operational continuity. Conversely, on days with limited nurse availability, more participants were assigned to the control group. This pragmatic approach preserved ecological validity by embedding group assignment within real-world service delivery constraints.
Registered nurses were blinded to the control group list and conducted intervention calls as part of their routine FHVC workload. Participants were unaware of the research component, ensuring naturalistic behavior.
Outcomes
Our primary outcome measure was the number of ED visits within 30 days of receiving the intervention, defined as any visit in which a participant registered in any of the 12 EDs within the Fraser Health region, regardless of whether they were ultimately seen by a clinician.
Secondary outcome measures included the following:
ED visits within 7 days of the intervention;
Hospital readmissions, at 7 and 30 days postintervention, defined as any admission to a hospital postdischarge; and
Participant experience, measured via a survey.
Sample Size Considerations
The sample size calculation was based on a retrospective analysis of EMRs from June 1, 2020, to May 31, 2021. This analysis estimated the average ED visits within 30 days of discharge before and after FHVC’s postdischarge calls were implemented (0.73 and 0.59 ED visits, respectively). To detect a statistically significant difference with 80% power and α=.05, a required sample size of 6930 participants (3465 per group) was calculated for 2 independent groups.
Procedures and Data Collection
FHVC nurses received standardized training to conduct postdischarge follow-up calls from a Clinical Nurse Educator, ensuring consistency in care delivery. Calls were conducted using standard FHVC telehealth systems, and data were recorded in a secure Excel file linked to the EHR.
During each call, FHVC nurses recorded participant information, including name, age, sex, phone number, LACE score, and discharging hospital, into a Microsoft Excel file stored on a secure network drive. Additional data included any identified knowledge gaps during the postdischarge call. A research assistant monitored data daily to ensure completeness and accuracy of data collection.
If participants were unreachable, the nurse left a voicemail message with the FHVC phone number, inviting the participant to call back if they needed support. Data on ED visits, hospital readmissions, LOS of initial hospitalization, city of residence, and the day of discharge were extracted from the EMR using unique identifiers.
All participants were invited via a telephone call to complete a patient experience survey 30 days after the intervention until 80 participants were reached for each of the intervention and control groups. Surveys were administered by a research assistant and a patient partner. The survey instruments differed by study arm to reflect the experience received (see Appendix S3 in for survey questions). Participants who received the postdischarge call from FHVC answered questions about the call itself, including its helpfulness in clarifying discharge instructions, medications, follow-up appointments, and confidence in managing care at home. Participants who did not receive a postdischarge call were asked parallel questions about their discharge experience, including understanding of instructions, medications, follow-up appointments, and confidence in self-management.
Statistical Analysis
The analysis was completed by a Fraser Health statistician using SPSS (Statistical Package for the Social Sciences) version 21.0 (IBM Corp). The primary analyses followed an intention-to-treat approach. Differences in demographic and outcome variables between groups were analyzed using chi-square tests for categorical variables and the Welch 2-tailed t tests for continuous variables. Mann-Whitney U tests were used where data were not normally distributed. Average levels of risk factors were compared between groups using relative risks, 95% CIs, and 2-tailed P values. To reduce the risk of type I error due to multiple comparisons, a Bonferroni correction was applied to the P values from unadjusted univariate tests conducted on demographic and clinical risk variables. This included both between-group comparisons (intervention vs control) and exploratory within-group comparisons (reached vs not reached in the intervention arm). Adjusted P values were reported where appropriate.
Negative binomial regression models were used to examine the relationship between the dependent variables (ie, the number of ED visits and count of readmissions at 7 and 30 d post call) and relevant predictors. This modeling approach was selected to account for the overdispersion in the data due to the high occurrence of zero values in the count data for ED visits and hospital admissions. Independent variables included intervention group, age, sex, LACE score, LOS of initial hospitalization, day of discharge of initial hospitalization, and geographical location of ED of initial hospitalization. Regression models were not corrected for multiple comparisons, as they represented prespecified primary analyses. Unlike univariate tests, regression coefficients are estimated jointly, inherently accounting for covariation among predictors. Therefore, corrections for multiple comparisons were not applied.
Incident rate ratios (IRRs) were reported to describe the association between the independent variables and the relative frequency of count of ED visits and count of readmissions at 7 and 30 days. A sensitivity analysis was conducted in which an outlier participant with 23 ED visits was recoded to the next-highest value observed in the dataset (13 visits). The results remained robust following this adjustment. Due to missing values in the initial LOS variable, 32 observations (9 in the control group and 22 in the intervention group) were excluded from the final regression models.
In addition to the primary and secondary outcomes, the number needed to treat (NNT) was calculated to further assess the potential clinical significance of the intervention []. NNT is a measure used to determine how many participants need to be treated with the intervention to prevent one additional adverse outcome, such as an ED visit or hospital readmission. The NNT was calculated for the primary outcome of ED visits and the secondary outcome of hospital readmissions at both 7 and 30 days after the follow-up call.
The formula used for calculating NNT is:
NNT=1/|CER – EER|
where CER is the control event rate (ie, the proportion of participants in the control group who experience the adverse outcomes), and EER is the experimental event rate (ie, the proportion of participants in the intervention group who experienced the adverse outcome). The calculated NNT values provide a clinical perspective on the effectiveness of the intervention, helping to assess how many participants need to receive the postdischarge follow-up call to prevent 1 additional adverse outcome.
Descriptive statistics for the participant experience survey were calculated using Microsoft Excel. No inferential tests were conducted because the survey questions differed between groups. The intervention group was asked whether the postdischarge call improved their understanding, and the control group was asked about their understanding of the initial discharge instructions; therefore, direct between-group comparisons were not possible.
Ethical Considerations
This study was reviewed and approved by the Fraser Health Research Ethics Board (number 2022192). Given that the study evaluated a quality improvement initiative embedded within routine operations and used deidentified secondary administrative data, the requirement for individual informed consent was waived by the ethics committees in accordance with institutional policy. All data were deidentified before analysis. No patient-identifiable information was shared outside the health authority. Data were stored on secure, password-protected servers in compliance with provincial privacy legislation. No financial or material compensation was provided to participants, as all activities represented standard care or evaluation of routine service delivery.
Results
Study Population
A total of 7091 participants were included in the study, with 3911 in the intervention group and 3180 in the control group (). The overall sample had a mean age of 68.1 (SD 13.74) years (95% CI 67.8‐68.4), and 47.2% (n=3349) were female.
Among the participants in the intervention group, 1752 fully completed the postdischarge call, while nurses were unable to reach the remainder directly. Of those who completed the call, 40% (n=701) had at least 1 care gap identified.
Figure 1. Flow diagram of participant inclusion and study design. This flowchart outlines participant selection for the retrospective cohort study evaluating the impact of nurse-led postdischarge telephone calls provided by Fraser Health Virtual Care (FHVC) on emergency department (ED) visits and hospital readmissions. The study included adult patients (≥18 y) discharged from acute care hospitals within Fraser Health, British Columbia, Canada, between January 2022 and December 2023.
Baseline Characteristics
Baseline characteristics for the intervention and control groups are presented in . After applying a Bonferroni correction for multiple comparisons (adjusted α=.0042 and adjusted P<.012), the only statistically significant difference was a higher proportion of weekend discharges in the intervention group (33.8% vs 21.5%; adjusted P<.012). No meaningful differences were observed in age, sex, LACE score, LOS, or hospital location. Within the intervention arm, baseline characteristics were similar between participants who completed the call and those who did not (Appendix S4 in ).
Table 1. Baseline characteristics of study sample. Characteristics of patients included in the retrospective cohort study assessing Fraser Health Virtual Care (FHVC)’s postdischarge telephone calls.
Intervention (n=3911)
Control (n=3180)
Difference statistics
Unadjusted P value
Bonferroni adjusted P value
Age, mean (SD)
67.7 (13.5)
68.6 (14.1)
6001487.5
.01
.132
Sex, n (%)
χ²=7.4
.006
.072
Female
1790 (45.8)
1559 (49)
Male
2121 (54.2)
1621 (51)
LACE score, mean (SD)
8.56 (4.42)
8.29 (4.53)
5943871
.001
.012
LOS days of initial hospitalization, mean (SD)
5.49 (6.94)
6.57 (9.70)
6001849
.05
.6
Discharge timing, n (%)
χ²=131.2
<.001
<.012
Discharged on weekend
1323 (33.8)
684 (21.5)
Discharged on weekday
2588 (66.2)
2496 (78.5)
Hospital location, n (%)
χ²=3.4
.06
.78
Rural or urban hospital
2278 (58.2)
1783 (56.1)
Metro hospital
1633 (41.8)
1397 (43.9)
aData include demographics, clinical risk factors (eg, LACE score and LOS), discharge timing, and hospital location. Comparisons are presented between the intervention group (received nurse-led call within 48 h postdischarge) and matched control group (no call), with difference statistics and P values.
bMann-Whitney U test.
cChi-square test. All degrees of freedom were 1.
dLACE: Length of stay, Acuity of admission, Comorbidities, and Emergency department use
eLOS: length of stay.
Primary Outcome: ED Visits
Participants in the intervention group had significantly fewer ED visits at both 7-day and 30-day postdischarge call compared to those in the control group. Within 7 days of the discharge call, 9.33% (365/3911) of intervention participants visited an ED, compared to 11.86% (377/3180) of control participants ().
The NNT to prevent 1 ED visit within 7 days post call was 40 (95% CI 2774). For ED visits within 30 days, NNT=86; however, the 95% CI crossed zero, indicating nonsignificance.
Table 2. Trial outcomes with unadjusted 7-day and 30-day emergency department (ED) visits and hospital readmissions following discharge, and counts and proportions of patients with ED use or hospital readmission after discharge among those who received a postdischarge telephone call (intervention) and those who did not (control) in Fraser Health, British Columbia, Canada (2022–2023).
Postdischarge call
Intervention (n=3911)
Control (n=3180)
Within 7 days of call
ED visits, n
427
472
ED use, n (%)
365 (9.33)
377 (11.9)
Hospital admissions, n
109
115
Hospital use, n (%)
106 (2.7)
109 (3.4)
Within 30 days of call
ED visits, n
1072
973
ED use, n
759 (19.4)
654 (20.6)
Hospital admissions, n
292
253
Hospital use, n (%)
257 (6.6)
214 (6.7)
Adjusted analyses confirmed that the intervention was associated with a significant reduction in 7-day ED visits (IRR 0.72, 95% CI 0.62‐0.84; P<.001) and a modest reduction at 30 days (IRR 0.88, 95% CI 0.78‐0.98; P=.02). Higher LACE scores were consistently associated with increased ED use. No significant associations were observed for age, sex, LOS, day of discharge, or hospital location ( and ).
Table 3. Negative binomial regression results for 7-day emergency department (ED) visits following discharge.
IRR (95% CI)
P value
Intervention
0.719 (0.617-0.837)
<.001
Age (y)
0.996 (0.990-1.001)
.11
Female (vs male)
0.886 (0.762-1.030)
.12
LACE score
1.051 (1.034-1.068)
<.001
LOS at initial hospitalization
0.992 (0.982-1.002)
.12
Weekday discharge (vs weekend)
0.982 (0.827-1.164)
.84
Metro hospital (vs rural or urban)
0.897 (0.769-1.045)
.16
aAdjusted IRR and 95% CIs for factors associated with ED visits within 7 days of hospital discharge among adult patients in Fraser Health, British Columbia (2022–2023). The model includes intervention exposure and demographic and clinical covariates.
bIRR: incident rate ratio.
cLACE: Length of stay, Acuity of admission, Comorbidities, and Emergency department use.
dLOS: length of stay.
Table 4. Negative binomial regression results for 30-day emergency department (ED) visits following discharge.
IRR (95% CI)
P value
Intervention
0.878 (0.783‐0.983)
.02
Age
0.991 (0.987‐0.995)
<.001
Female (vs male)
0.941 (0.841‐1.053)
.29
LACE score
1.082 (1.069‐1.095)
<.001
LOS at initial hospitalization
1.000 (0.993‐1.006)
.96
Weekday discharge (vs weekend)
0.957 (0.843‐1.086)
.50
Metro hospital (vs rural or urban)
0.897 (0.801‐1.006)
.06
aAdjusted IRR for ED visits within 30 days of hospital discharge among adult patients in Fraser Health, British Columbia (2022–2023), comparing those who received a postdischarge Fraser Health Virtual Care (FHVC) nurse call versus matched controls.
bIRR: incident rate ratio.
cLACE: Length of stay, Acuity of admission, Comorbidities, and Emergency department use.
dLOS: length of stay.
Secondary Outcome: Hospital Readmissions
There was no statistically significant reduction in hospital readmissions at 7 or 30 days. Within 7 days, 2.7% of intervention participants were readmitted versus 3.4% of controls (IRR 0.81, 95% CI 0.62‐1.06; P=.13). At 30 days, readmissions were 6.6% versus 6.7% (IRR 0.94, 95% CI 0.78‐1.14; P=.54). LACE score and LOS were significant predictors of readmission, while other covariates were not. NNT estimates to prevent one hospital readmission were 139 (7 days) and 625 (30 days), with 95% CIs crossing zero (; Appendix S5 in ).
Patient Experience Survey Results
Between June 14, 2022, and August 29, 2022, a total of 457 participants (control group: n=223; intervention group: n=264). The study design specified a target sample size of 80 participants per group, and recruitment was concluded once this threshold was reached, resulting in 160 participants (n=80 per group), yielding response rates of 36% in the control group and 30% in the intervention group. Among control group respondents, 67 (83.8%) participants were between the ages of 50 and 70 years, 43 (53.8%) were male, and 51 (63.8%) identified as White. Among intervention group respondents, 56 (70%) participants were between the ages of 50 and 70 years, 45 (56.3%) were male, and 57 (71.3%) identified as White.
Participants in the intervention group reported that the postdischarge call improved their understanding of hospital discharge instructions (n=46, 57.5% agreed) and 40% (n=32) stated that the call provided additional information they did not receive at the time of discharge. Most participants found the postdischarge call helpful in answering their questions (n=33; 41.3% strongly agreed) and 46.3% (n=36) felt more confident managing their own health care after discharge. Nearly all participants viewed the postdischarge call as a valuable service (n=40, 50.6% strongly agreed; n=36, 45.6% agreed). Overall, 71.6% of (n=53) participants in the intervention group visited a primary care provider for follow-up care after discharge.
Among participants in the control group, 47.5% (n=38) strongly agreed that they clearly understood the hospital discharge instructions, and 46.3% (n=37) agreed that they were satisfied with the information provided. Additionally, 51.3% (n=41) felt confident managing their health at home. In total, 60.8% (n=45) of participants in the control group visited a primary care provider for follow-up care after discharge. See Appendix S3 in for full results from patient experience surveys.
Discussion
Overview
This study evaluated a 1-time, nurse-led postdischarge follow-up call delivered through an integrated virtual care program. The intervention was associated with modest improvements in early postdischarge outcomes, with participants in the intervention group experiencing significantly fewer ED visits at both 7 and 30 days. However, hospital readmission rates were not significantly affected.
The observed 28% relative reduction in 7-day ED visits and 12% reduction in 30-day ED visits highlight the clinical relevance of the intervention, supported by the NNT estimates which showed that 39 participants needed to receive the intervention to prevent one 7-day ED visit, and 83 patients to prevent one 30-day ED visit. These are clinically meaningful numbers, especially in the context of high hospital discharge volumes, where even modest improvements can translate into substantial system-wide benefits. While hospital readmission reductions were numerically favorable, they did not reach statistical significance, potentially due to lower event rates and limited power. Alternatively, while a postdischarge phone call can clarify instructions, reduce anxiety, and address basic care gaps, a single call may be insufficient to address the complex medical and social factors that contribute to hospital readmissions [,] and patients with elevated LACE scores may require more comprehensive or repeated interventions to meaningfully reduce readmissions.
Patient Experience
Participants receiving postdischarge phone calls reported overall satisfaction with the intervention and found that the calls provided them with additional information, reduced their concerns, and gave them more confidence to manage their own health care at home (Appendix S3 in ). Interestingly, participants in the control group also reported satisfaction with the discharge information they received, suggesting that unrecognized gaps may remain without structured follow-up. During the postdischarge calls, FHVC nurses asked participants to explain their discharge plan, which often revealed missing or misunderstood information. Nurses followed a standard script which covered essential postdischarge topics. Through this process, 40% of participants in the intervention group were identified as having at least 1 care gap. It is plausible that some participants in the control group had similar gaps, but without prompting, they were not aware of them at the time of the survey, and therefore felt they could manage adequately post discharge. Additionally, 41% of control participants expressed that they would have appreciated FHVC contact information sooner, highlighting the potential value of proactive outreach.
Potential Mechanisms of Action
Follow-up calls likely operate through multiple mechanisms: reinforcing patient education, supporting medication adherence, addressing emotional concerns, and signaling coordinated care across the health system. The intervention may serve both as a direct support tool and as an organizational signal promoting better discharge and follow-up practices. While single-touch calls improved ED utilization, they appear insufficient to address complex factors driving hospital readmissions, underscoring the need for more intensive or repeated interventions for high-risk populations.
Several studies have demonstrated that patient education [] and medication adherence [,] are critical factors in reducing avoidable health care utilization, which may explain the observed reduction in ED visits in our study. Prior research has demonstrated that inadequate understanding of discharge instructions is a major driver of postdischarge complications and unplanned care use [,]. By reinforcing these instructions, postdischarge follow-up calls may have improved patient comprehension of their recovery plan, reduced knowledge gaps, and empowered patients to manage symptoms at home, thereby lowering the need for ED visits. In addition, the calls may have alleviated anxiety and promoted confidence in self-management [] by providing reassurance and tailored guidance, thereby reducing the likelihood of seeking avoidable emergency care.
Medication adherence is another well-documented challenge following hospital discharge, with nonadherence associated with increased ED visits and readmissions []. The follow-up calls offered a valuable opportunity to clarify prescriptions, address concerns, and reinforce adherence strategies. This may have helped prevent adverse events related to medication errors. Similar findings have been observed in previous studies where medication reconciliation and adherence support were associated with reductions in acute care use []. These results suggest that postdischarge calls extend beyond simple follow-up; they actively address gaps in understanding, medication adherence, and emotional well-being, contributing to their observed effectiveness in reducing ED visits.
Importantly, within the intervention arm, completing the call did not meaningfully change ED or readmission outcomes compared with participants who were not reached, suggesting that the benefits observed may reflect system-level effects of the outreach model rather than call completion alone. For example, the intervention may have functioned as a signal of coordinated care, reinforcing follow-up workflows, prompting timely triage, or improving discharge planning processes across the health system. Alternatively, exposure misclassification, where a participant assigned to the intervention group did not actually receive a call, may have diluted the measured effect of individual calls, meaning the observed reductions in ED visits reflect the broader impact of the intervention’s integration into routine care rather than direct participant-level engagement alone. Recognizing these mechanisms underscores that single-touch outreach can influence outcomes through organizational processes as well as patient-level interactions.
Clinical Implications
Postdischarge calls have been shown to enhance patient engagement with primary care providers, improve medication adherence, and contribute to better overall health outcomes []. Given the increasing difficulty in accessing primary care [,], these calls may serve as a low-barrier intervention to support care transitions and fill gaps in follow-up care.
Discharge calls can facilitate smoother transitions from hospital to home by proactively identifying and addressing common barriers to recovery. By intervening early, the discharge calls can reduce the risk of preventable complications and improve the overall patient experiences [] while also relieving pressures on overstretched health care systems [].
Reducing ED visits has important implications for health care systems, as ED overcrowding remains a critical issue []. A reduction in ED visits suggests that patients may be managing their conditions more effectively in outpatient settings, potentially leading to cost savings and improved resource allocation. Future research should explore whether postdischarge calls lead to increased engagement with primary care providers, potentially shifting health care utilization patterns.
Strengths and Limitations
Previous reviews, including 1 Cochrane review [] and 2 systematic reviews [,] have noted that many trials lacked sufficient statistical power, clearly defined sample size calculations, rigorous methodology, or standardized interventions. In contrast, our study addressed these limitations by using a larger sample size, informed by Fraser Health historical data. Additionally, we implemented a structured intervention that included standardized nurse training and call templates, ensuring consistency in care delivery across settings.
A major strength of this trial was its integration into an existing digital health care service. FHVC was already operational before the study, meaning that nurses conducting the calls had prior experience and received training from a clinical nurse educator. This level of standardization may have contributed to the observed effectiveness of the intervention, differentiating our study from others that implemented newly introduced follow-up call programs. Conducted within an existing operational health care service, the study reflected real-world variations in patient care, staffing constraints, and service delivery. As a result, our findings represent an intervention that health care organizations could realistically implement to support patients’ transitions from hospital to home.
The broad eligibility criteria further enhance the generalizability of our findings. Although the study focused on high-risk patients, it included patients with a range of health conditions, demographics, and socioeconomic backgrounds. The standardized discharge call protocol was designed to be adaptable across clinical contexts, and a detailed version is provided for reference (see Appendix S2 in ).
A key limitation is the potential exclusion of patients without reliable phone access. Certain socioeconomic groups may have faced barriers to participating, including a lack of access to phones or data plans. Although FHVC implemented strategies to enhance accessibility, such as using plain language and integrating interpreters to support patients who do not speak English, these barriers remain a challenge for equitable access to virtual care.
Another limitation of this study was the low intervention exposure rate within the intervention group. While the analysis followed an intention-to-treat approach, a substantial proportion of participants did not answer the postdischarge call and therefore were not actually exposed to the intervention. This may have diluted the observed effect and may have underestimated the true impact of the intervention had more participants engaged. Future efforts should focus on improving patient engagement, such as further increasing awareness of the follow-up service at the point of discharge, to enhance reach and effectiveness.
Despite being guided by a sample size calculation, the study faced logistical challenges due to fluctuating discharge volumes and staffing availability. While the goal was to collect data for 58 days, recruitment extended to 84 days to achieve the desired sample size. Nurse capacity constraints also required adjustments to the intervention group sizes, leading to a control group that was smaller than the initially planned sample size (3180 instead of 3465) and an intervention group that was larger (3911 vs 3465). These adjustments reflect the realities of implementing research within an operational care model and underscore the need to balance methodological rigor with service delivery. These deviations from the original allocation plan may impact statistical power and group comparability and should be considered when interpreting results.
Future Directions
Overview
While this study provides strong evidence for the effectiveness of postdischarge follow-up calls, several areas require further exploration to optimize implementation, improve equity, and maximize impact. Future research should focus on leveraging emerging technologies, understanding the mechanisms driving intervention success, addressing disparities in access to virtual care, and evaluating cost-effectiveness. Additionally, qualitative and subgroup analyses may help further refine the intervention’s design and delivery to better meet the needs of diverse patient populations.
Leveraging Emerging Technologies for Enhanced Support
Artificial intelligence (AI) has the potential to improve the scalability and efficiency of postdischarge interventions by augmenting human-led care with data-driven insights. AI-driven decision support systems could help identify patients most likely to benefit from follow-up calls, thereby optimizing resource allocation and ensuring that high-risk individuals receive timely support. By using predictive analytics to prioritize outreach, health care systems could enhance the effectiveness of follow-up programs while also managing staff workload more efficiently.
Additionally, natural language processing technologies could be integrated into call workflows to assist nurses in real-time. These tools could provide structured prompts to ensure comprehensive patient assessments, summarize patient concerns for documentation, or generate automated follow-up messages tailored to each patient’s needs. For example, natural language processing could automatically flag patients with high LACE scores who have missed follow-ups, prompting timely outreach and helping prioritize those at greater risk of admission. Future studies should explore how AI can support, rather than replace, clinical decision-making—maintaining the essential human connection that characterizes high-quality transitional care. A hybrid model where AI improves workflow efficiency while nurses remain the primary point of engagement may offer an optimal balance between scalability and personalized care.
Understanding Mechanisms of Action and Patient-Centered Benefits
While this study demonstrated a reduction in ED visits, future research should explore the mechanisms underlying this effect. It remains unclear which components of the intervention, such as patient education, medication adherence support, emotional reassurance, or care coordination, or the simple act of receiving a call, contribute most to the observed improvements. Identifying the most influential elements would support refinement of the intervention to maximize its impact and cost-effectiveness. Involving patients in this refinement process through co-design of the call content or format can further enhance the relevance and effectiveness of the intervention, aligning it more closely with patient needs and preferences.
Beyond clinical outcomes, patient-reported experiences offer valuable insights into the intervention’s effectiveness. Future qualitative research should examine how follow-up calls influence patient confidence in managing their recovery, their perceived quality of care, and any remaining unmet needs following discharge. Additionally, understanding the perspectives of nurses and other health care providers delivering follow-up calls can help identify workflow challenges and opportunities for improvement. Research in this area could inform best practices for scaling and sustaining postdischarge calls while also minimizing provider burden and enhancing patient engagement.
Promoting Equity in Postdischarge Support
Ensuring equitable access to follow-up care remains a critical challenge. Patients from lower socioeconomic backgrounds, those with limited English proficiency, and individuals without reliable phone access are at risk of being disproportionately excluded from telephone-based interventions. As a result, those who are most vulnerable to hospital readmission may not receive the support they need. To effectively reach and support diverse populations, follow-up care must also be culturally appropriate and safe. Embedding cultural safety into the design and delivery of interventions can help build trust and improve engagement across communities.
Future research should explore alternative and complementary strategies to reach underserved populations. These may include text-based follow-ups, video consultations, or partnerships with community health workers who can provide in-person support. Additionally, health systems should investigate more seamless integration of interpreter services into virtual care workflows and evaluate the potential of multilingual AI-driven chatbots to help bridge communications barriers. Addressing these disparities is essential to ensure that all patients, regardless of socioeconomic status, digital access, or language, can benefit equitably from postdischarge support.
Economic Analysis of Postdischarge Follow-Up Calls
A critical next step is to conduct a cost-effectiveness analysis to determine whether the observed reduction in ED visits results in net cost savings for the health care system. By evaluating factors such as reduced hospital readmissions, decreased ED use, and the cost of nursing time invested in delivering the intervention, an economic evaluation can guide policy decisions and resource allocation for broader implementation.
In addition to understanding overall cost-effectiveness, future studies should assess differential outcomes across patient subgroups. Certain populations may derive more substantial benefit from follow-up calls, informing a more targeted and efficient use of resources. Conducting subgroup analyses based on factors such as age, comorbidities, hospital discharge diagnosis, and social determinants of health could help refine intervention targeting. For example, patients with chronic conditions such as heart failure or chronic obstructive pulmonary disease may benefit more from medication adherence support, while those with lower health literacy may require additional educational reinforcement. Identifying which subgroups experience the greatest reduction in ED visits or readmissions will enable a more tailored approach, ensuring that resources are directed toward those who need them most.
Conclusions
This study suggests that proactive, digitally enabled outreach may support safer care transitions and reduce early ED utilization, even when delivered as a pragmatic, single-touch intervention within routine clinical operations. The findings highlight the potential for this low-cost, scalable intervention to support safer care transitions, particularly in healthcare systems where timely access to primary care remains a challenge. While the intervention did not significantly reduce hospital readmissions, its impact on ED use underscores its value in improving short-term outcomes and alleviating pressure on acute care services. Future studies should investigate whether certain patient subgroups derive greater benefit and explore ways to improve accessibility for populations with limited phone or digital access.
The authors thank the patients and the Fraser Health Virtual Care nurses that participated in this study.
This work was supported by the Fraser Health Strategic Priorities Grant and the Health Research Foundation of Innovative Medicines Canada Team Grant in Virtual Care. The funders had no role in the study design, data collection, analysis, interpretation, writing of the manuscript, or the decision to submit the paper for publication.
Due to conditions of the informed consent obtained from participants, the institutional and Ministry of Health ethical requirements do not permit us to share participant data from this study.
SD contributed to conceptualization, design, methodology, data curation, writing of the manuscript, and project administration. AA contributed to data curation, project administration, investigation, data acquisition, data analysis, and writing of the manuscript. M Montenegro contributed to methodology, data curation, data analysis, software, and writing of the manuscript. M Maitland contributed to conceptualization, design, methodology, and funding acquisition. SC contributed to software and data analysis. SJ contributed to design, methodology, and project administration. HS contributed to design and methodology. DC contributed to investigation and review and editing of the manuscript. JMR contributed to writing. M MacPherson contributed to writing of the manuscript. DB contributed to the review and editing of the manuscript. MN-vV contributed to conceptualization, design, methodology, and supervision. All authors read and approved the final manuscript.
Two authors (MN-vV and SJ) are employed by Fraser Health Virtual Care, the program responsible for implementing the intervention examined in this study, and therefore may be perceived as having an interest in positive outcomes. All other authors declare no financial or nonfinancial competing interests.
Edited by Alicia Stone, Naomi Cahill; submitted 11.Jul.2025; peer-reviewed by Leah Shafran Topaz, Nkemchor Chidubem Favour; final revised version received 19.Dec.2025; accepted 24.Dec.2025; published 17.Mar.2026.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in the Journal of Medical Internet Research (ISSN 1438-8871), is properly cited. The complete bibliographic information, a link to the original publication on https://www.jmir.org/, as well as this copyright and license information must be included.
The Nissan Murano is seen at the New York International Auto Show on April 16, 2025.
Danielle DeVries | CNBC
DETROIT — Nissan Motor plans to join fellow Japanese automakers Toyota Motor and Honda Motor in exporting U.S.-produced vehicles to Japan following changes to the country’s vehicle import rules reached through a trade deal last year by the Trump administration.
The company on Tuesday said it will import the midsize Nissan Murano, built in Smyrna, Tennessee, to Japan beginning early next year. It marks the first American-made Nissan sold in Japan since the 1990s, according to a Nissan spokeswoman.
“With the introduction of this model, Nissan aims to further strengthen its product lineup in Japan and meet the diverse needs of Japanese customers,” Nissan CEO Ivan Espinosa said in a statement.
Nissan is the latest Japanese automaker to announce such plans after changes to regulations meant automakers could more easily import vehicles from the U.S. to Japan. Those rules were put in place as part of a trade deal that also included easing U.S. tariffs enacted by President Donald Trump.
Under the new Japanese regulations that were confirmed last month, U.S.-made vehicles don’t have to meet the country’s vehicle certification as long as they comply with American standards.
Nissan confirmed plans to import the Murano from the U.S. with the steering wheel on the left-hand side of the vehicle, which is typical for Americans but not in the Japanese market.
Automakers typically have to tailor vehicles to meet safety and other regulations for different countries globally. They can range from things such as lighting and side mirrors to more complex parts such as the location of the steering wheel.
Toyota, Honda and Nissan stocks
Nissan’s decision follows Toyota announcing plans in December to begin exporting the Camry sedan, Highlander SUV and Tundra pickup from the U.S. to Japan beginning this year.
Honda — Japan’s second-largest automaker behind Toyota — earlier this month also announced plans to export the U.S.-built Acura Integra Type S and Honda Passport TrailSport Elite SUV to Japan beginning in the second half of this year.
While plans for such exports from the U.S. to Japan likely help with trade relations between the countries, the number of vehicles to be imported may not be meaningful, experts said.
About 95% of the Japanese market is made up of locally produced vehicles, leaving less than a quarter of a million units for imports from all around the world, and a majority of those are from Germany, according to Sam Fiorani, vice president of global vehicle forecasting for AutoForecast Solutions.
Vehicles sold under U.S. brands, including models built in other countries, are a small fraction of that group, including roughly 8,700 Jeeps and 500 Cadillacs, according to Fiorani.
Many of the vehicles planned to be imported to Japan also are considered big or not mainstream for Japanese consumers, according to Stephanie Brinley, a principal automotive analyst at S&P Global Mobility.
“These vehicles are still — with the exception of the Integra — are relatively large for Japan. I think they’re still going to be niche, low-volume products within that market,” she said. “But because they are a little bit different and a little bit bigger, they can position them as a special halo product in Japan.”
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Kindley Re Ltd., a Bermuda-domiciled life and annuity reinsurance company established by Kuvare Holdings in partnership with global investment manager Davidson Kempner Capital Management LP has raised an additional $250 million of equity capital from institutional investors to expand its franchise.
Kuvare Holdings, a technology-enabled specialist in life and annuity insurance and reinsurance solutions, launched the sidecar-like venture back in 2023, after an initial $400 million capital raise.
Kindley Re brings a complementary source of capital from third-parties to help Kuvare expand its underwriting business, by co-investing alongside the parent into qualifying new life and annuity opportunities it has sourced.
To-date, Kindley Re has invested some of the initial fund raise by entering into reinsurance agreements with Kuvare, to participate in qualifying deals including flow reinsurance transactions and block reinsurance transactions.
That original capital raise supported reinsurance of U.S. and Asian liabilities, originated in partnership with Kuvare and now the new equity raise will enable Kindley Re to become even more useful to its parent, in providing a third-party capitalised source of companion reinsurance capacity.
Kindley Re has now raised $250 million of additional equity capital commitments, in a raise supported by a group of institutional investors across the U.S., Latin America, Europe, and Asia, the company has reported.
The capital raise is expected to support the strengthening of its ability to expand its reinsurance franchise and new growth opportunities alongside Kuvare.
Kindley Re Ltd. is a Class E licensed, Bermuda-domiciled life and annuity reinsurance company.
Its launch followed the trend for life and annuity re/insurers to launch sidecar-like reinsurance structures, that provide investors a way to tap into the returns of the life reinsurance asset class and augment the capacity of the re/insurance sponsor at the same time, all while leaning on third-party investor appetite.
Vehicles like Kindley Re enable the sponsoring entities to double-down on the the return drivers of their businesses, leveraging investor appetite for returns from the underwriting and investment side of re/insurance, while utilising third-party capital to support their stature in the reinsurance marketplace.
The life and annuity space is all about scale and stature with deal sizes particularly large, so structures like Kindley Re help life and annuity specialists increase their relevance with clients, help them access deals they may otherwise have been able to enter into, all while sharing the rewards with third-party investors.
Law school professors can use AI-powered tools that require minimal technical expertise to create and deploy in order to help improve students’ legal reasoning and skills by simulating courtroom scenarios
Key insights:
Creating prototypes of IP-protected teaching tools— Law school faculty can build working AI teaching tool prototypes in one to two hours without IP worries because key optional settings enable a closed system to ensure professors’ intellectual property remains protected.
Strong prompting skills create faster prototypes — The best instructions initially set the AI’s character, explains what the AI needs to accomplish, lists which documents to reference exclusively, describes how the response should be formatted, and mentions any applicable legal jurisdiction limits.
Feedback from students is positive — Students’ responses show AI simulators reduce anxiety and build confidence by providing unlimited low-stakes practice opportunities that make legal concepts more digestible through active dialogue rather than passive reading.
Law schools face a persistent challenge on how to provide individualized skills practice when one professor must serve many students. And today’s traditional legal education offers limited opportunities for students to practice oral arguments, evidentiary objections, and witness examinations. Indeed, the repetition necessary to build authentic courtroom skills does not scale easily with law professors in the classroom alone.
To address this challenge, Prof. Alexandria Serra at the University of Missouri–Kansas City School of Law pioneered custom-built tools that simulate trial judges, three-panel appellate courts, witnesses, and evidentiary objection scenarios. Prof. Serra has seen firsthand how these tools give students unlimited, low-stakes practice opportunities that reduce their anxiety while building confidence in their legal reasoning and judgement.
Building your first AI learning tool, step by step
Creating custom AI teaching tools requires far less technical expertise than most professors would assume. As Prof. Serra explains, if you have a general idea of what you want the tool to accomplish, then “you can have a working prototype in less than two hours from idea to execution.”
The process begins with choosing a large language model (LLM) platform, such as ChatGPT, Claude, or Gemini, and securing a paid subscription, which most law schools will provide, she explains. During the sign-up process, optional settings enable a closed system to ensure law professors’ intellectual property is not shown to the students and is not used to train the LLMs.
Prof. Alexandria Serra
Next, you should gather class materials, including slides, case files, manuals, and problems the professor has already created. After that, it is necessary to define one specific use case, such as an evidentiary objections practice tool, a Socratic method simulator, or a client interview assistant.
The building process itself takes about one to two hours and requires no coding skills. “You just start talking to the LLM like you are training a teaching assistant to do exactly what you want to do,” Prof. Serra adds.
Having built many tools, she highlights three critical components that are necessary for the efficient, useful, and flexible prototype. These include:
1. Prompting skills
Effective prompting is key to generating a good prototype. According to Prof. Serra, the ideal prompt includes defining the AI’s role (You are a trial judge in a federal district court), specifying the task the AI should deliver, identifying which documents to use exclusively, describing the desired output format, and including any jurisdictional constraints.
2. Multimodal features in AI tools
Most platforms allow for voice-activated chat mode, in addition to typing back and forth, which helps students respond out loud in real time. Custom AI tools also have shareable links, which enables easy deployment to students. Once a student engages with the tool, they can send back a transcript of the interaction. Some platforms even allow shareable audio files so students can get feedback from their professors on skills performance, not just content.
3. Verifying reliability
Evaluating the quality of the AI output is important but naturally varies by use case. For classroom tools, Prof. Serra recommends deploying prototypes quickly and using students as testers. If the tool produces outputs with inaccuracies, she encourages students to bring these errors to class for discussion. That way, everyone learns how to critically diagnose problems with AI outputs. A variety of problems cause AI inaccuracies — the AI itself, poor prompting, incorrect legal reasoning, or incomplete training.
For wider deployment without the builder’s direct oversight, Prof. Serra recommends an extended period of testing and iteration. Her tool, MootMentorAI, which simulates a three-judge appellate panel for first-year law students preparing for oral argument, is one example. Because MootMentorAI was developed for use by a colleague, Prof. Serra worked with a research assistant to conduct 80 simulations over the course of a semester — 40 from the plaintiff’s perspective and 40 from the defendant’s perspective — to verify reliability and improve performance before deployment without her supervision.
Overcoming adoption barriers among peers
Faculty resistance remains the most significant barrier to deploying AI-enabled teaching tools in legal education. “There’s lots of faculty pushback, distrust, and a healthy dose of skepticism with AI,” Prof. Serra acknowledges, arguing that even so, AI-powered tools are teaching assets for all law school courses. “Even in doctrinal classes that run on traditional Socratic dialogue, professors can still use AI to reinforce learning outside the classroom through tools, such as podcast-style lectures, a multiple-choice practice assistant, tools to enable issue-spotting, and essay practice tied to course fact patterns.”
Common concerns among law school faculty include confidentiality, intellectual property protection, fear of revealing exam content, and perceived lack of technical expertise. However, Prof. Serra points out that these fears often stem from her colleagues’ misunderstanding of how closed systems work. Indeed, if privacy settings are correctly deployed, uploaded materials will not be used to train public models and students cannot access source documents.
Indeed, the most effective strategy for overcoming resistance is personal demonstration, she says, noting that she frequently sits down with colleagues virtually to build tools based on the colleague’s own use case. She’s built everything from a Startup CEO simulator for a business course, to an interview assistant for Career Services, to a simulated forensics expert for students to cross-examine. This grassroots approach, combined with speaking at conferences and identifying super fans who can champion the technology, gradually builds institutional buy-in, she adds.
Multifaceted student feedback
Student feedback has been overwhelmingly positive, with learners describing how AI simulators make legal skills training more accessible, more engaging, and less intimidating. In fact, students are often surprised by how convincingly AI tools can simulate judges, witnesses, and other real-world lawyering scenarios. They also appreciate having permission to use AI as a legitimate learning aid.
They also report that real-time interaction makes course concepts more digestible because these tools turn learning into an active dialogue rather than passively staring at a casebook. Finally, students say the simulators reduce anxiety before oral arguments or presentations by enabling unlimited, low-stakes repetition that builds confidence and keeps practice from feeling overwhelming.
Clearly, AI tools are quickly becoming essential learning infrastructure, and legal education cannot afford to treat them as optional add-ons if it expects to stay relevant. As a growing chorus of educators and employers warns that institutions must evolve, the real question is whether schools will build responsible, faculty-guided systems fast enough to meet students where the profession is headed.
When deployed thoughtfully, these platforms can scale individualized skills training, deepen engagement beyond the casebook, and build durable confidence that law students can carry into their future legal practice.
The stock market’s solid start to the week may signal investors aren’t appreciating the risks tied to the U.S.-Iran war, according to Goldman Sachs. Stocks rose broadly on Monday. The S & P 500 climbed 1%, and the Nasdaq Composite advanced 1.2%. The Dow Jones Industrial Average ended the day up more than 300 points, or 0.8%. The moves came as oil pulled back after Treasury Secretary Scott Bessent told CNBC that the U.S. is letting oil tankers from Iran pass through the Strait of Hormuz. Crude was also pressured by a report that said the U.S. would announce a group of countries to escort ships through the Strait. Still, some are wary of this reaction. “I worry the stock market is underestimating the potential downside tails,” Tony Pasquariello, global head of hedge fund coverage at Goldman Sachs, wrote in a note to clients. “The market is certainly smarter than I am, but I’m surprised that market participants aren’t more concerned.” .SPX 5D mountain SPX 5-day chart Indeed, there are signs that risks persist. While reports emerged of the escort coalition in the Middle East, President Donald Trump himself suggested it wasn’t quite ready yet . “We have some [countries] that are really enthusiastic. They’re coming already. They’ve already started to get there,” Trump told reporters on Monday. “We’ll give you a list. Some are very enthusiastic, and some are less than enthusiastic, and I assume some will not do it.” On top of that, Monday’s bounce wasn’t overly convincing from a volume standpoint. The SPDR SD & P 500 ETF (SPY) , one of the most widely traded funds in the market, traded 71.3 million shares Monday. That’s below its 30-day average volume of 88.5 million. The Invesco QQQ Trust , which tracks the Nasdaq-100, also had light volume with 44.4 million shares; its 30-day average sits at 71.5 million. And while the S & P 500 continues to hold above its key 200-day moving average, Rob Ginsberg of Wolfe Research thinks financials need to recover before a meaningful rally takes place. The S & P 500 financials sector is down 4% this month and is “deeply oversold,” the strategist wrote to clients. “We’ve been laser-focused on their troubling performance for quite some time, and if the market is going to make a powerful stand at its 200-day, this needs to be the one to show us the way.”
Company tops global soundbar sales, strengthening its audio portfolio with premium models and an expanded 2026 lineup
Coupled with 20 years of leadership in the global TV market, achievement establishes Samsung as the leader in home entertainment
Samsung Electronics Co., Ltd. today announced that it has maintained its leadership in the audio-visual sector as the world’s top soundbar brand for the 12th year in a row.
According to new research from Future Source, Samsung captured 21.5% of global soundbar revenue and 19.7% of unit volume in 2025, continuing its leadership streak that began in 2014. This milestone, along with two decades of global TV leadership[1], reinforces Samsung’s position at the forefront of the home entertainment industry.
Samsung’s sustained success in the soundbar market is driven by advanced audio technology, immersive sound and seamless integration with Samsung TVs. Building on this foundation, Samsung will expand its 2026 audio lineup with new products that deliver cinema-quality sound tailored to different living environments.
The lineup will include:
HW‑Q990H flagship soundbar, the successor to the HW‑Q990F
All‑in‑one soundbar HW‑QS90H, exceptional sound that is flexible so it can be wall mounted or sit independently
Erwan Bouroullec‑designed Music Studio 7 and Music Studio 5 Wi‑Fi speakers
“At Samsung, we take special pride in our soundbar brand and see it as a way to bring premium sound experiences to homes everywhere,” said Hun Lee, Executive Vice President of the Visual Display (VD) Business at Samsung Electronics. “Being named the top soundbar brand in the world for the 12th consecutive year is not just a tremendous honour but a testament to our commitment to premium home entertainment.”
[1]Omdia Q4 2025 Public Display Report, by unit sales.
India’s Prime Minister Narendra Modi, seventh left, poses for photographs with chief executive officers of various AI groups during the AI Summit in New Delhi, India, Thursday, Feb. 19, 2026. (Indian Prime Minister’s Office via AP)
Global AI summits have increasingly embraced the language of multistakeholder governance, but meaningful participation by civil society and academic actors remains limited. Across the series of AI summits — from Bletchley and Seoul to Paris and New Delhi — governments have gradually expanded opportunities for engagement with researchers, civil society organizations, and other stakeholders. These efforts have helped bring issues such as democratization, sovereignty, equity, and inclusivity into global AI governance discussions. Yet the ability of non-state and non-corporate actors to shape agendas and outcomes has remained constrained.These summits are often in the nature of trade shows showcasing industrial prowess rather than forums for substantive governance conversations.
The New Delhi AI Impact Summit Declaration, signed by more than 90 countries, including China and the United States, continued this trajectory by formally recognizing international cooperation and multistakeholderism. The 2026 India AI Impact Summit also created additional avenues for participation, particularly for civil society groups, researchers, and academics from the Majority World. However, the inclusion of these themes in summit agendas and declarations has not yet translated into meaningful influence over decision-making.
If global AI governance is to address real-world impacts — both positive and negative — the architecture and institutional processes of these Summits must evolve. Multistakeholder participation for civil society groups and academic actors should move beyond representation toward active involvement in agenda-setting and decision-making. This is especially true for those from the Global Majority, who face additional barriers to participation and power. To allow for truly meaningful, multistakeholder governance, the path to the upcoming UN Global Dialogue on AI Governance and the 2027 Global AI Summit in Geneva must be open, inclusive, and rights-focused, and prioritize a bottom-up civil society agenda.
Thematic priorities of AI Summits: From the UK to India and beyond
The previous three Summits in Bletchley, Seoul, and Paris focused on frontier risks, safety research, building safety networks, and advancing public interest AI. As the first summit hosted in a Global Majority country, the India AI Impact Summit shifted the global discourse to prioritize perspectives and needs of the Global Majority, integrating diverse perspectives into the official program.
While the New Delhi AI Impact Declaration is widely welcomed for its focus on sovereignty, democratizing access to AI resources and infrastructure, supporting locally relevant innovation, and strengthening resilient AI ecosystems, it falls short of addressing human rights or establishing mechanisms to track the implementation of voluntary commitments. Democracy and sovereignty are words increasingly used by the White House and US AI companies to position their products and services as more rights-respecting and competitive than their Chinese alternatives. Without targeted autonomy, the Global Majority runs the risk of renting Big Tech’s models.
Although multiple initiatives announced at the India Impact Summit are still in their early stages of implementation and are, again, voluntary and non-binding, it is noteworthy that multistakeholder collaboration is emphasized across multiple deliverables. In practice, the commitments could create a framework for cooperation rooted in inclusive, democratized AI. However, with the next summit being hosted by Switzerland, it is necessary to ensure that the thematic focus on the needs and issues of the Global Majority remains part of the core agenda of global AI governance. The answer lies in the architecture of the Summits.
Evaluating the summit architecture
To date, the architecture and organizational processes of these Summits have lacked coherence, offering civil society and academic stakeholders only a limited role in shaping agendas and outcomes. This inconsistency is evident across the Summit series: the Bletchley Summit had limited civil society participation; the Paris Summit utilized a multistakeholder steering committee and working groups with variable impact and restricted access to the Main Summit.
Ahead of the Delhi Summit, the Government of India established working groups (the outcomes of which are available on the IndiaAI website), expert engagement groups, and accredited pre-events organized and hosted by a range of stakeholders. Civil society sessions were accredited and integrated into the main Summit agenda and as satellite events, including our multistakeholder side event Reinforcements and Learning: Multistakeholder Convening on AI Governance, which convened over 400 leading academic, civil society, company, and government experts, and formed part of our broader MAP-AI project activities in New Delhi. The summit was also open to participation by the general public.
Yet, as with previous summits, the Delhi Summit’s broader participation did little to connect academic and civil society discussions to actual decision-making on the main agenda and outcomes. Space was definitely created for civil society participation at the India Summit, but the contours of inclusion weren’t negotiated; they were granted. For instance, on the day of the Prime Minister’s speech, with heads of state and senior executives in attendance, civil society was not permitted to attend.
Unfortunately, promises around Global Majority leadership did not translate into meaningful action, either. With the lasting image of the India AI Impact Summit being the Indian Prime Minister holding hands with mostly US Big Tech CEOs, who were all men.
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Across all summits, a persistent disconnect remains between the government decision-making track and civil society groups or academic mechanisms. To shift these vital voices from the periphery to the core, future Summits must move beyond simple participation toward shared spaces and “mingled tracks” that bring together governments, companies, and civil society in deliberative spaces. True multistakeholder outcomes require an exchange of perspectives that transcends panel discussions, allowing for real, integrated input from government, industry, and academia alike.
To enable this, the following issues must be addressed:
Lack of a governing framework: The current summit model operates on an ad-hoc basis, lacking a comprehensive governing framework, a central secretariat, or a coordinating body. This institutional vacuum creates a gap in predictable “continuity” between host nations. For example, Switzerland was only confirmed as the 2027 host in New Delhi, and the United Arab Emirates has announced that it will co-host 2027 and host the 2028 Summit, but this has not been confirmed. Without a transparent process for selecting future hosts or defining a multi-year agenda, civil society is forced into a cycle of reactive engagement. This unpredictability hinders sustained, long-term engagement, both substantively, financially, and logistically.
An accountability deficit: In the absence of formal monitoring and evaluation mechanisms, the commitments made at each Summit risk becoming performative and influenced by the shifting sands of geopolitics and corporate interests. There is currently no accountability framework to track progress on deliverables from one Summit to the next. For stakeholders engaging in each Summit, this raises fundamental questions about the efficacy of their participation and demands.
Procedural ambiguity for multistakeholder participation: The procedural pathways for integrating non-governmental and non-corporate input into concrete outcomes remained undefined. There is a focus on enabling participation, but avenues for meaningful influence on agendas, process, and outcomes are often opaque and inconsistent, leading to last-minute engagement efforts. The lack of a standardized process for receiving and synthesizing multistakeholder contributions, and a roadmap for it, leads to inconsistent participation. Long-established Internet Governance processes around multistakeholder participation through the World Summit on the Information Society (WSIS), the Internet Governance Forum (IGF), and NetMundial and the Sao Paulo Principles offer important lessons and pathways for incorporating meaningful multistakeholder participation.
Limited engagement: While India has set a valuable precedent by focusing on the Global Majority, it is unclear whether that priority will be retained as the next few global AI governance gatherings shift back to the North. Both logistically and substantively, Majority World participation, especially from civil society and academia, might drop in Geneva without dedicated efforts. Meanwhile, while civil society has been provided more space at and around the last two Summits, a “participation paradox” persists: civil society is increasingly invited to speak at sessions and panels but remains largely excluded from agenda-setting and decision-making.
These systemic barriers reveal a disconnect between rhetoric and reality: while the language of a multistakeholder approach and an agenda of inclusivity, social empowerment, and access is adopted, the actual agency of underrepresented voices remains curtailed. This curtailment occurs at a critical juncture, where multistakeholder input is essential as AI technologies and their applications evolve at breakneck speed.
This rapid advancement, further complicated by deepening geopolitical uncertainty and the increasing use of AI in armed conflict, raises fundamental questions about acceptable use, liability for harm, the necessary guardrails and checks and balances, and ultimately who gets to define them. These questions demand rigorous deliberation by diverse voices, particularly those most directly impacted by the technology. Consequently, we must design inclusive multistakeholder processes that bring together a plurality of contexts, values, experiences, and expertise and can navigate both hyper-fast development cycles and new use cases, as well as a landscape of fractured global relationships.
Future course
As the center of gravity for AI governance shifts from New Delhi to Geneva, the international community faces a critical moment. The challenge now is to ensure that the AI governance agenda, discourse, and ultimately the frameworks that emerge, reflect and address the needs of and impact on the more than 80% of the world’s population that lives in the Global Majority. This must be achieved by centering the human rights framework, enabling continuity and accountability, and by governance frameworks that address real-world impacts by enhancing multistakeholder participation.
To facilitate this evolution, the Centre for Communication Governance at National Law University Delhi (CCG) and Global Network Initiative have developed a Reflections and Recommendations brief. This framework serves as a blueprint for ensuring that AI governance conversations and processes include diverse perspectives, particularly from the Global Majority, are grounded in real-world contexts and impacts, prioritize a bottom-up civil society agenda, and result in legitimate outcomes, focusing on nine priorities.
It is clear that building and sustaining meaningful participation will require more than simply funding travel and organizing events. Enabling meaningful multistakeholder participation requires elevating Global Majority priorities with contextual nuance, convening diverse stakeholders on equal footing across the AI ecosystem, and integrating rigorous policy analysis with deep technical understanding. To enhance the impact of civil society and the Global Majority on AI governance, there is a need to support community and coordination, civil society agenda-setting and substantive advocacy, and targeted research and peer learning.
The next two years offer a critical opportunity to emphasize and institutionalize the agency of underrepresented voices. Ultimately, the legitimacy of the global AI governance architecture will be measured by its ability to operationalize the rhetoric of multistakeholderism. This requires a shift from symbolic inclusion to transparent, accountable, bottom-up, rights-driven frameworks that give those most impacted by AI not only an equal seat at the table but also an opportunity to write the recipe.
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