The study was conducted in the Department of Emergency Medicine, Linquan County People’s Hospital, Fuyang, Anhui, China. The study protocol was reviewed and approved by the Ethics Committee of Linquan County People’s Hospital (Approval No. 24XNLC-HL1015). Written informed consent was obtained from all participants before enrollment. All procedures involving human participants were conducted in accordance with institutional ethical requirements and applicable ethical principles.
Study setting and participant identification
The study was conducted as a single-center longitudinal observational investigation in the Department of Emergency Medicine at Linquan County People’s Hospital, Fuyang, Anhui, China. Participants were recruited between January 2024 and January 2026 and were followed from the post-emergency-treatment baseline through 1 month after discharge.
Convenience sampling was used to identify eligible patients admitted with acute myocardial infarction (AMI). The same eligibility criteria and screening procedures were applied to all potential participants. Because convenience sampling may introduce selection bias, this potential source of bias was considered when interpreting the generalizability of the findings.
A total of 287 patients were screened, of whom 27 were not enrolled. Eight patients had experienced a previous myocardial infarction, six were unable to complete the study assessments because of impaired consciousness or cognitive function, five had other organic heart diseases, four had malignant tumors, multiple organ failure, or other severe systemic diseases, and four declined participation. The remaining 260 patients were enrolled in the study.
Eligibility criteria and baseline definition
Patients were included if they had an established clinical diagnosis of AMI, were experiencing their first episode of myocardial infarction, were aged ≥18 years, had intact consciousness and cognitive function sufficient to understand and complete the study assessments, and provided written informed consent. Patients with other organic heart diseases, malignant tumors, multiple organ failure, or other severe systemic organic diseases were excluded.
Enrollment was restricted to patients with first-onset myocardial infarction to reduce heterogeneity associated with previous infarction, prior revascularization, chronic post-infarction functional impairment, and pre-existing adaptations in self-care or rehabilitation, all of which could independently influence baseline nursing dependency and subsequent trajectory patterns.
T1 was defined as the time point following successful emergency treatment and recovery of consciousness, when the participant was able to complete the required assessments reliably.
Demographic and cardiovascular-related clinical data collection
A study-specific general information questionnaire was used to collect age, sex, body mass index (BMI), marital status, cardiac function classification, myocardial infarction type, reperfusion treatment strategy, and history of underlying diseases. Demographic and psychosocial information was obtained through questionnaire assessment and medical record review, as appropriate. Cardiovascular-related clinical characteristics, including cardiac function classification, myocardial infarction type, reperfusion strategy, and history of underlying diseases, were extracted from the medical records for the index hospitalization using predefined definitions. Cardiac function classification was extracted from the index-hospitalization medical record and grouped as Class I–II or Class III–IV for analysis. Myocardial infarction type was classified as ST-segment elevation myocardial infarction (STEMI) or non-ST-segment elevation myocardial infarction (NSTEMI) based on the diagnosis recorded during the index hospitalization. History of underlying diseases was coded dichotomously as no (0) or yes (1), with “yes” indicating that at least one predefined chronic comorbid condition was documented in the medical history.
Percutaneous coronary intervention (PCI) and thrombolytic therapy were recorded according to the treatment actually received during the index hospitalization rather than the intended treatment plan. The original continuous values for age and BMI were retained for statistical analysis.
Repeated nursing dependency assessment
The Care Dependency Scale (CDS5) was administered at T1. The scale contains 15 items. Each item was rated from 1 (completely dependent) to 5 (almost independent), yielding a total score ranging from 15 to 75. Higher scores indicated greater independence and lower nursing dependency. According to the established CDS classification, scores of 60–69 indicate a limited degree of care dependency, whereas scores of 70–75 indicate near independence; therefore, a total CDS score <70 was considered indicative of nursing dependency in the present study4,5.
The CDS assessment was repeated on day 3 after admission (T2), at discharge (T3), and 1 month after discharge (T4). The same instructions, item order, scoring rules, and assistance procedures were used across all assessments to minimize measurement inconsistency. The T4 assessment was conducted during the scheduled 1-month post-discharge follow-up, either in person at the outpatient clinic or by telephone when an in-person visit was not feasible. In both settings, a trained member of the research team administered all CDS items using the same standardized instructions, item order, and scoring criteria.
All 260 enrolled participants completed the CDS at all four time points, and no participants were lost to follow-up during the 1-month observation period.
Baseline psychosocial assessment
The 17-item Hamilton Depression Rating Scale (HAMD-17)6 was administered once at T1. Items 1–3, 7–11, 15, and 17 were scored from 0 to 4, whereas items 4–6, 12–14, and 16 were scored from 0 to 2. Item scores were summed to obtain a total score ranging from 0 to 54, with higher scores indicating more severe depressive symptoms.
The Generalized Anxiety Disorder-7 (GAD-7)7 was administered once at T1. Each of the seven items was scored from 0 (not at all) to 3 (nearly every day), resulting in a total score ranging from 0 to 21. Higher scores indicated more severe anxiety symptoms.
The Social Support Rating Scale (SSRS)8 was administered once at T1. The scale consisted of 10 items. Items 1–4 and 8–10 were rated on a 4-point scale from 1 to 4; item 5 was scored from 1 to 4 according to the reported level of support; and items 6 and 7 were scored according to the number of available sources of support. The total score ranged from 12 to 66, with higher scores indicating greater social support.
All CDS and psychosocial assessments were administered or supervised by trained members of the research team. Before participant enrollment, assessors received standardized training on questionnaire administration, item interpretation, permitted assistance, and scoring procedures. The same standardized instructions, item order, and scoring criteria were used throughout the study. The same assessor was not required to evaluate an individual participant at every time point; consistency across assessors was maintained through standardized training and uniform assessment procedures. Participants were asked to complete the questionnaires independently whenever possible. When participants experienced difficulties with reading, comprehension, or writing, standardized one-to-one assistance was provided without suggesting responses, interpreting items on the participant's behalf, or altering the participant’s responses.
Data quality control and missing-data handling
Before questionnaire administration, participants were informed about the study purpose, completion procedures, and confidentiality requirements. Standardized instructions and identical assessment procedures were used for all participants. Completed questionnaires were checked immediately for omitted or clearly invalid entries. When an item was left unanswered, the participant was asked to review the omitted item and, if willing, provide a response. When questionnaire assistance was required, study staff did not suggest, interpret, or supply responses on the participant’s behalf. Clinical variables were extracted using predefined definitions, and completed forms were verified before data entry.
All 260 participants completed the CDS assessments at T1–T4, with no loss to follow-up. Longitudinal CDS data and the demographic, clinical, and psychosocial variables included in the reported analyses were complete. Therefore, all 260 participants were included in the analyses, and no data imputation was required.
Growth mixture modeling of longitudinal CDS scores
Growth mixture modeling (GMM) was performed using Mplus version 8.3. An unconditional GMM without covariates was fitted, with CDS_T1, CDS_T2, CDS_T3, and CDS_T4 entered as continuous manifest variables.
One- through five-class solutions were fitted sequentially using robust maximum likelihood estimation (MLR). To reduce the risk of convergence to a local maximum, 1,000 random sets of starting values were generated, and the best 200 were retained for final-stage optimization. For each solution, normal termination, replication of the best log-likelihood across random starts, and the absence of inadmissible parameter estimates were confirmed.
The Akaike Information Criterion (AIC), Bayesian Information Criterion (BIC), sample-size-adjusted BIC (aBIC), entropy, Lo-Mendell-Rubin adjusted likelihood-ratio test (LMR-LRT), and bootstrap likelihood-ratio test (BLRT) were recorded for each solution. Lower AIC, BIC, and aBIC values were interpreted as indicating better relative model fit, whereas entropy values closer to 1 indicated clearer class separation.
Each k-class solution was compared with the corresponding k − 1 solution using the LMR-LRT and BLRT. The final model was not selected solely on the basis of decreasing information criteria; convergence stability, class size, posterior membership probabilities, parsimony, and clinical interpretability were also considered. Each participant was assigned to the class with the highest posterior membership probability, and class-specific average posterior probabilities were calculated as an additional measure of classification quality.
Analysis of repeated CDS measurements
To evaluate within-participant changes in CDS scores across T1, T2, T3, and T4 in the overall cohort, a one-way repeated-measures analysis of variance (RM-ANOVA) was performed with assessment time as the within-subjects factor. The assumptions of approximate normality and sphericity were assessed. Sphericity was evaluated using Mauchly's test, and Greenhouse–Geisser-corrected results were used when the sphericity assumption was violated. All tests were two-sided, and P < 0.05 was considered statistically significant.
Univariate comparisons across trajectory classes
Analyses other than GMM were performed using IBM SPSS Statistics version 26.0. Age, BMI, HAMD-17, SSRS, and GAD-7 scores were analyzed as continuous variables without categorization.
Approximately normally distributed continuous variables were expressed as mean ± standard deviation and compared across the four trajectory classes using one-way analysis of variance. Categorical variables were expressed as participant counts and compared using the Pearson chi-square test. All P values were two-sided, and P < 0.05 was used as the threshold for identifying variables for inclusion in the initial multivariable model.
In the univariate analysis, age, marital status, cardiac function classification, myocardial infarction type, PCI, thrombolytic therapy, HAMD-17 score, SSRS score, GAD-7 score, and history of underlying diseases met the P < 0.05 criterion and were therefore entered into the initial multivariable model. Sex and BMI did not meet this criterion.
Multinomial logistic regression and model diagnostics
The four trajectory classes were treated as a nominal outcome, and multinomial logistic regression was performed rather than binary logistic regression. C1 (High Independence-Slow Improvement) was designated as the reference outcome category.
All variables with P < 0.05 in the univariate analyses were included in the initial model. Backward likelihood-ratio selection was then applied, with variables showing P > 0.10 sequentially removed. Statistically meaningful main effects were retained in the final model.
Multicollinearity was assessed using tolerance and variance inflation factor (VIF) values. In the final analysis, tolerance values ranged from approximately 0.81 to 0.97, and VIF values ranged from 1.03 to 1.24, indicating no substantial multicollinearity.
Interaction testing was restricted to prespecified clinically plausible terms to reduce the risk of overfitting. Three prespecified interactions—age × history of underlying diseases, marital status × SSRS score, and HAMD-17 score × GAD-7 score—were evaluated individually using likelihood-ratio tests. The corresponding P values were 0.655, 0.301, and 0.908, respectively; therefore, none of the interaction terms were retained.
Overall model performance was evaluated using the likelihood-ratio test against the intercept-only model; Pearson and deviance goodness-of-fit tests; Cox-Snell, Nagelkerke, and McFadden pseudo-R2 statistics; classification accuracy; convergence; and assessment of complete or quasi-complete separation.
Adjusted odds ratios (ORs) with 95% confidence intervals (CIs) were reported for all final predictors for the C2 versus C1, C3 versus C1, and C4 versus C1 comparisons. Wide CIs were interpreted as indicating limited precision rather than definitive evidence of large effect sizes.
Sample-size considerations and reporting
No single universal sample-size threshold was applied to the GMM. Sample adequacy was considered in relation to model complexity, class proportions, class separation, missing-data patterns, entropy, posterior probabilities, and convergence9.
No formal a priori simulation-based power calculation was performed because the study was an exploratory longitudinal investigation based on the eligible population available during the predefined recruitment period. The final four-class solution comprised 66, 54, 90, and 50 participants and yielded an entropy value of 0.879, with average posterior probabilities ranging from 0.871 to 0.927.
For multinomial logistic regression, sample adequacy was assessed with respect to the number of participants in each outcome category and the number of candidate predictor parameters10. Because some trajectory classes were relatively small, the regression analysis was interpreted as an exploratory association analysis rather than as the development of a definitive prediction model.
The observational study was reported in accordance with the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) framework, including the study design, setting, participant flow, data sources, potential sources of bias, study size, statistical methods, missing data handling, main results, limitations, and generalizability.