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Echinococcosis is a parasitic disease that poses a significant threat to human health and constitutes a global public health concern (1). Medication serves as one of the primary treatments, with albendazole considered the first-line drug (2-3). Present evidence indicates that Chinese mainland experiences the highest prevalence of echinococcosis (4). To alleviate the economic burden on patients and enhance treatment efficacy, China initiated “The National Project for Echinococcosis Control and Prevention” in 2008, offering free albendazole for patients undergoing medical treatment and mandating regular patient management. This study examined and investigated 899 patient files of individuals receiving and having received albendazole treatment, registered at the CDC across 10 endemic counties in Sichuan, Gansu, and Xinjiang provincial-level administrative divisions (PLADs) in 2019. The objective was to evaluate patient management quality, identify issues, and recommend viable strategies and measures. Among 634 assessable patient files, 71.60% of patients demonstrated a ratio of actual follow-up times to theoretical times below 0.8, and 71.46% of patients exhibited a ratio of actual reexamination times to theoretical times below 0.8. The proportion of individuals with a ratio of actual follow-up times to theoretical times decreased as the duration of albendazole treatment increased (χ²=229.394, P<0.001), as did reexamination rates (χ²=195.144, P<0.001). These findings suggest that relevant authorities should focus on improving the quality of patient management.
According to “The National Project for Echinococcosis Control and Prevention,” the CDC is responsible for establishing patient files upon initial diagnosis of echinococcosis. These files should include basic personal information, disease characteristics, and the date of initial diagnosis. Furthermore, it is mandated to record all follow-ups and reexaminations during the treatment period. Based on these findings, the therapeutic effects are evaluated, and the medical treatment plan may be adjusted as necessary (5). Follow-up assessments are conducted every three months to monitor patient medication adherence and to encourage corresponding reexaminations. Additionally, imaging reexaminations for patients undergoing albendazole treatment are recommended every six months.
In this study, we randomly selected 10 endemic counties in 2019 to examine the treatment of patients with relatively complete patient files. The selected counties included Daofu County, Ganzi County, and Ruoergai County in Sichuan Province; Huining County, Tianzhu County, Zhang County, and Maqu County in Gansu Province; and Gaochang District, Jimusar County, and Fukang City in Xinjiang Uygur Autonomous Region. We employed cluster sampling to investigate all patients treated with albendazole in these endemic counties. Data were collected from patient files, including administrative entry dates, actual follow-up occurrences, imaging reexaminations, and the duration of albendazole therapy.
The duration of albendazole therapy was calculated in months based on administrative entry dates and investigation dates. Durations of less than 15 days were excluded from the analysis. Due to missing mandatory data (e.g., administrative entry dates), we were unable to calculate the duration of albendazole therapy for some patients. Theoretical follow-up occurrences were computed based on follow-up frequency every three months. To evaluate follow-up, we calculated the ratio of actual to theoretical follow-up occurrences (Rf). The assessment of imaging reexaminations was calculated similarly by determining Rr. Additionally, we calculated the ratio of the actual duration of albendazole therapy to the recommended duration of therapy (Rm).
For statistical analysis, we utilized Epidata (version 3.1, EpiData Association, Odense, Denmark) and SPSS (version 22.0, IBM Corporation, Armonk, US).
In this study, a total of 899 patients from 10 endemic counties received albendazole treatment. The integrity of each patient file was assessed during the evaluation process. Out of the 899 patient files, 265 (29.48%) were found to have missing mandatory information and were consequently excluded from statistical analysis. Ultimately, 634 valid patient files (70.52%) were considered for further examination in this research.
Among the 634 files analyzed, 41 were found to be without follow-up records, resulting in a follow-up rate of 93.53% (593/634). The majority of Rf values fell within the range of 0.3≤Rf<0.5, accounting for 35.17%, followed by the range 0.5≤Rf<0.8, accounting for 25.55%. Only 21.92% of patients had Rf values ≥0.8. When stratified according to the theoretical duration of albendazole treatment, Rf values ≥0.8 were observed in 95.24% (20/21), 88.00% (44/50), 69.39% (34/49), 12.75% (26/204), 5.12% (15/293), and 0 (0/17) of patients for those treated with albendazole for less than 1 year, 1–2 years, 3–4 years, 5–6 years, 7–9 years, and ≥10 years, respectively. The proportion of patients with Rf values ≥0.8 significantly decreased as the duration of albendazole treatment increased (χ2trend=229.394, P<0.001) (Table 1). The recorded rate of reexamination was 94.64% (600/634). The Rr was mainly concentrated 0.3≤Rr<0.5, accounting for 41.17%, and 0.5≤Rr<0.8, accounting for 21.61%. Only 23.19% of patients had Rr≥0.8. Among patients taking albendazole for less than 1 year, 1–2 years, 3–4 years, 5–6 years, 7–9 years, and ≥10 years, the percentages of patients with Rr≥0.8 were 100.00% (21/21), 84.00% (42/50), 57.14% (28/49), 10.78% (22/204), 11.26% (33/293), and 5.88% (1/17), respectively. As the treatment duration increased, the proportion of patients with Rr≥0.8 significantly decreased (χ2trend=195.144, P<0.001) (Table 1).
Duration of albendazole
therapy (year)Total
(N)Follow-up (N, %) Reexamination (N, %) Rf<0.3 0.3≤Rf<0.5 0.5≤Rf<0.8 Rf≥0.8 Unrecorded R<0.3 0.3≤Rr<0.5 0.5≤Rr<0.8 Rr≥0.8 Unrecorded < 1 21 0 (0.00) 0 (0.00) 1 (4.76) 20 (95.24) 0 (0.00) 0 (0.00) 0 (0.00) 0 (0.00) 21 (100.00) 0 (0.00) 1− 50 0 (0.00) 0 (0.00) 4 (8.00) 44 (88.00) 2 (2.00) 0 (0.00) 1 (2.00) 4 (8.00) 42 (84.00) 3 (6.00) 3− 49 0 (0.00) 4 (8.16) 7 (14.29) 34 (69.39) 4 (8.16) 3 (6.12) 4 (8.16) 10 (20.41) 28 (57.14) 4 (8.16) 5− 204 35 (17.16) 76 (37.25) 56 (27.45) 26 (12.75) 11 (5.39) 14 (6.86) 99 (48.53) 59 (28.92) 22 (10.78) 10 (4.90) 7− 293 28 (9.56) 135 (46.08) 94 (32.08) 15 (5.12) 21 (7.17) 22 (7.51) 157 (53.58) 64 (21.84) 33 (11.26) 17 (5.80) ≥10 17 6 (35.29) 8 (47.06) 0 (0.00) 0 (0.00) 3 (17.65) 16 (94.12) 0 (0.00) 0 (0.00) 1(5.88) 0 (0.00) Total 634 69 (10.88) 223 (35.17) 162 (25.55) 139 (21.92) 41 (6.47) 55 (8.68) 261 (41.17) 137 (21.61) 147 (23.19) 34 (5.36) χ2 229.394 195.144 P-value* <0.001 <0.001 Note: N represents the total number of patients.
Abbreviation: CI=confidence interval; Rf=the ratio of actual to theoretical follow-up occurrences; Rr=the ratio of actual to theoretical reexamination occurrences.
* P-values were compared at a significance level of 0.05.Table 1. Number and percentage (%) of echinococcosis patients treated with albendazole, stratified by duration of therapy, across ten endemic counties in 2019.
Among 593 patients with follow-up records, 65.94% (91/138) of patients with Rf≥0.8 had the Rm≥0.8, which was significantly higher than that of patients with other ratios (χ2=281.745, P<0.001) (Table 2). For reexamination, 87.05% (121/139) of the patients with Rf≥0.8 had the Rr≥0.8, which was significantly higher than that of patients with other ratios (χ2=825.136, P<0.001) (Table 3).
Follow-up Total (N) Medication (N, %, 95% CI) χ2 P* Rm=0 0<Rm<0.3 0.3≤Rm<0.5 0.5≤Rm<0.8 Rm≥0.8 Unrecorded Rf<0.3 69 8 (12.50, 4.17–20.83) 27 (42.19, 29.75–54.62) 23 (35.94, 23.86–48.02) 6 (9.38, 2.04–16.71) 0 5 281.745 <0.001 0.3≤Rf<0.5 223 15 (8.29, 4.23–12.34) 35 (19.34, 13.53–25.15) 63 (34.81, 27.80–41.81) 60 (33.15, 26.23–40.07) 8 (4.42, 1.40–7.44) 42 0.5≤Rf<0.8 162 21 (13.13, 7.84–18.41) 15 (9.38, 4.81–13.94) 42 (26.25, 19.36–33.14) 53 (33.13, 25.75–40.50) 29 (18.13, 12.09–24.16) 2 Rf≥0.8 139 0 0 2 (1.45, 0.57–3.47) 45 (32.61, 24.69–40.53) 91 (65.94, 57.94–73.95) 1 Total 593 44 (8.10, 5.80–10.41) 77 (14.18, 11.24–17.12) 130 (23.94, 20.34–27.54) 164 (30.20, 26.33–34.08) 128 (23.57, 19.99–27.15) 50 Note: N represents the total number of patients. "Unrecorded" indicates a lack of medication records with corresponding follow-up data. Chi-square tests were utilized to determine the significance levels across varying ratio distributions.
Abbreviation: CI=confidence interval; Rf=the ratio of actual to theoretical follow-up occurrences; Rm=the ratio of the actual duration of albendazole therapy to the recommended duration of therapy.
* P-values were compared at the 0.05 significance level.Table 2. Follow-up and medication analysis for echinococcosis patients treated with albendazole in ten endemic counties, 2019.
Follow-up Total (N) Reexamination (N, %, 95% CI) Unrecorded χ2 P* Rr<0.3 0.3≤Rr<0.5 0.5≤Rr<0.8 Rr≥0.8 Rf<0.3 69 29 (42.65, 30.59–54.71) 39 (57.35, 45.29–69.41) 0 0 1 825.136 <0.001 0.3≤Rf<0.5 223 22 (10.50, 6.03–14.06) 191 (87.21, 82.76–91.67) 5 (2.28, 0.29–4.28) 1 (0.46, 0.04–1.36) 4 0.5≤Rf<0.8 162 4 (2.50, 0.05–4.95) 22 (13.75, 8.36–19.14) 115 (71.88, 64.83–78.92) 19 (11.88, 6.81–16.94) 2 Rf≥0.8 139 0 1 (0.72, 0.07–2.14) 17 (12.23, 6.72–17.74) 121 (87.05, 81.40–92.70) 0 Total 593 55 (9.39, 7.02–11.75) 253 (43.17, 39.15–47.20) 137 (23.38, 19.94–26.82) 141 (24.06, 20.59–27.53) 7 Note: N represents the total number of patients. “Unrecorded” indicates the absence of reexamination and follow-up records. Chi-square tests were utilized to determine the significance levels among various ratio distributions.
Abbreviation: CI=confidence interval; Rf=the ratio of actual to theoretical follow-up occurrences; Rr=the ratio of actual to theoretical reexamination occurrences.
* P-values were compared at the 0.05 significance level.Table 3. Analysis of Follow-up and reexamination for echinococcosis patients treated with albendazole in 10 endemic counties, 2019.
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