Skip to main content
  • Research article
  • Open access
  • Published:

Effectiveness of joint 3 + 1 malaria strategy along China–Myanmar cross border areas

Abstract

Background

Cross-border malaria in Laiza City of Myanmar seriously affected Yingjiang County of China and compromised reaching the goal of malaria elimination by 2020. Since 2017, a pilot project on 3 + 1 strategy of joint cross-border malaria prevention and control was carried out for building a malaria buffer in these border areas. Here, 3 were the three preventive lines in China where different focalized approaches of malaria elimination were applied and + 1 was a defined border area in Myanmar where the integrated measures of malaria control were adopted.

Methods

A 5-year retrospective analysis (2015 to 2019) was conducted that included case detection, parasite prevalence and vector surveillance. Descriptive statistics was used and the incidence or rates were compared. The annual parasite incidence and the parasite prevalence rate in + 1 area of Myanmar, the annual importation rate in Yingjiang County of China and the density of An. minimus were statistically significant indictors to assess the effectiveness of the 3 + 1 strategy.

Results

In + 1 area of Myanmar from 2015 to 2019, the averaged annual parasite incidence was (59.11 ± 40.73)/1000 and Plasmodium vivax accounted for 96.27% of the total confirmed cases. After the pilot project, the annual parasite incidence dropped 89% from 104.77/1000 in 2016 to 12.18/1000 in 2019, the microscopic parasite prevalence rate dropped 100% from 0.34% in 2017 to zero in 2019 and the averaged density of An. Minimus per trap-night dropped 93% from 1.92 in June to 0.13 in September. The submicroscopic parasite prevalence rate increased from 1.15% in 2017 to 1.66% in 2019 without significant difference between the two surveys (P = 0.084). In Yingjiang County of China, neither indigenous nor introduced case was reported and 100% cases were imported from Myanmar since 2017. The averaged annual importation rate from 2015 to 2019 was (0.47 ± 0.15)/1000. After the pilot project, the annual importation rate dropped from 0.59/1000 in 2016 to 0.28/1000 in 2019 with an overall reduction of 53% in the whole county. The reduction was 67% (57.63/1000 to 18.01/1000) in the first preventive line, 52% (0.20/1000 to 0.10/1000) in the second preventive line and 36% (0.32/1000 to 0.22/1000) in the third preventive line. The averaged density of An. Minimus per trap-night in the first preventive line dropped 94% from 2.55 in June to 0.14 in September, without significant difference from that of + 1 area of Myanmar (Z value = − 1.18, P value = 0.24).

Conclusion

The pilot project on 3 + 1 strategy has been significantly effective in the study areas and a buffer zone of border malaria was successfully established between Laiza City of Myanmar and Yingjiang County of China.

Peer Review reports

Background

Although, significant progress has been documented in the National Malaria Elimination Programme, cross-border/imported malaria remains a major challenge in malaria elimination in China. China 1–3–7 malaria strategy which refers case reporting within 1 day, case confirmation and investigation within 3 days, and focus response within 7 days has led to significant achievements and milestones in malaria control to elimination [1,2,3]. Its performance and key technical specification had remarkable impact in shrinking the national map of indigenous malaria from 762 to 2 counties and with 4262 cases to 3 cases from 2010 to 2016 respectively [4, 5]. In 2016, the World Health Organization (WHO) identified 21 countries, including China, as those on track to reach the goal of malaria elimination by 2020 [6].

Yunnan Province of China (YNC) shares a land border of 4060 km with Myanmar, Lao PDR and Vietnam in the Greater Mekong Sub-region. Among them, 18 counties in the West of YNC are adjacent to 5 special regions in the North of Myanmar with a land border of 1997 km. Myanmar is still one of the counties with highest malaria burden in the world [6], especially in the 5 special northern regions due to the limited health resources [7, 8]. In the 18 counties of YNC, most malaria cases are imported from the neighbor owing to intensive and regular daily cross-border activities. Consequently, curbing and controlling China–Myanmar cross-border malaria has become a major challenge to malaria elimination in YNC [9,10,11].

WHO defines border malaria as malaria transmission or potential transmission that takes place across or along boundaries between countries sharing a land border, it includes movement of infected people crosses boundaries, and/or mosquito transmission crosses or occurs along boundaries [12]. In order to reduce the malaria burden in China–Myanmar border area, an effective joint cross-border malaria prevention and control mechanism was set up between YNC and Myanmar since 2007, supported by the sixth and tenth round of China malarial project in the Global Fund to Fight AIDS, Tuberculosis and Malaria (refer to as GF malaria program) [13,14,15,16,17,18,19,20]. It was comprised of bilateral malaria programs and capacity transfer, as well as exchange of epidemic information [13, 15, 17], YNC’s provision of malaria capacity transfer and training, and establishment of 66 malaria consultation posts in the 18 border counties to detect and treat malaria for entry people, and to deliver a malaria protective pack for exit people [19, 20]. Myanmar’s establishment of 80 malaria medical stations in the 5 special regions was to carry out malaria case detection and management, provide distribution of long-lasting insecticidal nets (LLINs) or insecticide treated nets (ITNs) and promote health education [14, 16]. These integrated approaches led to significant achievements including the reduction of annual parasite incidence (API) from 41.7/1000 in 2008 to 7.1/1000 in 2013 in Myanmar side, and from 1.9/1000 in 2006 to 0.09/1000 in 2013 in China side. The reduction in malaria burden was 89% and 95%, respectively [20]. However, these milestones and achievements were not sustained due to the GF Malaria Program interruption for China in January 2014. As a remedy a high-level bilateral memorandum of understanding between China and Myanmar was signed in Tengchong City of YNC in 2016 and a new joint action plan for fighting malaria in both border areas was proposed to accelerate malaria elimination in China and rollback malaria in Myanmar.

Laiza City (LZC) of Myanmar is the political center of Kachin Special Region II (KSR II) and shares a land border of 20.5 km with Nabang Township of Yingjiang County (YJC) of YNC. After the regional conflict in KSR II in 2012, more than 30,000 internally displaced persons (IDP) migrated to LZC and resettled along the boundary. This greatly aggravated the malaria burden in both sides, resulting in the malaria incidence of KSR II rebounding from 2.1% in 2012 to 5.1% in 2016 [18], and the number of reported malaria cases in YJC sharply raised from 58 (23 indigenous cases) in 2012 [15] to 186 (1 indigenous case) in 2016, which accounted for 59.23% of the total reported cases in YNC in 2016. This was the only county where the number of reported cases raised rather than dropped since the National Malaria Elimination Programme launched in YNC in 2010 and local transmission continued to 2016 [5]. YJC has become the most challenging areas for achieving the goal of malaria elimination in China.

A pilot new joint cross-border malaria prevention and control project termed 3 + 1 strategy was initiated for establishing a buffer zone of border malaria in these areas since 2017. Here, + 1 was a catchment area in LZC of Myanmar (refer to as + 1 area), a defined region with a length of 20.5 km and a width of 2.5 km along the boundary, where the implementation of joint working group and adoption of integrated malaria control and elimination measures were aimed at reinforcing the existing local GF malaria programs. That included funding and technical assistance, capacity transfer and training early case detection and management, focus response, vector surveillance and control, health education, and radical treatment. 3 were to establish three preventive lines (TPLs) in YJC of China and to take the focalized approaches of national 1–3–7 strategy in each line. The first preventive line (1st PL) was the same defined region in the border areas of YJC corresponding to + 1 area of Myanmar, where the core interventions were vector surveillance and control, entry-exit person management, reactive and proactive case detection aiming at reducing the risk of case importation and local transmission interruption. The second preventive line (2nd PL) included other border areas in YJC besides 1st PL with core interventions including proactive malaria case detection and mobile population management in preventing transmission re-establishment. The third preventive line (3rd PL) covered the non-border areas including downtown of YJC where the core interventions were passive case detection for early detection and prompt treatment to maintain zero indigenous case.

This study was to assess the impact of joint 3 + 1 strategy and to share the learned experiences and lessons for accelerating malaria elimination agenda in the Greater Mekong Sub-region.

Methods

Study areas and population

The township and its county where the most imported malaria cases were reported in YNC in 2016, as well as the region of Myanmar within 2.5 km deep from the border line with the enrolled township of YNC were selected as the study areas. The study areas were the catchment areas of pilot project based on 3 + 1 strategy. 1st PL of YJC covered all 10 natural villages in Nabang Townships with population of about 2000. 2nd PL covered 51 administrative villages in 8 border townships of YJC with population about 147,000. 3rd PL covered 27 administrative villages in 6 non-border townships and downtown of YJC with population about 160,000. + 1 area of Myanmar covered the urban city of LZC, 4 natural villages, a high school and 2 camps of IDP, with a population about 20,000. Figure 1 shows a map of the study area of the pilot project on 3 + 1 strategy.

Fig. 1
figure 1

The map of study area of Pilot project on 3 + 1 malaria strategy. The map was depicted by us with ArcMap 10.7 version

Data resources and collection

Case detection

In LZC of Myanmar, the data of routine malaria and population size from January 1st, 2015 to December 31st, 2019 were collected from the office of GF malaria program in KSR II that monthly collected at grass-root health facilities via the health information system which established and maintained by GF malaria program since 2007 [20]. Data of confirmed cases and blood examination in + 1 area were extracted from the monthly report of Laiza central hospital (that including the data of LZC hospital), the camp clinic of Je Yang Hka and the camp clinic of Hpum Lum Yang. In YJC of China, Data of registered malaria cases from January 1st, 2015 to December 31st, 2019 were collected from the information management system specific to malaria elimination [1] and nationwide notifiable infectious diseases reporting information system [21]. The data of blood examination were extracted from the monthly report of each sentinel hospital that collected by County Center for Disease Control and Prevention (CDC) as part of GF malaria program management since 2003. Data of population size were extracted from the statistical yearbook of YJC (Additional file 1).

Determination of parasite prevalence

The parasite prevalence rate of + 1 area of Myanmar was surveyed at the beginning (April 2017) and the end (December 2019) of the pilot project in the 2 IDP camps, using a novel real-time quantitative PCR-based technique termed capture and ligation probe-PCR (CLIP-PCR) [22, 23]. Each participant’s body temperature was measured and 2 dried blood spots were collected. If the body temperature was higher than 37.5 °C or a fever occurred within the past week, the participant was immediately tested with a rapid diagnosis test (RDT, Wondfo Pf/Pan-LDH, China, lot number W05460602WC). One of 2 dried spotted bloods was tested by CLIP-PCR the next day in a molecular screen laboratory set up in the Nabang Township Hospital in 1st PL of YJC by the joint working group. All positives of CLIP-PCR or RDT were followed up with microscopy examination.

Vector surveillance

The data of + 1 area of Myanmar were collected from the monitoring records of the joint working group whom conducted periodic vector surveillance from June to September in 2018 and 2019. Ja Htu Kawng Village and 2 IDP camps were selected as capture sites, and then a house or a shelter was fixed as a capture point in the East, West, North, South and Middle of each capture site. Briefly, CDC light trap was hanged in indoor of each point; a 3-overnight capture was conducted in every 15 days from June to September and started before implementing indoor residual spraying (IRS) in June. The data of 1st PL of YJC were collected from county CDC, which carried out the national malaria vector surveillance project in 1st PL of YJC since 2015 with the same measures as + 1 area of Myanmar. The data of Anopheles minimus (An. minimus) females were extracted.

Statistical analysis

The databases were generated with Microsoft Excel 2010 and analyzed with Statistical Product and Service Solutions (SPSS) software version 20. Descriptive statistics was used and the statistically significant differences (SSD) of incidence or rate were compared with chi-square test and odds ratio (OR) with 95% confidence interval (CI). The level of significance was set at p value ≤ 0.05 and (1-OR) multiply 100 were used to indicate the degree of reduction or increment. To assess the case detection, API (number of new parasitological confirmed malaria case per 1000 population per year [24]) with 95% CI was computed as a key indicator in + 1 area of Myanmar, whereas annual importation rate (AIR, number of registered to imported case per 1000 population per year) with 95% CI was computed after getting rid of indigenous cases in YJC of China and TPLs. Both SSD were analyzed by comparing with last year and between 2019 and 2016, respectively. Annual blood examination rate (ABER), malaria test positivity rate (MTPR) and proportion of Plasmodium vivax (P. vivax) were also evaluated. The parasite prevalence rate (PPR, number of positive cases per 100 investigated participants) with 95% CI was calculated by using PCR, microscopic and submicroscopic, SSD were compared between the submicroscopic PPR of the two surveys. The monthly density (number of females per trap per night per month) of An. minimus was calculated and its reduction rate was calculated by using the averaged density in June and September between 2018 and 2019. The correlation between monthly density and number of malaria cases was measured with bivariate Pearson correlation, and SSD of the density between + 1 area of Myanmar and 1st PL of YJC was compared with rank sum test of nonparametric tests.

Results

Case detection

In + 1 area of Myanmar, a total of 5847 cases were confirmed during 2015 to 2019, in which P. vivax accounted for 96.27% (5629/5847) and P. falciparum 3.73% (218/5847). The averaged API was (59.11 ± 40.73)/ 1000, all of API had SSD compared with the previous year and between 2019 and 2016. The API dropped from 104.77/1000 in 2016 to 12.18/1000 in 2019 with a reduction of 89% (95% CI 88–91%, Table 1). In YJC of China, a total of 737 cases were registered from 2015 to 2019, in which 98.37% (725/737) was P. vivax and 1.63% (12/737) was P. falciparum; 0.95% (7/737) was indigenous cases and 99.05% (730/737) was imported cases. Among the seven indigenous cases, six were in 2015 (five in 1st PL and one in 2nd PL) and one was in 2nd PL in 2016. There have been neither new indigenous cases nor introduced cases since 2017. Among the 730 imported cases, only one case of 3rd PL came from Thailand in 2015, the rests imported from Myanmar. The proportion of reported cases by TPLs in the total cases of YJC was 56.99% of 1st PL, 14.52% of 2nd PL and 28.49% of 3rd PL. The averaged AIR was (0.47 ± 0.15)/1000, all had SSD compared between AIR in 2019 and 2016.The AIR dropped from 0.59/1000 in 2016 to 0.28/1000 in 2019 with a reduction of 53% (95% CI 39–63%) in YJC, meanwhile, it dropped from 57.63/1000 to 18.01/1000 with a reduction of 67% (95% CI 52–77%) in 1st PL, from 0.20/1000 to 0.10/1000 with a reduction of 52% (95% CI 10–75%) in 2nd PL and from 0.32/1000 to 0.22/1000 with a reduction of 36% (95% CI 3–57%) in 3rd PL, respectively (Table1). The trend of case detection in the study areas from 2015 to 2019 were depicted in Fig. 2.

Table 1 The results of case detection in each study area of the pilot project
Fig. 2
figure 2

The trend of annual parasite incidence in + 1 area of Myanmar, and the annual importation rate and cases composition in Yingjiang Country of China from 2015 to 2019. a The composition of imported cases in the three preventive lines from 2015 to 2019. b The trend of API in + 1 area of Myanmar and AIR in the three preventive lines and Yingjiang County from 2015 to 2019. Note (1) API annual parasite incidence; (2) AIR annual importation rate

Determination of parasite prevalence

In the first survey in April 2017, a total of 5570 participants including 37 febrile subjects were screened and 3 were RDT positives among the febrile ones. A total of 83 were found positive by CLIP-PCR, giving a PCR PPR of 1.49% (95% CI 1.17–1.81%, Table 2). Among the 83 PCR positives only 19 were positive by microscopy and all were P. vivax, giving a microscopic PPR of 0.34% (95% CI 0.19–0.49%), and 77.10% (64/83) of all infections were negative by microscopy with a submicroscopic PPR of 1.15% (95% CI 0.87–1.43%). The 3 RDT positives were both positive by PCR and microscopy. In the second survey in December 2019, a total of 1992 participants were screened and no one was RDT positive. 33 CLIP-PCR positives were identified with a PCR PPR of 1.66% (95% CI 1.1–2.22%). All 33 were microscopic negative, thus 100% of all infections were submicroscopic. The averaged PCR PPR was 1.58% in + 1 area. There was no SSD between the submicroscopic PPR of the two surveys and the microscopic PPR was reduced by 100%.

Table 2 The results of parasite prevalence survey in + 1 area of Myanmar

Vector surveillance

A total of 440 female anopheles belonging to 10 species were captured in 2018 and 2019, which included An. minimus, An. sinensi, An. jeyporiensis, An. maculatus, An. culicifacies, An. subpictus, An. barbirostris, An. barbumbrosus, An. messeae and An. bengalensis. In which An. minimus and An. sinensis were malaria vectors and accounted for 66.14% (291/440) and 3.64% (16/440), respectively. An. minimus accounted for 63.70% (186/292) in + 1 area of Myanmar and 70.95% (105/148) in 1st PL of YJC. After pilot project, the averaged monthly density of An. minimus per trap-night dropped from 1.92 in June to 0.13 in September with a reduction of 93% in + 1 area of Myanmar, and from 2.55 in June to 0.14 in September with a reduction of 94% in 1st PL of YJC. The monthly density of An. minimus in + 1 area of Myanmar had a significant positive correlation with monthly number of malaria case (r = 0.74, p = 0.04), but no correlation was found in 1st PL of YJC (r = 0.45, p = 0.25). There was no SSD between the densities of both sides. The trend of averaged monthly density of An. minimus and monthly number of malaria cases was summarized in Fig. 3.

Fig. 3
figure 3

The trend of the averaged monthly density of A. minimus and No. of monthly malaria cases in June to September in 2018 and 2019. Note All house indoor residual spraying in the middle of June

Discussion

It is important to note that the National Malaria Control Programme in Myanmar was launched in 2016 and its goal is to eliminate malaria by 2030 [25, 26]. However, National Malaria Elimination Programme in China was initiated in 2010 and its elimination goal is by 2020 [1,2,3]. It is a 10-year difference involving distinct stages in achieving the goal of elimination malaria between China and Myanmar. Although the Myanmar national programme has included KSR II, the support from national programme barely covered KSR II in Myanmar due to the conflict with central government since 2012 [27]. This situation resulted in an imbalance of border malaria control capacities between China and Myanmar, and malaria from KSR II threatens the border areas of YNC.

In order to reduce malaria transmission and enhance the control capacities in KSR II, the pilot project on 3 + 1 strategy of joint cross-border malaria prevention and control was initiated in both sides and supported by local funds. Due to limited funding and human recourses, + 1 area of Myanmar and 1st PL of YJC was set in a defined region, the width was limited to 2.5 km from boundary that was based on the fact that An. Minimus is dominant malaria vector in this area [28,29,30], with its maximum flight distance being 2.32 km [31, 32]. The purpose was to prevent mosquito transmission cross or along boundary by reducing vectorial capacity and building a flight buffer.

In 2016 in the + 1 area of Myanmar, the API unusually increased 2.31 times higher than 2015 (OR 95% CI 2.13–2.50, p value < 0.001), matching the WHO description on malaria outbreak (Fig. 2 and Table 1) [33]. Usually, malaria outbreaks in the Greater Mekong Sub-region are mostly ascribed to population movement and rarely to climatic factors [25]. In spite of the fact that difference of population between 2015 and 2016 was little (Table 1), and the rate of bednet ownership and proportion (97.3% in 2013) of sleeping under bednet was high [27, 34], especially sleeping under LLINs/ITNs (76.1% in 2013) [27], malaria outbreak unexpectedly occurred during the implementation of local GF malaria program in 2016. Several reasons could explain this, including that most of male adult conscribed into the ethnic army and stationed in the forest where malaria transmission risk was high [25], and when returning home they carried malaria back to communities. Another possibility was that usage of LLINs had expired [27]. When scaling up the proportion of LLINs distribution, coverage and use in the catchment areas of Myanmar was during the tenth round China GF malaria program from 2011 to 2013, and those LLINs expired by 2015 [27]. The IDPs moving into local GF malaria program did not have enough LLINs to replace them again and rarely implemented IRS and treated bednets due to funding gaps, leading to potential rebound of malaria transmission to pre-existing level [23].

Our findings showed that 96.27% of confirmed cases was P. vivax in the studied area, which is more difficult to control or eliminate than P. falciparum due to its several distinct biological characteristics [35], such as gametocytes in peripheral blood being matured to transmit to merozoites before symptoms appear; P. vivax malaria parasite density being more likely too low to be detected by microscopy or RDT; and hypnozoites in liver cell causing multiple relapse and requiring a 14-day-course treatment of primaquine which patients may not fully adhere. Our implemented pilot project had remarkable results in controlling malaria outbreak in + 1 area of Myanmar, most likely because of core WHO recommended malaria interventions and classical Chinese measures such as radical treatment at the resting stage [24, 35] (Table 1).

In the first year (2017) of the pilot project, vector control in + 1 area of Myanmar was one net per bed to distribute new LLINs provided by Health Poverty Action (HPA). IRS and vector surveillance were not carried out due to preparation of materials and documents, other interventions were performed since April 2017. Our findings showed the API in + 1 area of Myanmar in 2017 had SSD than 2016 (p value = 0.026). This meant the results of malaria control in + 1 area of Myanmar in the first year was effective, but the API only reduced by 7% (95% CI 1–13%), malaria transmission was still high. In the middle of June in the second (2018) and third (2019) years, all houses in + 1area of Myanmar and 1st PL of YJC were simultaneously treated with IRS using high-efficiency cypermethrin with WHO recommended dosage [36], and malaria vector was periodically monitored from the early of June to end of September, while the other interventions were maintained the same as 2017. The results of malaria control in + 1 area of Myanmar in the past two years had notable achievements, as API was sharply reduced by over 60% due the combined effect of IRS and LLINs.

The proportion of An. minimus in the female anopheles in + 1 area of Myanmar was as high as 63.7% and had a positive correlation with number of malaria case (r = 0.74, p = 0.04), which unequivocally confirmed again that An. minimus was the predominant malaria vector in this area. Previous study showed this mosquito rests indoor, prefers human blood and the biting peaks are in the sunset and midnight [37]. In our study, we chose the monthly density of An. minimus to evaluate the effect of IRS and LLINs and used the averaged monthly density of 2018 and 2019 to eliminate the climate impact. Generally, IRS protects residents against this mosquito biting before going to bed by killing mosquito that rest indoor, whereas LLINs protect residents after they go to bed by killing mosquito that rest on bednets. Both interventions had high use coverage in + 1 area of Myanmar and might have resulted in significantly reduced vectorial capacity and transmission. Figure 3 showed the averaged monthly density of An. minimus sharply reduced in July after implementing IRS, with corresponding sharp reduction of the number of malaria cases in August. IRS and LLINs/ITNs are core interventions of vector malaria control recommended by WHO [24], both may be less effective in reducing P. vivax transmission. But our findings revealed that they had a significant positive effect in reducing An. minimus vectorial capacity and competency.

Measuring the accurate parasite prevalence in the low transmission areas can be challenging due to limited sensitivity of microscopy and RDT [24]. Using CLIP-PCR, a high-throughput and highly sensitive molecular assay with a limit of detection of 0.01 parasites/μl [22, 23], we showed that the averaged PCR PPR was 1.58% in + 1 area of Myanmar. Additionally, our finding indicated the averaged API in + 1 area of Myanmar was (59.11 ± 40.73) /1000 and ratio of P. falciparum/P. vivax was 0.04, therefore the area belongs to a very low transmission area according to the WHO category [24]. Furthermore, 64 of 83 PCR positives (77.10%) were submicroscopic infections (all were subsequently identified as P. vivax by fluorescence quantitative PCR), a rate similar to the submicroscopic P. vivax infection rate found by Moreira et al. [38] and Cheng et al. [39]. Our findings showed the PPR of microscopy was reduced by 100%, which proved the core interventions of case detection were very effective and local GF malaria program worked in a high ABER (Table 1). There was no SSD between submicroscopic PPR at the beginning and the end of the pilot project, supporting the notion of submicroscopic infection being as infectious parasite reservoir [41]. These findings prompted contextual adoption of targeted interventions to control or eliminate this infection reservoir. Examples of such interventions include tracking those who had the same trip as the case and administering the same treatment, administering a dose of chemprophylactics for case neighbors and families, or taking radical treatment for P. vivax case at the resting stage. Our finding also hinted that the source of infection still existed in + 1 area of Myanmar, once the vector control was weakened, malaria transmission could rebound again.

Interestingly, our findings showed that the number of cases reported by 1st PL accounted for 57% of the total cases in YJC and its AIR determined the trend of AIR in YJC. Meanwhile, Fig. 2 and Table 1 showed that except in 2018, the AIR in 1st PL reduced significantly correlating with the decrease of API in + 1 area of Myanmar (p value < 0.001), suggesting that most of the imported cases in 1st PL of YJC were from + 1 area of Myanmar, whereas 2nd PL and 3rd PL might come from Myanmar outside + 1 area. An explanation could be the annual cross-border population of YJC was relatively stable in recent years, and only small groups of population at risk (PAR) stayed overnight or lived abroad. Usually, PAR was certain residents of 1st PL and 2nd PL who long-rent the land of KSR II close to the border for crop cultivation, while a few of non-local and 3rd PL went to the interior of KSR II for planting and mining. However, among the border of 214.6 km between YJC and KSR II, only LZC was the most serious malaria epidemic area and transmission was perennial with seasonal peak due to low altitude and dense population, the other areas of KSR II were low epidemic areas and transmission was interrupted in the cold season due to high altitude. In particular, most of the PAR in 1st PL lived in foothill and lowland plantations within + 1 area of Myanmar had high malaria transmission, which were relatively isolated and far away from Burmese villages [27].

Also the malaria consultation post in 1st PL of YJC was still working normally which established by GF malaria program since 2007. Most of PAR would take a dose of chemprophylactics before leaving the country and the new LLINs were freely available. That was why the AIR in 1st PL from 2015 to 2017 showed little difference and did not change with API of + 1area of Myanmar, but it sharply reduced in API after implementing all house IRS in 2018, then stable in 2019 due to a part of PAR lived outside + 1 area of Myanmar where no IRS. The research also found that all had SSD compared AIR in YJC and TPLs between 2019 and 2016 and proved the strategy of TPLs and its targeted local community’s measures for each preventive line were effective.

Our study limitations include the average ABER was 40% of + 1 area and 66% of 1st PL, they were much higher than 2nd PL and 3rd PL due to the number of malaria tested in + 1 area including the number of tested in passive case detection and active case detection combined in report monthly. However, that number in TPLs was only passive case detection, not included active case detect. So, there was no comparability between + 1 area of Myanmar and TPLs of YJC. Furthermore, passive case detection in 1st PL detected all febrile patients, but 2nd PL and 3rd PL detected only 3 types of fever such as malaria fever, suspected malaria fever and fever of unknown cause. Bias due to the number of cases reported by 3rd PL was more than 2nd PL, this was because the rich people and non-local mobile population prefers to go to county-level hospitals where they could get better medical resources, as part of cases were transferred from 1st PL and 2nd PL to the county hospital for treatment. Additionally, although the malaria data in + 1 area of Myanmar were collected from the office of GF malaria program via the health information system, the data was monthly reported by the primary level and no any the detail information of individual case, therefore, the population information of the case cannot be further analyzed.

Conclusion

The 3 + 1 strategy has made remarkable achievements and a buffer zone of border malaria was successfully established between YJC of China and LZC of Myanmar. In + 1 area of Myanmar, the integrated malaria preventive and control measures achieved significant results with the API and microscopic PPR reduced by 89% and 100% respectively. In YJC of China, the focalized approaches of malaria elimination for each preventive line showed significant milestones in local transmission interruption since 2017 with a county-wide AIR reduction of 53%.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

ABER:

Annual Blood Examination Rate

AIR:

Annual Importation Rate

API:

Annual Parasite Incidence

CDC:

Center for Disease Control and Prevention

CI:

Confidence interval

CLIP:

Capture and ligation probe

GF:

Global Fund to Fight AIDS, Tuberculosis and Malaria

IDP:

Internally displaced persons

ITNs:

Insecticide treated nets

KSR II:

Kachin Special Region II

LLINs:

Long-lasting insecticidal nets

LZC:

Laiza City

MTPR:

Malaria Test Positivity Rate

OR:

Odds ratio

PAR:

Population at risk

PCR:

Polymerase chain reaction

PL:

Preventive line

PPR:

Parasite Prevalence Rate

RDT:

Rapid Diagnosis Test

SSD:

Statistically significant differences

TPLs:

Three preventive lines

WHO:

World Health Organization

YJC:

Yingjiang County

YNC:

Yunnan Province of China

References

  1. Zhou SS, Zhang SS, Zhang L, Rietveld AECR, Ramsay AR, Zachariah R, et al. China’s 1-3-7 surveillance and response strategy for malaria elimination: Is case reporting, investigation and foci response happening according to plan? Infect Dis Poverty. 2015;4:55.

    Article  Google Scholar 

  2. Cao J, Sturrock HJ, Cotter C, Zhou S, Zhou H, Liu Y, et al. Communicating and monitoring surveillance and response activities for malaria elimination: China’s “1–3–7” strategy. PLoS Med. 2014;11(5):e1001642.

    Article  Google Scholar 

  3. Lu GY, Liu YB, Beiersmann C, Feng Y, Cao J, Müller O. Challenges in and lessons learned during the implementation of the 1–3–7 malaria surveillance and response strategy in China: a qualitative study. Infect Dis Poverty. 2016;5:94.

    Article  Google Scholar 

  4. Yan J, Hu T, Lei ZL. The endemic situation and challenges of major parasitic diseases in China. Chin J Parasitol Parasit Dis. 2015;6:412–7 (In Chinese).

    Google Scholar 

  5. Zhang L, Feng J, Zhang SS, Jiang S, Xia ZG, Zhou SS. Malaria situation in the People’s Republic of China in 2016. Chin J Parasitol Parasit Dis. 2017;6:516–9.

    Google Scholar 

  6. World Health Organization. World Malaria Report. Geneva: World Health Organization; 2017.

    Google Scholar 

  7. Cui LW, Yan GY, Sattabongkot J, Cao YM, Chen B, Chen XG, et al. Malaria in the Greater Mekong Subregion: Heterogeneity and complexity. Acta Trop. 2012;121(3):227–39.

    Article  Google Scholar 

  8. Zhao Y, Zhao Y, Lv Y, et al. Comparison of methods for detecting asymptomatic malaria infections in the China–Myanmar border area. Malar J. 2017;16:159.

    Article  Google Scholar 

  9. Yang HL, Xiao N, Yang YM, Xu JW. Challenges, opportunities and strategies of malaria elimination along China–Myanmar and China–Laos Border. Chin Trop Med. 2017;4(321–24):35.

    Google Scholar 

  10. Gao Q. Opportunities and challenges of malaria elimination in China. Chin J Schisto Control. 2011;4:804–10 (In Chinese).

    Google Scholar 

  11. Feng J, Liu J, Feng XY, Zhang L, Xiao HH, Xia ZZ. Towards malaria elimination: monitoring and evaluation of the “1-3-7” approach at the China–Myanmar Border. Am J Trop Med Hyg. 2016;4:804–10.

    Google Scholar 

  12. World Health Organization. WHO Malaria Policy Advisory Committee (MPAC) meeting report. 2018.10

  13. Wang RB, Zhang QF, Feng J, Xia ZG. Assessment on the effect of malaria control in China–Myanmar border areas. Chin J Dis Control Prev. 2016;9:863–6 (In Chinese).

    Google Scholar 

  14. Luo J. Model of China-Myanmar Malaria Project and enlightenment for Chinese Health Aid Program. Chin J PHM. 2014;4:480–3 (In Chinese).

    Google Scholar 

  15. Lin YX, Zhou DL, Guo XR, Yu GC, Chen LF, Si ZS. Measures and effect of jointing prevention and control of malaria in the border region of China and Myanmar from 2008 to 2014. ChinTrop Med. 2016;1:52–5 (In Chinese).

    Google Scholar 

  16. Zhang J, Dong JQ, Li JY, Zhang Y, Tian YH, Sun XY, et al. Effectiveness and impact of the cross-border healthcare model as implemented by non-governmental organizations: case study of the malaria control programs by health poverty action on the China–Myanmar border. Infect Dis Poverty. 2016;5:80.

    Article  Google Scholar 

  17. Wang RB, Dong JQ, Xia ZG, Cai T, Zhang QF, Zhang Y, et al. Lessons on malaria control in the ethnic minority regions in Northern Myanmar along the China border, 2007–2014. J Infect Dis Poverty. 2016;5:95.

    Article  Google Scholar 

  18. Liu H, Xu JW, Yaw B. Malaria burden and treatment targets in Kachin Special Region II, Myanmar from 2008 to 2016: a retrospective analysis. PLoS ONE. 2018;13(4):e0195032.

    Article  Google Scholar 

  19. Zeng XC, Sun XD, Li JX, Chen MN, Deng DW, Zhang CL, et al. Assessment of malaria control consultation and service posts in Yunnan. P R China Infect Dis Poverty. 2016;5:102.

    Article  Google Scholar 

  20. Xu JW, Li Y, Yang HL, Zhang J, Zhang ZX, Yang YM, et al. Malaria control along China–Myanmar Border during 2007–2013: an integrated impact evaluation. Infect Dis Poverty. 2016;5:75.

    Article  Google Scholar 

  21. Yang WZ, Li ZJ, Lan YJ, Wang JF, Ma JQ, Jin LM, et al. A nationwide web-based automated system for early outbreak detection and rapid response in China. Western Pac Surveill Response J. 2011;2(1):10–5.

    PubMed  PubMed Central  Google Scholar 

  22. Cheng ZB, Wang DQ, Tian XY, Sun Y, Sun XD, Xiao N, et al. Capture and ligation probe-PCR (CLIP-PCR) for molecular screening, with application to active malaria surveillance for elimination. Clin Chem. 2015;61(6):821–8.

    Article  CAS  Google Scholar 

  23. Zhou YW, Lin ZR, Cheng ZB, Zheng Z, Zhou XW, Zhou ZY, et al. Efficacy of capture and ligation probe-PCR with pooling strategy in detection of Plasmodium spp. Chin J Parasitol Parasit Dis Aug. 2016;34(4):330–3 (In Chinese)).

    Google Scholar 

  24. World Health Organization. A framework for malaria elimination. 2017.

  25. World Health Organization. Strategy for malaria elimination in the Greater Mekong Subregion: 2015–2030.2015

  26. Hein ZNM, Maung TM, Aung PP, Mon NO, Han WW, Oo T, et al. Do we need to go further to train healthcare providers in the targeted regions for malaria elimination in Myanmar? A mixed-methods study. Trop Med Health. 2020;48:11.

    Article  Google Scholar 

  27. Liu H, Xu JW, Guo XR, Havumaki J, Lin YX, Yu GC, et al. Coverage, use and maintenance of bed nets and related influence factors in Kachin Special Region II, northeastern Myanmar. Malar J. 2015;14:212.

    Article  Google Scholar 

  28. Shi WQ, Zhou XJ, ZhangY Zhou XN, Hu N, Wang XZ, et al. Investigation on Malaria Vectors in Western Part of China–Myanmar Border. Chin J Parasitol Parasit Dis. 2011;29(2):134–7.

    Google Scholar 

  29. Yu G, Yan GY, Zhang NX, Zhong DB, Wang Y, He ZB, et al. The Anopheles community and the role of Anopheles minimus on malaria transmission on the China–Myanmar border. Parasit Vectors J. 2013;6:264.

    Article  Google Scholar 

  30. Wang Y, Zhong D, Cui L, Lee MC, Yang Z, Yan G, et al. Population dynamics and community structure of Anopheles mosquitoes along the China–Myanmar border. Parasit Vectors. 2015;8:445.

    Article  Google Scholar 

  31. Verdonschota PFM, Besse-Lototskaya AA. Flight distance of mosquitoes (Culicidae): a metadata analysis to support the management of barrier zones around rewetted and newly constructed wetlands. Limnologica. 2013;45(3):69–79.

    Google Scholar 

  32. Guerra CA, Reiner RC Jr, Perkins TA, Lindsay SW, Midega JT, Brady OJ, et al. A global assembly of adult female mosquito mark-release-recapture data to inform the control of mosquito-borne pathogens. Parasit Vectors J. 2014;7:276.

    Article  Google Scholar 

  33. World Health Organization. Malaria control in humanitarian emergencies: an inter-agency field handbook – 2nd ed. 2013.

  34. Zhou G, Lo E, Zhong D, Wang X, Wang Y, Malla S, et al. Impact of interventions on malaria in internally displaced persons along the China–Myanmar border: 2011–2014. Malar J. 2016;15:417.

    Article  Google Scholar 

  35. World Health Organization. Control and elimination of Plasmodium vivax malaria: a technical brief. 2015.

  36. WHO. WHO recommended insecticides for indoor residual spraying against malaria vectors. 2018; 9.

  37. Dong XS. The mosquito fauna of Yunnan Province. Kunming: Yunnan Science and Technology Press; 1993. p. 77–81 (in Chinese).

  38. Moreira CM, Abo-Shehada M, Price RN, Drakeley CJ. A systematic review of sub-microscopic Plasmodium vivax infection. Malar J. 2015;14:360.

    Article  Google Scholar 

  39. Cheng Q, Cunningham J, Gatton ML. Systematic review of sub-microscopic P. vivax Infections: prevalence and determining factors. PLoS Negl Trop Dis. 2015;8:9.

    Google Scholar 

  40. WHO. Policy brief on malaria diagnostics in low-transmission settings. 2014.

  41. WHO. Global technical strategy for malaria 2016–2030. 2015.

Download references

Acknowledgements

We would like to thank Mr. Xiao-tao Zhao for his assistance in making the map of study areas by using ArcMap 10.7 version and Associate Prof. Tambo Ernest for critical review of the manuscript. We are grateful to Health Department of Kachin Special Region II for agreement and support on this pilot project, the generous cooperation is the cornerstone of the success of this project.

Funding

The collection, analysis, interpretation of data and writing the manuscript were supported by the National Natural Science Foundation of China (Grant No. 81960374), the design and implementation of the study were supported by Yunnan Innovative Team of Key Techniques for Vector Borne Disease Control and Prevention (Grant No. 2019HC010), and the technology and kits of Capture and Ligation Probe-PCR in the study were supported by National Major Science and Technology Projects (Grant No. 2018ZX10101001).

Author information

Authors and Affiliations

Authors

Contributions

X-DS and H-NZ conceived and designed this project. Z-RL and S-GL organized and supervised the field implementation, Z-RL, S-GL, X-DS, X-RG, JY, PT, Q-YC, X-YS, C-LD, K-XD, H-WC and Y-BD performed the field works and collected data. ZZ and H-RP performed the PCR tests. Z-RL and X-DS and ZZ analyzed the data and wrote and revised the manuscript. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Xiao-dong Sun, Zhi Zheng or Hong-ning Zhou.

Ethics declarations

Ethics approval and consent to participate

For the routine data of malaria case and vector of the pilot project, Ethics Committee of Yunnan Institute of Parasitic Disease (YIPD, China) and the Health Department of KSR II of Myanmar approved the access and collection. Malaria parasite prevalence was tested by using CLIP-PCR as a part of this study, the Ethics Committee of YIPD approved the study [Reference number: YIPD-EC-2017 (4) and YIPD-EC-2019 (4)]. All participants were informed in native language and the written informed consent was obtained from individual before the two dried blood spots were collected. There was no participant’s personal identification information in this article.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Material 1.

 The Data of map about the study area of pilot project. Material 2. Data of Fig. 2. Material 3. Data of Fig. 3

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Lin, Zr., Li, Sg., Sun, Xd. et al. Effectiveness of joint 3 + 1 malaria strategy along China–Myanmar cross border areas. BMC Infect Dis 21, 1246 (2021). https://doi.org/10.1186/s12879-021-06920-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12879-021-06920-z

Keywords