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Article

Low Levels of Knowledge, Attitudes and Preventive Practices on Leptospirosis among a Rural Community in Hulu Langat District, Selangor, Malaysia

by
Noramira Nozmi
1,
Suhailah Samsudin
1,
Surianti Sukeri
2,
Mohd Nazri Shafei
2,
Wan Mohd Zahiruddin Wan Mohd
2,
Zawaha Idris
3,
Wan Nor Arifin
4,
Norazlin Idris
2,
Siti Nor Sakinah Saudi
1,
Nurul Munirah Abdullah
1,
Zainudin Abdul Wahab
5,
Tengku Zetty Maztura Tengku Jamaluddin
1,
Hejar Abd Rahman
6,
Siti Norbaya Masri
1,
Aziah Daud
2,
Malina Osman
1 and
Rukman Awang Hamat
1,*
1
Department of Medical Microbiology and Parasitology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Selangor 43400, Malaysia
2
Department of Community Medicine, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan 16150, Malaysia
3
Health Promotion Unit, Penang State Health Department, Floor 7, Bangunan Persekutuan, Jalan Anson, Penang 10400, Malaysia
4
Unit of Biostatistics and Research Methodology, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan 16150, Malaysia
5
Health Department of Federal Territory Kuala Lumpur & Putrajaya, Jalan Cenderasari, Kuala Lumpur 50590, Malaysia
6
Department of Community Health, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Selangor 43400, Malaysia
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2018, 15(4), 693; https://doi.org/10.3390/ijerph15040693
Submission received: 22 February 2018 / Revised: 30 March 2018 / Accepted: 4 April 2018 / Published: 6 April 2018
(This article belongs to the Section Health Behavior, Chronic Disease and Health Promotion)
Versions Notes

Abstract

:
Little is known on the knowledge, attitudes and preventive practices (KAP) of leptospirosis worldwide. This study embarked on assessing the KAP of leptospirosis among rural communities in Malaysia. A total of 444 participants (223 male; 221 female) aged between 18 and 81 years old were surveyed by using a self-administered questionnaire. A majority of participants had poor knowledge level (57.0%), unacceptable attitudes (90.3%) and unacceptable preventive practices (69.1%) on leptospirosis, and only 29.7% knew “rat-urine disease” as leptospirosis. Only 34.2% of the participants knew the bacteria could enter via wound lesions. Ethnicity and income were strongly associated with knowledge level and preventive practices, respectively (p-values < 0.05). As for attitudes, ethnicity, income and education type were significantly associated (p-values < 0.05). Only 36.5% of the participants were willing to see a doctor and did not mind if their house or surrounding area is dirty (59.7%). Surprisingly, only 32.9% had used rubber boots during floods. By logistic regression analysis, ethnicity was the only significant predictor for both knowledge level (an odds ratio (AOR) = 0.39, 95% confidence interval (CI) = 0.222–0.680) and preventive practices (AOR = 1.81, 95% CI = 1.204–2.734). Ethnicity (AOR = 0.40, 95% CI = 0.239–0.665), income (AOR = 1.58, 95% CI = 1.041–2.385) and education type (AOR = 3.69, 95% CI = 1.237–10.986) were strong predictors for attitudes. Among the KAP variables, attitude (AOR = 4.357, 95% CI = 2.613–7.264) was the only predictor for the preventive practices by logistic regression analysis. The KAP elements on leptospirosis are still lacking and poor health seeking behavior and attitudes are of our utmost concern. Thus, effective strategies should be planned to impart knowledge, and develop proactive approaches and good preventive modules on leptospirosis to this leptospirosis-prone community.

1. Introduction

Leptospirosis—a neglected zoonotic disease caused by pathogenic Leptospira strains—is now becoming a global threat for causing significant morbidity and mortality in humans in both rural and urban settings worldwide [1,2,3,4,5]. Recently, more than 300 serovars and 20 species of these pathogenic strains have been identified and mammals, including rodents, are among the important reservoirs known to harbor these spirochetes [6,7,8]. Human leptospirosis is acquired through direct or indirect contact with water or soil contaminated by the urine, blood or tissues of infected mammals [3,9]. The disease has a wide clinical spectrum ranging from asymptomatic to hemorrhagic phenomenon and even death [2]. Nonetheless, the clinical manifestations of human leptospirosis possess a significant challenge to clinicians in managing the disease, since other tropical diseases such as dengue and malaria rather share similar symptomatology and epidemiology, albeit the pathogenesis pathways are different [10,11].
Globally, leptospirosis is considered as a re-emerging infectious disease and more than one million cases have been reported every year with the estimated incidence of 0.1 to 975 cases per 100,000 population annually [1,12]. The disease burden is largely centered in tropical and subtropical regions such as Southeast Asia and also in Central and South America regions [13,14,15,16]. Several contributing factors have been highlighted for high morbidity and mortality rates in these regions. The geographical location with frequent rainfall and floods, climate change, high number of animal reservoirs, human activities and other socio-epidemiological influences are attributable to the high incidence of leptospirosis [13,17,18,19,20].
Several outbreaks have been reported following climate change and human activities in Malaysia. For instance, an Eco-Challenge held in Borneo Island has recorded 29 of 304 athletes from 26 countries contracted leptospirosis [21]. Another outbreak has been reported involving 46 boys and young adults aged 8 to 19 years old who swam in a creek in Sabah with one succumbed to leptospirosis [22]. As for the natural disasters, 20 human leptospirosis cases with two deaths were reported following the prolonged flood during monsoon season that hit Johor, Malaysia [23]. Recently, a few north-eastern states of Malaysia such as Kelantan and Selangor recorded a high number of human leptospirosis cases in 2014 due to flood as well [24].
With the wealth of scientific data, our understanding of leptospirosis in Malaysia seems to be significantly improved. However, in order to ensure good control and preventive measures, surveys of knowledge, attitude, and preventive practices (KAP) among the public are urgently needed. Information from these surveys could also provide strategies to improve or evaluate existing programs as well as to identify potential interventions for behavioral changes. It is known that knowledge levels and perceptions are important key drivers for positive behavior [25]. To date, data on KAP studies on leptospirosis among rural population are still lacking in Malaysia. Herein, we present findings obtained from our rural communities to determine the socio-demographic characteristics, levels of knowledge, attitude, and preventive practices of leptospirosis.

2. Materials and Methods

2.1. Sample

The study commenced in Hulu Langat District, Selangor from February 2016 and ended in June 2017. The population of Hulu Langat District is approximately 1,156,585 people [26]. Hulu Langat has three waterfalls which are Air Terjun Sungai Gabai, Air Terjun Sungai Lepoh, and Air Terjun Perdik. It also has six rivers which are Sungai Congkak, Sungai Tekali, Sungai Tekala, Sungai Langat, Sungai Lui, and Sungai Pangsun. This district has attracted many visitors from Selangor and other states of Malaysia for its majestic waterfalls and shallow rivers. Recently, it has been declared as one of the hotspot areas for leptospirosis [24]. Leptospirosis cases were recorded to be the highest among other states in 2015 (2610 cases) based on the data obtained from Selangor State Health Department Office. In addition, 48% of the total deaths due to leptospirosis in Selangor were reported in Hulu Langat. Approval to conduct the study was obtained from the Faculty of Medicine and Health Sciences Ethical Review Committee Board, Universiti Putra Malaysia (UPM/TNCPI/RMC/JKEUPM/1.4.18.2).

2.2. Study Design

The study utilized a cross-sectional study design.

2.3. Study Population

Selangor is divided by nine districts and Hulu Langat has 19 villages within its territory. The study locations (4 villages) were selected by simple random sampling using a computer random generator to avoid any potential biases. The list of the villages was obtained from Hulu Langat District and Land Office. The aim of the study was briefed to each individual occupant residing in the villages in the rural area. Those who did not fulfill the criteria such as non-permanent resident and aged less than 18 years old were excluded in the study. Those who were eligible and voluntarily agreed to participate were asked to give their written consent. Each participant was approached by the investigators to complete a set of questionnaires using hard copies. The questionnaires were designed in Bahasa Malaysia (a local dialect), labelled and kept in a sealed envelope to ensure the confidentiality.

2.4. Instrument

The study used a validated KAP questionnaire on leptospirosis in Malaysia which has been adopted and modified accordingly [27]. The content validity of the study instrument was performed by cross-checking and authentication from experts in the field of study. The questionnaire was pre-tested among 30 Hulu Langat rural residents before the commencement of the study. Cronbach’s Alpha coefficient with acceptable results were obtained (knowledge, α = 0.710; attitude, α = 0.837; and practices, α = 0.956). Collected data were obtained based on 4 categories: (1) socio-demographic characteristics, (2) source of information and (3) variables of knowledge, attitude, and preventive practices of leptospirosis. Rural community was defined as residents who live outside urban areas including settlements with a population less than 10,000 residents, agricultural areas, forest and water bodies [26]. The divorced individual was considered unmarried. Informal education was defined as an educational model that comes spontaneously during the learning process and does not necessarily have a pre-defined curriculum [28].
Awareness of the participants on leptospirosis was assessed if the study participants had heard of the “rat-urine disease” as well as the source of the information. The terminology of “rat-urine disease” was adopted as it is commonly used by the local media to represent leptospirosis. The participants were asked on 8 items about the causative agent, how leptospirosis could be diagnosed, how leptospirosis could be transmitted, how leptospirosis could be manifested in man and its complications, and preventive measures that could be taken for instance, avoid wading through flood and swimming in contaminated river, lake and others. Participants were given 3 options such as “Correct”, “Wrong” and “Do not know”. Each correct answer was given as 1, while a 0 score was given to wrong answer and do not know. Participants with the knowledge scores of 60% and above were considered as having good knowledge, while those who scored below 60% were categorized as having poor knowledge [29].
Attitudes related to leptospirosis were determined by assessing 16 items related to environmental exposures to leptospirosis and perception on wearing protective equipment as well as towards readiness of wearing protective equipment, avoidance of exposure, participation in control and prevention activities, and health seeking behaviors. The responses were gathered using a 5-point Likert scale where 5, 4, 3, 2 and 1 corresponded to strongly agree, agree, maybe, disagree and strongly disagree, respectively. As for the negative statements, the scales were reversely arranged and recorded. Those participants with attitude scores of 80% and above were categorized as having acceptable attitude, while those who scored below 80% were considered as having unacceptable attitude [30].
The preventive practice questions contained 17 items (ensuring no rats around their houses, avoidance of risky activities and behaviors, rubbish and waste management, hand hygiene practices, food hygiene practices, treatment obtained, and opting for clean restaurant). Participants were asked to give a response of “Not applicable”, “Never”, “Sometimes”, “Most of the time”, and “All of the time” and scored as “0”, “1”, “2”, “3” and “4”, respectively. Those participants that had scores 80% and above were categorized as having acceptable preventive practice, while those with scores lower than 80% were categorized as having unacceptable preventive practice [31].

2.5. Data Analysis

SPSS Version 23 statistical software (SPSS Inc., Chicago, IL, USA) was used for the data analysis. Descriptive statistics were used to determine the socio-demographic factors and the KAP scores. Associations between categorical variables were analyzed by Chi square. In all cases, p-value < 0.05 was considered to be statistically significant at 95% CI. As for the significant associations, logistic regression was used for the respective variables.

3. Results

3.1. Demographic Data

In total, 444 participants were involved in the study. Males and females participated almost equally (50.2% vs. 49.8%). The age of the participants ranged from 18–81 years old with the mean age of 34.1 (±14.6). Malays (83.1%) outnumbered the Chinese (2.9%), Indian (6.8%) and others (7.2%). A majority of the participants were married compared to unmarried (65.3% vs. 34.7%), and almost a quarter (23.8%) had two children. Most of the participants received formal education than non-formal one (96.8% vs. 3.2%). However, 37.4% of the participants were unemployed and 43.5% earned less than 1500 Malaysian ringgit. The socio-demographic characteristics of the participants are shown in the Supplementary Material (Table S1).

3.2. KAP on Leptospirosis

3.2.1. Awareness and Source of Information on Leptospirosis

A majority of the participants (87.4%) had heard about “rat-urine disease”. Most of the participants (75.5%) identified the television/radio as the main source of information. Almost half (51.0%) had the information from the newspaper. Only 17.8% and 15.5% obtained the information from the doctor and magazine, respectively. Sources of information are shown in the Supplementary Materials (Table S2).

3.2.2. Knowledge on Leptospirosis

Overall, 43% and 57% of the participants had good and poor knowledge levels, respectively. Only 29.7% of the participants knew “rat-urine disease” is also known as leptospirosis and 69.1% of the participants were not aware of it. For further analysis and discussion, we used leptospirosis to represent “rat-urine disease” which was perceived by the rural communities. Interestingly, 66.7% correctly responded to leptospirosis as a zoonotic disease and 58.6% knew that leptospirosis is caused by bacteria. The participants also knew that leptospirosis could be diagnosed by blood test (61.0%). Meanwhile, contaminated water and food were the most well known as the routes of transmission by 61.9% and 60.4% of the study participants, respectively. Only 34.2% of the participants knew the bacteria could enter the wound and 58.1% were not aware of it. Surprisingly, shaking hands with infected person was thought of as a route of transmission (12.8%). Regarding the signs and symptoms of leptospirosis, 68.0% and 52.5% of the participants knew fever and body ache are symptoms of leptospirosis. However, only 24.5% of the participants knew yellowing of the eyes is the sign of leptospirosis, and the majority of participants (66.4%) were not aware of it. As for the complications, only 39.0% and 36.9% of the participants knew leptospirosis could lead to kidney failure and liver damage, respectively.
Concerning the preventive practices of leptospirosis, a majority of the participants (81.3%) knew leptospirosis could be prevented by ensuring the residential area is free of rubbish, followed by drinking clean water supply (77.7%), practicing good personal hygiene (77.7%), not swimming in contaminated freshwater bodies (75.5%) and not wading through flood (67.1%). However, wearing rubber gloves as a protective measure was known by only 55.2% of the participants. Table 1 shows the participants’ knowledge of leptospirosis.

3.2.3. Attitudes on Leptospirosis

Regarding attitudes towards readiness of wearing protective equipment, only 37.8% and 33.3% of participants were strongly agreed and agreed, respectively, on the willingness of wearing gloves while collecting the rubbish. Half of the participants (50.7%) had strongly agreed to make sure the dustbin is always covered. Less than half of participants had strongly agreed to make sure their family members would participate in cleaning activities (46.2%), and participated in prevention and control activities initiated by the authority (45.0%). Only 36.5% had strongly agreed to see a doctor if the participants have fever during a leptospirosis outbreak. Astonishingly, more than half did not mind if the house or its surrounding area is dirty (59.7%) and did not care if the participants find rats in the house or its surrounding area (55.4%). Table 2 shows the participants’ attitudes related to leptospirosis.

3.2.4. Preventive Practices on Leptospirosis

With regard to cleaning activities as preventive measures 63.5%, 60.6% and 49.3% of the participants had washed their hands with a soap after handling the rubbish or waste, their cooking tools and cleaned the house area from any rubbish or waste, respectively. A small percentage of the participants (6.8%) had gone for a picnic at the contaminated river/lake/waterfall for the past six months. In addition, a majority of the participants (64.0%) had kept the food in a covered container and 61.3% of the participants had covered the dustbin to prevent rats. Less than half (42.6%) had covered the wound or small cut while handling the rubbish or waste. Surprisingly, only 32.9% of the participants had used rubber boots while wading through the flood (Table 3).

3.3. KAP Analysis with Other Parameters

The data analysis on knowledge level of leptospirosis showed that Malays had good knowledge level than non-Malays (46.6% vs. 25.3%; prevalence ratio (PR) = 1.840, 95% CI = 1.229–2.755). The association of knowledge level and other variables are shown in the Supplementary Materials (Table S3). A very good attitude was demonstrated among Malays than non-Malays (66.7% vs. 44.0%; prevalence ratio (PR) = 1.515, 95% CI = 1.162–1.976). In terms of income, those who earned RM1500 and more had acceptable attitudes compared to those who earned less than RM1500 (69.4% vs. 58.8%; prevalence ratio (PR) = 0.843, 95% CI = 0.748–0.950). Participants who received formal education had acceptable attitudes than those who received non-formal education (64.0% vs. 31.3%; prevalence ratio (PR) = 1.911, 95% CI = 1.341–2.721). Associations between the participants’ attitude according and their respective variables are shown in Table 4. As for the preventive practices against leptospirosis, those who earned RM1500 and more had higher level of acceptable practices than those who earned less than RM1500 (38.8% vs. 25.9%; prevalence ratio (PR) = 1.211, 95% CI = 1.054–1.391). The level of preventive practices and its socio-demographic variables are shown in the Supplementary Materials (Table S4).
In the logistic regression analysis (Table S5), ethnicity was the only significant predictor for knowledge where Malays had 2.6 times higher odds of having good knowledge compared to non-Malays (AOR = 0.39, 95% CI = 0.222–0.680). Malays also had 2.5 times higher odds of having acceptable attitudes than non-Malays (AOR = 0.40, 95% CI = 0.239–0.665). In addition, income and education type were also significant predictors for attitudes. Those who had an income of RM1500 and more were 1.6 times more likely to have acceptable attitudes than those who had less than RM1500 income (AOR = 1.58, 95% CI = 1.041–2.385). Meanwhile, those who had a formal education were 3.7 times more likely to have acceptable attitudes than non-formal one (AOR = 3.69, 95% CI = 1.237–10.986). Table 5 shows the logistic regression analysis predicting the attitude on leptospirosis. As for the preventive practices, income was the only significant predictor. Those who earned RM1500 and more had 1.8 times higher odds of having acceptable practices than those who earned less than RM1500 (AOR = 1.81, 95% CI = 1.204–2.734). The logistic regression analysis is shown in the Supplementary Material (Table S6).
Table S7 shows the associations between preventive practices and knowledge and attitudes of the rural communities. Participants with good knowledge had acceptable practices than those with poor knowledge (37.2% vs. 26.1%; prevalence ratio (PR) = 0.702, 95% CI = 0.532–0.926). In addition, an acceptable level of practices was observed among participants with acceptable attitudes than those with unacceptable attitudes (41.2% vs. 13.3%; prevalence ratio (PR) = 0.323, 95% CI = 0.214–0.489). However, attitude was the only predictor for the preventive practices of leptospirosis by logistic regression analysis (Table S8). Participants with acceptable attitudes had 4.4 times higher odds of having acceptable level of preventive practices than those who had unacceptable attitudes (AOR = 4.357, 95% CI = 2.613–7.264).

4. Discussion

Several sero-epidemiological studies have documented the possible association of leptospirosis with certain high risk occupations such as town service workers, soldiers, farmers, food-handlers and people who were involved in recreational activities [20,30,32,33,34]. However, studies to explore the knowledge, attitudes and preventive practices are still lacking. With an increasing trend of number of deaths due to leptospirosis reported annually, an urgent need to gather important data for effective control and preventive plans is imminent.

4.1. Knowledge of Leptospirosis on Etiological Agents, Modes of Transmission, Clinical Symptoms, Preventive Measures and Its Complications

As expected, a majority of the members in a rural community in the present study have heard of “rat-urine disease” (87.4%) and a high proportion of the study participants obtained the information from the television and radio (75.5%). However, almost 70% of our rural communities were unaware of the term leptospirosis. In contrast, 90% of urban slum dwellers were aware of leptospirosis [35]. In addition, a higher percentage (87.3%) of rural workers who had heard of leptospirosis by broadcast media were observed in The Philippines [31], but lower (57.0%) among farmers in Ubon Ratchathani province, Thailand [36]. The perception of the disease as “rat-urine disease” has been accepted by our community for many decades as the term was portrayed by Malaysian headlines and broadcast media in several outbreaks or cases involving campers, rescuers and armies, which could be sensational news [37,38]. However, since leptospirosis is not only caused by infected rats but also other mammals [39], accurate information is needed for better understanding of the disease so that effective preventive strategies can be implemented. Surprisingly, only 17.8% of the participants had heard it from doctors in the present study. This is in contrast with a study in Thailand where 94.2% of rural farmers obtained the information from hospital staff [36]. This could be explained by the high endemicity of leptospirosis in the studied area, thus, massive health campaigns could have been initiated for the farmers.
In general, a higher percentage of our rural communities had poor knowledge of leptospirosis than good knowledge (57.0% vs. 43.0%) with the mean knowledge score of 52.1 (SD ± 26.4). Interestingly, higher percentages of people had poor knowledge levels were reported in other studies locally and abroad. For instance, 98.0% and 87.2% of healthy individuals and town service workers had poor knowledge level, respectively [40,41]. However, the cut-off levels for the good knowledge were higher than the present study which could influence the percentages of poor knowledge levels in their studies. In Nigeria, 95.8% of abattoir workers had a poor knowledge level on leptospirosis [42]. Meanwhile, 80.0% of rural farmers in Buriram Province, Thailand had a poor level of knowledge [43]. However, this could be explained by a high percentage of villagers who only received primary school education and lower (73.0%) in their study. Additionally, 58.6% of our rural communities knew leptospirosis is caused by bacteria, and 66.6% of the participants were correctly identified leptospirosis as a zoonotic disease. Higher percentages of people’s understanding of the bacteria as the causative agents were reported in Thailand (77.9%) and The Philippines (91.0%) [36,44]. It seems that the level of knowledge varies according to the socio-demographic profile, geographical location and the type of methodology used.
Based on the data gathered from the questions on the transmission, 70%, 69.8% and 58.1% of members among our rural community were unaware of nose, eye and wounds, respectively as the entry points for Leptospira. This is very crucial as these people are living near to the freshwater bodies, and the tendency to get leptospirosis could possibly be high if the study participants are involved in any aquatic activities especially in areas where the environmental sanitation is poor [45]. In contrast, residents in The Philippines knew skin could be the portal of entry (85.8%) [46], and recent findings of rural people residing in 14 cities of The Philippines documented that leptospirosis could enter humans via skin abrasions (71.0%) and mucous membranes (57.0%) [44]. Sakinah et al. [40] reported 66.2% of healthy residents knew Leptospira could enter human body via skin cuts. Contaminated water/drinks could only be recognized by our rural communities in the present study as a medium for leptospirosis to enter human body (61.9%). In Brazil, however, only 31.1% of urban slum dwellers knew leptospirosis could be acquired this way [35]. In highly endemic areas in Thailand, contaminated water was regarded as the mode of acquisition by 97.1% of rural villagers [36]. Meanwhile, 57.9% and 25.4% of Sri Lankans who had been involved in leptospirosis outbreak could only recognize contaminated water and drinks, respectively as the modes of acquiring leptospirosis [47]. In the present study, 60.4% of rural villagers knew leptospirosis can be transmitted by contaminated food. Information on contaminated food as a potential source of leptospirosis is lacking in the literature. Only two local studies have documented among healthy population (75.4%) and town service workers (78.9%) [40,41]. It is worth noting that contaminated drinks and food are among the risk factors for leptospirosis [48]. Surprisingly, 62% and 25.5% of our rural communities did not know and wrongly answered, respectively to the question on shaking hands with infected person could transmit leptospirosis. In view of the lack of knowledge of some aspects of the entry points of leptospirosis in the present study, educational programs should be enhanced and specifically oriented to this rural community for the successful prevention of this deadly disease as reported in many reports [49,50].
As for the clinical manifestations of leptospirosis, a majority of our rural communities knew fever (68.0%) and body ache (52.5%) were the symptoms. Higher percentages of fever as the clinical symptom were observed in two studies in Sri langka (93.4% and 86.0%) [29,47]. However, similar finding was observed for the body ache in a study in Sri Langka (53.6%) [29]. Rural communities in the present study were not aware of jaundice as the clinical sign of leptospirosis (66.4%). This is in accordance with poor knowledge of liver damage as a complication of leptospirosis (36.9%) in the present study. Ironically, 14.6% of people who had experienced an outbreak of leptospirosis were still ignorance of jaundice as one of the clinical signs in Sri Langka [47]. Jaundice is a sign observed in patients with leptospirosis, and it is due the accumulation of bilirubin in the blood stream as a result of hepatocellular damage and hepatocyte apoptosis [51]. Death (80.4%) was highly regarded as the main complication, followed by difficulty in breathing (45.3%) in the present study. In contrast, 4.2% of urban slum dwellers in Brazil knew leptospirosis is the deadly disease [35].
Concerning knowledge of the preventive measures, the highest percentage was reported for keeping surrounding area free from the accumulation of rubbish or waste materials in the present study (81.3%). Similar percentages were observed on keeping good personal hygiene and clean water consumption (77.7% for each). Among communities in The Philippines, 98.0% of their participants knew maintaining good sanitation is important for the prevention [44]. Another communities in Catbalogan City, The Philippines also understood that maintaining the house clean (99.0%) and avoiding the stream water for drinking (73.0%) are also good preventive measures [46]. Rahim et al. [41] reported leptospirosis could be prevented by maintaining the cleanliness of house compound (92.1%). In the present study, avoiding the contaminated fresh water bodies (75.5%) and flood (67.1%) were understood as good preventive measures. Almost similar findings were observed among community residents in The Philippines, i.e., 78.0% and 69.0% of their study participants knew avoidance of going to rivers/streams after the flood and swimming in contaminated water with rat urine, respectively are good preventive practices [44]. A good understanding of appropriate precautionary measures is pivotal in alleviating the public from getting leptospirosis. This is clearly explained by many established reports. For instance, involvement in flood and its related aquatic activities are known to be risk factors for the transmission of leptospirosis [17]. Poor house hygiene and environmental sanitation were also responsible for the increased risk of leptospirosis due to the close proximity to uncollected trash and rodent infestations [8,52].

4.2. Attitudes and Preventive Practices on Leptospirosis

In general, the rural communities had unacceptable attitudes in the present study (90.3%). This is reflected by their unacceptable preventive practices (69.1%). Similar data were reported in other studies elsewhere [40,44]. On another note, good knowledge was not reflected by acceptable attitudes and practices for some variables in the present study. For instance, 46.2% and 49.3% of the study participants had strongly agreed to involve their family members in cleaning up their surrounding area and had always cleaned up their housing area, respectively, despite having a good understanding of its cleanliness for prevention (81.3%). Adequate knowledge was also not reflected in their preventive practices as only 39.4% of the participants in the present study had always ensured that there would be no rats around their house. Interestingly, a study in The Philippines demonstrated that despite almost 100% of respondents who had correct knowledge of the preventive measures, only 40.0% of their study participants had really practiced cleaning of their surrounding area [44]. In terms of personal protective equipment (PPE), 37.8% of the participants in the present study had strongly agreed on using gloves, however, only 26.4% of the participants had always used gloves in their actual practice. Our findings corroborate with other reports. Despite having correct knowledge of wearing boots, only 21.0% of the Filipinos used them [44]. There are few factors that have been hypothesized for these findings. For instance, lack of access to PPE was responsible for the low adoption of risk reduction methods by residents in Brazil [35]. Inadequate support for the daily garbage removal by local authorities might also influence the practice level in Brazil [35]. Thus, our rural communities might have encountered the same problems although no data is available to support our notions. Poor health seeking behaviors were also observed in the present study. Only 48.9% of rural communities had strongly agreed to see a doctor if they have fever, while only 40.8% of the participants had gone to see a doctor when they had fever during the leptospirosis outbreak. Commencing appropriate behavior change interventions would be a challenge to respective agencies if these parameters are not carefully evaluated. World Health Organization has recommended that targeting at the source of infection, the route of transmission and health education are important tools for effective prevention and control measures of leptospirosis [53].

4.3. Associations between KAP of Leptospirosis with Sociodemographic Factors

Malays were found to have significantly more knowledgeable and acceptable attitudes than non-Malays in the present study. Malays were 2.6 and 2.5 times more likely to have good knowledge and acceptable attitudes, respectively than their counterpart. This could be related to the high incidence of leptospirosis and outbreaks reported among Malays as compared to other ethnicities for a decade [54]. This could trigger them to appropriately response to the disease and be more aware as one of active coping strategies. Health warnings could increase people’s sensitivity to their susceptibility toward diseases [55]. However, no significant association was observed between black and other races of urban slum dwellers in Brazil [35]. Income and education type were significantly associated with attitudes in the present study. Members of rural community who received a formal education were 3.7 times more likely to have good knowledge than those who had non-formal education. This finding re-emphasizes the importance of education as individuals with higher education are able to collect, process and interpret information on healthy behaviors [56]. Lower educational level has been shown to be associated with higher risk of acquiring leptospirosis [57]. Thus, it is hoped that the delivery of health information should be accustomed to our rural communities with a low level of education in accessible and easy-to-understand formats. In addition, many flood victims (mainly rural folks) are gathered in temporary shelters where food and basic amenities are provided for free by the government in Malaysia. Thus, apart from giving physical and emotional support to these people, health information on infectious diseases can be initiated by the community volunteers to raise their awareness especially on minimizing the infection risks. Interestingly, higher income is related to acceptable preventive practices in the present study. Our finding is in concordance with a study among non-agricultural workers in The Philippines [31]. It is very important to note that socioeconomic backgrounds have been recognized as independent risk factors for leptospirosis among residents who live in poverty [52].
In the present study, those who had acceptable attitudes were 4.4 times likely to have acceptable preventive practices than those who had unacceptable attitudes. Available data on the relationships of knowledge, attitudes, and preventive practices of leptospirosis is still lacking. Nonetheless, differences in the causal associations of these parameters have been documented in several studies among zoonotic diseases. Some studies support the significant associations between knowledge and attitudes and preventive practices [58,59], while others do not yield significant associations [60,61].

4.4. Limitations

This study has several limitations which need to be highlighted. Findings of our study could not be broadly generalized to all of the rural communities in Malaysia as it was conducted in several rural districts in a state of Malaysia. Different sociocultural and economic backgrounds may give different results. Nonetheless, our findings could offer an insight on the strategies required to effectively address this deadly neglected disease as the number of deaths is increasing each year locally. In addition, since the self-administered questionnaire was used, the risk of having social desirability is anticipated. Moreover, the behavior changes especially on the attitude could not be evaluated as cross-sectional design was used in this study. The questions used were in a close-ended format which could be interpreted differently by the participants.

5. Conclusions

This study has demonstrated that the levels of knowledge, attitudes and preventive practices on leptospirosis among our rural communities are still low. Thus, there is an urgent call for the relevant authorities or stakeholders to develop more approachable health education programs or interventions for this group of people and the public at large. There is still a gap in knowledge of leptospirosis, especially on the awareness of the term leptospirosis, its modes of entry, its clinical manifestations and complications. Of our utmost concern, the preventive practices were poorly portrayed, especially on the use of PPEs. These findings could also provide an insight for various agencies such as health district or state offices, schools, universities as well as veterinary and agricultural departments to strengthen their communication and outreach strategy. Mutual involvement between community leaders or volunteers and health professionals should be encouraged to impart knowledge, to strategize and develop good action plans or preventive modules on leptospirosis. Thus, protective health behaviors can be adopted particularly in leptospirosis-prone areas and high-risk populations.

Supplementary Materials

The following are available online at https://www.mdpi.com/1660-4601/15/4/693/s1, Table S1: Socio-demographic characteristics of members of a rural community in this study; Table S2: Sources from which members of a rural community obtained the information on leptospirosis; Table S3: Knowledge level of leptospirosis in relation to socio-demographic variables; Table S4: Practices of rural communities relating to prevention of leptospirosis and its socio-demographic variables; Table S5: Multiple logistic regression predicting the knowledge level on leptospirosis; Table S6: Multiple logistic regression predicting the practices level on leptospirosis; Table S7: Association between preventive practices level and knowledge level and attitude of the rural communities related to leptospirosis; Table S8: Multiple logistic regression of knowledge and attitude predicting the practices level on leptospirosis.

Acknowledgments

The work presented in this manuscript was supported by the Ministry of Higher Education, Malaysia via the Long-Term Research Grant Scheme (UPM/700-2/1/LRGS/5526400) and (203/PPSP/6770003). We thank the Faculty of Medicine and Health Sciences, UPM; Ministry of Health, Malaysia; School of Medical Sciences, USM for their approval and support.

Author Contributions

Noramira Nozmi, Malina Osman, Aziah Daud and Rukman Awang Hamat conceived of and designed the experiment. Noramira Nozmi, Suhailah Samsudin, Siti Nor Sakinah Saudi and Nurul Munirah Abdullah performed the experiment. Noramira Nozmi, Surianti Sukeri, Mohd Nazri Shafei, Wan Mohd Zahiruddin Wan Mohd, Zawaha Idris, Wan Nor Arifin, Norazlin Idris, Malina Osman and Rukman Awang Hamat analyzed the data. Zainudin Abdul Wahab, Tengku Zetty Maztura Tengku Jamaluddin, Siti Norbaya Masri and Hejar Abd Rahman contributed analysis tools. Rukman Awang Hamat wrote the paper.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Costa, F.; Hagan, J.E.; Calcagno, J.; Kane, M.; Torgerson, P.; Martinez-Silveira, M.S.; Stein, C.; Abela-Ridder, B.; Ko, A.I. Global morbidity and mortality of leptospirosis: A systematic review. PLOS Negl. Trop. Dis. 2015, 9, e0003898. [Google Scholar] [CrossRef] [PubMed]
  2. Levett, P.N. Leptospirosis. Clin. Microbiol. Rev. 2001, 14, 296–326. [Google Scholar] [CrossRef] [PubMed]
  3. Bharti, A.R.; Nally, J.E.; Ricaldi, J.N.; Matthias, M.A.; Diaz, M.M.; Lovett, M.A.; Levett, P.N.; Gilman, R.H.; Willig, M.R.; Gotuzzo, E.; et al. Leptospirosis: A zoonotic disease of global importance. Lancet Infect. Dis. 2003, 3, 757–771. [Google Scholar] [CrossRef]
  4. McBride, A.J.A.; Athanazio, D.A.; Reis, M.G.; Ko, A.I. Leptospirosis. Curr. Opin. Infect. Dis. 2005, 18, 376–386. [Google Scholar] [CrossRef] [PubMed]
  5. Haake, D.A.; Levett, P.N. Leptospirosis in humans. Curr. Top. Microbiol. Immunol. 2015, 387, 65–97. [Google Scholar] [CrossRef] [PubMed]
  6. Bourhy, P.; Collet, L.; Brisse, S.; Picardeau, M. Leptospira mayottensis sp. nov., a pathogenic species of the genus Leptospira isolated from humans. Int. J. Syst. Evol. Microbiol. 2014, 64, 4061–4067. [Google Scholar] [CrossRef] [PubMed]
  7. Saito, M.; Villanueva, S.Y.; Kawamura, Y.; Iida, K.; Tomida, J.; Kanemaru, T.; Kohno, E.; Miyahara, S.; Umeda, A.; Amako, K.; et al. Leptospira idonii sp. nov., isolated from environmental water. Int. J. Syst. Evol. Microbiol. 2013, 63, 2457–2462. [Google Scholar] [CrossRef] [PubMed]
  8. Victoriano, A.F.; Smythe, L.D.; Gloriani-Barzaga, N.; Cavinta, L.L.; Kasai, T.; Limpakarnjanarat, K.; Ong, B.L.; Gongal, G.; Hall, J.; Coulombe, C.A.; et al. Leptospirosis in the Asia Pacific region. BMC Infect. Dis. 2009, 9, 147. [Google Scholar] [CrossRef] [PubMed]
  9. Adler, B.; de la Peña Moctezuma, A. Leptospira and leptospirosis. Vet. Microbiol. 2010, 140, 287–296. [Google Scholar] [CrossRef]
  10. Lau, C.; Smythe, L.; Weinstein, P. Leptospirosis: An emerging disease in travelers. Travel. Med. Infect. Dis. 2010, 8, 33–39. [Google Scholar] [CrossRef] [PubMed]
  11. Priya, S.P.; Sakinah, S.; Sharmilah, K.; Hamat, R.A.; Sekawi, Z.; Higuchi, A.; Ling, M.P.; Nordin, S.A.; Benelli, G.; Kumar, S.S. Leptospirosis: Molecular trial path and immunopathogenesis correlated with dengue, malaria and mimetic hemorrhagic infections. Acta Trop. 2017, 176, 206–223. [Google Scholar] [CrossRef] [PubMed]
  12. Cosson, J.F.; Picardeau, M.; Mielcarek, M.; Tatard, C.; Chaval, Y.; Suputtamongkol, Y.; Buchy, P.; Jittapalapong, S.; Herbreteau, V.; Morand, S. Epidemiology of Leptospira transmitted by rodents in Southeast Asia. PLoS Negl. Trop. Dis. 2014, 8, e2902. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Amilasan, A.S.; Ujiie, M.; Suzuki, M.; Salva, E.; Belo, M.C.; Koizumi, N.; Yoshimatsu, K.; Schmidt, W.P.; Marte, S.; Dimaano, E.M.; et al. Outbreak of leptospirosis after flood: The Philippines 2009. Emerg. Infect. Dis. 2012, 18, 91–94. [Google Scholar] [CrossRef] [PubMed]
  14. Hinjoy, S. Epidemiology of leptospirosis from Thai National Disease Surveillance System 2003–2012. OSIR 2014, 7, 1–5. [Google Scholar]
  15. Bahaman, A.R.; Ibrahim, A.L. A review of leptospirosis in Malaysia. Vet. Res. Commun. 1988, 12, 179–189. [Google Scholar] [CrossRef] [PubMed]
  16. Costa, F.; Martinez-Silveira, M.S.; Hagan, J.E.; Hartskeerl, R.A.; dos Reis, M.G.; Ko, A.I. Surveillance for leptospirosis in the Americas, 1996–2005: A review of data from ministries of health. Rev. Panam. Salud Publica 2012, 32, 169–177. [Google Scholar] [CrossRef] [PubMed]
  17. Kawaguchi, L.; Sengkeopraseuth, B.; Tsuyuoka, R.; Koizumi, N.; Akashi, H.; Vongphrachanh, P.; Watanabe, H.; Aoyama, A. Seroprevalence of leptospirosis and risk factor analysis in flood-prone rural areas in Lao PDR. Am. J. Trop. Med. Hyg. 2008, 78, 957–961. [Google Scholar] [PubMed]
  18. Pappachan, M.J.; Sheela, M.; Aravindan, K.P. Relation of rainfall pattern and epidemic leptospirosis in the Indian state of Kerala. J. Epidemiol. Community Health 2004, 58, 1054. [Google Scholar] [CrossRef] [PubMed]
  19. Lau, C.L.; Smythe, L.D.; Craig, S.B.; Weinstein, P. Climate change, flooding, urbanization and leptospirosis: Fueling the fire? Trans. R. Soc. Trop. Med. Hyg. 2010, 104, 631–638. [Google Scholar] [CrossRef] [PubMed]
  20. Thayaparan, S.; Robertson, I.; Fairuz, A.; Suut, L.; Abdullah, M. Leptospirosis: An emerging zoonotic disease in Malaysia. Malaysia J. Pathol. 2013, 35, 123–132. [Google Scholar]
  21. Koay, T.K.; Nirmal, S.; Noitie, L.; Tan, E. An epidemiological investigation of an outbreak of leptospirosis associated with swimming, Beaufort, Sabah. Med. J. Malaysia 2004, 59, 455–459. [Google Scholar] [PubMed]
  22. Sejvar, J.; Bancroft, E.; Winthrop, K.; Bettinger, J.; Bajani, M.; Bragg, S.; Shutt, K.; Kaiser, R.; Marano, N.; Popovic, T.; et al. Leptospirosis in “eco-challenge” athletes, Malaysian Borneo, 2000. Emerg. Infect. Dis. 2003, 9, 702–707. [Google Scholar] [CrossRef] [PubMed]
  23. Badrul Hisham, A.S.; Nor Azian Shaharom, C.M.D.; Marzukhi, M.I.; Norli, R.; Fatimah, O.; Kee, K.F.; Arbaiah, O.; Mohd Yusof Adam, A.M. Spectrum of flood-related diseases encountered during flood disaster in Johore, Malaysia. Malays. J. Community Health 2009, 15, 15–23. [Google Scholar]
  24. Ministry of Health Malaysia. Proceedings of the Environmental Health by Local Authorities. 2015. Available online: http://jkt.kpkt.gov.my/jkt/resources/PDF/Persidangan_2015/persidangan%20kesihatan/Prosiding%20Persidangan%20Kesihatan%20Persekitaran%202016.pdf (accessed on 12 December 2017).
  25. Larson, E.L.; Jacalyn, L.; Adler, L.M.; Blane, C. A multifaceted approach to changing handwashing behavior. Am. J. Infect. Control 1997, 25, 3–10. [Google Scholar] [CrossRef]
  26. Department of Statistics Malaysia. Report on Definition of Urban and Rural Areas in Population and Housing Census 2010. Available online: http://www.rurallink.gov.my/wp-content/uploads/2015/05/23.pdf (accessed on 22 December 2017).
  27. Zahiruddin, W.M.; Arifin, W.N.; Mohd Nazri, S.; Sukeri, S.; Zawaha, I.; Abu-Bakar, R.; Hamat, R.A.; Malina, O.; Jamaluddin, T.Z.M.T.; Pathman, A.; et al. Development and validation of a new knowledge, attitude, belief and practice questionnaire on leptospirosis in Malaysia. BMC Public Health 2018, 18, 331. [Google Scholar] [CrossRef] [PubMed]
  28. Ngulube, P. Handbook of Research on Social, Cultural and Educational Considerations of Indigenous Knowledge in Developing Countries, 1st ed.; IGI Global: Hershey, PA, USA, 2017; pp. 1–462. ISBN 9781522508380. [Google Scholar]
  29. Samarakoon, Y.M.; Gunawardena, N. Knowledge and self-reported practices regarding leptospirosis among adolescent school children in a highly endemic rural area in Sri Lanka. Rural Remote Health 2013, 13, 2360. [Google Scholar] [PubMed]
  30. Nazri, S.M.; Rahim, S.M.; Nor Azwany, Y.; Habsah, H.; Zahiruddin, W.M.; Aziah, B.D.; Zaliha, I.; Mohamed Rusli, A. Seroprevalence of leptospirosis among town service workers in Northeastern state of Malaysia. Int. J. Collab. Res. Intern. Med. Public Health 2012, 4, 395–403. [Google Scholar]
  31. Arbiol, J.; Orencio, P.M.; Romena, N.; Nomura, H.; Takahashi, Y.; Yabe, M. Knowledge, attitude and practices TOWARDS leptospirosis among lakeshore communities of Calamba and Los Baños, Laguna, Philippines. Agriculture 2016, 6, 18. [Google Scholar] [CrossRef]
  32. El Jalii, I.M.; Bahaman, A.R.; Mohd-Azmi, M.L.; Mutalib, A.R. Occurrence of human leptospirosis in Malaysia: A retrospective study. J. Trop. Biomed. 2000, 16, 1–5. [Google Scholar]
  33. Samsudin, S.; Masri, S.N.; Jamaluddin, T.Z.M.T.; Saudi, S.N.S.; Ariffin, U.K.M.; Amran, F.; Malina, O. Seroprevalence of leptospiral antibodies among healthy municipal service workers in Selangor. Adv. Public Health 2015, 2015, 1–6. [Google Scholar] [CrossRef]
  34. Suhailah, S.; Sakinah, S.N.S.; Malina, O.; Norliza, B.A.; Asyraf, N.M.; Fairuz, A.; Jamaluddin, T.Z.M.T.; Rukman, A.H.; Zahiruddin, W.M.; Shafei, M.N.; et al. Seroprevalence of Leptospira antibodies among market workers and food handlers in the Central State of Malaysia. Trop. Med. Int. Health 2018, 23, 327–333. [Google Scholar] [CrossRef]
  35. Navegantes de Araújo, W.; Finkmoore, B.; Ribeiro, G.S.; Reis, R.B.; Felzemburgh, R.D.; Hagan, J.E.; Reis, M.G.; Ko, A.I.; Costa, F. Knowledge, attitudes, and practices related to leptospirosis among urban slum residents in Brazil. Am. J. Trop. Med. Hyg. 2013, 88, 359–363. [Google Scholar] [CrossRef] [PubMed]
  36. Wongbutdee, J.; Saengnill, W.; Jittimanee, J.; Daendee, S. Perceptions and risky behaviors associated with leptospirosis in an endemic area in a village of Ubon Ratchathani Province, Thailand. Afr. Health Sci. 2016, 16, 170–176. [Google Scholar] [CrossRef] [PubMed]
  37. Sapian, M.; Khair, M.T.; How, S.H.; Rajalingam, R.; Sahhir, K.; Norazah, A.; Khebir, V.; Jamalludin, A.R. Outbreak of melioidosis and leptospirosis co-infection following a rescue operation. Med. J. Malaysia 2012, 67, 293–297. [Google Scholar] [PubMed]
  38. Hin, H.S.; Ramalingam, R.; Chunn, K.Y.; Ahmad, N.; Ab Rahman, J.; Mohamed, M.S. Fatal co-infection-melioidosis and leptospirosis. Am. J. Trop. Med. Hyg. 2012, 87, 737–740. [Google Scholar] [CrossRef] [PubMed]
  39. Bunnell, J.E.; Hice, C.L.; Watts, D.M.; Montrueil, V.; Tesh, R.B.; Vinetz, J.M. Detection of pathogenic Leptospira spp. infections among mammals captured in the Peruvian Amazon basin region. Am. J. Trop. Med. Hyg. 2000, 63, 255–258. [Google Scholar] [CrossRef] [PubMed]
  40. Sakinah, S.N.S.; Suhailah, S.; Jamaluddin, T.Z.M.T.; Norbaya, S.M.; Malina, O. Seroprevalence of leptospiral antibodies and knowledge, attitude, and practices of leptospirosis to non-high risk group in Selangor. Int. J. Public Health Clin. Sci. 2015, 2, 92–104. [Google Scholar]
  41. Rahim, M.; Aziah, B.D.; Nazri, M.S.; Azwany, Y.N.; Habsah, H.; Zahiruddin, W.M.; Zaliha, I.; Rusli, M.A. Town service workers’ knowledge, attitude and practice towards leptospirosis. Brun. Darus. J. Health 2012, 5, 1–12. [Google Scholar]
  42. Abiayi, E.A.; Inabo, H.I.; Jatau, E.D.; Makinde, A.A.; Sar, T.T.; Ugbe, D.A.; Kumbish, P.R.; Okewole, P.A. Knowledge, attitudes, risk factors and practices (KARP) that favor leptospiral infection among abattoir workers in North Central Nigeria. Asian J. Epidemiol. 2015, 8, 104–113. [Google Scholar] [CrossRef]
  43. Wiwanitkit, V. A note from a survey of some knowledge aspects of leptospirosis among a sample of rural villagers in the highly endemic area, Thailand. Rural Remote Health 2006, 6, 526. [Google Scholar] [PubMed]
  44. Guevarra, J.P.; Borja, M.P.; Napulan, R.M.; Gloriani, N.G.; Yoshida, S.-I. Knowledge, attitudes and practices of the community residents concerning the prevention and control of leptospirosis in the National Capital Region (NCR), Philippines. Acta Med. Philipp. 2016, 50, 129–135. [Google Scholar]
  45. Wynwood, S.J.; Graham, G.C.; Weier, S.L.; Collet, T.A.; McKay, D.B.; Craig, S.B. Leptospirosis from water sources. Pathog. Glob. Health 2014, 108, 334–338. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Quina, C.R.; Almazan, J.U.; Tagarino, J.B. Knowledge, attitudes, and practices of leptospirosis in Catbalogan City, Samar, Philippines. Am. J. Public Health Res. 2014, 2, 91–98. [Google Scholar] [CrossRef]
  47. Agampodi, S.B.; Agampodi, T.C.; Thalagala, E.; Perera, S.; Chandraratne, S.; Fernando, S. Do people know adequately about leptospirosis? A knowledge assessment survey in post-outbreak situation in Sri Lanka. Int. J. Prev. Med. 2010, 1, 158–163. [Google Scholar] [PubMed]
  48. Waitkins, S. Leptospirosis as an occupational disease. Brit. J. Ind. Med. 1986, 43, 721–725. [Google Scholar] [CrossRef]
  49. John, T.J. The prevention and control of human leptospirosis. J. Postgrad. Med. 2005, 51, 205–209. [Google Scholar] [PubMed]
  50. Cachay, E.R.; Vinetz, J.M. A global research agenda for leptospirosis. J. Postgrad. Med. 2005, 51, 174–178. [Google Scholar] [PubMed]
  51. Merien, F.; Truccolo, J.; Rougier, Y.; Baranton, G.; Perolat, P. In vivo apoptosis of hepatocytes in guinea pigs infected with Leptospira interrogans serovar icterohaemorrhagiae. FEMS Microbiol. Lett. 1998, 169, 95–102. [Google Scholar] [CrossRef] [PubMed]
  52. Reis, R.B.; Ribeiro, G.S.; Felzemburgh, R.D.; Santana, F.S.; Mohr, S.; Melendez, A.X.; Queiroz, A.; Santos, A.C.; Ravines, R.R.; Tassinari, W.S.; et al. Impact of environment and social gradient on Leptospira infection in urban slums. PLoS Negl. Trop. Dis. 2008, 2, e228. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. World Health Organization. Human Leptospirosis: Guidance for Diagnosis, Surveillance and Control; WHO: Geneva, Switzerland, 2003; Available online: http://apps.who.int/iris/bitstream/10665/42667/1/WHO_CDS_CSR_EPH_2002.23.pdf (accessed on 8 January 2018).
  54. Benacer, D.; Thong, K.L.; Min, N.C.; Bin Verasahib, K.; Galloway, R.L.; Hartskeerl, R.A.; Souris, M.; Mohd Zain, S.N. Epidemiology of human leptospirosis in Malaysia, 2004–2012. Acta Trop. 2016, 157, 162–168. [Google Scholar] [CrossRef] [PubMed]
  55. Schneider, T.R.; Salovey, P.; Pallonen, U.; Mundorf, N.; Smith, N.E.; Steward, W.T. Visual and auditory message framing effects on tobacco smoking. J. Appl. Soc. Psychol. 2001, 31, 667–682. [Google Scholar] [CrossRef]
  56. Groot, W.; van den Brink, H.M. What does education do to our health? Measuring the effects of education on health and civic engagement. In Proceedings of the Copenhagen Symposium, Amsterdam, The Netherlands, 1 January 2006; pp. 355–361. [Google Scholar]
  57. Dias, J.P.; Teixeira, M.G.; Costa, M.C.N.; Mendes, C.M.C.; Guimarães, P.; Reis, M.G.; Ko, A.; Barreto, M.L. Factors associated with Leptospira sp infection in a large urban center in Northeastern Brazil. Rev. Soc. Bras. Med. Trop. 2007, 40, 499–504. [Google Scholar] [CrossRef] [PubMed]
  58. Ali, A.; Ahmed, E.Y.; Sifer, D. A study on knowledge, attitude and practice of rabies among residents in Addis Ababa, Ethiopia. Ethiop. Vet. J. 2014, 17, 19–35. [Google Scholar] [CrossRef]
  59. Sambo, M.; Lembo, T.; Cleaveland, S.; Ferguson, H.M.; Sikana, L.; Simon, C.; Urassa, H.; Hampson, K. Knowledge, attitudes and practices (KAP) about rabies prevention and control: A community survey in Tanzania. PLoS Negl. Trop. Dis. 2014, 8, e3310. [Google Scholar] [CrossRef] [PubMed]
  60. Yboa, B.C.; Labrague, L.J. Dengue knowledge and preventive practices among rural residents in Samar Province, Philippines. Am. J. Public Health Res. 2013, 1, 47–52. [Google Scholar] [CrossRef]
  61. Abedi, A.; Khan, Z.; Ansari, A.; Amir, A. Sp5-23 is knowledge and attitude correlating with practices? A KAP study on dengue fever. J. Epidemiol. Community Health 2011, 65, A451. [Google Scholar] [CrossRef]
Table
Table 1. The knowledge of leptospirosis by participants in rural areas of Hulu Langat.
Table 1. The knowledge of leptospirosis by participants in rural areas of Hulu Langat.
QuestionCorrect n (%)Incorrect n (%)Do Not Know n (%)
Rat urine disease is also known as leptospirosis132 (29.7)5 (1.1)307 (69.1)
The disease is caused by a bacterium260 (58.6)41 (9.8)143 (32.2)
Infected animals could also infect man296 (66.7)36 (8.1)112 (25.2)
The disease is diagnosed by blood test271 (61.0)28 (6.3)145 (32.7)
The etiological agent may enter human body via:---
Wound site152 (34.2)34 (7.7)258 (58.1)
Eyes87 (19.6)47 (10.6)310 (69.8)
Nose92 (20.7)41 (9.2)311 (70.0)
Mouth142 (32.0)32 (7.2)270 (60.8)
Contaminated food268 (60.4)13 (2.9)163 (36.7)
Contaminated water/drinks275 (61.9)9 (2.0)160 (36.0)
Shaking hands with infected individuals57 (12.8)113 (25.5)274 (61.7)
An individual with leptospirosis would have:---
Fever302 (68.0)5 (1.1)137 (30.9)
Body ache233 (52.5)17 (3.8)194 (43.7)
Yellowing of the eyes109 (24.5)40 (9.0)295 (66.4)
The disease may cause---
Death357 (80.4)5 (1.1)82 (18.5)
Breathing difficulty201 (45.3)21 (4.7)222 (50.0)
Kidney failure173 (39.0)24 (5.4)247 (55.6)
Liver damage164 (36.9)25 (5.6)255 (57.4)
Leptospirosis can be prevented by:---
Ensuring your residential area free of rubbish361 (81.3)2 (0.5)81 (18.2)
Not wading through flood298 (67.1)21 (4.7)125 (28.2)
Practising good personal hygiene345 (77.7)7 (1.6)92 (20.7)
Drinking clean water supply345 (77.7)0 (0.0)99 (22.3)
Wearing rubber gloves245 (55.2)44 (9.9)155 (34.9)
Not swimming in contaminated river/lake or waterfall335 (75.5)9 (2.0)100 (22.5)
Table
Table 2. Attitudes of leptospirosis among participants.
Table 2. Attitudes of leptospirosis among participants.
ItemStrongly Disagree n (%)Disagree n (%)Maybe n (%)Agree n (%)Strongly Agree n (%)
I will wear gloves if I handle the rubbish16 (3.6)28 (6.3)84 (18.9)148 (33.3)168 (37.8)
I will make sure my dustbin is always covered13 (2.9)8 (1.8)70 (15.8)128 (28.8)225 (50.7)
I will participate in prevention and control activities offered by the authority13 (2.9)2 (0.5)90 (20.3)139 (31.3)200 (45.0)
I will make sure my family is involved in cleaning activities around the house12 (2.7)0 (0.0)72 (16.2)155 (34.9)205 (46.2)
I will inform the health authority if I find myself having signs/symptoms of leptospirosis12 (2.7)2 (0.5)100 (22.5)130 (29.3)200 (45.0)
I will make sure my family members are aware of contaminated river/lake/waterfall11 (2.5)3 (0.7)105 (23.6)138 (31.1)187 (42.1)
I am not worried if I wade through the flood21 (4.7)53 (11.9)152 (34.2)99 (22.3)119 (26.8)
I do not mind if there are rats in my house and its surrounding26 (5.9)14 (3.2)84 (18.9)74 (16.7)246 (55.4)
I will inform the health authority if a person is suspected of having leptospirosis18 (4.1)10 (2.3)120 (27.0)134 (30.2)162 (36.5)
I do not mind if my housing area is dirty17 (3.8)12 (2.7)81 (18.2)69 (15.5)265 (59.7)
I need to see a doctor if I am having fever during a leptospirosis outbreak13 (2.9)2 (0.5)88 (19.8)124 (27.9)217 (48.9)
I need to wear personal protective equipment (rubber boot, facial mask, and others) when I handle the rubbish13 (2.9)19 (4.3)114 (25.7)147 (33.1)151 (34.0)
I am not worried if I do not wear personal protective equipment (PPE) such as gloves, boots while handling the rubbish27 (6.1)36 (8.1)117 (26.4)83 (18.7)181 (40.8)
Table
Table 3. Preventive practices on leptospirosis among rural communities in Hulu Langat.
Table 3. Preventive practices on leptospirosis among rural communities in Hulu Langat.
Preventive PracticesNever n (%)Sometimes n (%)Most of the Time n (%)All the Time n (%)Not Applicable n (%)
I ensured no rats are found in my housing area19 (4.3)95 (21.4)66 (14.9)175 (39.4)89 (20.0)
I went for a picnic at places contaminated with leptospirosis (waterfall/river/lake) within the past six months236 (53.2)62 (14.0)5 (1.1)30 (6.8)111 (25.0)
I cleaned my housing area from any waste/rubbish15 (3.4)44 (9.9)77 (17.3)219 (49.3)89 (20.0)
I handled waste/rubbish despite having wounds/cuts on my hands/legs131 (29.5)118 (26.6)43 (9.7)61 (13.7)91 (20.5)
I ate food/consumed water while handling the waste/rubbish287 (64.6)40 (9.0)12 (2.7)16 (3.6)89 (20.0)
I washed my hands with a soap after managing waste/rubbish17 (3.8)35 (7.9)22 (5.0)282 (63.5)88 (19.8)
I wore the following PPE while handling the waste/rubbish:
Rubber gloves105 (23.6)85 (19.1)43 (9.7)117 (26.4)94 (21.2)
Rubber boots149 (33.6)78 (17.6)33 (7.4)73 (16.4)111 (25.0)
Long sleeve attires97 (21.8)77 (17.3)45 (10.1)117 (26.4)108 (24.3)
I kept my food in a covered container14 (3.2)20 (4.5)41 (9.2)284 (64.0)84 (18.9)
I went to see a doctor when I had fever during a leptospirosis outbreak49 (11.0)37 (8.3)59 (13.3)181 (40.8)118 (26.6)
I covered the dustbin to prevent rat infestations 12 (2.7)27 (6.1)50 (11.3)272 (61.3)83 (18.7)
I washed the can/drink box before drinking57 (12.8)38 (8.6)46 (10.4)219 (49.3)84 (18.9)
I washed the utensils before cooking14 (3.2)27 (6.1)45 (10.1)269 (60.6)89 (20.0)
I preferred a clean restaurant for meals9 (2.0)12 (2.7)43 (9.7)297 (66.9)83 (18.7)
I used a plaster on wounds or small cuts while handling the waste/rubbish31 (7.0)61 (13.7)66 (14.9)189 (42.6)97 (21.8)
I waded through floods without PPE146 (32.9)59 (13.3)40 (9.0)39 (8.8)160 (36.0)
I used a plaster on wounds or small cuts while wading through floods70 (15.8)63 (14.2)42 (9.5)103 (23.2)166 (37.4)
I smoked while handling the waste/rubbish185 (41.7)18 (4.1)15 (3.4)30 (6.8)196 (44.1)
Table
Table 4. Level of attitude among rural communities in relation to socio-demographic variables.
Table 4. Level of attitude among rural communities in relation to socio-demographic variables.
VariablesAttitude Leveln (%)x2pPrevalence Ratio (CI) #
Acceptable (%) Unacceptable (%)
Gender------
 Male132 (59.2)91 (40.8)223 (50.2)2.5490.1101.219 (0.955–1.555)
 Female147 (66.5)74 (33.5)221 (49.8)--
Age (in years)------
 <34147 (67.1)72 (32.9)219 (49.3)3.3990.0651.144 (0.991–1.321)
 ≥34132 (58.7)93 (41.3)225 (50.7)--
Ethnicity------
 Malay246 (66.7)123 (33.3)369 (83.1)13.714<0.001 *1.515 (1.162–1.976)
 Non-Malay33 (44.0)42 (56.0)75 (16.9)--
Income (RM) † ------
 <1500161 (58.8)113 (41.2)274 (61.7)5.0980.024 *1.348 (1.032–1.761)
 ≥1500118 (69.4)52 (30.6)170 (38.3)--
Education type------
 Formal274 (64.0)154 (36.0)428 (96.4)7.0920.018 *1.911 (1.341–2.721)
 Non-formal5 (31.3)11 (68.7)16 (3.6)--
* Significant at p < 0.05; † Malaysian Ringgit; # CI = confidence interval.
Table
Table 5. Multiple logistic regression predicting the attitude on leptospirosis.
Table 5. Multiple logistic regression predicting the attitude on leptospirosis.
Variableβp-ValueAdjusted Odds Ratio95% CI
Constant 0.0012.174-
Ethnicity
 Malay <0.001 *0.3990.239–0.665
 Non-Malay−0.919
Income (RM) †
 <1500
 ≥15000.4450.032 *1.5751.041–2.385
Education type
 Non-Formal
 Formal1.3050.019 *3.6861.237–10.986
Notes: Method = Enter; R2 = 72.0%; Overall percentage = 66.0%; * significant p < 0.05; † Malaysian Ringgit.

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MDPI and ACS Style

Nozmi, N.; Samsudin, S.; Sukeri, S.; Shafei, M.N.; Wan Mohd, W.M.Z.; Idris, Z.; Arifin, W.N.; Idris, N.; Saudi, S.N.S.; Abdullah, N.M.; et al. Low Levels of Knowledge, Attitudes and Preventive Practices on Leptospirosis among a Rural Community in Hulu Langat District, Selangor, Malaysia. Int. J. Environ. Res. Public Health 2018, 15, 693. https://doi.org/10.3390/ijerph15040693

AMA Style

Nozmi N, Samsudin S, Sukeri S, Shafei MN, Wan Mohd WMZ, Idris Z, Arifin WN, Idris N, Saudi SNS, Abdullah NM, et al. Low Levels of Knowledge, Attitudes and Preventive Practices on Leptospirosis among a Rural Community in Hulu Langat District, Selangor, Malaysia. International Journal of Environmental Research and Public Health. 2018; 15(4):693. https://doi.org/10.3390/ijerph15040693

Chicago/Turabian Style

Nozmi, Noramira, Suhailah Samsudin, Surianti Sukeri, Mohd Nazri Shafei, Wan Mohd Zahiruddin Wan Mohd, Zawaha Idris, Wan Nor Arifin, Norazlin Idris, Siti Nor Sakinah Saudi, Nurul Munirah Abdullah, and et al. 2018. "Low Levels of Knowledge, Attitudes and Preventive Practices on Leptospirosis among a Rural Community in Hulu Langat District, Selangor, Malaysia" International Journal of Environmental Research and Public Health 15, no. 4: 693. https://doi.org/10.3390/ijerph15040693

APA Style

Nozmi, N., Samsudin, S., Sukeri, S., Shafei, M. N., Wan Mohd, W. M. Z., Idris, Z., Arifin, W. N., Idris, N., Saudi, S. N. S., Abdullah, N. M., Abdul Wahab, Z., Tengku Jamaluddin, T. Z. M., Abd Rahman, H., Masri, S. N., Daud, A., Osman, M., & Awang Hamat, R. (2018). Low Levels of Knowledge, Attitudes and Preventive Practices on Leptospirosis among a Rural Community in Hulu Langat District, Selangor, Malaysia. International Journal of Environmental Research and Public Health, 15(4), 693. https://doi.org/10.3390/ijerph15040693

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