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JSM Ophthalmology

Vitamin A Deficiency and Malnourishment among Young Children in Papua New Guinea

Research Article | Open Access | Volume 5 | Issue 1

  • 1. Department of Ophthalmology and Visual Sciences, Kellogg Eye Center, USA
  • 2. Department of Ophthalmology, Royal Hobart Hospital, Australia
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Corresponding Authors
V. Swetha E. Jeganathan, Department of Ophthalmology and Visual Sciences, Kellogg Eye Center, 1000 Wall St, Ann Arbor 48105, Michigan, USA, Tel: 1-734-763-8122;
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2. McLaren DS, Kraemer K, Xerophthalmia. World Rev Nutr Diet. 2012; 103: 65-75.

3. Tanumihardjo SA. Vitamin A: biomarkers of nutrition for development. Am J Clin Nutr. 2011; 94: 658S-65S.

4. Chiu M, Dillon A, Watson S. Vitamin A deficiency and xerophthalmia in children of a developed country. J Paediatr Child Health. 2016; 52: 699-703.

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6. Arlappa N. Vitamin A deficiency control measures: importance of vitamin A supplementation as a public health policy in the Indian context. J Public Health Policy. 2013; 34: 538-548

7. Sherwin JC, Reacher MH, Dean WH, Ngondi J. Epidemiology of vitamin A deficiency and xerophthalmia in at-risk populations. Trans R Soc Trop Med Hyg. 2012; 106: 205-214.

8. West KP Jr. Vitamin A deficiency disorders in children and women. Food Nutr Bull. 2003; 24: S78-90.

9. Benn CS, Aaby P, Arts RJ, Jensen KJ, Netea MG, Fisker AB. An enigma: why vitamin A supplementation does not always reduce mortality even though vitamin A deficiency is associated with increased mortality. Int J Epidemiol. 2015; 44: 906-918.

10. Robert E Black, Cesar G Victora, Susan P Walker, Zulfiqar A Bhutta, Parul Christian, et al. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet. 2013; 382: 427-451.

11. WHO. Indicators for assessing vitamin A deficiency and their application in monitoring and evaluation intervention programmes. Geneva. World Health Organization, 1996.

12. Sommer A. Vitamin a deficiency and clinical disease: an historical overview. J Nutr. 2008; 138: 1835-1839.

13. Saraiva BC, Soares MC, Santos LC, Pereira SC, Horta PM. Iron deficiency and anemia are associated with low retinol levels in children aged 1 to 5 years. J Pediatr (Rio J). 2014; 90: 593-599.

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15. Müller I, Bockarie M, Alpers M, Smith T. The epidemiology of malaria in Papua New Guinea. Trends Parasitol. 2003; 19: 253-259.

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17. Oppenheimer S. Iron and infection: narrative review of a major iron supplementation study in Papua New Guinea undertaken by the Department of Tropical Paediatrics, Liverpool School of Tropical Medicine, 1979-1983, its aftermath and the continuing relevance of its results. Paediatr Int Child Health. 2012; 32: S21-29.

18. Breymann C. Iron Deficiency Anemia in Pregnancy. Semin Hematol. 2015; 52: 339-347.

19. Amoa AB, Lavu E, Ray U, Sapuri M, Kariwiga G, Heywood S. The aetiology of severe anaemia among antenatal patients of the Port Moresby General Hospital. P N G Med J. 2003; 46: 143-151.

20. Manning L, Laman M, Rosanas-Urgell A, Michon P, Aipit S, Bona C. Severe anemia in Papua New Guinean children from a malariaendemic area: a case-control etiologic study. PLoS Negl Trop Dis. 2012; 6: e1972.

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23. Friesen H, Vince J, Boas P, Danaya R. Protection of breastfeeding in Papua New Guinea. Bull World Health Organ. 1999; 77: 271-274.

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26. Augusto RA, Cobayashi F, Cardoso MA; ACTION Study Team. Associations between low consumption of fruits and vegetables and nutritional deficiencies in Brazilian schoolchildren. Public Health Nutr. 2015; 18: 927-935.

27. West KP, LeClerq SC, Shrestha SR, Wu LS, Pradhan EK, Khatry SK, et al. Effects of vitamin A on growth of vitamin A-deficient children: field studies in Nepal. J Nutr. 1997; 127: 1957-1965.

28. Jones KD, Berkley JA. Severe acute malnutrition and infection. Paediatr Int Child Health. 2014. 34: S1-S29.

29. Stevens GA, Bennett JE, Hennocq Q, Lu Y, De-Regil LM, Rogers L, Danaei G, et al. Trends and mortality effects of vitamin A deficiency in children in 138 low-income and middle-income countries between 1991 and 2013: a pooled analysis of population-based surveys. Lancet Glob Health. 2015; 3: e528-36.

30. Seed JR. Protozoa: Pathogenesis and Defenses, in Medical Microbiology, S. Baron, Editor. 1996: Galveston (TX).

31. Vince JD. Diarrhoea in children in Papua New Guinea. P N G Med J. 1995; 38: 262-271.

32. Poka H, Duke T. Clinical management of diarrhoea in children. P N G Med J. 2013; 56: 156-161.

33. Clasen TF, Kelly T Alexander KT, David Sinclair, Sophie Boisson, Rachel Peletz,Howard H. Chang, Fiona Majorin, et al. Interventions to improve water quality for preventing diarrhoea. Cochrane Database Syst Rev. 2015: CD004794

34. Ejemot-Nwadiaro RI, Ehiri JE, Dachi Arikpo,Martin M. Meremikwu,Julia A Critchley. Hand washing promotion for preventing diarrhoea. Cochrane Database Syst Rev. 2015: CD004265.

Keywords

Vitamin A deficiency , Xerophthalmia , Papua New Guinea , Children , Risk factors

Abstract

Context: Papua New Guinea (PNG) has been classified by the World Health Organization as a country where Vitamin A deficiency (VAD) exists. 
Aims: To determine the vitamin A status and identify risk factors of VAD in children aged between 6 months to 6 years in PNG.
Setting and Design: A cross-sectional study was carried out on randomly selected children ages 6 months to 6 years in the Ramu region of Madang Province in PNG. 
Methods and Material: Vitamin A status was assessed by clinical indicators (ocular signs of xerophthalmia), subclinical indictors (self-reported night blindness), biochemical indicators (serum retinol, beta carotene, retinol binding protein(RBP) levels, conjunctival impression cytology) nutritional indicators (breast feeding patterns, vitamin A rich food), anthropometric measures, and associated morbidity conditions (diarrhea, malaria). 
Statistical analysis used: Epi Info 6 (Center for Disease Control, Atlanta, USA).
Results: From 609 children enrolled in the study, the prevalence of serum retinol levels ? 0.7 mmol/L was 10.3% (n= 62.7). Night blindness was reported in 4 children with no xerophthalmia evident. The prevalence of stunting was 35.2% (n= 214.4) in 
our study. 
Conclusions: No evidence of clinical VAD was found, but subclinical VAD occurred at a level of mild-moderate public health importance in our study. Further studies need to be carried out to assess VAD in different regions in PNG.

Citation

Jeganathan VSE, Verma N (2017) Vitamin A Deficiency and Malnourishment among Young Children in Papua New Guinea. JSM Ophthalmol 5(1): 1047.

ABBREVIATIONS

CIC: Conjunctival Impression Cytology; CRP: C Reactive Protein Levels; DGLV: Dark Green Leafy Vegetables; EPI: Expanded Program For Immunization; PEM: Protein Energy Malnutrition; PMGH: Port Moresby General Hospital; PNG: Papua New Guinea; RBP: Retinol Binding Protein; VAD: Vitamin A Deficiency; WHO: World Health Organization

INTRODUCTION

Vitamin A is critical for children’s growth and deficiency of this nutrient can result in protein energy malnutrition (PEM), micronutrient deficiency, and infections, in addition to decelerated growth [1]. Xerophthalmia caused by a severe vitamin A deficiency (VAD), if untreated, can lead to corneal ulceration and night blindness [2]. Clinical VAD is noted with apparent xerophthalmia and serum retinol levels of < 0.35µmol [3,4]. Subclinical VAD effects such as night blindness are seen when levels of serum vitamin A are low enough to have adverse health consequences even if there is no evidence of clinical xerophthalmia [5,6]. VAD appears to increase the risk of death even before xerophthalmia is apparent clinically [6,7]. Children between the ages of 6 months and 6 years are highly vulnerable to VAD [8]. The effects of vitamin A status on childhood mortality depend on the severity and prevalence of pre-existing VAD, concomitant nutritional disorders, and co-exiting infections [9]. It is estimated that over one million deaths in children could be prevented each year with improvement to vitamin A nutrition [10]

Papua New Guinea (PNG) has been classified by the World Health Organization (WHO) as a country where VAD exists. The aim of this study was to establish the vitamin A status of children aged 6 months to 6 years in the Madang province in PNG and determine associated risk factors.

MATERIALS AND METHODS

Study population and sampling methods

A prospective cross-sectional study was performed in the lower and middle Ramu region of the Madang province of PNG, to evaluate the vitamin A status of children aged between six months and six years. An estimated 7000 children (age between 6 months and 6 years), live here in 11 different isolated villages, located in four regions (Anaberg, Kwanga, Bogen and Bunapas). In our study, we included via random selection 609 children age six to 72 months, located from the four regions to determine their vitamin A status. We excluded children with presence of obvious illness, diarrhea or major injuries, diarrhea or fever in the last 2 weeks, non-residents, children on medications, children whose age was unknown, those with incomplete forms / interviews and unreliable information from parent.

Households in the villages were randomly selected. When people in a village lived scattered over a big area, the selection procedures were adjusted and clusters of households and children were enrolled in the survey. Children were selected so that approximately 10% of children in each age group were represented. The survey was carried out by 4 teams consisting of two trained health workers in pediatric and ophthalmic examination, a nutritionist and a pediatrician. The teams were accompanied by a local health worker from the nearest health center.

Ethical clearance

Ethical approval for the study was obtained from the Ethics Committee of PNG National Department of Health prior to study commencement. When the survey team arrived in the village, the purpose of the study was explained to the village leaders and parental informed consent was obtained for their child’s study participation.

Interviews

Mothers were asked to bring their children to a central point (usually the local school). The interviews were held in the local language, where medical history, immunization status, diet and night blindness were ascertained. Night blindness was assessed in all children using the WHO (1996) questionnaire: Can your child see in the daytime? Can your child see at night? If the answer to question 2 was “yes”, the child would be asked “is your child different from other children in the village? Or “does your child have night blindness (translated locally to “aitutak long nait”)? A family history of night blindness was also assessed in everyone during screening. Additionally, a household information form collected further socioeconomic information. This survey at the household level used focus groups of women and elders to generate a list of important foods available in homes whether from the home garden, or sources outside the community.

Physical examination

After the interviews had been completed, the following anthropometric data was recorded: weight (kg), and height/ length (cm). A weighing scale was used for weight evaluation. Children below 2 years of age had their length measured. For those over 2 years of age, height was measured. The child was then examined by the local pediatrician and a trained ophthalmologist for xerophthalmia or any corneal lesions. 

Conjunctival impression cytology (CIC)

CIC was collected from 100 randomly selected children by the Ophthalmologist. The sampled cells were stained and evaluated for described histological changes that are specific for VAD at the Department of Pathology, Port Moresby General Hospital (PMGH)

Laboratory biochemical markers

Blood was taken with steel butterfly needles from an appropriate vein on the forearm or hand and put in a non-Zinc containing heparinized Vacutainer tubes. Serum retinol binding protein (RBP), prealbumin, total proteins, β-carotene, and hemoglobin levels were analyzed at PMGH. The serum retinol levels were measured at the Children’s Hospital in Westmead, Australia, using a high pressure liquid chromatography column as recommended by WHO (1996) [11].

Statistical analysis

The children’s questionnaires were checked for completeness and data was transferred from the individual and household questionnaires to Epi Info 6 Program (Center for Disease Control, Atlanta, USA) and Microsoft Excel. These two programs were used for data analysis. A P-value less than 0.05 was considered statistically significant.The prevalence of each indicator of VAD as suggested by WHO (1996) was calculated [11].

 

RESULTS

Six hundred and nine children were enrolled from 50 households in our study. 49.1% (n=299) came from Anaberg, 31.1% (n=189.4) from Bogen, 11.3% (n=68.8) from Bunapas and 8.5% (n=51.8) from Kwanga. 53.7% were male. The average age was 37.2 months. The mean age of the children was 34.3 months for boys and 34.9 years for girls.

History of night blindness and ocular signs

The prevalence of night blindness was 1.1%. These four children had no evidence of a fundus abnormality or a positive family history of the disease. Almost all (98%) of the children had normal eyes on external examination. 1.3% of them had purulent conjunctivitis. One child had nystagmus and 2 had corneal scars due to trauma. These were cross-checked and validated by the ophthalmologist

Biochemical indicators

The mean serum retinol level was 1.22µmol (σ = 0.481) and 15% of the children had a serum retinol < 0.70µmol. There was no statistically significant difference in the serum retinol levels of boys (1.153 µmol) and girls (1.274) (p-value 0.21). Twenty five percent of children with night blindness had a serum retinol of greater than 0.7µmol. The largest percentage of children with low serum retinol were in Anaberg (49.1%) There was no correlation between the serum retinol and the anthropometric parameters.

The mean βCarotene level was 0.502µmol; RBP 19.23 mg/L, prealbumin 137.2 mg/L, and total protein levels 70.4 mg/L. The mean hemoglobin was 92 g/L. There was a weak correlation between serum retinol and hemoglobin (r=0.17). The mean hemoglobin levels in children with serum retinol<0.7µmol was 8.75 g/L. There was no correlation between hemoglobin and serum retinol in children with serum retinol below 0.7 µmol. There was good correlation between serum retinol and RBP levels (r=0.51, r2 =0.26 95%CI 0.07 and 0.43). There was a significant correlation between RBP and prealbumin (r=0.54, r2 =0.29 95% CI 0.10 and 0.46).

CIC

Due to cost considerations, a total of 101 CIC smears were studied. 36 found to be unsatisfactory as the cells could not be studied properly due to paucity of the cells or poor staining.

Nutritional indicators

Breast feeding patterns: 41.5% of the children were still breast-feeding. The mean age of boys still breast-feeding was 20.4 months (n=26, 6.1-65 months) and girls (n=18, 5-53 months). In the younger age group, 93.1% of children below 18 months of age were being breast fed and the mean age of stopping breast feeding was 22.2 months (median 24 months, SD 11.09). Solids were introduced at a mean age of 4.9 months (SD 2.76, median 4 months, and range 3-12 months).

Vitamin A rich food intake: We found that 69.8% of children consumed dark green leafy vegetables (DGLV, AKA “kumu”) every day of the week. The mean number of days/week that kumu was eaten was 5.6 and less than 14.2% of children consumed DGLV less than 3 days/week. The mean serum retinol in children consuming DGLV < 3 days/ week was 1.033 µmol. Cooked bananas was a commonly consumed vegetable (70.2% ≥ 3 days/ week; mean 4.5 days/week). 55.7% of children ate fresh bananas > 3 days/week; mean 3.3 days/week). Sweet potatoes were eaten by 28.3% children ≥ 3 days/week). This is the same situation with pawpaw (2.6%> 3-days/week; mean 1.5). Carrots were not consumed by any of the children. Whole fish was consumed by 51.5% of children ≥ 3 times/week (mean 3.2). Chinese cabbage, tomatoes, pumpkin, pandanus, pineapples, guava, shellfish, avocado pears, whole milk and eggs were consumed infrequently or not at all.

Market, household food and safe water availability: Only 2% of the people depended on food obtained from the market. 68% of households had a regular income most of which was earned by selling produce in the local market. More than 75% had DGLV (kumu) and bananas growing in their garden, and more than 60% had corn, sweet potato, beans and pumpkins in their garden. Pawpaw and bananas were available to more than 80% of households on a regular basis. Only 28% of the households had access to safe water. The rest of them relied on the rivers and streams (38%), bore holes (4%) and unprotected wells (24%) for their water supply.

Anthropometric data: The prevalence of stunting was 35.2% (z score < -2 SD for height/age). 51.6% had a weight-for-age Z (WAZ) score of <-2 SD for weight/age. There was no correlation between weight for height and age, serum retinol, total protein, prealbumin and RBP. There was a positive correlation between weight for height and β Carotene (r=0.15) and hemoglobin (r=0.15) levels.

Morbidity

Disease rates: The one-week diarrhea prevalence in the population was 11.3%. The fever prevalence rate was 34%. The commonest infections encountered were those of the skin / upper respiratory tract (2.2%) and clinical malaria (3.3%). A positive malaria slide was encountered in 2.1% of the children.

Immunization: Only 12% of the children had complete immunization, and 53% incomplete while 34% was unknown. None of them were fully immunized against measles. The BCG vaccination coverage was 62.1%. Other immunizations included Sabine vaccination (51.5%), triple antigen (49.5%), hepatitis B - 3 doses (14.6%), and measles - 3 doses (2.9%).

DISCUSSION

Our study found no children with definite clinical eye signs of VAD, although 1.1% had night blindness, which is indicative of mild VAD in the population. The mean serum retinol level was 1.22µmol, and 15% of the children had a serum retinol < 0.70µmol, which is in keeping with a moderate level of VAD severity.

Sommer recommended that the cut-off values for each country be defined, taking into consideration the local characteristics of infections, PEM, etc [12]. Furthermore, Sommer suggested that a prevalence of >40% of serum retinol at 5% prevalence of serum retinol values at <0.35µmol and requires a sample size that is eight times smaller than when attempting to work with the 5% (0.35µmol) definition to define severely deficient populations [12]. These suggestions fit with our observations using the 0.7µmol cut-off for defining this population as moderately deficient.

The mean hemoglobin in our study was 92 g/L, which is low. We found a weak correlation between serum retinol and hemoglobin (r=0.17), which is in line with the findings of other studies [13,14]. Anemia is widespread in both boys and girls living in lowland areas, [15,16] and is amongst the top ten causes of admissions and deaths in health facilities for infants in PNG [17]. Anemia in a pregnant mother may have a profound effect on the outcome of the pregnancy, causing the infant to suffer from iron deficiency anemia right from the womb or from insufficient iron in the mother’s breast milk [18]. Most cases of anemia in PNG children are believed to be iron deficiency anemia caused by inadequate nutritional intake, repeated malaria attacks, hookworm infestations, or a combination of these factors that needs to be addressed [19, 20].

In our study, malnutrition was most often seen in the second and third years of life, which is the time when the mother is likely to be pregnant again and the child has been weaned from breastfeeding [21]. A weaning diet poor in vitamin A predicts a childhood diet that is also poor in vitamin A [22]. PNG promotes breastfeeding as the best source of nutrition for infants and actively discourages mothers from bottle feeding their babies [23]. It was the first country to enact the Breast Feeding Supplies (Control) Act in an effort to protect babies from infections, diarrhea, and malnutrition brought on by artificial feeding and as a measure to support and encourage traditional feeding practices [24]. The act prohibits the sale of feeding teats, bottles, and dummies without prescription [24]. Despite the legislation, more women are now choosing to bottle feed their babies, and they are obtaining bottles and formula without legally required prescriptions [24]. Weaning practices are important as the infrequent consumption of DGLV or yellow fruits is associated with a 4- to 6-fold increase in the risk of xerophthalmia, compared to the 2- to 3-fold increased risk from fish, meat, milk, and eggs [22].

According to the WHO guidelines, a low risk exists when vitamin A-rich foods are available in the home fewer than 3times per week for >75% of households [11]. The risk of VAD is greater when the consumption of foods of animal origin does not regularly occur [25]. In many villages in PNG, some fruit trees are considered “common property,” and mothers collect fruit for their household consumption. In our study, pawpaw and bananas were available to more than 80% of households on a regular basis whereascarrots were not consumed by any of the children as they are more commonly grown in higher altitude areas in the country. Fish were plentiful in the rivers and creeks, and tinned fish, canned meats, and cooking oils were also available in the store in the village.

The prevalence of stunting in our population was 35.2%. A ≥30% prevalence of stunting in children under 5 years indicates an area/population at risk of VAD [11]. Stunting (-2) at ≥10% in children under 5 years as a high-risk area/population for VAD [11]. We found a negative correlation (r=-0.14) between CRP and WHZ, indicating that children prone to acute infections had some degree of wasting. A positive correlation was found between WHZ and the β-carotene (r=0.15) and hemoglobin (r=0.15) levels. Better nourished children tended to eat more and had higher carotene levels. Innovative research is needed in PNG to assess micronutrient bioavailability and develop food fortificants that optimize the nutritional value of food.

The high incidence of diarrhea (11.3%) and fever (34%) in a growing child remains a problemand can cause malnutrition or worsen existing malnutrition [28]. Likewise, a child with malnutrition is more susceptible to infectious diseases, thereby triggering a vicious cycle [29]. Regardless, fever—irrespective of etiology and helminthic infection—usually depresses appetite, nutrient absorption, and circulating blood levels of vitamin A [30]. Diarrhea is a common cause of childhood death in PNG [31]. Diarrhea is a disease that reflects sanitation and hygiene conditions. Only about a quarter of the study population in PNG had access to safe water, while approximately 10% of the population had adequate means of excreta disposal. High rainfall and the mountainous terrain create the ideal conditions for fecal contamination of surface water, which is the most common source of drinking water in many communities throughout PNG [32]. The need to improve potable water supplies and sanitation in the villages is self-evident [33]. Educating parents on hand washing, food preparation, water purification, and improvements in sanitation in the home environment are essential for preventing diarrhea [32,34].

In our study, two patients had a positive malaria slide, with serum retinol levels ≥ 0.7µmol. In many areas of PNG, malaria is endemic and a major cause of infant and child mortality [15]. Children between the ages of three months and five years are in the greatest danger of contracting malaria, as they have insufficient immunity. The importance of malaria as a cause of low serum retinol in endemic areas such as parts of PNG and the impact of vector control programs on serum retinol require further study.

Immunization rates in children between 12 and 23 months were generally poor in the regions of our study, and none of the children were fully immunized against measles. The risk of VAD increases when coverage rates for full immunization, particularly for measles, falls below 50% in children 12 to 23 months old [11]. Following the WHO guidelines, this puts the whole population at risk of developing VAD [11]. As long as villages have no permanent health facilities and the measles case fatality ratio remains high, the case can be made for providing vitamin A supplementation along with the expanded program on immunization

CONCLUSION

In summary, our study found no evidence of clinical VAD among the children in PNG. However, subclinical VAD with concurrent malnourishment occurred at a level of mild to moderate public health importance, which warrants further attention. Measures to improve general nutrition and prevent infectious diseases seem to be the best way forward.

ACKNOWLEDGEMENTS

The authors thank Professor Frank Billson, Dr Hanny Friesen and Dr John Earl for their valuable help and support in completing this study.

Received : 19 Dec 2016
Accepted : 04 Jan 2017
Published : 06 Jan 2017
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Launched : 2014
JSM Surgical Oncology and Research
ISSN : 2578-3688
Launched : 2016
Annals of Food Processing and Preservation
ISSN : 2573-1033
Launched : 2016
Journal of Radiology and Radiation Therapy
ISSN : 2333-7095
Launched : 2013
JSM Physical Medicine and Rehabilitation
ISSN : 2578-3572
Launched : 2016
Annals of Clinical Pathology
ISSN : 2373-9282
Launched : 2013
Annals of Cardiovascular Diseases
ISSN : 2641-7731
Launched : 2016
Journal of Behavior
ISSN : 2576-0076
Launched : 2016
Annals of Clinical and Experimental Metabolism
ISSN : 2572-2492
Launched : 2016
Clinical Research in Infectious Diseases
ISSN : 2379-0636
Launched : 2013
JSM Microbiology
ISSN : 2333-6455
Launched : 2013
Journal of Urology and Research
ISSN : 2379-951X
Launched : 2014
Journal of Family Medicine and Community Health
ISSN : 2379-0547
Launched : 2013
Annals of Pregnancy and Care
ISSN : 2578-336X
Launched : 2017
JSM Cell and Developmental Biology
ISSN : 2379-061X
Launched : 2013
Annals of Aquaculture and Research
ISSN : 2379-0881
Launched : 2014
Clinical Research in Pulmonology
ISSN : 2333-6625
Launched : 2013
Journal of Immunology and Clinical Research
ISSN : 2333-6714
Launched : 2013
Annals of Forensic Research and Analysis
ISSN : 2378-9476
Launched : 2014
JSM Biochemistry and Molecular Biology
ISSN : 2333-7109
Launched : 2013
Annals of Breast Cancer Research
ISSN : 2641-7685
Launched : 2016
Annals of Gerontology and Geriatric Research
ISSN : 2378-9409
Launched : 2014
Journal of Sleep Medicine and Disorders
ISSN : 2379-0822
Launched : 2014
JSM Burns and Trauma
ISSN : 2475-9406
Launched : 2016
Chemical Engineering and Process Techniques
ISSN : 2333-6633
Launched : 2013
Annals of Clinical Cytology and Pathology
ISSN : 2475-9430
Launched : 2014
JSM Allergy and Asthma
ISSN : 2573-1254
Launched : 2016
Journal of Neurological Disorders and Stroke
ISSN : 2334-2307
Launched : 2013
Annals of Sports Medicine and Research
ISSN : 2379-0571
Launched : 2014
JSM Sexual Medicine
ISSN : 2578-3718
Launched : 2016
Annals of Vascular Medicine and Research
ISSN : 2378-9344
Launched : 2014
JSM Biotechnology and Biomedical Engineering
ISSN : 2333-7117
Launched : 2013
Journal of Hematology and Transfusion
ISSN : 2333-6684
Launched : 2013
JSM Environmental Science and Ecology
ISSN : 2333-7141
Launched : 2013
Journal of Cardiology and Clinical Research
ISSN : 2333-6676
Launched : 2013
JSM Nanotechnology and Nanomedicine
ISSN : 2334-1815
Launched : 2013
Journal of Ear, Nose and Throat Disorders
ISSN : 2475-9473
Launched : 2016
Journal of Pharmacology and Clinical Toxicology
ISSN : 2333-7079
Launched : 2013
Annals of Psychiatry and Mental Health
ISSN : 2374-0124
Launched : 2013
Medical Journal of Obstetrics and Gynecology
ISSN : 2333-6439
Launched : 2013
Annals of Pediatrics and Child Health
ISSN : 2373-9312
Launched : 2013
JSM Clinical Pharmaceutics
ISSN : 2379-9498
Launched : 2014
JSM Foot and Ankle
ISSN : 2475-9112
Launched : 2016
JSM Alzheimer's Disease and Related Dementia
ISSN : 2378-9565
Launched : 2014
Journal of Addiction Medicine and Therapy
ISSN : 2333-665X
Launched : 2013
Journal of Veterinary Medicine and Research
ISSN : 2378-931X
Launched : 2013
Annals of Public Health and Research
ISSN : 2378-9328
Launched : 2014
Annals of Orthopedics and Rheumatology
ISSN : 2373-9290
Launched : 2013
Journal of Clinical Nephrology and Research
ISSN : 2379-0652
Launched : 2014
Annals of Community Medicine and Practice
ISSN : 2475-9465
Launched : 2014
Annals of Biometrics and Biostatistics
ISSN : 2374-0116
Launched : 2013
JSM Clinical Case Reports
ISSN : 2373-9819
Launched : 2013
Journal of Cancer Biology and Research
ISSN : 2373-9436
Launched : 2013
Journal of Surgery and Transplantation Science
ISSN : 2379-0911
Launched : 2013
Journal of Dermatology and Clinical Research
ISSN : 2373-9371
Launched : 2013
JSM Gastroenterology and Hepatology
ISSN : 2373-9487
Launched : 2013
Annals of Nursing and Practice
ISSN : 2379-9501
Launched : 2014
JSM Dentistry
ISSN : 2333-7133
Launched : 2013
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