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Home gardening and access to animals in households with xerophthalmic children in rural Nepal

Anita V. Shankar, Joel Gittelsohn, Elizabeth K. Pradhan, Chandra Dhungel, and Keith P. West, Jr.

Anita V. Shankar, Joel Gittelsohn, Elizabeth K. Pradhan, and Keith P. West, Jr., are affiliated with the Division of Human Nutrition, Department of International Health, in the School of Hygiene and Public Health at the Johns Hopkins University in Baltimore, Maryland, USA. Chandra Dhungel is affiliated with the Nepal Nutrition Intervention Project-Sarlahi in Kathmandu, Nepal.

Mention of the names of firms and commercial products does not imply endorsement by the United Nations University.

Abstract

This case-control study compares the home garden and animal husbandry practices of households with and without xerophthalmic children in south-central Nepal, focusing on the relationship between these practices and household intake of vitamin A-rich foods. Eighty-one households with a child between the ages of one and six years diagnosed with xerophthalmia (cases) and 81 households with an age-matched, non-xerophthalmic child (controls) were studied. There was little difference between case and control households in the size of their gardens. However, case households were significantly less likely to plant carotenoid-rich vegetables from October to March than were control households (odds ratio, 0.39; 95% confidence interval, 0.16 to 0.96). The mean consumption of non-carotenoid-rich vegetables, but not of carotenoid-rich vegetables, increased linearly with garden size. Case households were significantly more likely than control households to rent domesticated animals from others (c2 = 5.91; p <.05). Control households were more likely than case households to own chickens and pigeons (c2 = 6.6-9.2; p <.05). During specific seasons, household meat consumption was significantly lower in case households, regardless of access to animals. Case households appeared to have significantly lower intakes of key vitamin A-rich foods, particularly green leaves and meat, regardless of their socio-economic level (as determined by ownership of material goods), access to animals, or availability of home gardens.

Introduction

In areas where vitamin A deficiency is a serious public health problem, childhood xerophthalmia is known to cluster at the regional, district, village, and household levels [1]. This clustering is thought to be the result of pockets of relative poverty and/or poor access to vitamin A-rich food sources [2-5]. Despite this, there are a number of households living in these same high-risk clusters that do not experience xerophthalmia. One explanation is that these households have developed strategies that allow greater access to vitamin A-rich foods.

Cultivation of home gardens and ownership of domesticated animals are potential ways of increasing household access to foods rich in vitamin A and carotenoids. Numerous attempts have been made to implement gardening programmes towards such a goal [6, 7]. Indeed, several studies have found that the presence of a home garden is a strong predictor of the quality of child nutrition, particularly during seasons when employment opportunities are few [8-10].

Although home gardens have been shown to provide a number of economic and dietary advantages to poor families, the evidence linking home gardens to reduced vitamin A deficiency in vulnerable household members is equivocal. In Bangladesh, analyses indicate that even a small household garden affords protection against childhood xerophthalmia [4]. More recent work from this region [11] shows that the variety of plants in a garden, and not its size, is associated with reduced risk of xerophthalmia. Other studies, however, show that vitamin A status may not improve despite successful home gardening efforts [12,13]. In West Java, well-off households (those with home gardens and land) were found to consume more of all nutrients than did poorer households, except for vitamin A and calcium [14].

Household-level interventions directed towards improving vitamin A status have focused on increasing plant sources of vitamin A by encouraging home gardens, which require a relatively small investment and can be a source of abundant carotenoid-rich foods. Domestic animals are an additional source of home food that intervention studies and programmes often overlook. Domestic animals provide milk, eggs, and meat that may help protect household members from vitamin A deficiency.

In this study we explore the variations in access to domesticated animals and differences in home gardening practices in households with and without xerophthalmic children in rural Nepal. These practices are then examined with respect to the changes in intake of carotenoid- and retinol-rich foods at the household level over a one-year period.

Methods

A community-wide ocular survey was conducted in January 1992 on 3,735 pre-school children living in three Village Development Committees with a population of approximately 15,000 in Sarlahi District in the central lowland region of Nepal. The survey identified 86 households with children aged 12 to 72 months who had clinical signs of xerophthalmia or a current history of night-blindness. Five households were lost because of migration or refusal to participate, resulting in 81 case households participating in the study. Thirty-three of the children had guardian-reported night-blindness alone, 33 had Bitot’s spots alone, and 10 children had both night-blindness and Bitot’s spots. The remaining five were diagnosed with corneal xerosis alone or with Bitot’s spots or night-blindness.

From the pool of neighbouring households (within 5 km of the case), 81 control households were selected that had a child of the same age as the case child (within three months) and a younger sibling of similar age (within four months), if a younger sibling was present in the case household. In control households, there were no clinical signs of xerophthalmia in any child in the household and no reported history of night-blindness in children or their mothers. Both case and control households were studied prospectively from March 1993 to June 1994.

A recall of home gardening practices was obtained from the head of the household, usually a male, three times during the year: April-May 1993 (three-month recall period), August-September 1993 (four-month recall period), and February-March 1994 (five-month recall period). For the purposes of this study, a home garden was defined to include all plants (fruits and vegetables) grown in and around the homestead. We used specific local terms to distinguish home gardens from agricultural plots. During each round of interviews, recall data were collected on which vegetable and fruit plants were grown in the home garden, the quantity grown, and about how much of the produce was consumed in the household. Harvesting and consumption of green leaves associated with gourds (such as pumpkin leaves) were also noted.

The size of the vegetable garden was calculated by summing the total plot sizes used for each type of plant grown. If one plot area was used for two different crops (planted simultaneously or at different times), the total garden size equalled twice the actual land area used by the plants. In addition, individual vines and plants, such as gourds and tomatoes, grown outside a formal plot were counted separately and assigned an average value of 0.5 square feet (464 cm²) per plant. As a result of varying planting and harvesting intervals during the recall period, the calculation of garden size is not representative of the actual amount of cultivated land.

Only fruit plants and trees that produced fruit during the year surveyed were counted. The informants were asked to recall all vegetables and fruit plants to which their family had access and from which they were able to obtain some produce, such as plants shared with relatives or neighbours. Fruits or leaves found in the wild were not included within our definition of home garden.

Possession of domesticated animals was determined once by a survey conducted with the head of the household in January 1993. In Nepal there are several forms of animal ownership, ranging from outright ownership to renting and raising animals for a pre-determined portion of the meat or milk produced. Ownership of an animal, for this study, means that the owner has access to all milk or eggs produced by the animal and all the meat if the animal is slaughtered. Rental of an animal means that part of the animal products are kept by the owner and part by the household renting the animal. The numbers of animals owned, rented from others, and rented to others were determined for each household.

Household dietary intake was assessed with a previously described seven-day food-frequency questionnaire [15]. The food-frequency questionnaire was administered four times during the year beginning in July 1993: July to September, October to December, January to March, and April to June. Dietary recalls were conducted on individuals knowledgeable about the household and the food intake of the children, usually the mothers. Household intake was defined as foods consumed by any member of the household, focusing on foods consumed during the primary mealtimes.

Fruits and vegetables were classified as carotenoid-rich or non-carotenoid-rich on the basis of regional and international food composition tables [16,17]. Vegetables classified as carotenoid-rich included dark-green leafy vegetables and ripe pumpkin; fruits classified as carotenoid-rich included papayas, mangoes, and jackfruit.

Matched-pair odds ratios and 95% confidence intervals were derived by conditional logistic regression to compare household characteristics according to xerophthalmia status. All odds ratios were adjusted for socio-economic status, which was a scaled variable based on the number of different types of material possessions not related to either home gardening efforts or the up-keep of animals. The final scale had eight items in currently usable condition: flashlights (one or more), watches (one or more), bicycles (one or more), armoires (one or more), beds (two or more), number of rooms in the house (two or more), a roof constructed of a material other than straw, and irrigation pump sets. The alpha coefficient for this scale was 0.78 and the mean score value was 3. Those households with a scale score equal to or greater than the mean were classified as having higher socio-economic status (a value of 1 in the regression equation); those below the mean were classified as having lower socio-economic status (a value of 0).

Odds ratios (OR) of less than 1 indicate that case households were less likely than controls to report a practice (e.g., intake of foods). For analyses that required further stratification of the data, unmatched-pair analyses were conducted. Analyses were carried out using SAS (SAS version 6.11, SAS Institute, Cary, NC, USA).

Oral informed consent was obtained from families before participation in the study. This study was approved by the Nepal Health Research Council in Kathmandu and the Committee for Human Research, Johns Hopkins University School of Hygiene and Public Health, Baltimore, Maryland, USA.

Results

Household gardening patterns

Table 1 lists the most common fruits and vegetables grown over the year by case and control households. The types of vegetables and fruits planted and picked differ little between the two groups. An exception, however, is munga, a type of long thin gourd, which was planted significantly more frequently in control households. No difference was noted in access to gardens: more than 97% of all study households reported access to some type of home garden during the year, approximately 95% (97% cases, 94% controls) of the households cultivated vegetables, and more than 81% (80% cases, 84% controls) produced fruits. Likewise, no difference was found in the percentage (which averaged 60%) of vegetable and fruit harvests that the household reported were completely consumed.

Garden size varied during the year, with the smallest gardens being planted from June to September and the largest from October to March. Table 2 compares case and control households with respect to garden size and composition according to season. There were no significant differences in garden size between case and control households over the whole year; however, control households tended to have larger gardens than case households from October to March (OR, 0.41; 95% CI, 0.17 to 1.01). From October to March only, control households were significantly more likely than case households to plant and consume at least one carotenoid-rich vegetable (OR, 0.39; 95% CI, 0.16 to 0.96). This difference is mainly a result of the greater number of garlic leaves and onion greens consumed in control households during this period.

TABLE 1. Percentage of households with access to garden vegetables and fruits during the year, according to case status

Common name

Scientific name

Cases (n = 79)

Controls (n = 77)

Vegetables


Sponge gourd

Luffa cylindrica

84

75


Green chilies

Capsicum annum grossa

72

64


Green peas

Pisum sativum

66

64


Gourd

Lagemaria siceraria

66

62


Potato

Impomea batas-convulacea

58

69


Pointed gourd

Trichosonthes dioica

58

66


Munga

Gourd, like Moringa oleifera

37

55a


Eggplant

Solanum melongena-solonacea

33

34

Carotenoid-rich vegetables


Pumpkin

Cucurbita minima

68

77


Garlic leaves

Allium sativum

57

65


Mustard leaves

Brassica compestris-cruciferae

46

51


Dhaniya leaves

Coriander sativum

32

34


Thadiya leaves

Name unknown

32

23


Radish leaves

Raphnum sativus-crucifera

25

32

Fruits


Banana

Musa sapientum

52

53


White guava

Psidium guajava

57

49


Custard apple

Annona squamosa

23

28

Carotenoid-rich fruits


Papaya

Carica papaya

71

65


Mango

Mangifera indica

52

56


Jackfruit

Artocarpus integrifolia

48

49

a. Statistically significant at p <.05.
Figure 1 shows the relationship between average cumulative garden size and vegetable consumption for the year for both vitamin A-rich foods and those lacking significant amounts of vitamin A. Pooled data were used for these comparisons, as garden size did not significantly differ between cases and controls. Consumption of non-vitamin A-rich vegetables was found to increase with garden size, whereas consumption of vitamin A-rich vegetables remained low across the observed range of garden sizes. A similar analysis was performed for fruit consumption (fig. 2). In this case, households without gardens had roughly half the mean intake of carotenoid-rich fruits as households with large gardens, although this difference was not statistically significant.

Patterns of animal husbandry

Table 3 compares case and control households with respect to their access to domesticated animals. Nearly all households (90% of cases and 95% of controls) had at least one animal in their home, and nearly 50% of case and control households had a milk-producing animal. However, case households were more likely than controls to have rented animals from others, especially cows. Moreover, nearly twice as many control households as case households had chickens, and three times as many control households as case households had pigeons. Chickens and pigeons are both good sources of vitamin A-rich eggs and meat, including liver.

FIG. 1. Average weekly household consumption of low-carotenoid (grey bars) and carotenoid-rich (black bars) vegetables by all study households over the year, according to size of vegetable garden. 1 katha = 0.083 acres = 0.034 hectares

TABLE 2. Matched-pair adjusted odds ratios of garden characteristics for case and control households

Garden characteristic

Feb-May 1993

Jun-Sep 1993

Oct 1993-Mar 1994

Case-control pairs (n = 78)
(%)

ORa

95% CI

Case-control pairs (n = 78)
(%)

OR

95% CI

Case-control pairs (n = 77)
(%)

OR

95% CI

Cumulative plot sizeb (> 1 katha of land)

63 59

1.49

0.74-3.02

22 16

1.80

0.75-4.32

58 71

0.41

0.17-1.01

> 10 single vines, bushes

44 49

0.84

0.44-1.61

62 58

1.27

0.62-2.62

43 46

0.95

0.47-1.94

> 10 harvesting fruit plants

17 21

0.86

0.36-2.02

33 41

0.87

0.45-1.69

22 36

0.67

0.33-1.35

Carotenoid-rich vegetables harvested and consumed in household

64 71

0.82

0.41-1.65

24 27

0.92

0.45-1.92

72 87

0.39

0.16-0.96c

Carotenoid-rich fruits harvested and consumed in household

39 45

0.82

0.43-1.57

39 45

0.70

0.36-1.39

47 42

1.40

0.74-2.65

a. OR, odds ratio; OR < 1 indicates that case households are less likely than control households to report a practice.

b. 1 katha = 0.083 acres = 0.034 hectares. Garden size includes calculation of single vines and bushes with designated plot size of 0.5 sq. ft. (464 cm2) per plant.

c. p <.05.

FIG. 2. Average weekly household consumption of low-carotenoid (grey bars) and carotenoid-rich (black bars) fruits by all study households over the year, according to number of fruit plants

Using household food-frequency data, table 4 examines differences in milk consumption by any household member in the previous week, stratified by access to milk-producing animals. Comparisons are made for three groups: (1) households with no milk-producing animals, (2) households with milk-producing animals (either rented or owned), and (3) households that owned but did not rent milk-producing animals (a subset of group 2). Preliminary unadjusted odds ratios indicated that regardless of access to milk-producing animals (rented or owned), case households were significantly less likely than control households to have consumed milk during the periods from July to September and from October to December (odds ratios ranged from 0.16 to 0.33). However, adjustment for socio-economic status removed any significant differences in milk consumption between case and control households.

Meat (including liver) and eggs are also good sources of pre-formed vitamin A. Animals most likely to be domesticated for consumption include chickens, pigs, goats, and pigeons. Table 5 compares case and control households with and without access to these animals with respect to their consumption of meat and eggs. Among households without access to animals, case households were much less likely to report consumption of meat or eggs in the preceding week than controls (odds ratios ranged from 0.07 to 0.69), with significant differences during the period from January to March. Among households with access to animals, case households were significantly less likely than controls to report consumption of meat or eggs in the preceding week during the period from October to December (OR, 0.41; 95% CI, 0.20 to 0.82).

Discussion

In this paper we differentiate households with a xerophthalmic child from those having a non-xerophthalmic child of the same age, with respect to two factors that could influence the intake of vitamin A-rich foods: home gardens and access to domesticated animals. After controlling for socio-economic status and season, the presence or absence of these factors was related to household intake of vitamin A-rich foods.

Previous dietary analyses from this study indicated that control households consumed more carotenoid-rich vegetables from July to December than case households [15]. The current data corroborate previous findings by showing that control households were more likely to consume carotenoid-rich vegetables from their gardens from October to March as well. The increased intake of carotenoid-rich foods found in the previous analyses may be due in part to the greater access to garden vegetables during certain months of the year.

TABLE 3. Percentage of case (n = 81) and control (n = 81) households raising animals, renting animals from others, or renting animals to others

Animal

Raising animals

Renting animals from others

Renting animals to others

Case

Control

Case

Control

Case

Control

Cows

25

26

11

0a

3

7

Bulls and calves

56

58

10

7

3

4

Buffaloes (female)

6

9

0

0

0

0

Buffaloes (males and calves)

21

35

9

9

3

5

Goats (female)

24

25

4

4

1

0

Goats (males and kids)

56

58

23

20

5

12

Pigs

4

6

2

0

0

2

Chickens

26

46a

6

5

1

4

Pigeons

6

20a

0

0

0

0

Any milk-producing animal (cows, buffaloes, goats)

48

47

15

4a

4

7

Any animal

90

95

43

31

11

24a

a. p <.05 (unmatched pair analyses).
TABLE 4. Non-adjusted and adjusteda odds ratios for milk consumption (at least once per household in the past week), based on access to milk-producing animals,b for cases and controls, according to year and months

Year and months

No access

Accessc

Owned animals

OR

95% CI

OR

95% CI

OR

95% CI

1993 Jul-Sep


Non-adjusted

1.25

0.48-3.23

0.32

0.12-0.80d

0.33

0.12-0.89d


Adjusted

1.07

0.45-2.51

0.73

0.34-1.57

0.61

0.26-1.43

1993 Oct-Dec


Non-adjusted

1.56

0.62-3.97

0.16

0.06-0.45d

0.21

0.07-0.61d


Adjusted

1.30

0.53-3.15

0.57

0.26-1.26

0.55

0.24-1.28

1994 Jan-Mar


Non-adjusted

1.10

0.37-3.30

0.41

0.16-1.02

0.46

0.17-1.23


Adjusted

0.96

0.33-2.78

0.79

0.33-1.90

0.82

0.31-2.15

1994 Apr-Jun


Non-adjusted

0.47

0.17-1.26

0.69

0.28-1.71

0.90

0.34-2.39


Adjusted

0.41

0.15-1.12

1.41

0.58-3.43

1.78

0.63-5.06

a. Odds ratios adjusted for socio-economic level as determined by a scaled variable of material possessions owned.

b. Female cows, buffaloes, and goats.

c. Households raising animals, either owned or rented.

d. p <.05.

TABLE 5. Non-adjusted and adjusteda ratios for consumption of meat or eggs (at least once per household in the past week), based on access to commonly used animals,b for cases and controls, according to year and months

Year and months

No access

Accessc

OR

95% CI

OR

95% CI

1993 Jul-Sep


Non-adjusted

0.42

0.08-2.33

0.60

0.28-1.26


Adjusted

0.69

0.14-3.29

0.69

0.34-1.38

1993 Oct-Dec


Non-adjusted

0.19

0.03-1.11

0.31

0.14-0.67d


Adjusted

0.34

0.06-1.92

0.41

0.20-0.82d

1994 Jan-Mar


Non-adjusted

0.07

0.01-0.47d

0.70

0.32-1.52


Adjusted

0.08

0.01-0.91d

0.77

0.37-1.63

1994 Apr-Jun


Non-adjusted

0.39

0.56-2.73

0.71

0.35-1.48


Adjusted

0.65

0.11-3.91

0.80

0.42-1.51

a. Odds ratios adjusted for socio-economic level as determined by a scaled variable of material possessions owned.

b. Pigeons, chickens, pigs, and goats.

c. Households raising animals, either owned or rented.

d. p <.05.

The likelihood of improving consumption of vitamin A-rich foods from the garden, however, is not dependent on garden size. Larger garden sizes were not found to be associated with reported intake of dark-green leafy vegetables and pumpkin. This result supports those of other studies [8,14] showing that higher economic status may not result in greater consumption of carotenoid-rich vegetables. On the other hand, there was a corresponding increase in the consumption of non-carotenoid-rich vegetables with garden size. As in other areas of South Asia, in Nepal dark-green leafy vegetables are often considered low-status foods, which may explain, in part, why increasing the areas of home gardens does not increase the number of times carotenoid-rich vegetables are eaten.

In this population, access to gardens was high and did not differ significantly between case and control households. Nevertheless, the mean consumption of carotenoid-rich fruits and vegetables was extremely low, averaging less than four times in the preceding week. We also found an increase in the consumption of all fruits as garden size increased. Additional efforts to promote home gardens will likely need to focus on greatly increasing the number of types of carotenoid-rich foods planted and consumed in the household.

Access to domesticated animals is another household strategy that may increase vitamin A intake at the household level but is often omitted from the home-gardening literature. In our sample, both case and control households had access to some type of domesticated animal. However, the form of ownership varied: case households were more likely to rent animals than to own them. In addition, control households were significantly more likely than case households to own chickens and pigeons. This may be indicative of the slightly better socio-economic status of the control households, a finding consistent with other research in the area [3].

In an effort to control for the effects of socio-economic status on diet, we devised a socio-economic status scale that could serve as a proxy for household income but would not include items on ownership of land or animals. When this variable was included in the regression analysis, we found that socio-economic status did influence the odds ratios of household milk consumption but not those of consumption of meat and eggs. In the case of milk consumption, the odds ratios adjusted for socio-economic status were higher (0.5 to 0.7) than the unadjusted odds ratios (0.2 to 0.3), which implies that although control households had greater reported milk intake than cases, this was probably due in part to the slightly higher economic status of these households.

This was not true with consumption of meat or eggs; case households consumed meat or eggs significantly less frequently than controls in certain seasons, regardless of access to animals or socio-economic status. In households with no access to animals, the odds ratios for consumption of meat or eggs were low (0.07 to 0.69), suggesting that control households, even those without direct access to meat or eggs at home, were still able to obtain and consume meat or eggs more often than case households.

As efforts continue to identify household strategies that increase the intake of vitamin A-rich foods [18, 19], understanding the intricacies of current household practices and their relationship to diet is critical. This study demonstrates that household-level access to home gardens or domesticated animals does not ensure that vulnerable members within the household will be able to obtain a diet adequate to prevent clinical signs of vitamin A deficiency. In addition, the size of a garden did not appear to be related to the intake of carotenoid-rich vegetables in this population. From previous analyses [15] we learned that case households and index children were significantly less likely to consume meat, liver, and eggs. This finding holds true in the current analysis, which indicates that other factors besides household access to domesticated animals or socio-economic level (as determined by ownership of material goods) may influence household intake during critical periods of the year. This study is a first step in examining household strategies and their effect on household intake. Further research to identify other types of household strategies and characteristics important for increased consumption of vitamin A-rich foods is warranted.

Acknowledgements

The study group in Sarlahi included the authors and Dr. Rajendra Pradhan, Dr. Subarna Khatry, Mr. Steven LeClerq, Mr. Sharada Ram Shrestha, Mr. Noor Nath Acharya, and Dr. R. P. Pokhrel. The study is a collaborative effort between the Johns Hopkins University, Baltimore, Maryland, USA, the Nepal Netra Jyoti Sangh (National Society for the Prevention of Blindness), and the Nepal Eye Hospital. The authors express their sincere appreciation and thanks to the DIVA interviewers, Shishir Shrestha, Ramekwal Chaudhary, Sulochana Chaudhary, and Ishwari Shrestha. The project was funded through Cooperative Agreement No. DAN 0045-A-00-5094-00 between the Center for Human Nutrition/Dana Center for Preventive Ophthalmology of the Johns Hopkins University and the Office of Health and Nutrition of the US Agency for International Development, with additional support from Task Force Sight and Life (Roche, Basel, Switzerland) and National Institutes of Health shared instrument grant No. S10-RR 04060.

References

1. Katz J, Zeger SL, West KP, Tielsch JM, Sommer A. Clustering of xerophthalmia within households and villages. Int J Epidemiol 1993; 22: 709-15.

2. Mele L, West KP Jr, Kusdiono, Pandji A, Nendrawati H, Tilden RL, Tarwotjo I. Nutritional and household risk factors for xerophthalmia in Aceh, Indonesia: a case-control study. Am J Clin Nutr 1991; 53: 1460-5.

3. Khatry SK, West KP Jr, Katz J, LeClerq SC, Pradhan EK, Wuls Thapa MD, Pokhrel RP. Epidemiology of xerophthalmia in Nepal. Arch Ophthalmol 1995; 113: 425-9.

4. Cohen N, Jalil MA, Rahman H, Matin MA, Sprague J, Islam J, Davison J. Landholding, wealth and risk of blinding malnutrition in rural Bangladeshi households. Soc Sci Med 1985; 21: 1269-72.

5. Sommer A, West KP Jr. Vitamin A deficiency: health, survival and vision. New York: Oxford University Press, 1996.

6. Swedberg EA, Stetson V, Adrian JM, Zayan A. Multiple approaches to vitamin A (abstract). Report of the XVI IVACG Meeting, Chiang Rai, Thailand. Washington, DC: Nutrition Foundation, 1996: 92.

7. Talukder A, Bloem MW Home gardening activities in Bangladesh. Dhaka: Helen Keller International, 1992.

8. Kumar SK. Role of the household economy in child nutrition at low-incomes: case study in Kerala. Occasional Paper No. 95. Ithaca, NY, USA: Department of Agricultural Economics, Cornell University, 1978.

9. Ensing B, Sangers S. Home gardening in a Sri Lankan wet zone village: Can it contribute to improved nutrition? Wageningen, Netherlands: Wageningen Agricultural University, 1986.

10. Immink MDC, Sanjur D, Colon M. Home gardens and the energy and nutrient intakes of women and pre-schoolers in rural Puerto Rico. Ecol Food Nutr 1991; 11: 191-9.

11. Talukder A, Islam N, Tabibul AK, Desilles S, Bloem MW. Results and lessons learned from Helen Keller International’s home gardening activities in Bangladesh (abstract). Report of the XVI IVACG Meeting, Chiang Rai, Thailand. Washington, DC: Nutrition Foundation, 1994:92.

12. Smitasiri S. Nutri-action analysis: going beyond good people and adequate resources. Bangkok: Amarin Printing and Publishing Public Company, 1994.

13. Smitasiri S. Advocating a multidimensional evaluation approach for comprehensive nutrition communication programs. INMU Special Publication Series No. 1. Bangkok: Institute of Nutrition, Mahidol University, and UNICEF East Asia and Pacific Regional Office, 1994.

14. Abdoellah OS, Marten G. The complementary roles of home gardens, upland fields, and rice fields for meeting nutritional needs in West Java. In: Marten GG, ed. Traditional agriculture in South-east Asia: a human ecology perspective. Boulder, Col, USA: Westview, 1986: 293-325.

15. Shankar AV, West KP Jr, Gittelsohn J, Katz J, Pradhan R. Chronic low intakes of vitamin A-rich foods in households with xerophthalmic children: a case-control study in Nepal. Am J Clin Nutr 1996; 64: 242-8.

16. Gopalan C, Ramasastri BV, Balasubramanian SC. Nutritive value of Indian foods. Hyderabad: National Institute of Nutrition, 1989.

17. West CE, Poorvliet E. The carotenoid content of foods with special reference to developing countries. Alexandria, Va, USA: VITAL, International Science and Technology Institute, 1993.

18. Stoler A. Garden use and household economy in rural Java. Bull Indones Econ Stud 1978; 14: 85-101.

19. Wasantwisut E, Attig G. Empowering vitamin A foods: a food-based process for Asia and the Pacific region. Bangkok: Institute of Nutrition, Mahidol University, 1995.


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