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6. FEVER AND MALARIA (FORTNIGHTLY FEVER SURVEYS)
6.1.STlJDY AREA:
Fortnightly fever survey was carried out initially in 22 villages
in Jeypore zone for a period of one year (19871. The result of this
study was compared with that obtained by the national programne in the
same villages in previous years I1984 - 1986). For comparison of
seasonality and spatial distribution of malaria, fever surveys were
subsequently [between March, 1988 and February, 19891 carried out in 8
villages of Jeypore (Borigumna PHC: 2 each of tophill, foothill,
riverine and plain) and 4 villages of Malkangiri zone (Mlkangiri PHC:
1 each of the above types). The description and the basis of
classification of these villages have been given earlier (chapter: 5).
6.2. METFDDS OF SLRWY AND ANALYSES OF DATA:
Surveillance workers visited each household in the villages at
fortnightly intervals. All febrile persons, those giving history of
febrile spell in between visits and those afebrile but had complaints
of mild illness such as headache, body ache, nausea, vomiting,
diarrhoea, feverishness etc. at the time of visit were subjected to
finger prick blood examination. ?he last group of persons were included
in the survey since i t is necessary to examine these persons in usual
malaria surveillance, as per WI recarmendations [Black, 1968). As the
sanpling was essentially biased (cases of fever and other mild
illness), no m i n i m target was fixed. Informal consent for obtaining
finger prick blood smear was taken from all individuals and in !he case
of children, from their parents/ guardians.
To study the actual coverage of population in the fever surveys,
presence/ absence of all family rncrbers was recorded every fortnight in
4 villages (one of each type) in Jeypore zone for d period of 10-12
months.
Clinical diagnosis of febrile/ afebrile persons was made by a *
physician in the 8 villages of Jeypore zone whenever possible. Blood
smear was collected from all these perems (if not covered by above
surveys). This was done to study the relationship between clinical
manifestations and parasitaemia.
The blood smears collected were dehemglobinised, stained by
Giemsa and examined for parasi taemia and its grade following standard
technique (Bruce-Chwatt, 1985; also see chapter: 5.2).
A cquter data base was created for the purpose of analyses.
Apart from calculation of parasite rate ( % positivity armng those
examined: same as slide pos~tivity rate or SPR), mnthly and annual
fever or parasite incidence was calculatcrl ! K i n g tho rollowing
fonrula:
Nunber rve * Incidence = --------------- X lODD
Population
*: tve for fever or parasites ( total/ individual species) in unit time
(imnth;year).
'Ihe above parmoter is ttst:d in cnnt rol l)rngr;mlrlc!s ;]nil nloasurt:s
the fever/parasi te load in the population, since the denaninator is
population (WHC), 1964: Molineaux g g . , 1988) . This is based on the
following assunptions.
(i) All fresh cases of malaria are sycqtomatic (present with fever
or other mild illnesses),
(ii 1 the entire population is covered in every visl t .
Standard statistical methods were employed for testing the
significance of association of parasitaernia with factors like age, sex
etc. (Chi square and Fisher's test as applicable).
6.3. RESULTS OF EVE3 SUFM3 I N 22 VILLAGES [INITIAL STUDIES
I N 1987) :
A total of 5,520 blood smear slides was collected frm febrile/
s ~ t m t i c persons in 22 villages (population = 15,303) in Jeypore
zone. Of these 1,364 124.7%) were found positive for malaria parasite
[P. falciparm = 1,054; 1. vivax = 280; E. malariae = 4 and mixed - infections = 26 ) . Comparison o f data obtained from the same 22 villages
by surveillance under national p r o g r m (average of 3 years: 1984 - 1986) and that obtained in present study (1987) is shown in Table: 35.
The parasite incidence per 1,000 population was 49.5 and 89.1, under
national programne and present study respectively. The annual parasite
incidence in the entire Rorigma R1C which covers these villages was
29.6 and 26.0 per 1 ,000 population i.1 1986 and 1987 respectively,
indicating that there was nn real increase in malaria incidence in the
whole area in 1987. The relative rise in annual incidence only in the
22 villages in 1987 unlike the other parts of the PHC could therefore
be a result of effective surveillance in the present study.
During the course of the study i t was observed that villages
located at the foothills weremoremalarious. Of the 22 villages 3 were
located in the foothills and rest 19 in the plains. Analyses of data
according to these two village types indicated that the annual fever
and parasite incidence in foothill villages (531.3 and 207.8 per 1,000
population respectively) were c:nnsiderably higher colnpared tn those
Page. .I46
Table: 35
Canparison of parasite incidence betwen national p r o a r m and present study in 22 villages of Borigumna HE.
Months National programn: data Prusent s tutly tla t a (average of 1984-1986) (1987)
BSC Ntnnber Incidence BSC Nwnber Incidence ---------- ------------ ---------- ---------- +ve Pf Pr Pf +ve Pf Pr Pf
Janurary February March April May June July August Septerlxrr October Noventer Decmher
Total 3085 757 636 49.47 41.56 5520 1364 1054 89.13 68.88
Pr: any parasite. Pf: P.falciparum BSC: Blood m a r s collected and examined Incidence calculated per 1.000 population (total population = 15,303)
Page. .I47
located in plains (330.0 and 67.8 per 1,000 population respectively).
Hence in the next year, surveillance was carried out in 4 different
types of villages in two zones (Jeypore and Malkangiri) to generate
data not only on the difference in parasite load but also on the
seasonal differences if any, betwnecn the tll f ferent ecntyr1c:s of villages
in the two zones.
6.4. RESULTS OF YEAR ROIIND FEVER SURVFiS IN 4 D I F m W GROUPS OF
V I L W E S IN ?WD ZONES (March, 1988 to February, 1989):
The age and sex distribution of the population and the s q l e in
the year round fever surveys in the 12 villages (March, 1988 to
February,l989) is shown in Table: 36. Age distribution of the sample
generally resenbled that of the population [Figure: 29).
Of the 4,783 cases examined, 1,517 (31.7%) had malaria parasite
in their peripheral blood. The annual incidence of fever wes 528/1.000
population. The annual parasite incidence (API) was 167.5/1,000
population. All four species of human malarial parasites including P.
ovale (which was hitherto not recorded in any other part of India) were - detected in this locality. P. falciparm was detected in 1,158 (76.3%
of all +ves), P. in 217 (14.3% of all +ves), P. malariae in 23
(1.5% of all +ves) and P. ovale in 4 (0.26% of all +ves) persons. Mixed
infection with more than one parasite was recorded in 127 (8.4% of all
+vee) of cases and a n~ajority (102) of these had infectlonvith
Plasmdlum ovale, hltherto not recorded In India, was detected In =and foothlll vlllsges or Koraput (Section:
6 . 4 ) .
Page. . I48
Table: 36
Age specific coverage of sample in fever surveys of 12 villages in Koraput.
Age Population size Sample size %mple as % of in years* population in each
age class
Male Female Total Male Female Total Male Ferrlale Total
Total 4485 4572 9057 2320 2463 4783 51.73 53.87 52.81
*Lower limit of age class not included
Page. .I49
Age class in years*
PIOIRB: 29. Comparison of age distribution of sample in fever 8urveys with age structure of the population in 12 villages of Koraput.
Lower l i z f age class not included.
Page. . lSO
falciparm and s.
6.4.1. Age spwcific analysis of fever and parasitamia:
Age specific analysis indicated that the parasite rate [Table:
37) incrt~n~o~l ~ I V I I I I Inl,~l~l I I I V I I ~ t. I . I Z . ' l ' L 1 111 1.11~11 1 1 $ 1 [11:,11, 1 1 1 I ! , - L O ylr,il
age class (39.8%) and thereafter declined in adult age classes. The
ago specific rates for falciparlnn and reserrbled that of total
parasite rate (irrespective of species) except for the fact that
infants recorded higher rates compared to young children [Figure:
30A). Mixed infections were highest in infants which declined with age
[Figure: 30B, Table: 38). The analysis of age specific P. falciparm
gametocyte rate showed a peak in 1-2 year chlldren anddeclined
thereafter until 9-15 year age class. Young auults showed higher
gametocyte rate compared to older persons (Figure: 30C; Table: 37).
The pattern of age specific incidence (per 1,000 population in
each age class) was different from age specific parasite rate. The
pattern of incidence of fever and parasite was qualitatively similar.
Incidence increased from infant levels to reach a peak in children 1-2
years old, and declined thereafter till the adolescent age class to
stabilize in adults (Figure: 31 A; Table: 39). The patterns of
incidence of falciparm, and mixed infections were qualitatively
similar, but quantitatively at different levels (Figure: 31 A and B ) .
Parasite density index (PI>I) in the case of falciparm increased from
infant levels (2.25) to reach a peak density in 2-4 year age class
A 1 . PARASITE (TOTAL) 2. c. PALCIPARUI
-0--2- I ha.,--0'' 0----- 0-..
-.,,-----a I I I I 1
5. p. PALCIPARUM GrnTOCYTE
- 4 -
I I I I I
10 -
0 20 4 0 80 Age i n y e a r s
8 -
6 -
PICURB: 30. Age s p e c i f i c p a t t e r n s o f p a r a s i t e ( t o t a l ) , . P. f a l c i p a r u m . P . v i v a x , Mixed iril'ecLlon, Y. - -- - - - - -- fa l c iparum gametocytc r a t e s i n Lhe populaLion i n f e v e r s u r v e y s o f 1 2 v i l l a g e s i n Koraput.
4 . MIXED INFECTION RATE '
4 - 2 -
0 I I I I I
Page.. 153
Table: 38
Age specific distribution of mixed infections in fever surveys in 12 villages of Koraput.
Age in No. of cases with Total MIX RT years* n~lxed ( 8 )
Pf+Pv Pf+Fm P v + m Pf+Pv+Rn Pf+Po Po+Pv Po+Pf+Pv
Pf : P. falciparm Pv : P. v i v a Rn : P. malariae Po : P, ovale MIX RT: % i m a f e c t i o n rate * Lower limit of age class not included
M e in years
FIGURE: 31. Age specific patterns of fever (1). total parasite (2). P. falciparur ( 3 ) . P. (4). mixed infection ( 5 ) . B. malariae (6) and-E. ( 7 ) incidence. and P. - - f ~ c i p a r u r (8) and E. ( 9 ) density index in fever surveys of 12 villages.
Page. .I56
12.66) and declined thereafter gradually. P. vivax also showed a trend
similar t o 1. falciparm, but the levels were always lower and the peak
density of this parasite was in 9-15 year age class (Figure: 31C).
Tnere was no distinct age specific pattern of incidence or density
index for P. malariae and P. ovale (Table: 3 7 1 , probably due to lower
nunber of cases detected.
6.4.2. Parasitaemia in females and males:
In the year round fever survey, the parasite rate (Table: 40)
was higher (34.5%) in males compared to fomales (2!1.1\,), however the
difference was not statistically significant ( P >0.05). Age specific
analysis indicated that there was a clear quantitative separation of
total parasite rate (irrespei:tive of species), fali:ipar~nn rate and
vivax rate in the sexes beyond 4-9 years age class (Y~gure: 32 A,B 6
C ) , though qualitatively the patterns were m r e or less similar for
both sexes. Significant difference (P <0.051 in total paras~te rate
(irrespective of species), falciparum rate and rate was observed
between the sexes in age classes 20-50, 30-40 and 20-40 years
respectively. No distinct pattern of difference was observed between
the sexes in falciparm gametocyte rate and in mixed infection [Figure:
32D and E). The parasite density index for falciparm, and
malariae (2.46, 2.05 and 1.82 respectively) was higher in males when
cunpared to females (2.34, 1.88, 1.67 respectively). The age specific
patterns for femles and males Were not dls11nc.t (Figure: 331, even
Page. .I58
J)-9\ SLIDE POSITIVITY I I - - P. PALCIPARU* I
years
0 2 0 9 0 60 Age in years
PICURE: 32. Comparison of age specific pattern of parasite (total: elide positivity, individual species and mixed infections) and 1. falciparum gametocyte rate between females (1) and males ( 2 ) in fever eurveys of 12 villages.
Page. .I59
h / '\.
b- - - - 0 2 - *-- --.--.- - -.- -'-• 1
- P. VIVAX - -
I I I I I
20 40 Age in years
PICURB: 33. Comparison of age specific parasite density index (PDI) between felales (1) and malee (2) in fever surveys of 12 villages in Xoraput.
Page. .I60
though males beyond 20 years generally recorded higher densities
canpared to females.
'Ihe annual fever incidence was 539 and 517 per 1.000 males and
females respectlvoly. Malns hnwovor rncnrrlnd hi 8hr:r AI'I 11 7H.f1/ 1,00111
h e n conpared to females [156.6/1.0001. ?he analysis of age specific
incidence showed that the pattern of incidence was qualitatively
similar for both the sexes but quantitatively males particularly in
adult age classes recorded higher parasite incidence compared to
females (Figure: 3 4 ) .
6 . 4 . 3 . Seasonal changes in fever and parasitaemia:
Analysis of seasonal changes in parasite rate (in all the 12
villages as a whole) showed that the malaria cases started increasing
from June to reach a major peak in July [rainy season), declined
Shdrply in August and started gradually increasing from October to
reach another peak in Deceder (winter season; Figure: 35). Cases of
falciparum and were recorded throughout the year. ?he seasonal
pattern of falciparum was qualitatively similar to total parasite rate
[irrespective of species), since this was the predominant parasite
species. Seasonal changes in P. were not as distinct as in the
case of P. falciparum. Cases of P, malariae were recorded between July
and February (highest proportinn was recordod in Vct~ruary). Cases of E.
ovale were recorded between kcember and February (Table: 41 1. Cases of
Page. ,161
\ "! -
P. FALCIPARUW - -
MIXED INPECTION
20
"B= An, , = m , m
FIGURE: 34. Comparison of age specific patterns of incidence between females ( 1 )
and males (21, in fever surveys of 12 villages.
Page. .I62
60 1. PARASITE (TOTAL) 2. 1. PUCIPARUII
40 -
J P H A I I J J A (Month)
FIGURE: 35. Seaeonal patterns of parasite (total), P. falciparum. P. vivax and g. falciparum gametocyte rates in fever - - surveys in 12 villages in Koraput.
Page. . I63
Table: 41
Seasonal changes i n p a r a s i t e r a t e s i n f eve r surveys i n 1 2 v i l l a g e s of Koraput.
Month No. SPR PFX WR examined ( % I % ( % I
January 324 37.96 28 .70 4 .94 February 206 26 .70 19 .42 1 .94 March 302 24.50 16.56 5.fi3 Apri l 278 26.62 17 .63 6.83 b Y 305 22.62 16.39 4.92 June 333 28.83 16 .52 8 .11 J u l y 626 54.63 46.01 4 . 9 5 August 571 22.77 18 .39 2 . 8 0 Septerrher 608 20.89 15 .63 3 .13 October 422 26.78 18.25 3 .32 Novernber 402 33.08 28 .11 3 .48 December 406 44.58 35.22 3.45
M POR M I X RT PFGR ( 8 1 ( % I ( % I ( 8 )
Tota l 4783 31.72 24.21 4 .31 0 .48 0 .06 2.66 2.97
SPR : S l i d e o o s i t i v i tv r a t e PFR E . fa lc iparum r a i e WR g, = ? a t e EM? P. malar iae r a t e POR P. ovale r a t e M I X RTT M w i n f e c t i o n r a t e PFGR P. fa lc iparum gametocyte r a t e ,
Page. ,164
mixed infect ions were recorded throughout the year and the occurrence
of these were highest in DcrcMber (Table: 41). P. falciparun gamtocyte
rate was lowest in April and a clear peak was observed in January
(Figure: 3 5 ) .
Seasonality of fever and parasite incidence (per 1,000
population) in all the villages was also studied (Figure: 36).
Incidence of fever was lowest in February, which increased gradually
to reach a peak in July and remained more or less stable until
Septmer to decline gradually thereafter. Seasonal pattern of
parasite incidence on the other hand resembled that of parasite rate:
there was a major peak in July and another in Oecerber. The seasonal
pattern of falciparun incidence resehled that of total parasite
incidence. P. % also prevailed throughout the year, its incidence
being highest in July. Incidence of both malarlae and was low and
therefore, no distinct seasonality could be made out (Table: 42).
Seasorlality of infant parasite rate was also analyzed to know
the period of transmission. I t was observed that malaria parasite was
detected in infants throughout the year and there were two distinct
peaks, one in Aug~lst and the other in December (Table: 43). While
falciparm cases were detected throughout the year (highest in Apri 1) ,
viva cases were recorded from May t o August, and from October to - January (highest in August). P. malariae cases were recorded betwen
PICURE: 36. Seasonal changes In fever ( 1 ) . total parasite ( 2 ) P. falclparum ( 3 ) and _P. -x (4) incidence in 12 village^ of Koraput.
Page. . I67
Table: 43
Seasonal changes of parasite rate and density index in infants in fever surveys in 12 villages of Koraput.
m n t h No. examined
- - -
January 19 February 11 March 8 Apri 1 6 May 18 June 2 1 July 20 August 26 Septerrber 18 October 22 November 21 December 17
SPR ( % )
47.37 27.27 25.00 33.33 16.67 28.57 20.00 50.00 22.22 27.27 33.33 52.94
PFR ( % 1
10.53 18.18 25 .OO 33.33 11.11 14.29 10.00 30.77 22.22
9.09 23.81 23.53
PFGR [ % )
50.00 50.00
0.00 0.00 0.00
33.33 0.00
25.00 0.00
50.00 20.00
0.00
TOTAL 207 32.85 18.36 8.70 2.42 0.48 18.42
sPR : Slide positivity rate PFR : P. falciparum rate PVR : g. rate FMR : P. malariae rate mt : r . ovalo rate PFGR: P. falciparum gametocyte rate
Page. .I68
Novmbr and February, their occurrence being highest in January. One
case of P. was recorded in Decewer. The pattern of seasonal
incidence of parasitaemia in infants generally reserrbled that of infant
parasite rate (Figure: 37; Table: 44).
6.4.4. Spatial distribution of parasitaemia:
The annual parasite rate was compared between the four groups of
villages in two geographic zones (Table: 45). Tophill villages in both
zones recorded higher parasite rates (above 50%) compared to the other
types of villages. Though the tophill village in Malkangiri recorded a
higher parasite rate 159.81%) compared those in Jeypore (51.2%), the
difference was not statistically significant ( P >0.051. The foothill
villages in both zones recorded slrnilar parasites rates: 43.9% and
42 .2% in Jeypore and blalkangiri respectively ( P >0.05). The villages
in plains in Jeypore recorded significantly higher parasite rate
118.9%) compared to that 113.8%) in Malkangiri zone ( P t0.051. The
riverine village in Malkangiri recorded a very high parasite rate
(45.0%) compared to those in Jeypore (17.0%) and the difference between
the zones was statistically significant ( P c0.05). The annual
falciparum and rates were higher in the tophill villages compared
to the other groups of villages in both the zones. Whlle P. malariae
was detected in all the groups of villages in both zones, P, &was
detected only in the top and foothill villages in Jeypore. Mixed
infections were recorded in a1 1 groups of villages and their occurrence
Page. .I69
J P H A n s J A S O N D (Month)
PICURE: 37. Seaeonal patterns of fever (1). total Parasite (2). P. falciparum (3) and g. rival ( 4 ) incidence in in- - fante in fever surveys in 12 villages of Koraput.
Page. ,172
was highest in the tophill villages in both zones. P. falciparm
gmtocyte rate was higher in all the groups of villages in J w o r e
canpared to Malkangiri zone. Tophill villages recorded the highest
falciparm garnetocyte rates in respective zones .
Parasite rate in 2-9 year children is used to classify areas
under degrees of endmici ty (Bruce-Chwat t , 1985 ; Pampana. 1969). '1he
annual parasite rates in this age class indicated that, while the
tophill and foot hill villages in .Jeypore zone were hyperendmic
[parasite rates of 73.3% and 50.9% respectively), the riverine villages
were mesoendmic (parasite rate 11.7%1 and the plain villages were
hypoendmic (parasi te rate 6.6%). In Malkangiri zone, though the
parasite rates [in this age class1 were different compared to Jeypore,
the levels of endemicity were similar. The tophill and foothill
villages were hyperendemic (parasite rates of 59.4% and 58.3%
respectively), the riverine village was mesoendemic (parasite rate of
50%) and the plain village was hypoendemic (parasite rate of 9.6%).
The incidence [per 1,000 population) of fever and parasite in
different groups of villages in two zones are shown in Table: 46.
Highest incidence of fever and falciparum infection was recorded in the
foothill village in Malkangirl. Parasite incidence was the highest in
the tophill village in the same zone. Incidence of vivax, malariae and
ovale infections was highest in tophill villages of Jeypore zone. The -
incidence of mixed infection was the highest in the tophill village in
Malkangiri.
The age specific parasite rates in the different groups of
villages are canpard in Figure: 38. In the tophill villages in Jeypore
zone, the infant par~si te rate was fifi.08, anrl i t incrt:ils~~d tn rc:ach a
p a k level of 81.5% in 1-2 year old children and declined sharply
thereafter in adult age classes. In foothill villages the infant
parasite rate was 21.0%, and increased to reach a peak level of 53.7%
in 4-9 year age class (a shift of peak age cmpared to tophill
villages) and declined gradually thereafter (Figure: 38 A ) . The
difference in the age prevalence curves between the two villages is
distinct. The patterns for the riverine and plain villages in Jeypore
zone w r e similar (Figure: 38 8 ) . The parasite rates increased
gradually in childhood to reach peak levels in juveniles and young
adult age classes (the peak for riverine villages was 36.8% in 15-20
year age class and that for plain villages was 37.2% in 20-30 years age
class) and declined gradually in older age classes (a minimal rise was
also evident in old age class of beyond 50 years).
In the tophill village in Malkangiri, the peak parasite rate was
in the 1-2 year age class (as in the case of tophill villages in
Jeypore zone) and it declined thereafter to stabilize in adult age
clpsses (Figure: 38 C ) . The age specific patterns of parasite rate in
the foothill and the riverine villages (Figure: 38D) w r e similar and
reflected a situation midway betwen top and foothill v!!lages in
M L K A N C I R I *
e 60
M L K M C I R I
40
30
.- Age in years
PICURE: 3R. Comparison of age specific patterns of parasite rate in tophill (1). foothill (21, riverine (3) and plain ( 4 ) villages in the two zones in lever sruveye of loraput.
& tbe number of cases with fever was low, wider class intervals were selected.
Jeypore zone. In the plain village in Malkangiri zone, the peak
prevalence was observd in 9-15 year age class (Figure: 38D1, following
which i t declined gradually in adults. Adults recorded higk~er parasite
prevalence canpared to young children as was also observed in the plain
villages in Jeypore.
Comparison of the age specific incidence in the different groups
of villages in the two zones was also done (Figures: 39 6 40). The
patterns of parasite incidence in the tophill villages in both the
zones and the riverine village in Malkangiri zone were qualitatively
similar: the peak incidence was in toddlers (children 1-2 years old).
following which there was a sharp decline in adult age classes.
Quantitatively however, tophill villages in Jeypore zone recorded
higher incidence ccmpared to the others. In the foothill villages in
both the zones, the parasite incidence increased from infant level to
reach a peak in juveniles (4-9 year old: note the shift in peak age
class cqared to the tophill villages), following which, i t gradually
declined to r m i n more or less stable in the adult age classes. In the
plain and riverine villages in Jeypore zone, the level of parasite
incidence in adults was higher canpard to children. The age specific
pattern of parasite incidence was at a low level in the plain village
in Malkangiri and i t was not distinct. (Note that the Y scale for the
figures are different, since i t was not possible to present all with
sant, scale).
It was also observed that children below 9 years suffered m r e
than one attack of malaria annually (recording incidence of 1,000 to
Page. .I77
TOPHILL
Age in yearn
FIGURE: 39.1. Patterns of age specific incidence of fever (11, total parasite ( 2 ) . z. falciparun ( 3 ) . P. vivax ( 4 ) and P. malariae (5) in top- hill and foothill villages in Jeypore zone.
(example 1 in "Y" axis = 1,000)
Page. .I78
H
Age i n years
PICURB: 39.2. Patterns of age spec i f i c incidence of fever (1 ) . to ta l parasite ( 2 ) . P. faleiparum ( 3 ) . P. vivax ( 4 ) and E. malariae ( 5 ) i n plain and riverine v i l l ages i n Jeypore zone.
Page. . I 7 9
TOPHILL
1.0
'1
- -.----,-- --v , ' 0.0 . 0 20 40 60 0 20 40 60
Age i n years
PICURB: 40.1. Patterm of age spec i f i c incidence of fever (1) total parasite ( z ) , P. falciparum ( 3 ) . P. vivax ( 4 1 and P. nalariae (5) in tophil l and - - - - foo th i l l v i l lages i n Malkangiri zone.
*(example 1 i n "Y" axle = 1,000)
PLAIN
0.5 l 0 L 2
PLAIN
0 .1 I- ,, . &&<%g::&:- -. - - - 7-8-;e;
0 20 11 0 60 i n years
PIOURE: 40.2. Patterns of age spec i f i c incidence of fever (11, to ta l parasite (21, P . falciparum ( 3 1 , P. vivax ( 4 ) and P. malariae ( 5 ) i n plain and riverine v i l l ages i n llaltangiri zone.
(example 1 i n "Yo a x i s = 1,000)
3,000/1,000 children) in the first group of villages 1 tophill in both
zones and riverine in Malkangiri), which reflected the high degree of
malaria transmission. The other observation from the above patterns of
incidence is that, in the villages with high degree of transmission
(tophill in both zones and riverine in Malkangiri) the separation
b t w e n the age profiles of fever and parasite incidence was relatively
narrow and there was a striking resemblance in the patterns of both
[Figures: 39.1 A , 40.1 A, 40.2 G). n i s was not so in the other groups
of villages. Thus the fever incidence in the 'first group of villages
1 tophill in both zones and riverine in Malkangiri) could reflect the
pattern of malaria incidence, while i t was not so in the other groups
of villages. In fact, the wide separation between fever and parasite
incidence in plain villages (Figures: 39.2 E, 40.2 E ) indicated that
most cases of fever in these villages are due to causes other than
malaria.
The age specific patterns of falciparun density index in
different groups of villages is s h m in Figure: 41. In the tophill
villagas in Jeypore zone and the foothill villages in both the zones,
the parasite density levels were higher in children compared to adults
(marked in f o m r cqared to latter). On the other hand, in the plain
and riverine villages in Jeypore zonqadults generally recorded higher
density cmared to children betwen 4-15 years. In the other villages
the patterns were not very distinct.
JKYPORB
" 0
IULXANCIRI*
2
0 - 1
0 20 4 0 60 Age i n years
FIGURE: 4 1 . Comparison o f pat terns o f age a p e c i f i c P. falciparum p a r a s i t e d e n s i t y index i n the t o p h i l l ( 1 ) . f o o t h i l l (2), r i v e r i n e ( 3 ) and p l a i n ( 4 ) v i l l a g e s i n f e v e r sruveys i n two zones of Koraput.
As t h e number o f c a s e s wi th f e v e r was low, wider c l a s s I n t e r v a l s were s e l e c t e d .
8r
Seasonality of parasi to rates in different groups of villages
was also canpard. In Jeypore zone, all four groups of villages
recorded the major peak during rainy season in July (the peak was sharp
in rivtrrine and foot hill villages) and a second peak was observd
during winter [Cecmber - January). The seasonality of P, falciparm
generally resMnbled the pattern for total parasite rate. Peak
rate was observed between March and June (March in foott~ill, April in
plain, and, June in tophill and riverine) prior to falciparum peak
(Figure: 42). The seasonality of malaria in Malkangin villages was
different (Figure: 43). In top and foot hill villages the peak was in
winter (October - January). However, there was s m d~fference in their
seasonal patterns. While in the tophill village no malaria case was
recorded between February and Apri 1 , in the foothill vi 1 lage cases were
recorded throughout the year. The pattern in the tophill village was
not distinct, possibly due to the variations in sample size (depending
on the number of fever cases) in different months. In the plain
village, two distinct peaks, a major one in Deceher and the other in
March were observed. The seasonality in thy riverine village was not
distinct, though cases were recorded throughout the year.
Seasonality of parasite incidence in the different groups of
villages was also canpared (Figures: 44 6 45). In all the groups of
villages in Jeypore zone, the seasonality of malaria incidence
readled that of parasite rate. While the major peak in top and
foothill villages was in July, i t was in Septtrnber in plain and
Page. .I84
J P I I A I I J J A S O N D J P M A M J J A S O N D (Month) (Month)
PIGURU: 42. Comparison of seasonal patterns of to ta l parasite (11, !. s- par- ( 2 ) , 1. ( 3 ) and P . malariae ( 4 ) rates between four - group8 of v i l l ages i n Jeypore zone.
PICURB: 43. Comparison of seasonal patterns of t o t a l parasite (11, P. f a l c i - parum ( 2 ) . 11. ( 3 ) and E. m l a r i a e ( 4 ) rates between four - di f f erent groups o f v i l l a g e s i n llalkangiri zone.
Page. ,186
J P X A M J J A S O N D J P M A M J J A S O N D (Nonth1 (Month)
PICURB: 44. Comparison of seasonal patterns o f fever (1). to ta l parasite ( 2 ) . P. Palciparum ( 3 ) and P. ( 4 ) incidence i n 4 different groups - - of v i l l ages i n Jeypore zone.
3 a
0
,a 30
O. 1 no k 60 Ci
0 50 $ 30 0
8 3 0 0
J F M A M J J A S O N D J F M A M J J A S O N D (Month) (Month)
PICURB: 45. Comparison of seasonal patterns of fever (1 ) . total parasite ( 2 ) . P. falciparum (3) and P. vivax ( 4 ) incidence in 4 different groups - - of villages in Mlkangiri zone.
riverine villages. In Melkangiri, the seasonality of parasite incidence
was distinct unlike the seasonality of parasite rate (compare Figures:
43 6 45). In the tophill village, twa distinct peaks were observed: one
in June (sharp) and the other in January. A distinct peak was observed
in March in the plain village and in the foothill village, parasite
incidence increased from May onwards to reach peak levels between
Novder and January. The seasonal pat tern of parasite incidence in the
riverine village showed the major peak in October.
Seasonality of parasite rate/incidence was also studied for
individual villages in both the zones. I t was observed that the
patterns varied betwen the villages, even within the same ecotype/zone
(Figures: 46 6 4 7 ) .
6.4.5. Incidence of fever and parasitaemia in different
c m u n i ties:
The data collected in the initial fever survey in the22
villages (1987) was further analyzed for incidence of fever and
parasi tamia in the different ccmnunities. The results indicated that
both fever and parasite incidence varied widely in the different
tribal/ other cmnities (Table: 47). Both fever and parasite
incidence were higher in Cmothios and Paikas canpared to Porojas.
100
5 0 MLKANCIRI JBYPORE 1
0 JEYPORB 2
FOOTHILL
A
80
40 JBYPORB 1 JEYPORB 2
O MALKAMCIRI
- U
6 0
4 0 20
*AUANCIRI
j 0 JBYPORE 1 JBYPORE 2
L
PLAIN
A
60
40 JBYPORB 1
20 JBYPORB 2
0 MALKANCIHI
J P l A l J J A S O N d ( M o n t h )
PICURB: 46. C o m p a r i s o n o f s e a a o n a l p a t t e r n o f p a r a s i t e r a t e i n t h e i n d i v i d u a l v i l l a g e s (1 v i l l a g e i n m l k a n g i r i z o n e a n d 2 v i l l a g e s i n J e y p o r e zone , i n e a c h o f t he g r o u p s ) i n f e v e r s u r v e y s o f KoSaPUt.
{,The o r d e r o f t h e v i l l a g e s i n t h e 4 g r o u p s h a v e b e e n ' m ~ . r * e l ~ ~ o t t d l l ' l c ~ ~ c ~ ~ l l y Lor c l a t . l L y )
FOOTHILL
r-- -1 u
2 100
g MALKANCIRI 0 50 JEYPORE 2
f 0 JEYPORE 1
MALKANGIRI JEYPORE 1
20
10 JEYPORE 1 JBYPORE 2 lALKANGlRI
0
J P M A M J J A S O N D (Month)
PICURE: 47. Comparison of seasonal pattern of parasite incidence in the individual villages (1 village in Nalkangiri and 2 villages in Jeypore zone, in each of the groups) in fever survey8 of Koraput.
(The order of the villages in the I groups have been arranged differently for clarity)
Page.. 191
Table: 47
Caparison of fever and parasite incidence among different tribes4 camunities in fever surveys in 22 villages in Koraput (19871.
Tribe/ Population Incidence per 1,000 population PFGR cannunity size ( 8 )
Fever Parasite
Age in years
Poroja 1 4 9 1 2847 102 .0 131.7 34.2 43.2 D M b o 920 1744 130 .4 1 8 2 . 9 37.0 51.6 Chnathio 3 9 1 678 496.2 697.6 104.9 182.9 Pa i ka 1 0 1 248 386.1 467.7 138.6 197 .6 Tant i 116 210 336.2 261.9 94.8 52.4 Mali 179 312 217.9 333.3 50.3 80.1
PFGR: g. falciparm gametocyte rate
Page. ,192
6.4.6. Actual coverage of population in the fever surveys:
In the 4 villages (one of each type) the actual presence or
absence of individuals in the village at the time of surveillance was
mnitored (for 10 to 12 mnths). On an average, the total absentees per
visit (fortnightly) ranged between 28.0% of population in the village
in plain8 to 56.09 of population in the tophill village (Table: 481.
Approximately 5.6% of the population had left the village temporarily
for few days due to various reasons. Of the absentees a majority
(81.2%) had left the village for their daily work and earning. The
exact reasons for the high absentee rate in the tophill village is not
known. Since the villages are located in remte areas, people tend to
leave the village earlier compared to other villages for daily work.
The other possibility is the delayed arrival of the surveillance
workers in these villages due to practical constraints in reaching the
villages (long distance and poor cmunication facilities].
nough no seriously il l or febrile person was expected to have
left the village during the survey, i t was possible that some
individuals who were absent had febrile at tacks in between visits of
the surveillance worker or had mild illness and early manifestations of
malaria and these persons were not covered under surveillance as they
were not available at the time of house visit.
Page. .I94
6.4.7. Relationship between clinical presentations and
parasi t aemia:
The relationship between individual clinical manifestations and
parasitaemia was also studied. For this purpose the parasite rate in
persons having only single syrrptcm was analyzed (Table: 491, Though
persons with fever or vmiting recorded relatively higher parasite
rates, parasitaemia was detected in persons with any of the synptoms.
The P. falciparun density index was also high for cases with vomiting
and fever (Table: 49). The mean duration of fever was 4.37 days.
Analysis of symptoms apart from fever showed that, while there was
significant association between vomiting, head~che and diarrhoea with 2
P. falciparun parasi taemia (vmi ting: X ~ 4 2 . 3 3 , I' = 0.(11)1); headache: -2 2 X = 5.81; P = 0.016; diarrhoea: X = 4.34, P = 0.0371, other
2 symptoms had a poor association (nausea: X = 0.01, P = 0.931; body
2 ache X = 0.33. P = 0.566).
Clinical diagnosis prior to blood smear examination was made in
888 persons. Of the 327 persons diagnosed to be suffering from typical
malarial attack, 140 (42.8%) shaved peripheral blood parasltaemia. Of
the rest 561 persons, who were clinically diagnosed to be suffering
f r m illnesses other than malaria, 66 (11.76%) had parasitaemia [Table:
50). The parasite rates in these two groups were significantly
different [P <0.05).
Page. .I95
Table: 49
Canparison of parasite rate in patients with different clinical manifestations.
Clinical No. No. Parasite PDI Pf manifestations* examined +ve rate ( $ 1
Fever Headache Diarrohea Body ache Nausea Vomiting
PDI Pf: Parasite density index in P.falciparwn cases * Only persons having single manifestation have bean
considered
Table: 50
Comparison of parasite rate in cases with different clinical diagnosis.
Clinical diagnosis
No. No. +ve for Parasite examined parasite rate ( 8 1
Malaria 327 140 4 2 . 8
Other diseases
Respiratory infection 253 25 9.9 Skin diseases 181 17 9 . 4 Malnutrition 5 0 11 22.0 Gastroenteritis 30 4 1 3 . 3 Arthralgia 32 3 9.4 Viral fever 15 6 40.0
Total 888 206 23.2
Page. .I97
6.5. DISCUSSION:
Ihe results of the year round fever survey in the 22 villages in
Jeypore zone indicated that all were endemic for malaria. Caparison of
results showed that the surveillance under the national programne was
effective in detecting only about 55% of malaria cases (since the W1
in present study was 89.1 as against 49.5 per 1,000 population under
the national progrm). Problems relating to efficiency of case
detection under the nat iondl prngrarmne is well hr~uwn ISharmna g.,
1983; Choudhury, 1984; Anonpus, 1985a). This appears to be one of the
most important factors responsible for the persistence of malaria in
this district (see chapter: 10).
The results in the sor:ond year of the study revealed the
presence of all four human malarial parasites in the locality. Hitherto
there was no scientific evidence of presence of P. ovale in any part of
Irvlia (Choudhury, 1985b). Neither this parasite nor P. malariae (which
is known to be prevalent in this locality from early part of the
century: Perry, 1914; Senior White, 1937a; Senior White, 1938) have
been recorded under the national p r o g r m . The importance of P.
malariae has been discussed earlier (chapter 5.4). Endemic foci of P.
ovale are restricted mostly to parts of Africa (Garnham, 1966; Onori,
1967; Armstrong, 1969; hblineaw and Gramiccia, 1980), though this has
been detected occasionally in other parts of the world (Millan and
Kelly, 1967; Cadigan and Dssowi tz, 1969; Scmboon and Sivasomboon, 1983;
Sher g g., 1988: Storey g g., 1989). This parasite is known to be
highly susceptible to cheimtherapy (Loban and Polozok, 1985). The
presence of this parasite in remte tophill villages indicated the
inadequacy of case detection and treatment in these areas. Presence of
all the four h m n malarial parasites together with several vectors (9
known vectors are prevalent in the locality: VCRC annual report; 1989)
indicated the high malariousness of the area.
Presence of infants wi th parasi taelnia thrtnlghnut the year
indicated perennial transmission. The results also indicated the
possibility of Lwo pcnh Irdnsi~iissio~~ [~crlr~rls: OIII: 1 1 1 1 111wi11y 1110 o~~sc:l
of rains during July - August and another in winter, between Noverber and January.
Analysis of annual fever survey data confirmed the spatial
heterogeneity of malaria in the locality. The problem of malaria varied
k,th qualitatively and quantitatively, not only between the two
physiographic zones but also between ecotypes of villages within the
zones. The patterns of age specific parasite rate and incidence in the
different groups of vil lagcs indicated difference iii degrees of
transmission (Viswanathan, 1!151: Mol ineaux, I I I R H 1. 'lhose pat terns in
Koraput district could be classified into three types (see Figures: 38,
39 and 40):
(1). The pattern in tophill villages in both zones and riverine
village in Malkangiri indicated high degree of transmission
(since parasite rates in children below 5 years was very high)
and high level of acquired i m n i ty ( the sharp decline in
parasite rate in adults is indicative of this).
(ii). The other eno of the spectrum is represented by the pattern in
plain villages in both zones and riverine village in Jeypore
zone, where the transmission was relatively at a lower level
(gradual rise in parasite rate in childhood to reach peak levels
in young adolescent/adult age classes, depending probably on the
degree of exposure).
(iii). In betwen the above two extrms lies the pattern observed in
foothill villages in both zones, where the transmission was
moderate (resulting in shifting of peak age to 4-9 years) and
level of acquired imnity was lower canpared to tophills (since
adult parasite rates were relatively higher].
Viswanathan (19511 had classified endmicities according to the
patterns of age specific parasite rate. According to his classification
the pattern in tophill village in Jeypore zone indicated holoendmic
situation and that in Malkangiri indicated hyperendemic situation.
Foothill villages in both zones and riverine village in Malkangiri
S h m d a pattern which indicated a highly endemic situation. The
pattern in all other groups of villages indicated mesoendtmic
situation. m e thtrorot lcal pat turns prr~jrosr:[l by Vlswanalhan arrl
presented for camparison [Figure: 4 8 ) .
Page. .ZOO
0 5 10 15 Age in years
PIGURB: 48. Patterns of age specific parasite prevalence to illustrate the transmission at different levels of endemicity: hypoendemic (1). mesoendemic ( 2 ) . highly endemic (3). hyperendemic ( 4 ) . holoendemic (5) and superendemic (6) situation (as per Visranathan. 1951).
There was no agreement between endmicities of different groups
of villages as determined by mass blood surveys (chapter: 5 . 3 . 4 : Table:
191 and fewr surveys. Inclusion of asyqtamtic individuals in mass
survey unlike in fever survey is possibly responsible for this
difference. Again there was no complete agreement in the degrees of
endemicities in different groups of villages by child spleen and
paras1 te rates (Chapter 5 . 3 . 4 ) . These findings highlight the
difficulties in interpretation of results obtained by different
surveys. Problems in classifying areas under different degrees of
endemicities are known (Iyengar and Sur, 1929: Viswanathan. 1951;
Pampana, 1969; Bruce-Chwatt , 1985).
The seasonality of malaria also clearly varied in the two
physiographic zones and the four ecotypes of villages. ?his showed the
necessity for planning of control measures separately for different
localities. The time and frequency of residual insecticide spray have
to be adjusted according to transmission seasons. The wide separation
between the profiles of fever and parasite incidence particularly in
plain villages indicated that pres~mptive treatment CII all tcver caries
is not warranted in these villages. The insistence of imparting
presunptive treatment to all febrile cases leads to over consmption of
antimalarials (Najera, 1989).
Unlike in the case of mass blood surveys (chapter: 5.3.31, there
was no significant difference in parasite rates between the sexes in
the annual fever survey. While the former was a random survey, the
latter was a biased survey for fever cases. Whether the difference is
due to this reason or othenvise is not known.
Results of mass blood survey had shown high prevalence of
parasi taemia among the aborigine tribals (Bondas and Porojas; see
chapter:5.3.5). Bondas were not included in the fever survey. Porojas
however, recorded low parasite incidence when compared to others in the
fever survey. This again could be due to the difference in sampling in
two surveys. I t is possible that many Porojas circulated parasite, but
were asymptanatic and they were detected only in mass survey but not in
fever survey.
Following the failure of eradication programnes, i t has been
advocated to reconsider malaria as another disease entity particularly
in areas where the resources do not permit ef Sect ive surveillance
(WD, 1986a; Hays, 1989, bblineaux, 1989). In such situation, one has to
depend on the clinical findings for malaria case rietr:ction. The present
study revealed that the parasite rate in cases presenting with symptms
other than fever was also high in Koraput. Further, the manifestations
due to P. falcipsrum may be varied and typical malarial fever
periodicity takes time to establish (Bruce-Chwatt , 1985; Loban and
Polozok, 1985), hence the clinical diagnosis can be improved by looking
for fever with other associated symptms. A chination of
manifestations such as fever, headache and vmiting seem to be a useful
indicator of falciparun malaria. The type of manifestation could also
be dependent on the innune status of individuals as suggested by the
difference in parasite density index in different manifestatibns.
Relationship between parasite density and clinical manifestations is
well known (Sinton g g.. 1931: Pazzaglia and Wot~dwarrl. 11102: I.oban
and Polozok. 1985; Richards etg. , 1988a).
API has been used as a yard stick for deciding the nature of
control measures under the national progranane (Pat tanayak and Roy,
1980; S h a m , 1984a; also chapter: 4). The present study revealed that
a large proportion of the population was not available at the time of
survey. It was possible that some of them may have had mild illness (in
spite of which they go out to earn their livelihnod due to poverty) and
these persons were missed. Ibis not only lowered the reliability of API
as an indicator of malaria, but also could have resulted in
accmlation of parasite load in the comnity favouring the
persistence of the problem.