1
HsiaoA, etal. BMJ Open 2022;12:e052337. doi:10.1136/bmjopen-2021-052337
Open access
Economic impact of cholera in
households in rural southern Malawi: a
prospective study
Amber Hsiao ,1 Enusa Ramani,1,2 Hye- Jin Seo,3 GiDeok Pak,4 Dan Vuntade,5
Maurice M’bang’ombe,6 Bagrey Ngwira,5 Wilm Quentin,1 Florian Marks ,7,8
Vittal Mogasale 2
To cite: HsiaoA, RamaniE,
SeoH- J, etal. Economic
impact of cholera in households
in rural southern Malawi: a
prospective study. BMJ Open
2022;12:e052337. doi:10.1136/
bmjopen-2021-052337
►Prepublication history and
additional supplemental material
for this paper are available
online. To view these files,
please visit the journal online
(http://dx.doi.org/10.1136/
bmjopen-2021-052337).
BN since deceased.
Received 13 April 2021
Accepted 08 March 2022
For numbered affiliations see
end of article.
Correspondence to
Dr Vittal Mogasale;
vmogasale@ gmail. com
Original research
© Author(s) (or their
employer(s)) 2022. Re- use
permitted under CC BY.
Published by BMJ.
ABSTRACT
Introduction Cholera remains a significant contributor
to diarrhoeal illness, especially in sub- Saharan Africa.
Few studies have estimated the cost of illness (COI) of
cholera in Malawi, a cholera- endemic country. The present
study estimated the COI of cholera in Nsanje, southern
Malawi, as part of the Cholera Surveillance in Malawi
(CSIMA) programme following a mass cholera vaccination
campaign in 2015.
Methods Patients ≥12 months of age who were recruited
as part of CSIMA were invited to participate in the COI
survey. The COI tool captured household components
of economic burden, including direct medical and non-
medical costs, and indirect lost productivity costs.
Results Between April 2016 and March 2020, 40 cholera
cases were enrolled in the study, all of whom participated
in the COI survey. Only two patients had any direct medical
costs and five patients reported lost wages due to illness.
The COI per patient was US$14.34 (in 2020), more than
half of which was from direct non- medical costs from
food, water, and transportation to the health centre.
Conclusion For the majority of Malawians who struggle
to subsist on less than US$2 a day, the COI of cholera
represents a significant cost burden to families. While
cholera treatment is provided for free in government- run
health centres, additional investments in cholera control
and prevention at the community level and financial
support beyond direct medical costs may be necessary to
alleviate the economic burden of cholera on households in
southern Malawi.
INTRODUCTION
Cholera is an infection of the intestine caused
by the bacterium Vibrio cholerae that leads to
acute, rapidly dehydrating diarrhoeal disease.
Annually, an estimated 2.86 million cases of
cholera occur in cholera- endemic countries
that result in 95 000 deaths.1 A recent study
estimated that cholera is especially pervasive
throughout sub- Saharan Africa (sSA) where
the human and economic burden of cholera
is greatest, with more than 200 million people
living in areas where cholera is present. Of
these 200 million, 87 million live in areas with
high incidence, defined as >1 case per 1000
people per year.2
While improvements to water, sanitation
and hygiene (WASH) are the best long- term
solution for preventing more diarrhoeal
diseases, these measures remain unavailable
to large proportions of people in sSA, espe-
cially among those living in flood- prone rural
areas. The availability of low- cost inactivated
oral cholera vaccines (OCVs) since 2011
has significantly changed the landscape and
provided a cost- effective short- to- middle- term
approach for cholera prevention and control.3
A number of mass vaccination campaigns—
many of which have taken place in sSA—
have demonstrated that it can be successfully
administered in a variety of settings, including
high- risk settings to prevent an impending
outbreak, or to quickly halt the transmission
of an ongoing outbreak.4 5
In Malawi specifically, cholera has been
reported since the 1970s and is endemic to
the country.6–8 The extent of the cholera
burden in the country has not been well
documented due to the lack of sustainable
diagnostic and surveillance capacity.
One of the worst cholera outbreaks to
date occurred in January 2015 following the
nation’s worst floods in history, which affected
more than 1.1 million people in the Southern
Region and displaced at least 230 000 people
STRENGTHS AND LIMITATIONS OF THIS STUDY
⇒We recruited patients who were cholera- confirmed
at the time they first sought care and interviewed
them regarding costs incurred due to illness with-
in 7 days following their initial health facility visit,
which limited recall bias.
⇒The sample size was relatively small, which limits
the generalisability of the findings.
⇒The cost of illness estimate is likely to be an under-
estimate as it only includes out- of- pocket expendi-
tures of patients who sought care.
2HsiaoA, etal. BMJ Open 2022;12:e052337. doi:10.1136/bmjopen-2021-052337
Open access
from their homes.9 Within a month of the flood, cholera
cases were being reported in Nsanje and Chikwawa, two
of the worst- hit districts in southern Malawi. The flooding
led to a multistakeholder response to coordinate a reac-
tive OCV mass vaccination campaign in the region.10
Due to the lack of diagnostic capacity, cholera cases were
being diagnosed based on clinical presentation as per the
WHO and national guidelines.11
The OCV mass vaccination campaign was then imple-
mented primarily in Nsanje, which was identified as having
the highest burden of cholera based on prior years’ data
provided by the Malawian Ministry of Health (MOH).
From 30 March 2015 to 23 April 2015, the International
Vaccine Institute (IVI), MOH, WHO and John Snow, Inc
coordinated a reactive mass vaccination campaign that
targeted 160 000 people (320 000 total doses of the OCV
Shanchol (Shantha Biotechnics Pvt, Ltd., India) over
1 year of age. Those living in high- risk areas of Nsanje—
namely, those living in internally displaced camps and
surrounding villages—were the primary targets.10
In the course of a 4- year effort to strengthen cholera
surveillance capacity and infrastructure in Nsanje
following the mass vaccination campaign, we investi-
gated the cost of illness (COI) of cholera for patients who
sought care. Only one study to date has reported on the
COI from cholera in southeastern Malawi (Lake Chilwa
in the districts of Machinga and Zomba).12 The objec-
tive of this study is to provide additional field data on the
economic burden of cholera in Malawi from a household
perspective.
METHODS
As part of the Cholera Surveillance in Malawi (CSIMA)
programme, cholera surveillance was conducted across
22 Nsanje (population >292 000) and 18 Chikwawa
(population >533 000) healthcare facilities from 5 April
2016 to 31 March 2020. IVI staff trained health surveil-
lance assistants (HSAs) and health workers at all Nsanje
and Chikwawa facilities to identify patients who sought
care for acute watery diarrhoea. HSAs are community
health facilitators who live in the area served by the local
healthcare facility who are involved in activities such as
WASH and general health promotion.
Patients who met the inclusion criteria (who were
eligible to receive OCV based being at least 12 months
of age at the start of the vaccination campaign, and
presented to an Nsanje health facility with acute watery
diarrhoea indicative of cholera as defined by the WHO11)
were invited to participate in the diarrhoeal surveil-
lance study. Participants who provided informed written
consent provided a stool specimen to perform a rapid
diagnostic test (RDT) for cholera (Crystal VC RDT; Arkray
Healthcare Pvt, India; previously Span Diagnostics, Surat,
India) and/or a stool sample for culture confirmation at
the national reference laboratory in Lilongwe. The use of
RDTs has been accepted for use by the Malawi MOH, and
there is documented experience with this test kit in other
settings.13 14 While the use of the RDT is not intended to
be a substitute for stool culture, the use of the kit in this
setting ensured that one would not miss any potential
cholera cases during the early surveillance period while
logistics for stool transportation and culture were being
set- up.
Between 6 April 2016 and 12 December 2017, culture-
confirmed and RDT- positive cholera cases were recruited
for the overall study, as well as the COI survey compo-
nent. However, due to low recruitment numbers of RDT-
confirmed and/or culture- confirmed cholera cases,
in part due to limited availability of RDT kits and stool
collection logistical challenges, the inclusion criteria were
expanded from 12 December 2017, through 31 March
2020, to include clinically diagnosed cholera cases in an
outbreak situation to avoid missing potential cases.
While cholera vaccines were administered to residents
in both Nsanje and Chikwawa, the majority of doses were
administered to residents of Nsanje. Thus, only patients
recruited from Nsanje health centres were invited for
the COI portion of the study. The COI from a house-
hold perspective was assessed for patients who provided
written informed consent (regardless of vaccination
status). The COI tool (online supplemental material)
was developed based on a tool that IVI had previously
used for other COI studies, with further refinements
using the guidelines for cost collection in cholera studies
provided by the WHO.15 16 The survey tool captured
household components of economic burden, divided
further into direct medical costs (DMCs), direct non-
medical costs (DNMCs) and indirect costs (ICs) (as
done in the previous studies17), with the payer being the
patients themselves or caregivers/helpers of the patient
(eg, relatives). Experienced interviewers were trained on
how to administer the survey and all survey responses
were validated by the University of Malawi Polytechnic
and MOH collaborators to ensure they were appropriate
for the local context.
A series of a maximum of three interviews were
planned for the COI assessment, with day 0 (ie, day of
diagnosis) being the day of the patient’s health facility
visit: at day 0–7, day 13–15 (beyond the mean duration
of an episode of cholera illness) and day 20–22. To mini-
mise recall bias, the first interview took place as soon as
cholera was confirmed either by a test or a clinician, with
a maximum of 7 days following the first healthcare facility
visit. If a patient preferred to be interviewed while at the
healthcare facility, the trained interviewer conducted the
first COI interview at the time of the initial outpatient or
inpatient visit. Patients who were not feeling well enough
were contacted by an HSA to schedule a future interview
time. Trained interviewers would then visit the patient’s
home at the scheduled time to conduct the first interview.
At the end of each COI assessment, patients were asked
whether they felt they had fully recovered from cholera.
If the patient reported still being ill, the next interview
was scheduled; otherwise, no additional interviews were
conducted.
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HsiaoA, etal. BMJ Open 2022;12:e052337. doi:10.1136/bmjopen-2021-052337
Open access
At each of the interviews, patients (or parent/guardian)
were asked how much money they spent during each
of their visits to a healthcare facility or other treatment
locations (eg, a traditional healer) since becoming ill,
including any visits that may have occurred prior to the
study enrolment date. DMCs included out- of- pocket
payments for services, prescription drugs and any other
health facility fees. DNMCs included transportation and
food expenses incurred by the patient and/or caregivers
who went to the health facility with the patient.
Finally, IC accounted for the patients’ and/or care-
givers’ productivity losses incurred due to lost wages. We
calculated productivity losses using three scenarios based
on (1) self- reported wage losses, (2) minimum wage per
day for all workers between 14 and 50 years of age (the
legal minimum and old- age pension eligibility age18) who
did not report wage losses and (3) minimum wage per
day for all patients >5 years of age who did not report
wage losses, given evidence from Africa that children are
often involved in economic activities that add to a family’s
income.19
In all scenarios, if patients and/or caregivers reported
wage losses, these were calculated based on self- reported
daily lost productivity (half or full days of work lost due
to taking care of the ill patient) and daily wages. For
patients and caregivers who did not report wage losses
(ie, scenarios 2 and 3), we applied the minimum wage of
1346.16 Malawian kwacha (MWK) per day (US$1.83/day
as of 1 January 2020) to account for the monetary value
of productivity losses.20 Productivity losses were not calcu-
lated for caregivers who indicated that they did not cut
back on their usual activities had they not been caring for
the patient. They were also not calculated for caregivers
who reported no income lost (eg, a caregiver who is dedi-
cated to unpaid housework).
Costs were collected in MWK, inflated to 2020 MWK
using World Bank inflation data,21 and converted to
2020 US$ (736.5803 MWK=US$1 on 31 March 2020).22
All analyses were conducted in Stata/IC 13.1 (College
Station, Texas, USA) and Microsoft Excel.
Patient and public involvement
Patients including their caretakers were involved in this
study as participants in the COI interviews. Costs related
to cholera illness were collected from the participants
after obtaining informed consent. The public was not
involved in this study. Patients and the public were not
involved in study development, defining the research
question and study design, recruitment and the conduct
of the study. Early findings of the study were disseminated
through a workshop attended by country policymakers,
health managers and health facility staff.
RESULTS
During our surveillance period, 2201 individuals met the
diarrhoeal illness criteria for stool collection and testing
for cholera in Nsanje. Of these patients, 40 (1.8%) were
identified as cholera cases and were recruited for the
surveillance study. On the day of their health facility visit,
all 40 patients also consented for COI interview. Table 1
summarises selected demographic characteristics, as well
as OCV statuses, of all cases.
Of the 40 cases, 31 (78%) were seen in an outpatient
setting. Duration of illness was 5 days (min–max: 2–17
days) in the outpatient setting and 8 days (min–max: 2–19
days) in the inpatient setting. Most patients (n=34) had
fully recovered by the time the first interview occurred
(scheduled within 7 days of recruitment day 0); 6 patients
had a second interview (at day 13–15) and none required
a third interview. A higher proportion of inpatient cases
were males, whereas outpatient cases were majority
female. Of the 40 cases, 4 were identified clinically, 9
using RDT and 27 using culture confirmation. A larger
proportion of children were seen in the inpatient setting,
compared with outpatient.
The direct and IC of cholera per patient was US$14.34
when averaged across all patients, with the largest propor-
tion of costs (57.9%) being from DNMCs (food, water
and transportation) (table 2). DMCs for drugs and
consumables were zero for nearly all patients; only two
patients seen in the inpatient setting had any drug costs
of US$11.17 (8229 MWK) and US$1.19 (875 MWK) each,
both of whom were seen at a private Christian Health
Association of Malawi (CHAM) facility; these two patient
costs increased the overall average across the cohort to
US$0.31.
Patient and caregiver food costs were US$0.95 and
US$1.61 on average, respectively. Roundtrip transporta-
tion costs were relatively lower for patients at US$1.84,
compared with caregiver transportation costs at US$3.91.
Transportation time on average per patient was 112 min
roundtrip (min, max: 10–360).
We also performed various scenario analyses for ICs
(table 3), where costs were only averaged across patients
and caregivers with non- zero productivity losses in each
scenario. Eight patients were excluded from wage loss
calculations due to missing age or birthdate. Thirty- four
patients had at least one caregiver provide care during
their illness, with a total of 53 caregivers across all patients.
Caregivers only reported whether they were children or
adults (ie, exact ages or birthdates were not ascertained);
all caregivers reported being adults who we assumed were
of working age.
In scenario 1, productivity losses (lost wages) due to
being sick for the duration of illness were US$10.60 on
average (n=5) for patients who reported wage losses,
though one patient reported receiving paid sick leave for
this time (US$10.89), which would reduce the average
to US$10.53 (n=4). Only 15 caregivers (who cared for
eight patients) reported US$6.36 on average in lost wages
due to missing work. In scenario 2, where the minimum
wage was assumed for all patients (n=11) and caregivers
(n=45) of working age, productivity losses were US$8.83
for patients and US$3.94 for caregivers on average. In
scenario 3, where the minimum wage was assumed for all
4HsiaoA, etal. BMJ Open 2022;12:e052337. doi:10.1136/bmjopen-2021-052337
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patients >5 years of age (n=19), productivity losses were
US$9.78 for patients on average. In this scenario anal-
ysis, there were two patients aged 5–14 years (US$14.16
on average) and five patients aged ≥60 years (US$8.59 on
average). Caregiver costs in scenarios 2 and 3 were the
same (US$3.94) since all caregivers were adults.
Half of all patients (n=20), and two- thirds of inpatients
(n=6), reported having to borrow money from someone
to pay for healthcare, food or transportation as a result
of having cholera (table 4), but most did not have to sell
personal belongings to pay for care. Experiencing at least
some food insecurity in the past year (defined as going
without food at least once in the past 3 months) was an
issue for a large proportion of patients (n=28).
DISCUSSION
Our study estimated patient and caregiver costs associ-
ated with seeking healthcare for the treatment of severe
diarrhoeal illness diagnosed as cholera in Nsanje. We had
few diarrhoeal cases overall. The cost of cholera illness
per patient was US$14.34, with the largest proportion of
costs being from DNMCs (food, water and transporta-
tion) (US$8.30), followed by indirect productivity losses
(US$5.73) in our primary analysis, where costs were aver-
aged across all patients in our cohort.
The majority of our patients were not admitted during
their visit to the health centre. Patients who sought care
in the outpatient setting were symptomatic an average of
1.4 days prior to seeking care. Patients who were admitted
were sick for an average of 2.8 days prior to seeking care
and had an inpatient stay of 2 days. Our patient popu-
lation was slightly skewed towards females and of those
whose age was reported, most patients were adults aged
18 and older. The majority of patients were not vacci-
nated during the OCV campaign in 2015.
Overall, only two patients with cholera had any DMCs;
one was seen in the outpatient setting (875 MWK or
US$1.19) and the other was admitted to a private CHAM
facility (8229 MWK or US$11.17). This finding was
expected, as cholera treatment is provided free of charge
in Malawi. On average, patients and their caregivers
spent US$8.61 in direct costs (US$0.31 in medical costs
and US$8.30 in non- medical costs, including those with
zero costs), almost all of which was due to food and/or
water and transportation costs. In our scenario analysis
Table 1 Demographic and medical characteristics of
cholera cases in Nsanje District, Malawi, 2016–2020
Outpatient
n (%)
Inpatient
n (%)
Total*
n (%)
Total 31 (78) 9 (22) 40 (100)
Sex
Male 9 (29) 6 (67) 15 (38)
Female 17 (55) 3 (33) 20 (50)
Unknown/missing 5 (16) 0 (0) 5 (13)
Age
<5 years 10 (32) 4 (44) 14 (35)
≥5 years to <18 years 2 (6) 1 (11) 3 (8)
≥18 years to <35 years 9 (29) 0 (0) 9 (23)
≥35 years 3 (10) 3 (33) 6 (15)
Unknown/missing 7 (23) 1 (11) 8 (20)
Level of education
Never went to school 13 (42) 3 (33) 16 (40)
Preschool 2 (6) 0 (0) 2 (5)
Completed primary 10 (32) 3 (33) 13 (33)
Completed secondary 2 (6) 0 (0) 2 (5)
Unknown/missing 4 (13) 3 (33) 7 (18)
Employment status
Works for a wage 5 (16) 0 (0) 5 (13)
Does not work for a
wage
26 (84) 9 (100) 35 (88)
Average inpatient stay,
days (min–max)
– 2 (1–4) –
Average number of
symptomatic days prior
to seeking medical care
(min–max)
1.4 (0–4) 2.8 (1–8) 1.7 (0–8)
Average number of days
sick with cholera
5 (2–17) 8 (2–19) 6 (2–19)
Method of transportation
for patients to health
centre
Walked 9 (29) 1 (11) 10 (25)
Biked 12 (39) 5 (56) 17 (43)
Motorcycle 3 (10) 1 (11) 4 (10)
Minibus 5 (16) 1 (11) 6 (15)
Private car 1 (3) 0 (0) 1 (3)
Hired canoe 1 (3) 0 (0) 1 (3)
Ambulance (from MOH) 0 (0) 1 (11) 1 (3)
Vaccination status (OCV
in 2015)
Not vaccinated 16 (52) 5 (56) 21 (53)
One dose 5 (16) 1 (11) 6 (15)
Two doses 6 (19) 0 (0) 6 (15)
Unknown/missing 4 (13) 3 (33) 7 (18)
Cholera confirmation
Continued
Outpatient
n (%)
Inpatient
n (%)
Total*
n (%)
Rapid diagnostic test 5 (56) 4 (44) 9 (22)
Lab culture
confirmation
25 (93) 2 (7) 27 (68)
Clinically identified 1 (25) 3 (75) 4 (10)
*Sum of percentages may exceed 100 due to rounding.
MOH, Ministry of Health; OCV, oral cholera vaccine.
Table 1 Continued
5
HsiaoA, etal. BMJ Open 2022;12:e052337. doi:10.1136/bmjopen-2021-052337
Open access
when only those with self- reported wages are consid-
ered, only five patients with cholera (all outpatient cases)
reported productivity losses of US$8.83 on average, and
15 caregivers of patients reported wage losses, averaging
US$3.93. In our scenario analysis, where we applied
the minimum wage to all patients and caregivers who
Table 2 Mean direct and indirect costs (MWK and USD 2020) for cholera cases in Nsanje District, Malawi, 2016–2020*
(averaged across all 40 patients)
Inpatient (n=9) Outpatient (n=31) Total costs (n=40)
% of
total
2020 MWK
(min, max)
2020 USD
(min, max)
2020 MWK
(min, max)
2020 USD
(min, max)
2020
MWK
2020
USD
Direct, medical costs 97 0.13 265 0.36 228 0.31 2.2
Drugs and
consumables†
97 (0–875) 0.13 (0–1.19) 265 (0–8229) 0.36 (0–11.17) 228 0.31 2.6
Direct, non- medical costs 9703 13.17 5073 6.89 6115 8.30 57.9
Patient food and/or
water
505 (0–1353) 0.69 (0–1.84) 753 (0–6148) 1.02 (0–8.35) 697 0.95 6.6
Patient transportation
(roundtrip)
2007 (0–8750) 2.73 (0–11.88) 1161 (0–9836) 1.58 (0–13.35) 1352 1.84 12.8
Caregiver food and/or
water
1332 (0–2734) 1.81 (0–3.71) 1143 (0–12 686) 1.55 (0–17.22) 1186 1.61 11.2
Caregiver transportation
(roundtrip)
5858 (0–13 525) 7.95 (0–18.36) 2016 (0–8346) 2.74 (0–11.33) 2880 3.91 27.3
Indirect (productivity
losses)‡
489 0.66 5304 7.20 4221 5.73 40.0
Patient 0 (0–0) 0 (0–0) 1259 (0–12 519) 1.71 (0–17.00) 976 1.32 9.2
Caregivers 489 (0–2213) 0.66 (0–3.00) 4045 (0–70 526) 5.49 (0–95.75) 3245 4.41 30.7
Total mean costs§ 10 289 13.97 10 643 14.45 10 563 14.34 100.0
*All costs by category are averaged over the total number of patients in each category (ie, patients or caregivers with zero costs are not
excluded in the average).
†Only two patients (one inpatient, one outpatient) had any DMCs, but costs are averaged over the total number of patients.
‡Productivity losses are averaged over the total number of patients in each category (not averaged over the total number of caregivers); six
outpatients and two inpatients had caregivers who reported wage losses, but wages are averaged over the total number of outpatients (n=31)
and inpatients (n=9).
§Costs are first summed across categories for each patient and averaged across total patients.
DMCs, direct medical costs; MWK, Malawian kwacha.
Table 3 Scenario analyses of mean indirect costs for cholera cases with reported wage losses and assuming minimum wage
in Nsanje District, Malawi, 2016–2020
Scenario 1: among those
with self- reported wages
only*
Patients: n=5
Caregivers: n=15 % of
total
indirect
costs
Scenario 2: self- reported +
minimum wage for patients
aged 15–50 years
Patients: n=11
Caregivers: n=45 % of
total
indirect
costs
Scenario 3: self- reported +
minimum wage for patients
aged >5 years
Patients: n=19
Caregivers: n=45 % of
total
indirect
costs
2020 MWK
(min, max)
2020 USD
(min, max)
MWK
(min, max)
2020 USD
(min, max)
MWK
(min, max)
2020 USD
(min, max)
Indirect, productivity losses
Patients* 7807
(5008–12
519)
10.60
(6.80–17.00)
63 6506
(2692–12 519)
8.83
(3.66–17.00)
69 7161
(2019–16 154)
9.78
(2.74–21.93)
71
Caregivers 8558
(823–25
039)
6.36
(1.12–33.99)
38 5306
(823–25 039)
3.94
(1.12–33.99)
31 5306
(823–25 039)
3.94
(1.12–33.99)
29
Total indirect
costs
16 365 16.96 11 812 12.77 12 467 13.72
*All 5 patients who worked for a wage were outpatient.
MWK, Malawian kwacha.
6HsiaoA, etal. BMJ Open 2022;12:e052337. doi:10.1136/bmjopen-2021-052337
Open access
theoretically could be contributing to economic activities
(ie, household work), indirect productivity losses were as
high as US$9.78 per patient and US$3.94 per caregiver.
This latter scenario may overestimate the number of indi-
viduals who experience productivity losses and the actual
economic impact, though the average productivity losses
(US$13.72) were lower than in the self- reported wage
scenario ($16.96).
The overall costs found in our study are substantially
less than one study previously reported in rural Malawi.12
Ilboudo et al reported household costs of US$65.60 in
2016 (US$106.16 in 2020). They reported a much larger
proportion of hospitalised cases: their study sampled 100
cases (which estimated 9% of the overall caseload from
the cholera outbreak), 90 of whom were hospitalised,
whereas we only had 7 hospitalised cases (17.5% of total
cases). Transportation costs in our study were also lower
for both patients and caregivers compared with their
study, which may be attributable to differences in trans-
portation methods and travel distances to health centres.
The largest differences in costs between our study and
Ilboudo et al were in food and lost productivity costs,
likely also driven by the fact that their study had more
hospitalised cases that required more expenses over
several days. Their reported ICs of patient’s productivity
were a larger portion of overall costs (35.1% compared
with our 9.2%), which may be attributed to their study
cohort having longer inpatient stays. The caregiver lost
productivity costs as a proportion of overall costs were
lower in their study (23.5% compared with our 30.7%).
Differences in productivity costs may be attributed to
several reasons, such as differences in wages in Nsanje
versus Machinga and Zomba districts, unemployment
rates and other socioeconomic factors. The differences
may also be attributed to the severity of illness, potentially
attenuated by vaccination. Ilboudo et al assessed costs of
illness from patients who had cholera in the ±1 week prior
to and after the OCV campaign that was underway (which
followed the cholera outbreak). Thus, the proximity in
timing to the outbreak may have meant that few individ-
uals had any immunity to cholera and may have experi-
enced more severe symptoms, whereas in our population,
OCV coverage and immunity was likely higher. Given the
relatively small sample size in both studies, however, more
data are needed from the region to understand why these
costs differed more than other cost components.
We also assessed financial and food insecurity for cases.
Half of our cases had to borrow money from someone
to pay for costs associated with their cholera illness and
treatment, which is similar to the proportion reported by
Ilboudo et al. A large proportion of our cases also faced
food insecurity at some point in the prior year.
Table 4 Financial and food insecurity of cholera cases in Nsanje District, Malawi, 2016–2020
Outpatient (n=31) n (%) Inpatient (n=9) n (%) Total (n=40) n (%)
Borrowing money to pay for healthcare services
Did not borrow money 17 (55) 3 (33) 20 (50)
Borrowed money from a family member 6 (19) 0 (0) 6 (15)
Borrowed money from a friend 4 (13) 5 (56) 9 (23)
Borrowed money from a cooperative 0 (0) 1 (11) 1 (3)
Borrowed money from a neighbour 1 (3) 0 (0) 1 (3)
Borrowed money from the village chief 1 (3) 0 (0) 1 (3)
Borrowed money from boss/employer 1 (3) 0 (0) 1 (3)
Borrowed money from church 1 (3) 0 (0) 1 (3)
Sold items to pay for healthcare services
Did not sell anything 29 (94) 4 (44) 33 (83)
Rented out rice and maize plots 0 (0) 4 (44) 4 (10)
Sold radio 1 (3) 0 (0) 1 (3)
Sold livestock 1 (3) 1 (11) 2 (5)
Frequency of household going without food in the
past year
Never 4 (13) 1 (11) 5 (13)
Once every 3 months 7 (23) 1 (11) 8 (20)
Once per month 3 (10) 2 (22) 5 (13)
Twice per month 2 (6) 1 (11) 3 (8)
Once per week 8 (26) 1 (11) 9 (23)
Almost every day 3 (10) 0 (0) 3 (8)
Unknown/missing 4 (13) 3 (33) 7 (18)
7
HsiaoA, etal. BMJ Open 2022;12:e052337. doi:10.1136/bmjopen-2021-052337
Open access
Our study had several limitations. One limitation was the
late start of cholera surveillance (April 2016) relative to
the cholera outbreak (approximately February 2015), in
response to which a vaccination campaign was conducted
(March/April 2015). It is possible that some postvaccina-
tion campaign cholera cases may have occurred in the
year prior to the start of cholera surveillance, particularly
during the November 2015 to April 2016 rainy season;
these cases would not have been included in this study.
The study was also not able to collect COI data from
Chikwawa residents and infants <12 months, which may
have provided different cost estimates. Given the small
number of cholera cases, even after expanding the case
criteria to clinically diagnosed cases (of which there
were only 4), it may not be representative of the general
Nsanje population, particularly those who were sick and
did not seek care. It is also possible that patients may have
shown up for care but were undiagnosed or misdiagnosed
for reasons such as diagnostic sensitivity. While we were
unable to assess any patterns or variation in the use of the
three testing methods (RDT, culture or clinically identi-
fied) by the health centre, it is possible that our recruited
patient cohort is biased towards health centres that were
better equipped to test, recruit and treat patients. For
example, many of the more remote health centres in
Nsanje lacked toilets or latrines for proper stool collec-
tion and have limited access to electricity to ensure the
viability of stool samples, which may have limited the
sensitivity of the stool culture result. Apart from the logis-
tical challenges of recruitment, the area also has a high
number of migrants from Mozambique; migrants may be
less likely to seek care due to several reasons, including
language barriers, discrimination due to cultural differ-
ences, and fear of deportation.23
Health facility costs were also not included in our
costing, which may be a significant portion of the total
costs as most patients reported US$0 in DMCs. A recent
study in rural Malawi estimated that the average treatment
cost to a health facility for a hospitalised cholera case was
US$59.70 in 2016 (US$96.61 in 2020).12 A separate study
on cholera treatment costs at the facility level at this study
site has estimated an economic cost of US$41.86 in 2018
(US$50.79 in 2020) and a financial cost of US$25.43 in
2018 (US$30.85 in 2020).24 Finally, there was the poten-
tial for recall bias, especially for patients who may have
had costs prior to the initial visit to the health centre from
which they were recruited for the study. For costs incurred
from the day of enrolment onward, we attempted to mini-
mise the potential for recall bias by following up first
within a week of the initial visit.
Despite the limitations, our study provides one of the
few COI studies of cholera illness in sSA from the house-
hold perspective. More studies are needed to more fully
evaluate the cholera costs of illness in Malawi. Currently,
spending on health accounts for less than 10% of country
revenues—below the 15% target set by the Abuja Declara-
tion to which Malawi is a signatory.25 Healthcare financing
in Malawi is also unpredictable and unsustainable given
the country’s reliance on development partners’ contri-
butions that account for nearly two- thirds of total health
expenditure.26 Our study supports the need for further
spending in the health sector; for example, building and
staffing additional health centres that reduce the amount
of time patients have to travel could reduce the cost
burden on patients.
While the study was not designed to assess vaccine effec-
tiveness, our surveillance efforts may also be a positive
indication that the cholera vaccine may be associated with
a reduction in the burden of cholera in the middle- term,
as most of our cases were unvaccinated (while approxi-
mately half of the Nsanje population received the cholera
vaccine). Since this study was conducted, in recogni-
tion of the high incidence of cholera and the need for
additional tools to address the burden, the government
of Malawi integrated OCVs into its national cholera
control plan in 2017,27 and there have been several OCV
campaigns implemented since.10 28 Alternatively, given
that cholera often occurs cyclically, it is possible that the
time period during which surveillance occurred was a low
or no cholera transmission interval. Ultimately, investing
more heavily in WASH infrastructure would be the most
effective, though more costly, solution in the long- run to
avert cholera.
In a country where the gross domestic product per
capita per day is less than US$2 (US$625 annually in
2020), a family who has to spend US$14 on average for
cholera illness will very likely have to make financial sacri-
fices to access treatment. Even though the DMCs associ-
ated with cholera care are low, the patient (who is willing
and able to go to the health centre) must bear a high
burden of DNMCs and indirect lost productivity costs.
For those who do not have the means of even going to
a health facility to seek care, the consequences are likely
even more severe; for example, the death of a family
member whose wages supported the family has significant
long- term impacts beyond a single cholera episode.
In conclusion, we find that households face a significant
cost burden when one falls sick with cholera. These costs
are significantly high to warrant additional investments in
the health system to avert future cases of cholera.
Author affiliations
1Department of Health Care Management, Technische Universität Berlin, Berlin,
Germany
2Policy and Economic Research, International Vaccine Institute, Seoul, The Republic
of Korea
3Epidemiology, Public Health, Impact, International Vaccine Institute, Seoul, The
Republic of Korea
4Biostatistics & Data Management, International Vaccine Institute, Seoul, The
Republic of Korea
5Department of Environmental Health, University of Malawi the Polytechnic,
Blantyre, Malawi
6Ministry of Health Malawi, Lilongwe, Malawi
7Epidemiology, Public Health, Impact, International Vaccine Institute, Gwanak- gu,
The Republic of Korea
8Cambridge School of Clinical Medicine, Cambridge Biomedical Campus,
Cambridge Institute of Therapeutic Immunology and Infectious Disease,
Cambridge, UK
8HsiaoA, etal. BMJ Open 2022;12:e052337. doi:10.1136/bmjopen-2021-052337
Open access
Contributors AH and VM conceptualised the study, led the protocol development,
field training and survey implementation in collaboration with H- JS, GDP, DV, MM,
BN, FM and ER. Data collection was supervised by DV, MM and BN, and monitored
by GDP, AH, VM, ER and H- JS. Data analysis and interpretation were done by AH
supported by VM and WQ. The manuscript was written by AH, supported by VM and
WQ. All authors have reviewed, edited and approved the final manuscript. AH and
VM are the guarantors and take full responsibility for the finished work and/or the
conduct of the study, had access to the data, and controlled the decision to publish.
Funding This research was conducted by International Vaccine Institute and
funded by Bill & Melinda Gates Foundation (OPP38590) and the UK Foreign,
Commonwealth and Development Office and Wellcome (214662/Z/18/Z). The
International Vaccine Institute acknowledges its donors including the Republic of
Korea, Swedish International Development Cooperation Agency and Republic of
India.
Competing interests None declared.
Patient and public involvement Patients and/or the public were involved in the
design, or conduct, or reporting or dissemination plans of this research. Refer to the
Methods section for further details.
Patient consent for publication Consent obtained directly from patient(s).
Ethics approval This study was approved by the National Health Sciences
Research Committee (NHSRC) of the Ministry of Health in Malawi (protocol
#16/2/1547; approval #1547) on 29 March 2016. The International Vaccine
Institute’s (IVI) Institutional Review Board (IRB) approved the study on 6 April
2016. All participants (or a parent/guardian) provided written informed consent
prior to interviews. For patients aged <12 years, consent was provided by the
parent/guardian, and in these cases, the patient/caregiver provided the interview
responses. For patients aged 12–17 years, ascent was provided by both the parent/
guardian and child. Adults aged ≥18 years provided consent directly. The IVI IRB and
the NHSRC approved the modification to expand to inclusion of clinically diagnosed
cases on 31 May 2017 and 31 July 2017, respectively. Training of all health
surveillance assistants on the modification occurred on 12 and 13 December 2017,
and the data collection continued until 31 March 2020.
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement All data relevant to the study are included in the
article or uploaded as supplementary information.
Supplemental material This content has been supplied by the author(s). It has
not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been
peer- reviewed. Any opinions or recommendations discussed are solely those
of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and
responsibility arising from any reliance placed on the content. Where the content
includes any translated material, BMJ does not warrant the accuracy and reliability
of the translations (including but not limited to local regulations, clinical guidelines,
terminology, drug names and drug dosages), and is not responsible for any error
and/or omissions arising from translation and adaptation or otherwise.
Open access This is an open access article distributed in accordance with the
Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits
others to copy, redistribute, remix, transform and build upon this work for any
purpose, provided the original work is properly cited, a link to the licence is given,
and indication of whether changes were made. See:https://creativecommons.org/
licenses/by/4.0/.
ORCID iDs
AmberHsiao http://orcid.org/0000-0003-2295-0886
FlorianMarks http://orcid.org/0000-0002-6043-7170
VittalMogasale http://orcid.org/0000-0003-0596-8072
REFERENCES
1 Ali M, Nelson AR, Lopez AL, etal. Updated global burden of cholera
in endemic countries. PLoS Negl Trop Dis 2015;9:e0003832.
2 Lessler J, Moore SM, Luquero FJ, etal. Mapping the burden
of cholera in sub- Saharan Africa and implications for control:
an analysis of data across geographical scales. Lancet
2018;391:1908–15.
3 Hsiao A, Hall AH, Mogasale V, etal. The health economics of cholera:
a systematic review. Vaccine 2018;36:4404–24.
4 Hsiao A, Desai SN, Mogasale V, etal. Lessons learnt from 12 oral
cholera vaccine campaigns in resource- poor settings. Bull World
Health Organ 2017;95:303–12.
5 Pezzoli L, Oral Cholera Vaccine Working Group of the Global Task
Force on Cholera Control. Global oral cholera vaccine use, 2013-
2018. Vaccine 2020;38 Suppl 1:A132- A140.
6 Msyamboza KP, Kagoli M, M'bang'ombe M, etal. Cholera outbreaks
in Malawi in 1998- 2012: social and cultural challenges in prevention
and control. J Infect Dev Ctries 2014;8:720–6.
7 Swerdlow DL, Malenga G, Begkoyian G, etal. Epidemic cholera
among refugees in Malawi, Africa: treatment and transmission.
Epidemiol Infect 1997;118:207–14.
8 World Health Organization. Cholera country profile. Malawi, 2010.
9 Government of Malawi. Malawi 2015 floods post disaster needs
assessment report 2015.
10 Msyamboza KP, M'bang'ombe M, Hausi H, etal. Feasibility and
acceptability of oral cholera vaccine mass vaccination campaign
in response to an outbreak and floods in Malawi. Pan Afr Med J
2016;23:203.
11 World Health Organization. Ending Cholera—A global roadmap to
2030, 2017.
12 Ilboudo PG, Huang XX, Ngwira B, etal. Cost- of- illness of cholera
to households and health facilities in rural Malawi. PLoS One
2017;12:e0185041.
13 Mukherjee P, Ghosh S, Ramamurthy T, etal. Evaluation of a rapid
immunochromatographic dipstick kit for diagnosis of cholera
emphasizes its outbreak utility. Jpn J Infect Dis 2010;63:234–8.
14 Sinha A, Sengupta S, Ghosh S, etal. Evaluation of a rapid dipstick
test for identifying cholera cases during the outbreak. Indian J Med
Res 2012;135:523–8.
15 World Health Organization, Department of Immunization Vaccines
and Biologicals. Guidelines for estimating the economic burden of
diarrhoeal disease, with focus on assessing the costs of rotavirus
diarrhoea. Geneva, Switzerland, 2005.
16 Poulos C, Riewpaiboon A, Stewart JF, etal. Costs of illness due to
endemic cholera. Epidemiol Infect 2012;140:500–9.
17 Lee J- S, Mogasale V, Lim JK, etal. A multi- country study of the
economic burden of dengue fever based on patient- specific field
surveys in Burkina Faso, Kenya, and Cambodia. PLoS Negl Trop Dis
2019;13:e0007164.
18 US Social Security Office of Retirement and Disability Policy. Social
security programs throughout the world: Africa, 2019. Available:
https://www.ssa.gov/policy/docs/progdesc/ssptw/2018-2019/africa/
malawi.html
19 Chima RI, Goodman CA, Mills A. The economic impact of malaria in
Africa: a critical review of the evidence. Health Policy 2003;63:17–36.
20 WageIndicator. org. Minimum Wage – Malawi, 2020. Available: https://
wageindicator.org/salary/minimum-wage/malawi/archive/20200101
[Accessed 1 Feb 2022].
21 The World Bank. Inflation consumer prices (annual %) – Malawi.
Available: https://data.worldbank.org/indicator/FP.CPI.TOTL.ZG?
locations=MW [Accessed 31 Jan 2022].
22 Reserve Bank of Malawi. Exchange rates. Available: https://www.
rbm.mw/Statistics/MajorRates [Accessed 31 Jan 2022].
23 Legido- Quigley H, Pocock N, Tan ST, etal. Healthcare is
not universal if undocumented migrants are excluded. BMJ
2019;18:l4160.
24 Morgan W AL, Hutubessy R, etal. Cost of treatment of cholera in
rural Malawi health facilities. (under preparation).
25 World Health Organization. The Abuja declaration: ten years on 2011.
Available: http://www.who.int/healthsystems/publications/abuja_
declaration/en/
26 Ministry of Health. Malawi health sector strategic plan II, 2017- 2022,
2017. Available: https://extranet.who.int/countryplanningcycles/
sites/default/files/planning_cycle_repository/malawi/health_sector_
strategic_plan_ii_030417_smt_dps.pdf [Accessed 20 Jan 2022].
27 M'bangombe M, Pezzoli L, Reeder B, etal. Oral cholera vaccine in
cholera prevention and control, Malawi. Bull World Health Organ
2018;96:428–35.
28 Sauvageot D, Saussier C, Gobeze A, etal. Oral cholera vaccine
coverage in hard- to- reach fishermen communities after two mass
campaigns, Malawi, 2016. Vaccine 2017;35:5194–200.