Abstract

Measles deaths highlight immunization program gaps. In the Child Health and Mortality Prevention Surveillance study in Mali, we observed a rise in under-5 measles-related deaths in 2022 that corresponded with increased measles cases at the same time and a decline in measles vaccine coverage in Mali in 2020.

As a highly contagious, vaccine-preventable disease with an estimated reproductive number of 12–18, the occurrence of measles and measles-related fatalities within a community serves as a sensitive indicator of suboptimal vaccination coverage [1, 2]. In 2019, approximately 69 800 children under the age of 5 years died from measles, with a disproportionate burden falling on sub-Saharan Africa (SSA), accounting for 78% of the global deaths [3].

Despite collective commitments from all World Health Organization (WHO) regions to eliminate measles by administering 2 doses of measles-containing vaccine (MCV) at age 9 and 15 months in areas with active measles transmission, and at 12 and ≥15 months in low-risk settings [4, 5] no region has experienced sustained elimination. Nevertheless, 83 individual countries achieved the goal in 2022 [6]. Achieving 95% vaccination coverage for both doses is imperative to interrupt measles transmission and attain herd immunity [7, 8].

The occurrence of measles deaths indicates that a substantial number of cases are occurring within the community [9]. However, incidence rates are difficult to estimate because of variable case fatality rates resulting from factors such as MCV dose receipt, nutritional status, age, and wealth index. Here, we describe measles-related deaths that occurred in the Child Health and Mortality Prevention Surveillance (CHAMPS) study in Bamako, Mali, in the context of local measles disease epidemiology, the pandemic of COVID-19, and MCV coverage in Mali during the same period.

METHODS

The CHAMPS network is a surveillance system to track the causes of death for stillbirths and children younger than 5 years of age at demographically characterized sites in Mali, Ethiopia, Sierra Leone, Mozambique, Kenya, South Africa, and Bangladesh, and the study methods were previously described [10–13]. Briefly, within a subset of deaths in which parental consent is obtained, we conduct minimally invasive tissue sampling to obtain biopsies of internal organs and collect whole blood, cerebrospinal fluid, as well as nasal, oral, pharyngeal, and rectal swabs. The specimens undergo evaluation through quantitative polymerase chain reaction using multiplexed TaqMan Array Cards, culture, histopathology with special stains, and immunohistochemistry as appropriate. Clinical history is gathered from medical records and verbal autopsies [14]. These data are reviewed by a panel of expert clinicians, pathologists, epidemiologists, and laboratorians using a standardized Determination of Cause of Death adjudication process in which the causal chain is determined per International Classification of Diseases and the WHO death certificate criteria, including the designation of an underlying and intermediate cause of death [15, 16]. In Mali, CHAMPS cause-of-death assessments are conducted in Bamako, covering Djikoroni-para and Banconi from 2017, with Sebenikoro added in 2022.

To provide a contextual backdrop for the CHAMPS measles deaths in Mali, we conducted a descriptive study by reviewing routine data from the Mali Ministry of Health, focusing on laboratory-confirmed measles cases detected during routine surveillance and MCV coverage. Additionally, we examined standardized measles incidence and MCV coverage rates from the WHO and United Nations International Children's Emergency Fund (UNICEF) [17]. In Mali, the administration of the first dose of MCV (MCV1) occurs at 9 months, followed by a second dose (MCV2) between 15 and 18 months of age.

RESULTS

Between August 2017 and December 2022, CHAMPS-Mali conducted minimally invasive tissue sampling on 562 children. Among these, 485 underwent the Determination of Cause of Death process, whereas 77 are pending adjudication. Eight (1.6%) children were identified as having measles in the causal chain of their death distributed across the years 2017 (1 case), 2018 (1 case), 2021 (2 cases), and 2022 (4 cases). The children's ages ranged from 4 months to 5 years; 5 cases were female. Of the 6 children who were age-eligible for MCV, 3 were unvaccinated, and vaccination status for the remaining 3 was unknown. Two children contracted measles at 4 and 8 months of age, before the age of routine measles vaccination. For all the children, the immediate cause of death was sepsis or pneumonia with measles infection as an underlying or morbid condition. All children had malnutrition as a morbid, underlying, or other significant condition and 5 children had concurrent gastroenteritis. The cases are summarized in Table 1.

Table 1.

Measles Deaths in CHAMPS—Clinical Case Summaries

Date of DeathAgeSexHIV DNA PCRNutritional StatusaMCV StatusClinical PresentationMeasles Positive TestsbPathology ReportImmediate Cause Of DeathcMorbid ConditioncUnderlying Conditions/Other Significant Conditionsc
November 20172 y, 11moFNegWHZ: −4.86
WAZ: −5.28
LAZ: −3.53
HCAZ: −2.45
MUAC Z: −4.18
UnkNot availableBlood
CSF
Lung
ONP
Lung: neutrophilic interstitial pneumonitis.
Evidence of Escherichia. coli and Klebsiella pneumoniae in vessels
Liver: moderate steatosis (small and large droplet)
CNS: intravascular fibrin thrombi and evidence of E coli and K pneumoniae
Sepsis (E coli)Sepsis (K pneumoniae)Measle/severe malnutrition
June
2018
3 y, 9moFNegWHZ: −2.41
WAZ: −0.85
LAZ: 1.25
HCZ: −0.12
MUAC Z: −0.08
NoFever, cough, difficulty breathing, rash, diarrhea, vomiting, oral mycosis, night sweats, loss of consciousness, convulsion, agitation, nightmares, chest pain, dysphagia, odynophagiaBlood
CSF
Lung
ONP
Lung: bronchopneumonia and aspiration pneumonia with mixed bacteria and gastrointestinal contents. Evidence of measles virus, Streptococcus species and Hemophilus influenzae.
Liver: mild sinusoidal leukocytosis
Polymicrobial pneumonia (H influenzae, S pneumoniae)Measles/ Rickets, Enteritis, use of traditional medication
September 20211 y, 4moMNegWHZ: −3.88
WAZ: −3.22
LAZ: 0.95
HCZ: −2.9
MUAC Z: −3.22
UnkFever, cough, difficulty breathing, rash, diarrhea, vomiting, oral mycosis, night sweats, loss of consciousness, convulsion, discoloration of eyes, distended abdomen.Blood
Lung
ONP
Lung: interstitial pneumonitis, and bronchopneumonia. Evidence of measles, Klebsiella species and Streptococcus species.
Liver: mild congestion and large droplet steatosis, focal intravascular bacteria.
Polymicrobial sepsis (K pneumoniae, S. aureus, Moraxella catarrhalis)Bacterial and viral pneumonia (K pneumoniae, S aureus, M catarrhalis, measles).
Gastroenteritis
Measles/severe malnutrition
November 2021∼2yFNegWHZ: −2.64
WAZ: NA
HAZ: NA
HCZ: NA
MUAC Z: NA
NoFever, cough, pruritis, boils on the skin, diarrhea, edema of the limbs, face swelling, anal prolapse, foot ulcer, weight loss, polydipsiaBlood
ONP
Lung: inadequate sample
Liver: severe steatosis and sinusoidal leukocytes
Polymicrobial sepsis (E coli/Shigella,
Pseudomonas aeruginosa, S pneumoniae,
M catarrhalis)
Measles
Shigellosis with rectal
prolapse
Diarrhea
Kwashiorkor/
bullous impetigo
February 2022<5yFNegWHZ: −2.9
WAZ: NA
HAZ: NA
HCZ: NA
MUAC Z: NA
UnkNot availableBlood
CSF
Lung
ONP
Lung: interstitial pneumonitis, and bronchopneumonia. Evidence of Klebsiella species and Streptococcus species.
Liver: mild congestion and mild steatosis
Pneumonia (K pneumoniae and S pneumoniae)Moderate malnutritionMeasles/disseminated herpes simplex virus 1 infection
March
2022
11moMUnkWHZ: −3.22
WAZ: −4.12
HAZ: −3.64
HCZ: −3.53
MUAC Z: −1.53
NoFever, cough, difficulty breathing, rash, diarrhea, night sweats, runny nose, sunken eyes.Blood
Lung
ONP
Lung: interstitial pneumonitis, and bronchopneumonia. Evidence of Streptococcus species.
Liver: mild congestion and severe steatosis.
CNS: intravascular leukocytosis
Pneumonia (S pneumoniae and Group A streptococcus [GAS])Sepsis (Staphylococcus aureus, S pneumoniae, GAS, and E coli/Shigella)
Severe malnutrition
Diarrhea
Measles
May
2022
4moMUnkWHZ: −3.73
WAZ: −5.03
HAZ: −3.68
HCZ: −2.07
MUAC: −5.58
NAFever, coughBlood
Lung
Lung: bronchopneumonia. Evidence of cytomegalovirus (CMV), gram-variable rods and Pneumocystis jiroveci (PJP).
Liver: mild congestion, severe steatosis, and sinusoidal leukocytosis
CNS: intravascular leukocytosis
Polymicrobial sepsis (S pneumoniae, P aeruginosa, K
pneumonia, M catarrhalis, Acinetobacter
baumanii, E coli/Shigella)
Disseminated measles.
Enteric infection (Norovirus,
campylobacter)
Pneumonia
(S pneumoniae measles, PJP)
Severe malnutrition (acute on chronic)
Immunodeficiency of unknown cause
May
2022
8moFUnkWHZ: −3.51
WAZ: −2.24
LAZ: 0.69
HCZ: −0.68
MUAC Z: −2.95
NACough, difficulty breathing, rash, diarrheaBlood
Lung
ONP
Lung: interstitial pneumonitis. Evidence of Hemophilus species
Liver: mild congestion and mild steatosis.
Pneumonia (H influenzae)Moderate malnutrition
Diarrhea
Measles
Date of DeathAgeSexHIV DNA PCRNutritional StatusaMCV StatusClinical PresentationMeasles Positive TestsbPathology ReportImmediate Cause Of DeathcMorbid ConditioncUnderlying Conditions/Other Significant Conditionsc
November 20172 y, 11moFNegWHZ: −4.86
WAZ: −5.28
LAZ: −3.53
HCAZ: −2.45
MUAC Z: −4.18
UnkNot availableBlood
CSF
Lung
ONP
Lung: neutrophilic interstitial pneumonitis.
Evidence of Escherichia. coli and Klebsiella pneumoniae in vessels
Liver: moderate steatosis (small and large droplet)
CNS: intravascular fibrin thrombi and evidence of E coli and K pneumoniae
Sepsis (E coli)Sepsis (K pneumoniae)Measle/severe malnutrition
June
2018
3 y, 9moFNegWHZ: −2.41
WAZ: −0.85
LAZ: 1.25
HCZ: −0.12
MUAC Z: −0.08
NoFever, cough, difficulty breathing, rash, diarrhea, vomiting, oral mycosis, night sweats, loss of consciousness, convulsion, agitation, nightmares, chest pain, dysphagia, odynophagiaBlood
CSF
Lung
ONP
Lung: bronchopneumonia and aspiration pneumonia with mixed bacteria and gastrointestinal contents. Evidence of measles virus, Streptococcus species and Hemophilus influenzae.
Liver: mild sinusoidal leukocytosis
Polymicrobial pneumonia (H influenzae, S pneumoniae)Measles/ Rickets, Enteritis, use of traditional medication
September 20211 y, 4moMNegWHZ: −3.88
WAZ: −3.22
LAZ: 0.95
HCZ: −2.9
MUAC Z: −3.22
UnkFever, cough, difficulty breathing, rash, diarrhea, vomiting, oral mycosis, night sweats, loss of consciousness, convulsion, discoloration of eyes, distended abdomen.Blood
Lung
ONP
Lung: interstitial pneumonitis, and bronchopneumonia. Evidence of measles, Klebsiella species and Streptococcus species.
Liver: mild congestion and large droplet steatosis, focal intravascular bacteria.
Polymicrobial sepsis (K pneumoniae, S. aureus, Moraxella catarrhalis)Bacterial and viral pneumonia (K pneumoniae, S aureus, M catarrhalis, measles).
Gastroenteritis
Measles/severe malnutrition
November 2021∼2yFNegWHZ: −2.64
WAZ: NA
HAZ: NA
HCZ: NA
MUAC Z: NA
NoFever, cough, pruritis, boils on the skin, diarrhea, edema of the limbs, face swelling, anal prolapse, foot ulcer, weight loss, polydipsiaBlood
ONP
Lung: inadequate sample
Liver: severe steatosis and sinusoidal leukocytes
Polymicrobial sepsis (E coli/Shigella,
Pseudomonas aeruginosa, S pneumoniae,
M catarrhalis)
Measles
Shigellosis with rectal
prolapse
Diarrhea
Kwashiorkor/
bullous impetigo
February 2022<5yFNegWHZ: −2.9
WAZ: NA
HAZ: NA
HCZ: NA
MUAC Z: NA
UnkNot availableBlood
CSF
Lung
ONP
Lung: interstitial pneumonitis, and bronchopneumonia. Evidence of Klebsiella species and Streptococcus species.
Liver: mild congestion and mild steatosis
Pneumonia (K pneumoniae and S pneumoniae)Moderate malnutritionMeasles/disseminated herpes simplex virus 1 infection
March
2022
11moMUnkWHZ: −3.22
WAZ: −4.12
HAZ: −3.64
HCZ: −3.53
MUAC Z: −1.53
NoFever, cough, difficulty breathing, rash, diarrhea, night sweats, runny nose, sunken eyes.Blood
Lung
ONP
Lung: interstitial pneumonitis, and bronchopneumonia. Evidence of Streptococcus species.
Liver: mild congestion and severe steatosis.
CNS: intravascular leukocytosis
Pneumonia (S pneumoniae and Group A streptococcus [GAS])Sepsis (Staphylococcus aureus, S pneumoniae, GAS, and E coli/Shigella)
Severe malnutrition
Diarrhea
Measles
May
2022
4moMUnkWHZ: −3.73
WAZ: −5.03
HAZ: −3.68
HCZ: −2.07
MUAC: −5.58
NAFever, coughBlood
Lung
Lung: bronchopneumonia. Evidence of cytomegalovirus (CMV), gram-variable rods and Pneumocystis jiroveci (PJP).
Liver: mild congestion, severe steatosis, and sinusoidal leukocytosis
CNS: intravascular leukocytosis
Polymicrobial sepsis (S pneumoniae, P aeruginosa, K
pneumonia, M catarrhalis, Acinetobacter
baumanii, E coli/Shigella)
Disseminated measles.
Enteric infection (Norovirus,
campylobacter)
Pneumonia
(S pneumoniae measles, PJP)
Severe malnutrition (acute on chronic)
Immunodeficiency of unknown cause
May
2022
8moFUnkWHZ: −3.51
WAZ: −2.24
LAZ: 0.69
HCZ: −0.68
MUAC Z: −2.95
NACough, difficulty breathing, rash, diarrheaBlood
Lung
ONP
Lung: interstitial pneumonitis. Evidence of Hemophilus species
Liver: mild congestion and mild steatosis.
Pneumonia (H influenzae)Moderate malnutrition
Diarrhea
Measles

Abbreviations: CSF, cerebrospinal fluid; HCZ, head circumference Z score; LAZ, length for age Z score; MUACZ, mean upper arm circumference Z score; NA, nonapplicable; Neg, negative; ONP, oral, nasal, and pharyngeal specimen; Unk, unknown; WAZ, weight for age Z score; WHZ, weight for height Z score.

aNutritional status Z score interpretation: Mild malnutrition = −1.0 to −1.9; moderate malnutrition = −2.0 to −2.9; and severe malnutrition = ≥−3.0.

bTested through quantitative polymerase chain reaction using multiplexed TaqMan Array Cards, culture, histopathology with special stains, or immunohistochemistry.

cCausal death pathways as determined through the Determination of Cause of Death process: immediate cause of death = disease or condition that directly preceded or directly led to death; morbid condition = disease or condition that was the intermediate cause of death; underlying condition = disease or injury that initiated the train of events leading directly to death; other significant disease = condition not directly associated or in the causal chain of death, but still contributed to the death.

Table 1.

Measles Deaths in CHAMPS—Clinical Case Summaries

Date of DeathAgeSexHIV DNA PCRNutritional StatusaMCV StatusClinical PresentationMeasles Positive TestsbPathology ReportImmediate Cause Of DeathcMorbid ConditioncUnderlying Conditions/Other Significant Conditionsc
November 20172 y, 11moFNegWHZ: −4.86
WAZ: −5.28
LAZ: −3.53
HCAZ: −2.45
MUAC Z: −4.18
UnkNot availableBlood
CSF
Lung
ONP
Lung: neutrophilic interstitial pneumonitis.
Evidence of Escherichia. coli and Klebsiella pneumoniae in vessels
Liver: moderate steatosis (small and large droplet)
CNS: intravascular fibrin thrombi and evidence of E coli and K pneumoniae
Sepsis (E coli)Sepsis (K pneumoniae)Measle/severe malnutrition
June
2018
3 y, 9moFNegWHZ: −2.41
WAZ: −0.85
LAZ: 1.25
HCZ: −0.12
MUAC Z: −0.08
NoFever, cough, difficulty breathing, rash, diarrhea, vomiting, oral mycosis, night sweats, loss of consciousness, convulsion, agitation, nightmares, chest pain, dysphagia, odynophagiaBlood
CSF
Lung
ONP
Lung: bronchopneumonia and aspiration pneumonia with mixed bacteria and gastrointestinal contents. Evidence of measles virus, Streptococcus species and Hemophilus influenzae.
Liver: mild sinusoidal leukocytosis
Polymicrobial pneumonia (H influenzae, S pneumoniae)Measles/ Rickets, Enteritis, use of traditional medication
September 20211 y, 4moMNegWHZ: −3.88
WAZ: −3.22
LAZ: 0.95
HCZ: −2.9
MUAC Z: −3.22
UnkFever, cough, difficulty breathing, rash, diarrhea, vomiting, oral mycosis, night sweats, loss of consciousness, convulsion, discoloration of eyes, distended abdomen.Blood
Lung
ONP
Lung: interstitial pneumonitis, and bronchopneumonia. Evidence of measles, Klebsiella species and Streptococcus species.
Liver: mild congestion and large droplet steatosis, focal intravascular bacteria.
Polymicrobial sepsis (K pneumoniae, S. aureus, Moraxella catarrhalis)Bacterial and viral pneumonia (K pneumoniae, S aureus, M catarrhalis, measles).
Gastroenteritis
Measles/severe malnutrition
November 2021∼2yFNegWHZ: −2.64
WAZ: NA
HAZ: NA
HCZ: NA
MUAC Z: NA
NoFever, cough, pruritis, boils on the skin, diarrhea, edema of the limbs, face swelling, anal prolapse, foot ulcer, weight loss, polydipsiaBlood
ONP
Lung: inadequate sample
Liver: severe steatosis and sinusoidal leukocytes
Polymicrobial sepsis (E coli/Shigella,
Pseudomonas aeruginosa, S pneumoniae,
M catarrhalis)
Measles
Shigellosis with rectal
prolapse
Diarrhea
Kwashiorkor/
bullous impetigo
February 2022<5yFNegWHZ: −2.9
WAZ: NA
HAZ: NA
HCZ: NA
MUAC Z: NA
UnkNot availableBlood
CSF
Lung
ONP
Lung: interstitial pneumonitis, and bronchopneumonia. Evidence of Klebsiella species and Streptococcus species.
Liver: mild congestion and mild steatosis
Pneumonia (K pneumoniae and S pneumoniae)Moderate malnutritionMeasles/disseminated herpes simplex virus 1 infection
March
2022
11moMUnkWHZ: −3.22
WAZ: −4.12
HAZ: −3.64
HCZ: −3.53
MUAC Z: −1.53
NoFever, cough, difficulty breathing, rash, diarrhea, night sweats, runny nose, sunken eyes.Blood
Lung
ONP
Lung: interstitial pneumonitis, and bronchopneumonia. Evidence of Streptococcus species.
Liver: mild congestion and severe steatosis.
CNS: intravascular leukocytosis
Pneumonia (S pneumoniae and Group A streptococcus [GAS])Sepsis (Staphylococcus aureus, S pneumoniae, GAS, and E coli/Shigella)
Severe malnutrition
Diarrhea
Measles
May
2022
4moMUnkWHZ: −3.73
WAZ: −5.03
HAZ: −3.68
HCZ: −2.07
MUAC: −5.58
NAFever, coughBlood
Lung
Lung: bronchopneumonia. Evidence of cytomegalovirus (CMV), gram-variable rods and Pneumocystis jiroveci (PJP).
Liver: mild congestion, severe steatosis, and sinusoidal leukocytosis
CNS: intravascular leukocytosis
Polymicrobial sepsis (S pneumoniae, P aeruginosa, K
pneumonia, M catarrhalis, Acinetobacter
baumanii, E coli/Shigella)
Disseminated measles.
Enteric infection (Norovirus,
campylobacter)
Pneumonia
(S pneumoniae measles, PJP)
Severe malnutrition (acute on chronic)
Immunodeficiency of unknown cause
May
2022
8moFUnkWHZ: −3.51
WAZ: −2.24
LAZ: 0.69
HCZ: −0.68
MUAC Z: −2.95
NACough, difficulty breathing, rash, diarrheaBlood
Lung
ONP
Lung: interstitial pneumonitis. Evidence of Hemophilus species
Liver: mild congestion and mild steatosis.
Pneumonia (H influenzae)Moderate malnutrition
Diarrhea
Measles
Date of DeathAgeSexHIV DNA PCRNutritional StatusaMCV StatusClinical PresentationMeasles Positive TestsbPathology ReportImmediate Cause Of DeathcMorbid ConditioncUnderlying Conditions/Other Significant Conditionsc
November 20172 y, 11moFNegWHZ: −4.86
WAZ: −5.28
LAZ: −3.53
HCAZ: −2.45
MUAC Z: −4.18
UnkNot availableBlood
CSF
Lung
ONP
Lung: neutrophilic interstitial pneumonitis.
Evidence of Escherichia. coli and Klebsiella pneumoniae in vessels
Liver: moderate steatosis (small and large droplet)
CNS: intravascular fibrin thrombi and evidence of E coli and K pneumoniae
Sepsis (E coli)Sepsis (K pneumoniae)Measle/severe malnutrition
June
2018
3 y, 9moFNegWHZ: −2.41
WAZ: −0.85
LAZ: 1.25
HCZ: −0.12
MUAC Z: −0.08
NoFever, cough, difficulty breathing, rash, diarrhea, vomiting, oral mycosis, night sweats, loss of consciousness, convulsion, agitation, nightmares, chest pain, dysphagia, odynophagiaBlood
CSF
Lung
ONP
Lung: bronchopneumonia and aspiration pneumonia with mixed bacteria and gastrointestinal contents. Evidence of measles virus, Streptococcus species and Hemophilus influenzae.
Liver: mild sinusoidal leukocytosis
Polymicrobial pneumonia (H influenzae, S pneumoniae)Measles/ Rickets, Enteritis, use of traditional medication
September 20211 y, 4moMNegWHZ: −3.88
WAZ: −3.22
LAZ: 0.95
HCZ: −2.9
MUAC Z: −3.22
UnkFever, cough, difficulty breathing, rash, diarrhea, vomiting, oral mycosis, night sweats, loss of consciousness, convulsion, discoloration of eyes, distended abdomen.Blood
Lung
ONP
Lung: interstitial pneumonitis, and bronchopneumonia. Evidence of measles, Klebsiella species and Streptococcus species.
Liver: mild congestion and large droplet steatosis, focal intravascular bacteria.
Polymicrobial sepsis (K pneumoniae, S. aureus, Moraxella catarrhalis)Bacterial and viral pneumonia (K pneumoniae, S aureus, M catarrhalis, measles).
Gastroenteritis
Measles/severe malnutrition
November 2021∼2yFNegWHZ: −2.64
WAZ: NA
HAZ: NA
HCZ: NA
MUAC Z: NA
NoFever, cough, pruritis, boils on the skin, diarrhea, edema of the limbs, face swelling, anal prolapse, foot ulcer, weight loss, polydipsiaBlood
ONP
Lung: inadequate sample
Liver: severe steatosis and sinusoidal leukocytes
Polymicrobial sepsis (E coli/Shigella,
Pseudomonas aeruginosa, S pneumoniae,
M catarrhalis)
Measles
Shigellosis with rectal
prolapse
Diarrhea
Kwashiorkor/
bullous impetigo
February 2022<5yFNegWHZ: −2.9
WAZ: NA
HAZ: NA
HCZ: NA
MUAC Z: NA
UnkNot availableBlood
CSF
Lung
ONP
Lung: interstitial pneumonitis, and bronchopneumonia. Evidence of Klebsiella species and Streptococcus species.
Liver: mild congestion and mild steatosis
Pneumonia (K pneumoniae and S pneumoniae)Moderate malnutritionMeasles/disseminated herpes simplex virus 1 infection
March
2022
11moMUnkWHZ: −3.22
WAZ: −4.12
HAZ: −3.64
HCZ: −3.53
MUAC Z: −1.53
NoFever, cough, difficulty breathing, rash, diarrhea, night sweats, runny nose, sunken eyes.Blood
Lung
ONP
Lung: interstitial pneumonitis, and bronchopneumonia. Evidence of Streptococcus species.
Liver: mild congestion and severe steatosis.
CNS: intravascular leukocytosis
Pneumonia (S pneumoniae and Group A streptococcus [GAS])Sepsis (Staphylococcus aureus, S pneumoniae, GAS, and E coli/Shigella)
Severe malnutrition
Diarrhea
Measles
May
2022
4moMUnkWHZ: −3.73
WAZ: −5.03
HAZ: −3.68
HCZ: −2.07
MUAC: −5.58
NAFever, coughBlood
Lung
Lung: bronchopneumonia. Evidence of cytomegalovirus (CMV), gram-variable rods and Pneumocystis jiroveci (PJP).
Liver: mild congestion, severe steatosis, and sinusoidal leukocytosis
CNS: intravascular leukocytosis
Polymicrobial sepsis (S pneumoniae, P aeruginosa, K
pneumonia, M catarrhalis, Acinetobacter
baumanii, E coli/Shigella)
Disseminated measles.
Enteric infection (Norovirus,
campylobacter)
Pneumonia
(S pneumoniae measles, PJP)
Severe malnutrition (acute on chronic)
Immunodeficiency of unknown cause
May
2022
8moFUnkWHZ: −3.51
WAZ: −2.24
LAZ: 0.69
HCZ: −0.68
MUAC Z: −2.95
NACough, difficulty breathing, rash, diarrheaBlood
Lung
ONP
Lung: interstitial pneumonitis. Evidence of Hemophilus species
Liver: mild congestion and mild steatosis.
Pneumonia (H influenzae)Moderate malnutrition
Diarrhea
Measles

Abbreviations: CSF, cerebrospinal fluid; HCZ, head circumference Z score; LAZ, length for age Z score; MUACZ, mean upper arm circumference Z score; NA, nonapplicable; Neg, negative; ONP, oral, nasal, and pharyngeal specimen; Unk, unknown; WAZ, weight for age Z score; WHZ, weight for height Z score.

aNutritional status Z score interpretation: Mild malnutrition = −1.0 to −1.9; moderate malnutrition = −2.0 to −2.9; and severe malnutrition = ≥−3.0.

bTested through quantitative polymerase chain reaction using multiplexed TaqMan Array Cards, culture, histopathology with special stains, or immunohistochemistry.

cCausal death pathways as determined through the Determination of Cause of Death process: immediate cause of death = disease or condition that directly preceded or directly led to death; morbid condition = disease or condition that was the intermediate cause of death; underlying condition = disease or injury that initiated the train of events leading directly to death; other significant disease = condition not directly associated or in the causal chain of death, but still contributed to the death.

National data across all age groups in Mali for the same period showed a similar trend of increased frequency of laboratory-confirmed measles after 2020 (Figure 1). The reported measles cases decreased from 87 in 2016 to 26 in 2017 but then increased nearly 20-fold to 476 in 2018. The numbers remained stable thereafter, before doubling to 908 in 2021 and settling at 748 in 2022. The WHO/UNICEF estimates for measles incidence per 1 million population reflected this surge, rising from 1.3 cases in 2017 to 22.1 in 2019 and reaching 94.7 in 2021 before dropping to 33.9 in 2022 [17].

Reported measles cases and measles-containing vaccine coverage from Mali Ministry of Health administrative data. MCV2 was first introduced in 2019 in Mali. MCV1, measles containing vaccine 1; MCV2, measles containing vaccine 2; WHO, World Health Organization/United Nations International Children's Emergency Fund estimates of Mali measles-containing vaccine coverage.
Figure 1.

Reported measles cases and measles-containing vaccine coverage from Mali Ministry of Health administrative data. MCV2 was first introduced in 2019 in Mali. MCV1, measles containing vaccine 1; MCV2, measles containing vaccine 2; WHO, World Health Organization/United Nations International Children's Emergency Fund estimates of Mali measles-containing vaccine coverage.

Correspondingly, the periods of increased measles cases in 2017–2018 and 2020–2021 aligned with declines in MCV1 coverage (Figure 1). Mali's Ministry of Health reported consistent national MCV1 coverage exceeding 90% since 2016, except for dips in 2017 (83%) and 2020 (87%). WHO/UNICEF standardized estimates of MCV1 coverage in Mali mirrored this, holding steady at 70% since 2016 but dropping to 62% in 2020 [17]. Since the introduction of MCV2 into routine immunization in 2019, coverage has risen from 5.5% to 59% in 2022, as indicated by local data, aligning closely with WHO/UNICEF estimates of 4% and 44%, respectively, for the same period (Figure 1) [17]. Mali had 2 catch-up measles vaccination campaigns around our study period in 2015 and 2019 and had administrative coverage rates of 112.5% and 108.9%. Follow-up national administrative surveys reported coverage rates of 93.5% and 82.7%, respectively.

DISCUSSION

We report a notable increase in measles-related deaths among children younger than age 5 years old in 2022 compared with previous years in our study, corresponding to a surge in measles cases and a decline in MCV1 vaccine coverage in Mali. The deceased children were mainly very young with 25% being too young to be vaccinated, unvaccinated, and malnourished, and exhibiting measles-compatible symptoms complicated by bacterial pneumonia, gastroenteritis, and sepsis [18, 19]. Measles mortality rates are often challenging to accurately estimate because of the lack of mortality data, and varying reporting practices depending on factors such as community versus hospital deaths, age, nutritional status, associated complications, and country. Moreover, they are often underestimated in low- and middle-income settings [20]. Nonetheless, our 4 observed deaths in 2022 corroborate a manifold rise in measles community circulation in Bamako from 2019 to 2022 .

The increase in measles cases in 2022 was preceded by a 6% and 3% drop in WHO/UNICEF and Mali estimates of MCV coverage in 2020, pointing to immunization gaps as a potential contributing factor to the outbreak. The 2 notable events in 2020 were the COVID-19 pandemic, which was first detected in Mali in March of that year, and political instability that heightened during the national elections of 2020 [21, 22]. These 2 events likely led to insecurity and decreased vaccination session attendance, potentially increasing the pool of susceptible children to measles [23]. This is supported by global data that shows declination in routine childhood immunization coverage and outreach services globally during 2020 [24]. Notably, the MCV1 coverage rate reported by the WHO/UNICEF was lower than that reported by the Mali Ministry of Health. WHO/UNICEF estimates were based on coverage surveys and not country estimates because of inconsistencies in the country's data [23]. Still, the trend of the coverage is similar.

The resurgence of measles after the COVID-19 pandemic was not unique to Mali, with similar trends observed in other SSA countries. Liberia saw a >6-fold increase in its incidence of measles cases per 1 million population from 214 to 1565.2, which was associated with a drop in MCV1 coverage from 68% in 2019 to 61% in 2021 [17]. Other SSA countries that saw a significant increase in their measles incidence were Somalia, South Africa, Ethiopia, and Côte d'Ivoire, and the outbreaks were associated with MCV coverage rates that ranged from 46% to 85% [17, 25, 26]. Additionally, measles catch-up vaccination campaigns were delayed because of the COVID-19 pandemic [27]. In fact, in the general SSA region between 2019 and 2021, estimated annual measles cases and deaths increased by 22% and 8%, respectively, MCV1 coverage decreased from 70% to 68%, the number of countries with ≥95% coverage decreased from 6 to 3, and no country in the WHO African region had received verification of measles elimination [28]. This set back the measles elimination targets for the continent by several years [29]. Similar trends have been observed globally, and none of the WHO regions has recovered MCV coverage levels from 2019 [30].

Our data on measles deaths highlight the risk of measles faced by young infants during the “window of vulnerability” when maternal antibodies wane before vaccine eligibility at 9 months. It was previously shown in Mali that many infants are susceptible to measles before 9 months of age [31, 32]. However, routine immunization is not recommended for these younger children because of lower immunogenicity; therefore, achieving herd immunity is paramount to protect these vulnerable children from infection. Unfortunately, except for 2022, Mali's MCV1 coverage has fallen short of the 95% elimination vaccination coverage rate, with MCV2 coverage lagging further behind. Despite measles catch-up campaigns in 2015 and 2019, our data suggest ongoing community transmission. Further catch-up campaigns are needed, especially after 2020 when the rate of accumulation of susceptible cases may have been higher than previous years [24, 33]. Regular catch-up campaigns, including during immunization program disruptions, have proven effective in filling immunization gaps and controlling measles [34–37]. Our study captures measles deaths that may have otherwise gone unnoticed during routine surveillance. The main limitation is that it is descriptive and cannot establish a statistical association between the drop in MCV coverage and rise in measles cases. We do not have data on the reasons for missed vaccination in the CHAMPS measles cases. Nonetheless, our results tally with local data on measles transmission. The trends we report align with WHO/UNICEF standardized data and are consistent with measles outbreaks occurring in other similar settings.

CONCLUSION

Measles continues to circulate among infants and young children in Mali, as evidenced by our mortality surveillance, particularly following the decline in MCV coverage in 2020. It is imperative to implement catch-up immunization efforts to reach children who were inadvertently missed during routine vaccination activities.

Notes

Acknowledgments. The authors express gratitude to all participating families, the local communities, and the Mali Ministry of Health for supporting CHAMPS study activities. The authors also acknowledge the staff of the Centre pour le Développement des Vaccins-Mali who were instrumental in data collection and Andrew Lentinin for his help in creating the figure.

Financial support. This work was supported by the Bill & Melinda Gates Foundation [grant number OPP1126780 to K.L.K.]. Although the funder contributed to discussions regarding study design and data collection, they were not involved in conducting the study, managing, analyzing, or interpreting the data, preparing, reviewing, or approving the manuscript, nor in the decision to submit the manuscript for publication.

Data Availability. CHAMPS data are open access and datasets are available for download or request on www.champshealth.org.

Author Contributions. M.D.T., K.L.K., and S.O.S. conceived the study. A.M.B., J.J., D.S., N.K., S.S., F.C.H., C.T.T., A.T., C.B.T., B.G., and S.O.S. executed the study and collected data. N.N.N. and M.D.T. conducted the literature review, data analysis, and writing of the manuscript. All authors contributed substantially to the review, revision of the manuscript, and have read and approved the final manuscript.

Patient Consent Statement. Written consent for the CHAMPS study was obtained from the parents or guardians of the participants. CHAMPS was approved by the Faculté de Médecine, Pharmacie et Odonto-Stomatologie of Mali, the Ministry of Health of Mali, and the University of Maryland, Baltimore institutional review board.

References

1

John
J
.
Measles: a canary in the coal mines?
Indian J Pediatr
2016
;
83
:
195
6
.

2

Guerra
FM
,
Bolotin
S
,
Lim
G
, et al.
The basic reproduction number (R0) of measles: a systematic review
.
Lancet Infect Dis
2017
;
17
:
e420
8
.

3

Global Burden of Disease Collaborative Network.
Global burden of disease, measles—level 3 cause. 2020. Available at: https://www.healthdata.org/results/gbd_summaries/2019/measles-level-3-cause

4

World Health Organization
.
Measles vaccines: WHO position paper—April 2017
.
Wkly Epidemiol Rep
2017
;
17
:
205
28
.

5

World Health Organization
. Immunization agenda 2030. 2020. Available at: https://www.who.int/docs/default-source/immunization/strategy/ia2030/ia2030-document-en.pdf

6

Minta
AA
,
Ferrari
M
,
Antoni
S
, et al.
Progress toward measles elimination—worldwide, 2000–2022
.
MMWR Morb Mortal Wkly Rep
2023
;
72
:
1262
8
.

7

World Health Organization
. Measles and rubella strategic framework. 2021 Available at: https://www.who.int/publications/i/item/measles-and-rubella-strategic-framework-2021-2030

8

Moss
WJ
,
Strebel
P
.
Biological feasibility of measles eradication
.
J Infect Dis
2011
;
2041
(
Suppl 1
):
S47
53
.

9

Sbarra
AN
,
Mosser
JF
,
Jit
M
, et al.
Estimating national-level measles case–fatality ratios in low-income and middle-income countries: an updated systematic review and modelling study
.
Lancet Glob Health
2023
;
11
:
e516
24
.

10

Rakislova
N
,
Fernandes
F
,
Lovane
L
, et al.
Standardization of minimally invasive tissue sampling specimen collection and pathology training for the Child Health and Mortality Prevention Surveillance Network
.
Clin Infect Dis
2019
;
69
:
S302
10
.

11

Martines
RB
,
Ritter
JM
,
Gary
J
, et al.
Pathology and telepathology methods in the Child Health and Mortality Prevention Surveillance Network
.
Clin Infect Dis
2019
;
69
:
S322
32
.

12

Diaz
MH
,
Waller
JL
,
Theodore
MJ
, et al.
Development and implementation of Multiplex TaqMan array cards for specimen testing at Child Health and Mortality Prevention surveillance site laboratories
.
Clin Infect Dis
2019
;
69
:
S311
21
.

13

Salzberg
NT
,
Sivalogan
K
,
Bassat
Q
, et al.
Mortality surveillance methods to identify and characterize deaths in Child Health and Mortality Prevention surveillance network sites
.
Clin Infect Dis
2019
;
69
:
S262
73
.

15

Blau
DM
,
Caneer
JP
,
Philipsborn
RP
, et al.
Overview and development of the child health and mortality prevention surveillance determination of cause of death (DeCoDe) process and DeCoDe diagnosis standards
.
Clin Infect Dis
2019
;
69
(
Suppl 4
):
S333
41
.

16

World Health Organization
. The WHO application of ICD-10 to deaths during the perinatal period: ICD-PM. WHO. 2016 Available at: https://www.who.int/publications/i/item/9789241549752

17

World Health Organization
. WHO Immunization Data Portal. 2022. WHO immunization portal. Available at: https://immunizationdata.who.int/pages/coverage/mcv.html

18

Alves Graber
EM
,
Andrade
FJ
,
Bost
W
,
Gibbs
MA
.
An update and review of measles for emergency physicians
.
J Emerg Med
2020
;
58
:
610
5
.

19

Perry
RT
,
Halsey
NA.
The clinical significance of measles: a review
.
J Infect Dis.
2004
;
189
(
Suppl 1
):
S4
16
.

20

Cairns
KL
,
Nandy
R
,
Grais
RF
.
Challenges in measuring measles case fatality ratios in settings without vital registration
.
Emerg Themes Epidemiol
2010
;
7
:
4
.

21

Human Rights Watch. World Report 2021—Mali. 2021. Available at: https://www.hrw.org/world-report/2021/country-chapters/mali

22

Ahmed
A
,
Ly
MA
,
Diarra
BA
, et al.
Challenges to the implementation and adoption of physical distancing measures against COVID-19 by internally displaced people in Mali: a qualitative study
.
Confl Health
2021
;
15
:
88
.

23

World Health Organization
. Mali: WHO and UNICEF estimates of immunization coverage: 2022 revision. 2022. Available at: https://data.unicef.org/wp-content/uploads/cp/immunisation/mli.pdf.

24

Shet
A
,
Carr
K
,
Danovaro-Holliday
MC
, et al.
Impact of the SARS-CoV-2 pandemic on routine immunisation services: evidence of disruption and recovery from 170 countries and territories
.
Lancet Glob Health
2022
;
10
:
e186
94
.

25

Oduoye
MO
,
Zuhair
V
,
Marbell
A
, et al.
The recent measles outbreak in South African region is due to low vaccination coverage. What should we do to mitigate it?
New Microbes New Infect
2023
;
54
:
101164
.

26

Nchasi
G
,
Paul
IK
,
Sospeter
SB
,
Mallya
MR
,
Ruaichi
J
,
Malunga
J
.
Measles outbreak in sub-Saharan Africa amidst COVID-19: a rising concern, efforts, challenges, and future recommendations
.
Ann Med Surg (Lond)
2022
;
81
:
104264
.

27

Ho
LL
,
Gurung
S
,
Mirza
I
, et al.
Impact of the SARS-CoV-2 pandemic on vaccine-preventable disease campaigns
.
Int J Infect Dis
2022
;
119
:
201
9
.

28

Masresha
BG
,
Hatcher
C
,
Lebo
E
, et al.
Progress toward measles elimination - African region, 2017-2021
.
MMWR Morb Mortal Wkly Rep.
;
72
:
985
991
.

29

World Health Organization Africa
. Measles elimination by 2020: a strategy for the African Region. 2011. Available at: https://www.afro.who.int/sites/default/files/sessions/working_documents/AFR-RC61-8-Measles-elimination-by-2020—strategy-forthe-African-Region—with-Resolution.pdf

30

Minta
AA
,
Ferrari
M
,
Antoni
S
, et al.
Progress toward regional measles elimination—worldwide, 2000–2021
.
MMWR Morb Mortal Wkly Rep
2022
;
71
:
1489
95
.

31

Tapia
MD
,
Sow
SO
,
Medina-Moreno
S
, et al.
A serosurvey to identify the window of vulnerability to wild-type measles among infants in rural Mali
.
Am J Trop Med Hyg
2005
;
73
:
26
31
.

32

Dixon
MG
,
Tapia
MD
,
Wannemuehler
K
, et al.
Measles susceptibility in maternal-infant dyads—Bamako, Mali
.
Vaccine
2022
;
40
:
1316
22
.

33

Kreidl
P
,
Ammerer
D
,
Würzner
R
,
Luckner Hornischer
A
,
Von Laer
D
,
Borena
W
.
Measles elimination: identifying susceptible sub-populations to tailor immunization strategies
.
Viruses
2019
;
11
:
765
.

34

Clarke
A
,
Blidi
N
,
Yokie
J
, et al.
Strengthening immunization service delivery post Ebola virus disease (EVD) outbreak in Liberia 2015–2017
.
Pan Afr Med J
2019
;
33
:
5
.

35

Marin
M
,
Nguyen
HQ
,
Keen
J
, et al.
Importance of catch-up vaccination: experience from a varicella outbreak, Maine, 2002–2003
.
Pediatrics
2005
;
115
:
900
5
.

36

Simone
B
,
Balasegaram
S
,
Gobin
M
, et al.
Evaluation of the measles, mumps and rubella vaccination catch-up campaign in England in 2013
.
Vaccine
2014
;
32
:
4681
8
.

37

Zhang
RQ
,
Li
HB
,
Li
FY
,
Han
LX
,
Xiong
YM
.
Epidemiological characteristics of measles from 2000 to 2014: results of a measles catch-up vaccination campaign in Xianyang, China
.
J Infect Public Health
2017
;
10
:
624
9
.

Author notes

Potential conflicts of interest. All authors: No reported conflicts.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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