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Factors associated with sclerema in infants with diarrhoeal disease: a matched case-control study
Mohammod Jobayer Chisti1, Tahmeed Ahmed, Abu Syed Golam Faruque
1International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh. chisti@icddrb.org
Insights
Infants with diarrheal illness and sepsis who develop sclerema face higher mortality. Hypothermia and low serum protein/prealbumin levels are key indicators associated with sclerema in these infants.
Area of Science:
- Pediatrics
- Neonatology
- Infectious Diseases
Background:
- Sclerema neonatorum is a rare but serious condition affecting newborns.
- Diarrheal illness and clinical sepsis are common in infants, particularly in resource-limited settings.
- Identifying risk factors for sclerema in septic infants is crucial for timely intervention.
Purpose of the Study:
- To determine clinical and biochemical factors linked to sclerema in infants with diarrheal illness.
- To investigate the outcomes associated with sclerema in this vulnerable population.
Main Methods:
- A case-control study comparing 30 infants with sepsis and sclerema to 60 matched controls without sclerema.
- Analysis focused on variables including hypoxia, hypothermia, C-reactive protein (CRP), serum total protein, and prealbumin.
- Statistical methods included chi-square tests and t-tests/Mann-Whitney tests for comparing proportions and means.
Main Results:
- Infants with sclerema had a significantly higher case-fatality rate (30% vs. 2%).
- Adjusted analysis revealed that sclerema was associated with hypothermia (OR 11.6), lower serum total protein (OR 1.12), and lower prealbumin (OR 1.5).
Conclusions:
- Hypothermia, low serum total protein, and low prealbumin levels are significant factors associated with sclerema in infants with diarrheal illness and clinical sepsis.
- These findings highlight critical indicators for identifying infants at risk of developing sclerema.
Aim:
To identify clinical and biochemical factors associated with sclerema in infants with diarrhoeal illness, and their outcome.
Methods:
In this case-control study, we enrolled 30 infants with clinical sepsis with sclerema (cases) and another 60, age- and sex-matched infants with clinical sepsis but without sclerema (controls) from among those admitted to the special care unit (SCU) and longer stay unit (LSU) of the Dhaka Hospital of International Centre for Diarrhoeal Disease Research, Bangladesh (ICDDR,B) for their diarrhoeal illness from May 2005 through April 2006. Sclerema as the dependant variable while hypoxia, hypothermia, C-reactive protein (CRP) level, serum total protein and prealbumin level were the major independent variables compared in the analysis. Differences in proportions were compared by the chi-square test and differences of mean were compared by Student's t-test or Mann-Whitney test, as appropriate.
Results:
The case-fatality was significantly higher among the cases than the controls (30% vs. 2%, CI 2.9-565.5). After adjusting for confounders, infants with sclerema were more likely to be hypothermic (OR 11.6, 95% CI 1.1-126.5), and have lower serum total protein (OR 1.12, 95% CI 1.04-1.21) and prealbumin (OR 1.5, 95% CI 1.1-2.3).
Conclusion:
Diarrhoeal infants having clinical sepsis presenting with hypothermia, lower serum protein and prealbumin are prone to be associated with sclerema.
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