Abstract
Background
Children with Congenital Heart Disease (CHD) are at increased risk for severe acute malnutrition (SAM). We aimed to determine the magnitude and determinants of SAM among children with CHD in a tertiary hospital.
Methods
Retrospective cross-sectional study was conducted among children with CHD between 2016 and 2019. Clinical and anthropometric data were retrieved from medical records. Anthropometric assessment was done by using WHO standard growth curves. Data analysis was done using Statistical Package for Social Sciences V22. Statistical significance was set at p-value <0.05, and multivariable logistic regression was used to determine predictors.
Results
There were 2400 pediatric admissions during the study period, CHD accounted for 6.5%(156) of admissions. For review, 141 records were eligible. The gender distribution was comparable, males 51.1% (72). Infants (<12 months) and older children (≥12 months) accounted for 57.4% (81) and 42.6% (60) of study subjects, respectively. SAM was documented in 51.8% (73) of the study subjects, [95% CI: 44.7–60.2]. Infants had higher odds of SAM compared to children aged ≥12 months[adjusted odds ratio (AOR)= 4.48, 95%CI:2.07–9.70]. Anemic children had higher odds for SAM[AOR =3.76, 95% CI:1.54–9.18]. Children without acyanotic CHD with heart failure(HF) were 58% less likely to develop SAM[AOR= 0.42, 95% CI:0.19–0.96].
Conclusion
The burden of SAM among children with CHD is high. Younger age, anemia and acyanotic CHD with HF predicted SAM. Screening for anemia and targeted anthropometric assessment are recommended for early SAM detection.
Keywords: Congenital heart disease, severe acute malnutrition, Ethiopia
Introduction
Double burden of malnutrition with childhood undernutrition and adult obesity is documented in low and middle-income countries (1,2). Severe Acute Malnutrition (SAM) is considered when weight for height(WFH) is <-3 Z score, bilateral pitting edema or low mid upper arm circumference (MUAC) is documented(3). Malnutrition is a common problem among children with Congenital Heart Disease (CHD)(4). Stunting and wasting are reported in 37% and 7% of Ethiopian children under the age of five, respectively(5).
Several mechanisms are proposed for growth failure among children with CHD. Decreased intake, increased energy requirements and presence of pulmonary hypertension are the main factors leading to malnutrition. Decreased intake could be related to anorexia following the chronic hypoxemia, and several other immune and neurohormonal disturbances are also postulated(6–10). Early and timely CHD interventions are shown to improve the catch-up growth(11–13).
Malnutrition in CHD patients can be categorized into different groups depending on the presence or absence of cyanosis/pulmonary hypertension/heart failure. Several combinations including acyanotic patients with pulmonary hypertension (patients with left-to-right shunt and pulmonary hypertension), acyanotic patients without pulmonary hypertension and cyanotic patients are used(4, 14–16).
SAM was documented among 31–71.4% of children with CHD. Presence of anemia, age at presentation, low arterial oxygen saturation, heart failure, poor dietary history, pulmonary hypertension and lack of surgical interventions predicted SAM(4, 17–20). SAM is managed using the World Health Organization's (WHOs) treatment protocol(21). Preoperative nutritional care is highly recommended to improve the postoperative outcome of CHD (12). Treatment of CHD in most parts of Africa, including Ethiopia, is provided by overseas voluntary mission or humanitarian aid, and the majority of the patients do not have access to the service. Success of such treatment models in sustaining the care has been questioned, and reconsideration was suggested(22,23). Global call for coordination of such pediatric cardiac surgery mission efforts was also recommended(24). Evidence on CHD related SAM is scarce from Africa and absent from Ethiopia. We aimed to assess the magnitude and predictors of SAM among unoperated pediatric CHD.
Methods
Setting: The study was conducted at Hawassa University Comprehensive Specialized Hospital (HUCSH), Hawassa, 271km South of Addis Ababa, Ethiopia's capital. HUCSH is the first referral and teaching hospital in Southern Ethiopia. It serves a catchment population of over 18 million. It is a referral hospital for Southern Ethiopia and its neighboring regional states of Ethiopia. Pediatrics Department provides services for outpatient, emergency and admitted cases. There is an established therapeutic ward for care of children with SAM. SAM patients receive intensive care and followup by trained and dedicated nurses, intern and resident doctors, and pediatric consultant physicians. Admitted workup and treatment of CHD cases also include radiologic studies, echocardiographic imaging and laboratory tests.
Study design: Retrospective cross-sectional study on the medical records of CHD patients seen at HUCSH between 2016 and 2019
Study population: All pediatric patients, aged less than 14 years, with CHD who had received admitted care at HUCSH
Inclusion criteria: All children between 2months and 14 years of age with echocardiographic documented CHD
Exclusion criteria: Incomplete charts, children with comorbid condition like developmental delay, Downs Syndrome and other genetic abnormalities
Operational definitions: Moderate malnutrition was defined when weight for height (WFH), weight for age (WFA), and height for age (HFA) are between -3 and -2 Z-scores on WHO standard growth curves. On the other hand, SAM was considered when WFH was <-3 Z score, bilateral pitting edema or low mid upper arm circumference (MUAC) for age(3). Underweight and stunting were defined when the weight for age and height for age were < -2 Z scores, respectively. Wasting and severe wasting were considered when the weight for height was < -2 Z score and < -3 Z scores, respectively(25). Anemia was defined when hemoglobin concentration was <11g/dl, <11.5g/dl, and <12g/dl in under five years, 5–11 years and 12–14 years of age, respectively(26). Cardiomegaly was defined when cardiothoracic ratio was > 60% in neonates, and >55% in older children (27). Acyanotic CHD was defined as anatomic connection between the pulmonary and systemic circulations with left to right shunts (28). Cyanotic CHD was defined as heart lesions resulting in cyanosis owing to right sided heart obstructive lesions, left heart obstructive lesions, and mixing lesions(29). Infants are children below the age of one year(30).
Pulmonary hypertension (PH) was considered when the peak tricuspid regurgitation velocity was >2.8m/sec and other parameters like blunted inferior vena diameter respiratory cycle variation were present (31). Patients were grouped into different classes: group I, acyanotic CHD without heart failure or pulmonary hypertension; group II, acyanotic with heart failure; group III, acyanotic CHD with pulmonary hypertension; group IV, cyanotic CHD(16).SAM treatment outcome was assessed on hospital discharge and was defined as death or survival.
Sample size: A sample size of 114 was calculated using single population proportion formula with assumptions of 92% malnutrition proportion among CHD, 95% confidence interval with 5% margins of error (4).A total of 156 consecutive medical records were retrieved during study period from medical records archive, and fifteen were excluded due to incomplete information and documentation of syndromic or genetic abnormality diagnosis. Finally, one hundred forty-one medical records fulfilling the predefined criteria were selected and included in the study.
Study variables: The dependent variable was severe acute malnutrition. Age, sex, income, CHD type, pulmonary hypertension, nutritional history and heart failure were the independent variables.
Data collection: Structured questionnaire was prepared and data were collected from patient medical records. Socio-demographic data, anthropometric data, clinical, echocardiography results and summary of important laboratory findings were retrieved from the medical records of patients.
Data analysis: The collected data were analyzed using descriptive and inferential statistics. Statistical package for social sciences (SPSS) version 22 software was used to analyze the data. Frequencies and percentages were used to present categorical data. Parametric tests were used to assess the association between variables and outcome. Binary logistic regression was used to check the association between dependent and independent variables. Variables with Pvalue < 0.25 on binary logistic regression were used for multivariable logistic regression for controlling the possible effect of confounders. Finally, variables which had an independent association with SAM were identified on the basis of adjusted odds ratio(AOR), 95% CI and P-value < 0.05.
Ethical approval: Ethical approval and waiver of consent for the study was obtained from the Institutional Review Board of Hawassa University.
Results
Socio-demographic profile: There were 2400 pediatric admissions during the study period, and CHD accounted for 6.5% (156) of the admissions. One hundred forty-one medical records were eligible for review and included in the study. The gender distribution was comparable, males 51.1% (72) of study subjects. Most of the study subjects were from the Southern regional state of Ethiopia, 55.3% (78), while the remaining ones were from the neighboring Oromia regional state of Ethiopia, 44.7% (63). Infants (2–12 months) accounted for 57.4% (81) of the study subjects.
Anthropometric data: Underweight and moderate malnutrition by MUAC were documented in 70(49.6%) and 34(24.1%) of the study subjects, respectively. Stunting was reported in 42(29.8%) of the study subjects. SAM was reported in 53(37.6%) and 39(27.7%) of the study subjects using MUAC and WFH, respectively. SAM using both MUAC and WFH was documented in 73(51.8%) of the study subjects (Table 1).
Table 1.
Anthropometric parameter | Frequency | Percent |
Weight for age | ||
Normal | 60 | 42.6 |
Underweight | 70 | 49.6 |
Height for age | ||
Normal | 99 | 70.2 |
Stunted | 42 | 29.8 |
MUAC$ for age | ||
Severe malnutrition | 53 | 37.6 |
Moderate malnutrition | 34 | 24.1 |
Mild malnutrition | 11 | 7.8 |
Normal | 43 | 30.5 |
Weight for height | ||
Normal | 52 | 36.9 |
Wasting | 89 | 63 |
Severe wasting (by Weight for height) | ||
Yes | 39 | 27.7 |
No | 102 | 72.3 |
$SAM (WFH and MUAC*) | ||
Yes | 73 | 51.8 |
No | 68 | 48.2 |
&MUAC-mid upper arm circumference, $SAM-severe acute malnutrition, *WFH weight for height
Clinical data: Pulmonary hypertension was documented in 26(18.4%) of CHD, and moderate severity predominates, 12(46.1%). cardiomegaly and anemia were reported in 112(79.4%) and 39(27.7%) of the study subjects, respectively. The majority of the study subjects had been survived up on discharge, 123(87.2%). Most of the study subjects had acyanotic CHD with heart failure, 90(63.8%) (Table 2). The common types of CHD included ventricular septal defect, patent ductus arteriosus, tetralogy of fallot, endocardial cushion defect and atrial septal defects contributing to 79(56%), 16(11.3%), 15(10.6%), 13(9.2%) and 11(7.8%) of the study subjects, respectively. None of our study subjects had undergone surgical or definitive intervention for CHD.
Table 2.
Variable | Category | Frequency (N=141) | Percent |
Pulmonary Hypertension | Yes | 26 | 18.4 |
No | 115 | 81.6 | |
Severity of Pulmonary Hypertension | Mild | 5 | 19.2 |
Moderate | 12 | 46.1 | |
Severe | 9 | 34.6 | |
Cardiomegaly | Yes | 112 | 79.4 |
No | 29 | 20.6 | |
Pulmonary edema | Yes | 49 | 34.8 |
No | 92 | 65.2 | |
Anemia | Yes | 39 | 27.7 |
No | 102 | 72.3 | |
Acyanotic CHD% without &HF/PHTN* | Yes | 16 | 11.3 |
No | 125 | 88.7 | |
Acyanotic CHD with HF | Yes | 90 | 63.8 |
No | 51 | 36.2 | |
Acyanotic CHD with PHTN | Yes | 23 | 16.3 |
No | 118 | 83.7 | |
Cyanotic CHD without PHTN/HF | Yes | 26 | 18.4 |
No | 115 | 81.6 | |
Treatment outcome at discharge | Survived | 123 | 87.2 |
Died | 18 | 12.8 |
%CHD-congenital heart disease, &HF-heart failure, * PHTN-pulmonary hypertension
Magnitude and determinants of malnutrition: The overall magnitude of SAM in this study was 51.8%(73).
Bivariate analysis: From all variables analyzed, seven variables (age, sex, anemia, pulmonary hypertension, cardiomegaly, pulmonary edema, and acyanotic CHD with heart failure) were associated with SAM on bivariate analysis (Table 3). Variables with p-value < 0.25 were selected for multivariable analysis
Table 3.
Variable | Category | SAM# | $COR (95% %CI) | P. value | |
Yes | No | ||||
Age | ≥12 months | 20 | 40 | 1 | 0.000 |
2–12 months | 53 | 28 | 7.95(2.70–23.35) | ||
Anemia | Yes | 44 | 58 | 1 | 0.001 |
No | 29 | 10 | 3.82(1.68–8.66) | ||
Cardiomegaly | Yes | 61 | 51 | 1 | 0.21 |
No | 12 | 17 | 0.59(0.59–2.37) | ||
Acyanotic CHD^ with &HF | Yes | 19 | 32 | 1 | 0.05 |
No | 41 | 49 | 0.49(0.24–1.04) | ||
Yes | 16 | 10 | 1.62(0.68–3.88) | 0.27 | |
Pulmonary *HTN | No | 57 | 58 | 1 | |
Male | 40 | 32 | 1.36(0.70–2.64) | 0.35 | |
Sex | Female | 33 | 36 | 1 | |
Yes | 24 | 25 | 0.84(0.42–1.68) | 0.62 | |
Pulmonary edema | No | 49 | 43 | 1 |
^CHD-congenital heart disease, &HF-heart failure, *HTN-hypertension,#SAM-severe acute malnutrition, $COR-crude odds ratio, %CI- confidence interval
Multivariable analysis result: Infants (2–12 months) had four times higher odds of SAM compared to children aged 12 months and above[AOR =4.48, 95% CI: 2.07–9.70]. Those who had anemia were four times more likely to develop SAM compared to their counterparts, [AOR =3.76, 95% CI:1.54–9.18] whereas those who had no acyanotic CHD with HF were 58% less likely to have SAM compared to their counterparts [AOR =0.42, 95% CI: 0.19–0.96] (Table 4).
Table 4.
Variable | Category | SAM | AOR (95% CI) | P. value | |
Yes | No | ||||
Age | ≥12 months | 20 | 40 | 1 | 0.000 |
2–12 months | 53 | 28 | 4.48(2.07–9.70) * | ||
Anemia | Yes | 44 | 58 | 1 | 0.004 |
No | 29 | 10 | 3.76(1.54–9.18) * | ||
Cardiomegaly | Yes | 61 | 51 | 1 | 0.2 |
No | 12 | 17 | 1.86(0.71–4.87) | ||
Acyanotic CHD with HF | Yes | 19 | 32 | 1 | 0.04 |
No | 41 | 49 | 0.42(0.19–0.96) * |
Significant p-value <0.05, COR = Crude Odds Ratio, CI = Confidence interval, AOR = Adjusted Odds Ratio
Discussion
The magnitude of severe acute malnutrition among CHD in this study was 51.8%, 95% CI (44.7%–60.2%). This magnitude is lower than studies conducted in Egypt (71.4%) and Nigeria (61.2%). This difference could be due to the age of inclusion, settings and capacity of the institutions and design differences (17,18). Our report is higher than reports from Uganda(31.5%) and Iran (39.8%)(15,19). The higher figure in our study could be a reflection of the high national burden of malnutrition in Ethiopia(5). In the current study, different forms of malnutrition were documented. Underweight, stunting, and moderate and severe wasting were documented in 70(49.6%), 42(29.8%), 34(24.1%) and 16(11.1%) of the study subjects, respectively. Comparable results were reported from Uganda and Nigeria; undernutrition assessment in a tertiary hospital in Tanzania documented a similar pattern (18,19,32).A higher figure was reported from Iraq with underweight and wasting contributing to 32% and 65% of CHD(16). Nevertheless, this study only included infants as study subjects.
In this study, the majority of our study subjects had acyanotic congenital heart disease with heart failure. This is comparable to a previous report from the same hospital and a study done in Addis Ababa, Ethiopia(33,34). Heart failure is documented to result in energy imbalance in cardiac patients by increasing basal metabolic rate due to inflammation or chronic disease, and hence resulting in malnutrition(6, 7, 35). Additionally, children who had no acyanotic CHD with HF were 58% less likely to develop SAM compared to their counterparts. This is opposed to the evidence that cyanotic patients are at higher risk of growth failure due to prolonged hypoxemia(35,36). However, our report should be seen in light of the small size of cyanotic heart disease children in this study as the more severe cyanotic patients might have died early due to the natural course of the illness and/or lack of interventions.
In the current study, infants (2–12 months) were four times more likely to develop SAM compared to children of 12 months and above. This is consistent with reports from Nigeria and India(4,13). Infancy is linked with a higher energy demand for accelerated growth, and it is also the time where the risk for chest infection is very high owing to CHD related left to right shunts (35,38,39).
In this study, children who had anemia were four times more likely to develop SAM compared to their counterparts. This finding is consistent with reports from Nigeria and Uganda(18,19). Anemia could be a marker of underfeeding especially in children with CHD owing to the feeding challenges among them (35,38). Moreover, it is documented that anemia among children with severe acute malnutrition is of nutritional origin even demanding transfusion (40).
Our study has limitations. It is a retrospective and single center study, and several other determinant factors including intake and feeding pattern which assist in determining the primary nutritional issues were not assessed. It was also not possible to validate the documented anthropometric measurements. However, our study reports the magnitude and determinant factors for SAM among children with the non-intervened CHD in the Ethiopian setting. It also calls for timely attention to reverse the situation and to avert the productive loss in the long run.
In conclusion, a high severe acute malnutrition burden among children with congenital heart disease is documented. Young age, anemia and acyanotic CHD with HF were factors positively associated with severe acute malnutrition. Screening for anemia and targeted anthropometric assessment are recommended for better and early detection of SAM.
Acknowledgments
We thank all health professionals who cared for our study subjects.
References
- 1.Modjadji P, Madiba S. The double burden of malnutrition in a rural health and demographic surveillance system site in South Africa: a study of primary schoolchildren and their mothers. BMC Public Health. 2019;19(1):1087. doi: 10.1186/s12889-019-7412-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Perez-Escamilla R, Bermudez O, Buccini GS, Kumanyika S, Lutter CK, Monsivais P, et al. Nutrition disparities and the global burden of malnutrition. BMJ. 2018;361:k2252. doi: 10.1136/bmj.k2252. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.World Health Organization, author. WHO child growth standards and the identification of severe acute malnutrition in infants and children. A Joint Statement by the World Health Organization and the United Nations Children's Fund. Geneva: Switzerland: 2009. [PubMed] [Google Scholar]
- 4.Arodiwe I, Chinawa J, Ujunwa F, Adiele D, Ukoha M, Obidike E. Nutritional status of congenital heart disease (CHD) patients: Burden and determinant of malnutrition at university of Nigeria teaching hospital Ituku - Ozalla, Enugu. Pak J Med Sci. 2015;31(5):1140–1145. doi: 10.12669/pjms.315.6837. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Ethiopian Public Health Institute (EPHI) [Ethiopia] and ICF, author. Ethiopia Mini Demographic and Health Survey 2019: Key Indicators. Rockville, Maryland, USA: EPHI and ICF; 2019. [Google Scholar]
- 6.Menon G, Poskitt EM. Why does congenital heart disease cause failure to thrive? Arch Dis Child. 1985;60(12):1134–1139. doi: 10.1136/adc.60.12.1134. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Filippatos GS, Anker SD, Kremastinos DT. Pathophysiology of peripheral muscle wasting in cardiac cachexia. Curr Opin Clin Nutr Metab Care. 2005;8(3):249–254. doi: 10.1097/01.mco.0000165002.08955.5b. [DOI] [PubMed] [Google Scholar]
- 8.Salzer H R, Haschke F, Wimmer M, Heil M, Schilling R. Growth and nutritional intake of infants with Congenital Heart Disease. Pediatr Cardiol. 1989;10(1):17–23. doi: 10.1007/BF02328630. [DOI] [PubMed] [Google Scholar]
- 9.Mehrizi A, Drash A. Growth Disturbance in Congenital Heart Disease. J Pediatr. 1962;61:418–429. doi: 10.1016/s0022-3476(62)80373-4. [DOI] [PubMed] [Google Scholar]
- 10.Lees M H, Bristow J D, Griswold H E, Olmsted R W. Relative Hypermetabolism in infants with Congenital Heart Disease and Undernutrition. Pediatrics. 1965;36:183–191. [PubMed] [Google Scholar]
- 11.Cheung MM, Davis AM, Wilkinson JL, Weintraub RG. Long term somatic growth after repair of tetralogy of Fallot: evidence for restoration of genetic growth potential. Heart. 2003;89(11):1340–1343. doi: 10.1136/heart.89.11.1340. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Argent AC, Balachandran R, Vaidyanathan B, Khan A, Kumar RK. Management of undernutrition and failure to thrive in children with congenital heart disease in low- and middle-income countries. Cardiol Young. 2017;27(S6):S22–s30. doi: 10.1017/S104795111700258X. [DOI] [PubMed] [Google Scholar]
- 13.Vaidyanathan B, Nair SB, Sundaram KR, Babu UK, Shivaprakasha K, Rao SG, et al. Malnutrition in children with congenital heart disease (CHD) determinants and short term impact of corrective intervention. Indian Pediatr. 2008;45(7):541–546. [PubMed] [Google Scholar]
- 14.Varan B, Tokel K, Yilmaz G. Malnutrition and growth failure in cyanotic and acyanotic congenital heart disease with and without pulmonary hypertension. Arch Dis Child. 1999;81(1):49–52. doi: 10.1136/adc.81.1.49. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Tabib A, Aryafar M, Ghadrdoost B. Prevalence of Malnutrition in Children with Congenital Heart Disease. J Compr Ped. 2019;10(4):e84274. [Google Scholar]
- 16.Rabab Hasan Baaker AA-A, Ashraf Ahmad Kamel. Malnutrition and Growth Status in Patients with Congenital Heart Disease. The Iraq Postgraduate Medical Journal. 2008;7(2) [Google Scholar]
- 17.Hassan BA, Albanna EA, Morsy SM, Siam AG, Al Shafie MM, Elsaadany HF, et al. Nutritional Status in Children with Un-Operated Congenital Heart Disease: An Egyptian Center Experience. Front Pediatr. 2015;3:53. doi: 10.3389/fped.2015.00053. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Okoromah CA, Ekure EN, Lesi FE, Okunowo WO, Tijani BO, Okeiyi JC. Prevalence, profile and predictors of malnutrition in children with congenital heart defects: a case-control observational study. Arch Dis Child. 2011;96(4):354–360. doi: 10.1136/adc.2009.176644. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Batte A, Lwabi P, Lubega S, Kiguli S, Otwombe K, Chimoyi L, et al. Wasting, underweight and stunting among children with congenital heart disease presenting at Mulago hospital, Uganda. BMC Pediatr. 2017;17(1):10. doi: 10.1186/s12887-017-0779-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Venugopalan P, Akinbami FO, Al-Hinai KM, Agarwal AK. Malnutrition in children with congenital heart defects. Saudi Med J. 2001;22(11):964–967. [PubMed] [Google Scholar]
- 21.World Health Organization, author. Guideline: Updates on the management of severe acute malnutrition in infants and children. Geneva: World Health Organization; 2013. [PubMed] [Google Scholar]
- 22.Tefera E, Nega B, Yadeta D, Chanie Y. Humanitarian Cardiology and Cardiac Surgery in Sub-Saharan Africa: Can We Reshape the Model? World J Pediatr Congenit Heart Surg. 2016;7(6):727–731. doi: 10.1177/2150135116668834. [DOI] [PubMed] [Google Scholar]
- 23.Jivanji SGM, Lubega S, Reel B, Qureshi SA. Congenital Heart Disease in East Africa. Front Pediatr. 2019;7:250. doi: 10.3389/fped.2019.00250. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Polivenok I, Gelatt M, Cardarelli M. Cardiac surgical missions: what works, what does not, where we need to go from here. Curr Opin Cardiol. 2020;35(1):76–79. doi: 10.1097/HCO.0000000000000691. [DOI] [PubMed] [Google Scholar]
- 25.World Health Organization, author. Training Course on Child Growth Assessment. Geneva: Switzerland: 2008. [Google Scholar]
- 26.World Health Organization, author. Haemoglobin concentrations for the diagnosis ofanaemia and assessment of severity. Vitamin andMineral Nutrition Information System. Geneva: World Health Organization; 2011. (WHO/NMH/NHD/MNM/1 1.1)( http://www.who.int/vmnis/indicators/haemoglobin.pdf, Jan 5 2020) [Google Scholar]
- 27.Jayaprasad N. Heart failure in children. Heart Views. 2016;17(3):92–99. doi: 10.4103/1995-705X.192556. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Colombo Jamie N, McCulloch Michael A. Acyanotic Congenital Heart Disease: Left-to-Right Shunt Lesions. NeoReviews. 2018;19(7):375. [Google Scholar]
- 29.Galvis MMO, Mendez MD. StatPearls [Internet] Treasure Island (FL): StatPearls Publishing; 2020. Cyanotic Heart Disease. [Google Scholar]
- 30.World Health Organization, author. Consolidated ARV guidelines. Definition of key terms. 2013. ( https://www.who.int/hiv/pub/guidelines/arv2013/intro/keyterms/en/, April 14, 2020)
- 31.Galiè Nazzareno, Humbert Marc, Vachiery Jean-Luc, Gibbs Simon, Lang Irene, et al. 2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: The Joint Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS): Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT) European Heart Journal. 2015;37(1):67–119. doi: 10.1093/eurheartj/ehv317. [DOI] [PubMed] [Google Scholar]
- 32.Bashaka PJ, Sawe HR, Mwafongo V, Mfinanga JA, Runyon MS, Murray BL. Undernourished children presenting to an urban emergency department of a tertiary hospital in Tanzania: a prospective descriptive study. BMC Pediatr. 2019;19(1):327. doi: 10.1186/s12887-019-1706-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Gebremariam S, Moges T. Pediatric Heart Failure, Lagging, and Sagging of Care in Low Income Settings: A Hospital Based Review of Cases in Ethiopia. Cardiol Res Pract. 2016;2016:7147234. doi: 10.1155/2016/7147234. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Nigussie B, Tadele H. Heart Failure in Ethiopian Children: Mirroring the Unmet Cardiac Services. Ethiop J Health Sci. 2019;29(1):811–818. doi: 10.4314/ejhs.v29i1.2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Lewis KD, Conway J, Cunningham C, Larsen BMK. Optimizing Nutrition in Pediatric Heart Failure: The Crisis Is Over and Now It's Time to Feed. Nutr Clin Pract. 2018;33(3):397–403. doi: 10.1177/0884533617712502. [DOI] [PubMed] [Google Scholar]
- 36.Ulfah D, Lestari E, Salimo H, Widjaya S, Artiko B. The effect of cyanotic and acyanotic congenital heart disease on children's growth velocity. Paediatrica Indonesiana. 2017;57(3) [Google Scholar]
- 37.Costello CL, Gellatly M, Daniel J, Justo RN, Weir K. Growth Restriction in Infants and Young Children with Congenital Heart Disease. Congenit Heart Dis. 2015;10(5):447–456. doi: 10.1111/chd.12231. [DOI] [PubMed] [Google Scholar]
- 38.Das BB. Current State of Pediatric Heart Failure. Children (Basel) 2018;5(7):88. doi: 10.3390/children5070088. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Barton JS, Hindmarsh PC, Scrimgeour CM, Rennie MJ, Preece MA. Energy expenditure in congenital heart disease. Arch Dis Child. 1994;70(1):5–9. doi: 10.1136/adc.70.1.5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Thakur Neha, Chandra Jagdish, Pemde Harish, Singh Varinder. Anemia in Severe Acute Malnutrition. Nutrition. 2014;30(4):440–442. doi: 10.1016/j.nut.2013.09.011. [DOI] [PubMed] [Google Scholar]