Literature DB >> 33110806

Hypertension in pediatric patients admitted to inpatient ward at King Abdulaziz Universty Hospital in Saudi Arabia: Prevalence, causes, and outcomes.

Osama Safdar1, Reham AlJehani1, Mohammed Aljuhani1, Hajar AlGhamdi1, Arub Asiri1, Oyoon AlGhofaily1, Fatimah Hisan1, Ghidah Altabsh1.   

Abstract

BACKGROUND: The secondary hypertension (HTN) is the predominant form of HTN in pediatrics. Renal diseases and renovascular anomalies are the most commonly reported causes. In this study, we aimed to identify the prevalence, causes, and outcomes of secondary HTN in Saudi Arabia.
METHODS: A retrospective study was conducted among 3,640 pediatric patients aged between 0 and 18 years, admitted to the pediatric nephrology ward at King Abdulaziz University Hospital, Jeddah, Saudi Arabia. The study has been approved by the ethics review committee of King Abdulaziz University.
RESULTS: Prevalence of secondary HTN due to renal disease was (77.0%). Most of the cases were diagnosed with stage 5 renal disease (78.3%). Small kidney size was frequently diagnosed (n = 29, 11.9%), followed by large kidney size (n = 26, 10.7%). One third of the cases (n = 79, 32.4%) were under control, 49 (20.1%) lost follow-up, and 24 (10.1%) deceased. A total of 61 (33.1%) patients progressed to end-stage renal disease and patientswere managed by different types of treatments.
CONCLUSION: The prevalence of secondary HTN due to renal disease is considered to be high in pediatric patients admitted to King Abdulaziz University. Several renal diseases in the renal system are associated with secondary HTN mostly attriubuted to renal malformation. In addition, renal affection, cerebral infarction, bleeding, left ventricular hypertrophy, and valvular lesion are the highest reported complications in our population. Follow-up with ECHO and brain CT is highly recommended in pediatric HTN. Future studies on a larger sample and vigorous follow-up are recommended. Copyright:
© 2020 Journal of Family Medicine and Primary Care.

Entities:  

Keywords:  Hypertension; inpatient; outcomes; pediatric

Year:  2020        PMID: 33110806      PMCID: PMC7586632          DOI: 10.4103/jfmpc.jfmpc_214_20

Source DB:  PubMed          Journal:  J Family Med Prim Care        ISSN: 2249-4863


Introduction

Hypertension (HTN) is identified as persistent blood pressure values ≥the 95th percentile. Primary HTN has no definite secondary causes but multiple factors such as obesity, insulin resistance, impairment in sodium homeostasis, or renin-angiotensin system may be involved.[1] Secondary HTN, in contrast, is the predominant form of HTN, and the underlying etiology lies behind various secondary causes.[2] In a retrospective review, out of 275 hypertensive children, 57% had secondary HTN due to renal, cardiovascular, autoimmune, endocrine, gastrointestinal, hematological, medication-related orneurological causes.[3] Management guidelines of pediatric HTN were updated in 2017, the disease is recognized by elevated blood pressure >90th percentile; early detection and management measurements are essential to lessen the irreversible changes that could affect the cardiovascular system and renal system.[24] Calcium-channel blockers (CCB) and angiotensin-converting enzyme inhibitors (ACEI) are the most favorable therapy to lower blood pressure in pediatric.[45] However, secondary HTN was found to have a better response than primary HTN.[5] The complication of HTN are miscellaneous, HTN could be presented as hypertensive emergency that may involve severe kidney injury, affection of myocardium, and retinopathy.[6] In a retrospective study carried out on 246 children with sustained HTN, 35 patients were presented, for the first time, with complications of severe HTN such as congestive heart failure and encephalopathy. The underlying causes of HTN in is this study were attributed to renal, renovascular, or endocrine system disorders.[7] Pediatric population in the Kingdom of Saudi Arabia is highly susceptible to develop either primary or secondary HTN, hence regular screening is highly recommended. In a recent study that aimed outline the prevalence of risk factors of diabetes and HTN among school children in Kingdom of Saudi Arabia, 11.6% had body mass index (BMI) above the normal range and 43% had sedentary lifestyle.[8] In a cross-sectional study of 401 adolescents from Jeddah, the prevalence of HTN was 17.2%, pre-HTN was observed in 4.2%, and obesity was reported in 19.2%. In addition, the prevalence of hematuria and proteinuria were 17% and 10.2%, respectively.[9] In a recently published article, isolated systolic hypertension (ISH) was the most reported phenotype in obese children (24.3%).[10] However there are no studies assess the prevalence of HTN in pediatric patients addmitted to pediatric inpatient ward. Consequently, in our present study, we sought to assess the prevalence, causes, and outcomes of secondary HTN in pediatric patients admitted to King Abdulaziz University Hospital in Jeddah, Saudi Arabia between 2015 and 2019.

Material and Methods

Study setting

This is a retrospective study, conducted among 3,640 pediatric patients in the pediatric ward at King Abdulaziz University Hospital, Jeddah, Saudi Arabia. Patients aged 0–18 years of age were included. The study has been approved by the ethics review committee of King Abdulaziz University June 14, 2017. For the age group (1–13), the American Academy of Pediatrics (AAP) updated guidelines 2017 has been followed to diagnose HTN which is: Normal BP: <90th percentile. Elevated BP: ≥90th percentile to <95th percentile or 120/80 mmHg to <95th percentile or 130/80 to 139/89 mm Hg. Stage 1 HTN: ≥95th percentile to <95th percentile + 12 mmHg. Stage 2 HTN: ≥95th percentile +12 mmHg, or 2140/90 mm Hg. For the ≥13 age group, adolescent same as adults, American Heart Association (AHA) guidelines have eliminated the category of preHTN, categorizing patients as having either Elevated (120–129 and less than 80) or stage I HTN (130–139 or 80–89). While previous guidelines classified 140/90 mm Hg as stage 1 HTN, this level is classified as stage 2 HTN under the new guidelines.[4]

Data collection

Data were obtained by an electronic questionnaire from pediatric ER, pediatric medical ward, and Pediatric intensive care unit (ICU) files, in the period 2010–2018 at King Abdulaziz University Hospital. The questionnaire included information about gender, age at diagnosis, HTN causes, renal disease stage, blood pressure, HTN urgency, HTN emergency, complication, medical history, laboratory investigation, ultrasound, kidney size, renal disease characteristic, cardiovascular, CT brain, renal CT, medication, past history, and outcomes.

Data analysis

Data entry was performed by Microsoft Excel. Descriptive analysis was performed using the SPSS software. Qualitative variables were summarized by calculating the number and percent, whereas the median, 25th and 75th Quartile range were calculated for continuous variables.

Results

Out of 3,640 particpants, 244 met the criteria for the diagnosis of HTN, 86 patients (35.2%) were female and 158 (64.8%) were male, the mean age was 10 years. Third of the cases (n = 86, 35.2%) were diagnosed at the age between 0 and 2 years, then at the age 6 and 10 years (n = 64, 26.2%).

Prevalence of secondary HTN and its causes

The majority of the cases (n = 188, 77.0%) were secondary to kidney disease, then primary cause in (n = 23, 9.4%) cases. Most of the cases were diagnosed with stage 5 renal disease (78.3%). Less than half of the case were HTN urgency (n = 59, 24.2%) and HTN emergency (n = 49, 20.1%). Total of 170 (69.7%) patients did not perform CT brain, 40 (16.4%) had normal CT brain, only 34 (13.9%) had abnormal CT brain and only 4 (1.6%) cases had eye problems. The majority 236 (96.7%) of cases did not have any birth complications. Table 1 summarizes the demographic and baseline character of included patients. Past history of chronic illness is insulted in Figure 1, 48 (17.1%) had “nephrotic syndrome,” followed by 32 (11.4%) “Renal diseases,” then 12 (43%) “Hematological diseases.”
Table 1

The demographic and baseline character of included patients

Variable nPercentage
Gender
 Female8635.2
 Male15864.8
 Age by Median, (25th and 75th Quartile range)10.0(5, 15)
Age at diagnosis
 0-28635.2
 3-55020.5
 6-106426.2
 11-154116.8
 16-1831.2
HTN causes
 Cardiac20.6
 Neuroblastoma10.3
 Primary239.4
 Secondary (Endocrine)2.8
 Secondary (Kidney disease)18877.0
 Secondary (CNS)11c
 Secondary (medications)1.4
 Secondary to stress2.8
 Transient145.7
Renal disease stage
 Not applicable14157.8
 Stage 1104.1
 Stage 241.6
 Stage 352.0
 Stage 462.5
 Stage 57832.0
Blood pressure chart
 /A21688.5
 <95th1.4
 >95 centrile1.4
 >99th + 541.6
 110/130. 108/551.4
 120/671.4
 185/90. 160/681.4
 50th31.2
 5th1.4
 75th centrile1.4
 901.4
 93/1401.4
 95th41.6
 95th + 51.4
 99th1.4
 99th + 552.0
HTN urgency
 No18575.8
 Yes5924.2
HTN emergency
 No19579.9
 Yes4920.1
Complications
 Non23696.7
 hyaline membrane disease31.2
 prolonged ventilation >4 weeks1.4
 Sepsis41.6
CT brain final
 Not applicable17069.7
 Abnormal3413.9
 Normal4016.4
Eye examination
 Not applicable21487.7
 Blind31.2
 Fundis exam was performed, D, M, V WNL, pt not coaprative1.4
 Normal2610.7
Mode of delivery
 Unknown21286.9
 C/S83.3
249.8
GA
 Unknown23395.5
 24-281.4
 33-36104.1

C/S, cesarean section; SVD, spontaneous vaginal delivery; GA, gestational age

Figure 1

Frequencies of chronic illness in patients past history

The demographic and baseline character of included patients C/S, cesarean section; SVD, spontaneous vaginal delivery; GA, gestational age Frequencies of chronic illness in patients past history

Renal

Regarding laboratory and radiological investigations, there was a decrease in serum levels of P, K, and creatinine. While there was an increase in the levels of Calcium (Ca) electrolytes, Magnesium (Mg), glomerular filtration rate (GFR), GFR2, bicarb, and Albumin. On the other hand, the level of PH, RBCs, and protein decreased [Table 2].
Table 2

Laboratory investigation in included patients

VariableMedian25th and 75th Quartile range
Ca initial2.18(2.0,2.3)
Ca last2.24(2.0,2.3)
P initial1.57(1.3,1.9)
P last1.52(1.2,1.8)
K initial4.20(3.8,4.9)
K last4.0(3.6,4.4)
Ca initial electrolytes2.1(1.8,2.4)
Ca last electrolytes2.2(1.9,2.3)
Mg initial0.8(0.7,0.9)
Mg last0.9(0.7,1.0)
Alb initial27.0(17.0,33.0)
Alb last31.0(23.0,36.0)
RBCs initial2.0(0.9,10.0)
RBCs last2.0(1.0,14.0)
Protein initial2.0(1.0,3.0)
Protein last2.0(1.0,3.0)
Creatinine initial53.5(28.8,164.0)
Creatinine last50.0(30.0,269.0)
GFR initial95.7(45.1,146.9)
GFR last197.2(102.2,245.2)
PH initial7.33(7.2,7.4)
PH last7.34(7.2,7.4)
Bicarb initial23.0(18.0,25.6)
Bicarb last24.0(20.8,27.0)
GFR initial 27.5(2.7,15.3)
GFR last 29.1(1.4,15.1)
Laboratory investigation in included patients Total of 55 (22.5%) did not perform an ultrasound, normal ultrasound was noted in (45.1%), while bi-lateral hydronephrosis in (16.4%) and unilateral hydronephrosis in (6.6%), different findings are presented in Table 3.
Table 3

Ultrasound finding

VariablenPercentage
Not done5522.5
Normal11045.1
ARPCKD1.4
Atrophic left kidney1.4
bi-lateral hydronephrosis4016.4
Bilateral atrophy1.4
Bilateral Hydroureter1.4
bilateral minimal fullness of renal pelvis1.4
Bilateral small echogenic kidney with RT renal cortical cyst1.4
Bilateral small echogenic kidneys with mild to moderate ascites1.4
Bilateral small hydrocele1.4
Ectopic right kidney1.4
hyperechoic1.4
hyperechoic and multiple cyst on both1.4
Increase echogenesty bilatral1.4
increase Echogenicity1.4
increase echogenicty1.4
Increase right renal echogenicity1.4
Kidney stones1.4
Left multicystic kidney1.4
mild prominence of calyceal system1.4
Multiple cysts1.4
Polycystic kidney1.4
Severe Hydroureters1.4
small echogenic kidneys1.4
Stable polycrystic disease1.4
uni-lateral hydronephrosis166.6
Ultrasound finding Regarding kidney size, total of 56 (22.9%) showed that there is no data about kidney size, 121 (49.6%) had normal kidney size, while the rest 67 (27.5%) had different findings; small kidney size was frequently diagnosed (n = 29, 11.9%), followed by large kidney size (n = 26, 10.7%). Good corticomedullary differentiation was reported in (59%) while poor in (13.9%), absence of nephrocalcinosis in (73.8%) while it presented in only (2.5%). The majority of cases did not perform micturating cystourethrogram (MCUG) (n = 209, 85.6%), normal finding in (6.6%) while bilateral vesicoureteral reflux was present in 8 cases (3.3%) and unilateral vesicoureteral reflux in 4 cases only. Total of 85.1% did not perform dimercaptosuccinic acid (DMSA) scan, normal finding in (5.7%). Total of 218 (89.6%) did not perform CT renal, 5 (2.0%) had normal CT renal, while only 21 (8.4%) had different findings. Characteristic of renal imaging are presented in Table 4.
Table 4

Characteristics of renal imaging

VariablenPercentage
Kidney size
Normal12149.6
no data5622.9
5.6 × 3 cm size of the left kidney1.4
A large right sided abdominal mass is identified measuring approxumately 6.5 times 7.6 times 8.8 cm times in diameter, located in the expected region of the right adrenal gland1.4
Big2610.7
Lt kidny atrophied, Rt kidny enlarged1.4
Minimal increase in the size1.4
Relatively increased1.4
right kidney only1.4
Right kidneys is small1.4
Rt is small1.4
Rt. is small, Lt. is big1.4
Small2911.9
The right is normal1.4
The right kidney enlarged1.4
With cyst measures 0.5 cm1.4
Chorticomedullary differentiation
NA5723.3
Normal1.4
cortical thickness2.8
Cortical thickness of 0.81.4
Good14459.0
good in the right2.8
increased cortical echogenicity1.4
Irregular outline with multiple diverticulae1.4
Mild cortical increase echogenicity with no dilation or stones1.4
Poor3413.9
Nephrocarcinosis
Absent 18073.8
N/A5823.7
Present 62.5
MCUG
Not applicable20985.6
Normal166.6
bi-lateral vesicoureteral reflux83.3
Bladder is distended and elongated1.4
Grade 5 right sided vesicoureteric reflux1.4
Grade V1.4
Neurogenic bladder1.4
Neurogenic bladder with no vesicoureteric reflux1.4
Normal but the patient may have neurogenic bladder1.4
Obstruction1.4
Uni-lateral vesicoureteral reflux41.6
DMSA
Normal145.7
Not applicable21785.1
bi-lateral scarring52.0
evidance of bilatral renal impairment, wore on the left side1.4
no evidence of functioning tissue at the left side on the right side1.4
Right double moiety collecting system with dilated non obstructed system and preserved split function1.4
Right normal/left multicystic dysplastic kidney1.4
small rt kidney but no scar1.4
uni-lateral scarring31.2
Renal CT
No CT21889.6
Normal 52.0
Abdominal fluid pressing on the liver -kidneys the lungs are not remarkable1.4
Atrophied kidney1.4
bi lateral hydronephrosis1.4
Bilateral atrophied kidneys1.4
Bilateral PKD1.4
Bilateral small atrophied kidneys with multiple cystic lesion1.4
both kidneys normal in size, with bilateral sever hydronephrosis no stones1.4
Hydronephrosis due to staghorn stone in left kidney1.4
Left adrenal neuroblastoma with enlarged paraaortic and iliac lymph nodes1.4
markedly enlarged with ca deposition, poor corticomed differentiation and stretched deformed renal pelvis ( polycystic kidney disease )1.4
Medullary nephrocalcinosis with renal stones1.4
Multiple variable in size cortical cysts1.4
No renal vein thrombosis, small bowel edema and mild free fluid1.4
normal, high density in the cortex1.4
Rt kidney enlarge and severe hydronephrosis lef kidney with multiple cysts1.4
Severe hydronephrosis and hydroureter1.4
Splenomegaly1.4
The left side horseshoe kidney concerning for residual or recurrent tumor1.4
The right kidney has been surgically removed with no evidance of residual tumor or recurrence. Two cortical lesions seen in the left kidney.1.4
Unremarkable1.4
Variable sizes stone in the lower pole right kidney1.4
Characteristics of renal imaging

CVS

The results in Table 5 summarize findings in CVS; there were 157 (65.5%) cases who did not perform ECHO, 52 (21.3%) had normal echo, while only 35 (13.2%) had different findings presented in the table; left ventricular hypertrophy in 10 cases followed by valvular lesion in six cases and PDA in two cases.
Table 5

CVS finding

VariablenPercentage
No ECHO15765.5
Normal5221.3
7 mm fenestrated ASD shunting left to right1.4
Cardiomyopathy1.4
Coarctation of aorta1.4
Dilated left ventricle and left atrium1.4
IVC thrombus1.4
Left ventricular dilation1.4
Left ventricular hypertrophy104.1
Left ventricular hypertrophy + valvular lesion1.4
Mild peripheral pulmonary stenosis1.4
Minimal pericardial effusion and minimal pericardial thickening1.4
Patent foramen ovale1.4
PDA2.8
Pericardial effusion1.4
TGA,PDA S/P ARTERIAL switch operation1.4
Tof dialted RV + pulmonary atresia/s/p tof repair and tricuspid valve repair and lpa unifocalization1.4
Valvular lesion62.5
Valvular lesion, TOF1.4
vsd1.4
CVS finding

Brain

The results in Table 6 summarize the findings in the brain; there were 169 (69.3%) patients who did not perform CT brain, 40 (16.4%) had normal finding, while only 35 (14.3%) had different findings; infarction in six cases and bleeding in two cases.
Table 6

Brain finding

VariablenPercentage
N/A16969.3
Normal4016.4
Associated with mass effect and midline shift - bilateral diffuse brain edema1.4
Atrophic brain changes1.4
Atrophy1.4
Bilateral focal area of vasogenic edema1.4
Bilateral globus palledi calcification likely related to renal disease and hemodialysis1.4
Bilateral occipital and temporal hypodensitis likely representing PRES disease1.4
bleeding2.8
Brain atrophic changes in form of dilated ventricle1.4
Could be A recent ischemic event, further evaluation by MRI is recommended1.4
Deep white matter hypodensity due to metabolic imbalance1.4
diffuse axonal injury1.4
Dilatation of lateral and 3rd ventricles1.4
Dilated lateral and third ventricle1.4
Early edema1.4
hypoxic ischemic injury1.4
Hyrdocephalous1.4
infarction62.5
Internal placment of Lt posterior parietal VP shunt - fullness of the 4th ventricle and the foramen magnum - interval increase of the size of the ventricular system interval increase in the degree of hydrocephals involving the lateral ventricle1.4
Large left retrocerebellar cyst in posterior fossa1.4
Lt parietemloral and Rt temporal occipital subgleal fluid collection most likely related to fluid infusion1.4
Marked thinning of the carpus callosum1.4
mass in the left cerebral hemisphere1.4
No intracerebral hematoma or extra Axial collection1.4
non communicating hydrocephalus1.4
There is interval development of relatively large right occipital cortical and subcortical hypodensity and smaller one on the left side1.4
There’s a Lt parietal subcortical hypodensity with no mass effect in the ajacent sulci or midline shift its likely a chronic brain insult. No evidence of acute brain insult1.4
Tiny dense focus on the right cerebral lair hemisphere1.4
Widining of extraaxsial space1.4
Brain finding

Medication

Only 11 (2.6%) patients did not receive any medications, while the rest received different type of medications; 134 (31.3%) received “ACE inhibitors,” followed by 123 (28.7%) administered “Diuretics (furosemide),” then 106 (24.8%) had “Ca- channel blockers.” Figure 2.
Figure 2

Frequencies of medications used in patients

Frequencies of medications used in patients

Disease progression and outcomes

One-third of the cases (n = 79, 32.4%) were under control while 49 (20.1%) lost follow-up and 24 (10.1%) deceased. Total of 61 (33.1%) were progressed to end-stage renal disease and patients were managed by different types of treatments; 20 cases were managed by medications, 19 cases were managed by hemodialysis, and 17 cases were managed by peritoneal dialysis [Table 7].
Table 7

Disease progression and outcomes

VariablenPercentage
Controlled 7932.4
Deceased2410.1
Did surgery1.4
Loss of follow up4920.1
Progressed to end stage renal disease, patient was managed by CIC1.4
Progressed to end stage renal disease, patient was managed by hemodialysis197.8
Progressed to end stage renal disease, patient was managed by kidney transplantation41.6
Progressed to end stage renal disease, patient was managed by medications208.2
Progressed to end stage renal disease, patient was managed by peritoneal dialysis177.0
Recovered 114.5
Transient41.6
Uncontrolled156.1
Disease progression and outcomes

Discussion

There is a lack of knowledge regarding th eprevalence of HTN in children of Saudi Arabia. This study findings document the prevalence, causes, and outcomes of HTN in pediatric patients presented in the inpatient ward. Out of 244 included patients, 188 cases had HTN secondary to renal disease with a prevalence of 77.0% while the prevalence of primary HTN was 9.4%. Half of the patients were diagnosed in the first 5 years. Nephrotic syndrome and renal diseases were the most frequent chronic illness that had been reported, which explain the abnormalities in renal imaging and renal function test. However, the reported data are not integral andimportant investigations were not performed such as eye examinations, assessment of kidney size, and ECHO. Our results are consistent with the current literature; in age group up to 6 years, renal disorders followed by coarctation of the aorta are the most commonly reported causes, followed bythe renal parenchymal disease in older age.[11] In another study in the southwestern United States, out of 132 children with HTN, 67% was due to renal or renovascular diseases such as renal artery thrombosis, cystic kidney disease, glomerulonephritis, and reflux nephropathy.[12] In another study, underlying causesof secondary HTN in 242 patients were mostly due to chronic glomerulonephritis (49.2%), followed by coarctation of aorta, (53.3%) then obstructive uropathy (15.8%) and reflux nephropathy (12.2%) in contrast to low prevalence of thrombotic microangiopathy (6.1%) and renovascular disease (5.7%).[7] In a retrospective study in Thailand among 66 children, the prevalence of secondary HTN was 79.1% and most patients were asymptomatic, renal parenchymal diseases were identified in 62.7% and coarctation of the aorta was detected in 3.0% only.[13] Previous studies have revealed that many factors are associated with the high rates of HTN such as age, sex (male) or obesity. In another study of 25,309 children and adolescents aged 7–18 years, the prevalence of obesity and HTN were 3.7% and 4.9%, respectively. A multicenter study by Narang et al. concluded that age, sex, socioeconomic status, and geographical distribution had an impact on the prevalence of HTN.[14] In 2017, Das Mk et al. reported that the prevalence of HTN raises with BMI and age. More specefically, the prevalence of HTN among under weight was 14.6% compared to 20.6% among normal weight persons.[15] In a cross-sectional study in northern India among 1,085 school children aged from 11 to 17 years, the prevalence of HTN and overweight were 5.9% and 3.5%, respectively.[16] However, Sumboonnanonda et al. found that BMI more than 25 is not reliable to differentiate primary and secondary HTN, since there is no significant difference between them.[13] In general, systemic HTN could affect the cardiovascular system. In our study, left ventricular hypertrophy and valvular lesions were the highest abnormality reported, even with a few event and small prevalence reported. In a cross-section study on hypertensive young patients, 17% had concentric left ventricular hypertrophy.[17] However, Lesiman et al. found a humble relationship between blood pressure variability and left ventricular hypertrophy in primary and secondary HTN; however, secondary HTN was associated with increased sleep period diastolic standard deviation.[18] Further, regular screening for elevated blood pressure and preventable measurement to control weight, reduce salt intake, encourage healthy dietary habits and active lifestyle are all recommended to avoid the complications of pediatric HTN.[1] The main aim of healthcare practitioners in the management of pediatric secondary HTN is to normalize the blood pressure below the 90th percentile and closely monitor any potential target organ damage.[19] However, there is no preferred antihypertensive medication, but it is recommended to start with the lowest dosage of the antihypertensive medication till target blood pressure is reached. If still target blood pressure is not achieved with the maximum dosage of a single medication, a second medication with complementary action should be added.[19] In our study, the majority of patients were treated by angiotensin-converting enzyme inhibitor (ACEI), since it was found to be a good choice for a child with proteinuria due to renal disease.[19] Also, the highest percentage of patients who progressed to end-stage renal disease were managed by medications. Beside pharmacological therapy, lifestyle modification could be effective to decline the blood pressure. Significant reduction in blood pressure in adolescent was accomplished bymaintaining the DASH diet (Dietary Approaches to Stop HTN) versus standard diet.[20] It is worth mentioning that evidence-based information and statistics about pediatric HTN would help the policymakers and all healthcare practitioners in the effective management of HTN and associated comorbidities. The National Institute of Health (NIH) of the USA has reported that at least once annual evaluation of blood pressure and checking the elements of anthropometry are warranted.[2122] Our study has some limitations: (1) it was carried out as a single-center, (2) participants were only inpatients cases, (3) investigations performed were not sufficient to evaluate and investigate the complications of HTN, and (4) there were some missing data from specific profiles.

Conclusion

The prevalence of secondary HTN due to renal disease is considered to be high in pediatric patients admitted to King Abdulaziz University. Several renal diseases in the renal system are associated with secondary HTN mostly attriubuted to renal malformation. In addition, renal affection, cerebral infarction, bleeding, left ventricular hypertrophy, and valvular lesion are the highest reported complications in our population. Follow-up with ECHO and brain CT is highly recommended in pediatric HTN. Future studies on a larger sample and vigorous follow-up are recommended.

Recommendations

Follow-up extended studies with ECHO, eye examination and brain CT are highly recommended in pediatric HTN Studies with larger sample and multi-centers approach are recommended.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.
  18 in total

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3.  Clinical Practice Guideline for Screening and Management of High Blood Pressure in Children and Adolescents.

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Review 4.  Pediatric hypertensive emergencies.

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5.  Sustained hypertension in children.

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6.  Etiology of sustained hypertension in children in the southwestern United States.

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7.  Association between DASH diet (Dietary Approaches to Stop Hypertension) and hypertension in adolescents: A cross-sectional school-based study.

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8.  Redefining hypertension in children and adolescents: A review of the evidence considered by the European Society of Hypertension and American Academy of Pediatrics guidelines.

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Authors:  Rajiv Narang; Anita Saxena; Ankush Desai; Sivasubramanian Ramakrishnan; Rajendra S Thangjam; Snehal Kulkarni; Kedareshwar Narvencar; Ana K Jacques' E Costa; Amit Dias; Ritesh Sukharamwala; John Cleland
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