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Renal Function in Childhood Dengue Hemorrhagic Fever. Fungsi Ginjal pada Demam Berdarah Dengue Anak

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Dedi Rachmadi, Engkie A Djauharie, Dany Hilmanto, Nanan Sekarwana

Department of Child Health

Faculty of Medicine Universitas Padjadjaran-Rumah Sakit Dr. Hasan Sadikin Bandung

Absract

Dengue hemorrhagic fever (DHF) is the dengue virus infection characterized by plasma leakage as a result of

increased vascular permeability. Consequently, it will influence renal function especially in dengue shock syndrome (DSS). The aim of this study was to assess glomerular filtration rate (GFR) in DHF and DSS. A descriptive study

with cross sectional design was performed in all DHF children who were admitted to Department of Child Health

Dr. Hasan Sadikin Hospital Bandung, from October 2003 to January 2004. Diagnosis of DHF was confirmed

by WHO criteria. The patients were divided into DHF group (grade I and II) and DSS group (grade III and IV).

Glomerular filtration rate was calculated by Schwartz formula from creatinine serum level. The distribution of sex, age, and nutritional status were using chi-square test and the proportion of GFR was used t test. From 68 subjects, 41 (60%) were diagnosed as DHF and 27 (40%) as DSS. There were no significant difference in distribution of sex, age, and nutritional status between DHF and DSS group, each p value was >0.05. Mean GFR in all subjects, DHF, and DSS group were 155.9±47.8, 152.3±49.2, and 161.3±45.9, consecutively. The proportion of GFR between DHF and DSS group was 137.50 (94.8–1318.2) vs. 155.38 (89.2–261.9), p=0.322. In conclusions, all subjects have normal GFR, there is no difference of GFR between DHF and DSS group. [MKB. 2011;43(2S):44S–7]. Key words: Dengue hemorrhagic fever (DHF), dengue shock syndrome (DSS), glomerular filtration rate (GFR)

Fungsi Ginjal pada Demam Berdarah Dengue Anak

Abstrak

Demam berdarah dengue (DBD) merupakan infeksi virus dengue, ditandai dengan kebocoran plasma akibat peningkatan permeabilitas vaskular. Berkurangnya aliran darah ke ginjal akan mempengaruhi fungsi ginjal,

terutama pada sindrom syok dengue (SSD). Tujuan penelitian ini untuk menilai laju filtrasi glomerulus (LFG)

pada DBD dan SSD. Penelitian deskriptif dengan rancangan potong silang pada penderita DBD yang datang ke

Departemen Ilmu Kesehatan Anak RS Dr. Hasan Sadikin Bandung, periode Oktober 2003–Januari 2004. Diagnosis

DBD berdasarkan kriteria WHO. Subjek dibagi dalam grup DBD (derajat I dan II) dan SSD (DBD derajat III dan

IV). Penilaian LFG dihitung dari kadar kreatinin serum dengan rumus Schwartz. Perbandingan distribusi jenis

kelamin, usia, dan status nutrisi pada kedua kelompok menggunakan uji chi-kuadrat, sedangkan untuk proporsi

LFG dengan uji t. Dari 68 subjek, grup DBD 41 (60%) dan grup SSD 27 (40%). Tidak ada perbedaan distribusi jenis kelamin, usia, dan satus nutrisi antara grup DBD dan SSD, masing-masing dengan nilai p>0,05. LFG rata-rata grup gabungan, DBD, dan DSS berturut-turut 155,9±47,8; 152,3±49,2; dan 161,3±45,9. Proporsi LFG antara grup DBD dan SSD 137,50 (94,8–131,82) vs 155,38 (89,2–26,9), p=0,322. Simpulan, semua subjek penelitian mempunyai LFG normal dan tidak ada perbedaan antara DBD dan SSD. [MKB. 2011;43(2S):44S–7].

Kata kunci: Laju filtrasi glomerulus (LFG), demam berdarah dengue (DBD), sindrom syok dengue (SSD)

Korespondensi: Dr. Dedi Rachmadi, dr., Sp.A(K), M.Kes, Departemen Ilmu Kesehatan Anak Fakultas Kedokteran Universitas Padjadjaran-Rumah Sakit Dr. Hasan Sadikin, jalan Pasteur No. 38 Bandung 40163, telepon (022) 2035957,

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Introduction

Dengue virus infection clinically manifests as dengue fever (DF), dengue hemorrhagic fever (DHF) or dengue shock syndrome (DSS). Dengue hemorrhagic fever (DHF) and DSS are the severe manifestation of dengue virus infection characterized by plasma leakage as a result of increased vascular permeability. Following this leakage, hypovolemic and decrease renal blood perfusion occurs as a consequence of a plasma

volume loss. Consequently, it will influence glomerular filtration rate (GFR) especially in

severe DHF (grade III and IV).

Dengue hemorrhagic fever is a sporadic fever disease, which is characterized by hemorrhage, tends to produce shock and might death.1,2 Capillary

damage allows fluid, electrolyte, and protein to leak into extravascular spaces. This internal redistribution of fluid results in hemoconcentration

and hypovolemia. Hemoconcentration in DHF

patients occur more than 20%.1 Shock is the most

feared complication for DHF patients.3 Shock in

DHF is caused by hypovolemia, and hypovolemia will cause a decrease of cardiac output which in

turn will decrease renal blood flow (RBF). This

reduce in RBF from hypovolemia means that the

fluid balance control system does not work well,

it will lead to renal dysfunction and even acute kidney injury.4

In recent years there has been an increasing report of unusual manifestation of dengue viral infection including renal system involvement. Renal involvement in several cases has been reported usually accompanied with acute kidney injury with or without shock, hemolysis, rhabdomyolysis, and sepsis.3,5 There are a few reports about renal

function in patients with dengue hemorrhagic fever (DHF). Renal dysfunction is manifested by an increase in serum creatinine concentration. Even so, the duration needed from hypovolemia to renal dysfunction is uncertain.4 This study will assess

and wantto know the difference renal function by

examining creatinine level in patients with DHF and DSS when diagnosed for the first time.

Methods

This was an analytic descriptive study with a cross sectional design. The amount of sample

was based on a confidence interval of 95% and a power test of 80%. The subject of this study

were all pediatric DHF patients hospitalized at the Pediatric Department of Dr. Hasan Sadikin Hospital Bandung, from October 2003 to January 2004.

The subject of DHF was fulfilled by WHO

clinical and laboratory criteria, whose parents willing to join and sign the informed consent. The

exclusion criteria for this study were the patients had already received intravenous fluid therapy

by the time DHF was diagnosed, children with dehydration due to diarrhea and vomiting and those with renal disease.

All subjects’ identity was filled, including the general characteristics of name, age, sex, address,

and nutritional status. Dengue hemorrhagic fever

patients were classified as DHF or DSS group. The

serum creatinine concentration was measured by the Jaffe method on admission (from Outpatient or Pediatric Emergency Department) and then the

GFR was calculated by the Schwartz formula.

Ethical approval for this study was obtained from the Ethic Committee of the Faculty Medicine of Padjadjaran University/Dr. Hasan Sadikin Hospital Bandung.

The distribution of sex and nutritional

status in both groups were compared using chi-square test, while the age, length of fever before admitted to hospital, and hematocrit using t test. Data analysis was conducted descriptively for

mean and standard deviation. To compare GFR

value means between DHF and DSS groups were used t test, and p values <0.05 were considered to

indicate statistical significance. Statistic package for social sciences (SPSS) 17.0 computer program

was used to analyze data from this study.

Results

A total number of 68 children with DHF and DSS fulfilled the enrollment criteria.

Statistical analysis shows there were no

difference in distribution of sex, age, and

nutritional status, length of fever before admitted to hospital and hematocrit from both DHF and DSS groups. The difference of platelet count

in DHF and DSS was significant (Table 1). All subjects had normal GFR. There was no difference of mean GFR between DHF and DSS

group (Table 2).

Discussion

The World Health Organization criteria for

dengue hemorrhagic fever are fever (2–7 days),

minor or major hemorrhagic manifestations, thrombocytopenia (<100,000/mm3), and objective

evidence of increased capillary permeability (hematocrit increased >20%). Dengue shock syndrome should fulfill these criteria plus

hypotension or narrow pulse pressure (<20 mm

(3)

Hg).1,3 All of these features were present in our

described patient studies.

The GFR is clinically important because it

is a measurement of renal function. Measuring serum creatinine is a simple test and it is the most commonly used indicator of renal function.6

Creatinine, as a waste product of metabolism, is

not reused by the body and is normally excreted exclusively by the kidney. Creatinine is also

produced naturally by the body (creatinine is a break-down product of creatine phosphate,

which is found in muscle). It is freely filtered by

the glomerulus, but also actively secreted by the peritubular capillaries in very small amounts such that creatinine clearance overestimates actual

GFR by 10–20%.6 Serum creatinine concentration

will be affect by the following variables: sex, age,

weight, nutritional status, and race.7 In this study

shows there were no difference in distribution of

sex, age, and nutritional status from both DHF

and DSS groups.

The results of this study found that GFR

of DHF and DSS patients were within normal

values according to age and sex. There was no difference in GFR between DHF and DSS patients, p=0.322 (Table 2). It was not in

accordance with the theory that hypovolemia occurred in DHF and DSS patients may caused a major circulation disturbance in all organs including kidney.4,5 Hypovolemia that occurred in

DHF and DSS would cause a decrease in cardiac output which in turn will decrease renal blood

flow (RBF). In more severe cases when degree of plasma leakage is to greater extent, the patients

will have clinical signs of shock. In contrast with our study, the previous studies from small series of patients or case reports. Tanphaichitr et al7 found one case of transient azotemia and

one case of acute renal failure (ARF) among

17 patients with DHF. Mendez and Gonzales8

found 1.6% of (ARF) among 617 children with DHF in Colombia. Lee et al9 reported 4.9% of

ARF in 81 Chinese patients suffering from DHF/

DSS and Abboud10 reported 5% of ARF in DHF.

Other studies, there were eight cases of acute

kidney injury (AKI) reported in patients with

DF5,11 and DSS.3,12 More recently, there were 15

cases of nephropathy dengue has been reported.13

Mostly dengue infection induced renal injury accompanied with syok, rhabdomyolysis, and hypotension. Chotmongkol and Sawanyawisuth14

reported of dengue infection induced renal injury, there was a case of dengue infection induced glomerulonephritis without shock, hypotension, or rhabdomyolysis.

It was assumed that the hypovolemia or shock in our study was so brief that the decreased RBF does not persist, so the circulation system can function well causing no renal damages. It was probably caused by the short lived hypovolemia in DHF patients and the renal autoregulation system causing the kidney as the last organ to be affected by hemodynamic dysfunction.15

According to Vogt and Avner,4 the time needed

from hypovolemia to cause renal dysfunction is still uncertain.

There were no reduces and differences of GFR

in DHF and DSS patients at the time of diagnosis.

Table 1 Characteristics of DHF and DSS

DHF DSS p

Sex, n

Male

Female 1625 1314 *0.457

Age, mean (years) 7.6 8.4 0.337

Nutritional status, n PEM

Non PEM 1328 89 *0.856

Length of fever before admitted to hospital, mean (days) 4.0 4.3 0.329

Hematocrit, mean (%) 41.98 42.22 0.833

Platelet, mean/mm3 96517 69037 0.007

p = t test, *chi-square test

Table 2 GFR in DHF and DSS GFR (n=41)DHF (n=27)DSS Combination(n=68) p* Mean (SD) Median Range 152.30 (49.20) 137.50 94.88–318.21 161.31 (45.88) 155.38 89.17–261.90 155.88 (47.77) 141.89 89.17–318.21 0.322 *Mann Whitney test

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The affect of hypovolemia in renal function could not be determined based on serum creatinine level at the time the diagnosis of DHF was

confirmed. Creatinine will not be raised above the normal range until 60% of total kidney function

is lost.6 To ascertain the renal function in DHF

and DSS patients, a more accurate examination

is necessary and repeated that measurement during the course of the illness is needed. Further

study with serial GFR and serum creatinine level

evaluation is needed to make the natural history of DHF and DSS clear. We concluded that there

are no increases and differences of GFR on DHF

and DSS patients at the time of diagnosis.

References

1. World Health Association. Dengue guideline

for diagnosis, treatment, prevention, and control. 3rd edition. Geneva: World Health

Association; 2009.

2. Gibbons RV, Vaughn DW. Dengue: an

escalating problem. BMJ. 2002;324:1563–6.

3. Karakus A, Banga N, Voorn GP, Meinders AJ.

Dengue shock syndrome and rhabdomyolisis.

Neth J Med. 2007;65:78–81.

4. Vogt BA, Avner ED. Renal failure. In:

Behrman RE, Kliegman RM, Arvin AM,

eds. Nelson textbook of pediatrics. 17th ed.

Philadelphia: WB Saunders Co. 2004. p.

1767–71.

5. Nair VR, Unnikrishnan D, Satish B, Sahadulla MI. Case report acute renal failure in dengue fever in the absence of bleeding manifestations or shock. Infect Dis Clin

Pract. 2005;13:142–3.

6. Friedman A. Laboratory assessment and investigation of renal function. In: Avner

ED, Harnon WE, Niaudet P, Yashikawa N,

editors. Pediatric nephrology. 6th ed. Berlin

Heidelberg: Springer-Verlag. 2009. p. 491–

504.

7. Tanphaichitr VS, Chonlasin R, Suwantol

L, Pung-Amritt P, Tachavanich K, Yogsan

S, et al. Effect of red blood cell

glucose-6-phosphate dehydrogenase deficiency on

patients with dengue hemorrhagic fever. J

Med Assoc Thai. 2002;85(Suppl. 2):S522–9. 8. Mendez A, Gonzalez G. Dengue haemorrhagic

fever in children: ten years of clinical

experience. Biomedica. 2003;23:180–93.

9. Lee IK, Liu JW, Yang KD. Clinical

characteristics and risk factors for con-current bacteremia in adults with dengue

hemorrhagic fever. Am J Trop Med Hyg. 2005;72:221–6.

10. Abboud O. Tropical acute renal failure.

3rd Congress of Nephrology in Internet.

(accessed January 2007). Available from:

http:/www.uninet.edu/cin2003/conf/aboud. html.

11. Wiersinga WJ, Scheepstra CG, Kasanardjo

JS, de Vries PJ, Zaaijer H, Geerlings SE.

Dengue fever-induced hemolytic uremic

syndrome. Clin Infect Dis. 2006;43:800–1.

12. Davis JS, Bourke P. Rhabdomyolysis associated with dengue virus infection. Clin

Infect Dis. 2004;38:e109–11.

13. Kimmel PL, Moore J Jr. Viral

glomerulonephritis. In: Schrier RW, editor.

Disease of the kidney and urinary tract. 8th

edition. Philadelphia: Lipincott Williams and Wilkins; 2007. p. 1478–80.

14. Chotmongkol V, Sawanyawisuth K. Case report dengue hemorrhagic fever with

encephalopathy in an adult. Am J Trop Med Hyg. 2004;35:160–3.

15. Greenbaum LA. Pathophysiology of body

fluids and fluid therapy. In: Behrman RE,

Kliegman RM, Jenson HB, editors. Nelson

textbook of pediatrics. 17th ed. Philadelphia:

WB Saunders Co; 2004. p. 191–245.

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Dzulfikar D. Lukmanul Hakim, Wiwin Winiar, Herry Garna

Departemen Ilmu Kesehatan Anak, Fakultas Kedokteran, Universitas Padjajaran-Rumah Sakit Dr.

Hasan Sadikin Bandung

Abstrak

Virus dengue dapat menyebabkan infeksi pada semua kelompok usia dengan manifestasi klinis beragam mulai dari asimtomatik, ringan, sampai berat yang biasanya merupakan kasus fatal. Dengue berat ditandai dengan kebocoran plasma, hemokonsentrasi, dan gangguan hemostasis. Penelitian ini bertujuan untuk mengetahui karakteristik penderita dengue berat yang dirawat di ruang Pediatric Intensive Care Unit (PICU) RS Dr. Hasan Sadikin sejak Januari 2009 sampai Desember 2010. Penelitian dilakukan secara retrospektif deskriptif berdasarkan data dari rekam medis penderita. Sebanyak 21 penderita dengue berat dirawat selama 2 tahun, 15/21 penderita perempuan

dan 6/21 laki-laki, serta 5/21 anak meninggal dunia selama dirawat dengan sebab kematian tersering sindrom

syok dengue (SSD) dan kogagulopati intravaskular diseminata (KID). Sebagian besar penderita berusia 1−5 tahun

dengan status gizi baik. Hepatomegali ditemukan pada semua penderita dengan hematokrit rata-rata 38%. Pada penelitian ini, manifestasi klinis dengue berat berupa SSD (15/21), KID (11/21), ensefalopati (6/21), efusi pleura

(5/21), miokarditis (3/21), serta acute respiratory distress syndrome (3/21). Simpulan, dengue beratlebih banyak didapatkan pada anak perempuan, usia 1–5 tahun, serta status gizi baik. Manifestasi klinis dengue berat yang

dominan berupa syok, koagulasi intravaskular diseminata, dan ensefalopati. [MKB. 2011;43(2S):48S–52]. Kata kunci: Dengue berat, karakteristik, pediatric intensive care unit

Characteristic of Severe Dengue Hospitalized

in Pediatric Intensive Care Unit

Abstract

Dengue viral infections affect all age groups and produce a spectrum of clinical illness that ranges from asymptomatic to severe and occasionally fatal disease. Severe dengue characterized by plasma leakage, hemoconcentration, and hemostatic disorder. The aim of this study was to know the characteristic of severe dengue patients admitted to Pediatric Intensive Care Unit (PICU) Dr. Hasan Sadikin Hospital Bandung during January 2009 to December 2010. This was a retrospective descriptive study based on the data collected from the medical records.

Twenty-one severe dengue cases in two years was admitted 15/21 females and 6/21 males, and 5/21 of them died during

hospitalization because of dengue shock syndrome (DSS) and disseminated intravascular coagulation (DIC). Most of them were 1−5 years old with good nutritional status. Hepatomegaly was found in all cases with mean

hematocrit was 38%. In this research, the most manifestation of severe dengue were DSS (15/21), DIC (11/21), encephalopathy (6/21), pleural effusion (5/21), myocarditis (3/21), and acute respiratory distress syndrome (3/21).

In conclusions, severe dengue more common in girls, 1–5 years old, and well-nourished children. The most common clinical manifestation of severe dengue were shock, disseminated intravascular coagulation, and encephalopathy.

[MKB. 2011;43(2S):48S–52].

Key words: Characteristic, pediatric intensive care unit, severe dengue

Korespondensi: Dzulfikar Djalil, dr., Sp.A(K), M.Kes, Departemen Ilmu Kesehatan Anak Fakultas Kedokteran Universitas Padjadjaran-Rumah Sakit Dr. Hasan Sadikin, jalan Pasteur No. 38 Bandung 40163, Indonesia, telepon (022) 2035957,

Gambar

Table 1 Characteristics of DHF and DSS

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