Cargando…

Tumor lysis syndrome in pediatric acute lymphoblastic leukemia at tertiary care center

OBJECTIVES: Tumor lysis syndrome (TLS) is common complication of acute lymphoblastic leukemia (ALL). It is characterized by presence of two or more of hyperkalemia, hyperuricemia, hyperphosphatemia and hypocalcemia. TLS may cause acute kidney injury (AKI), arrhythmias and seizures. Our objective was...

Descripción completa

Detalles Bibliográficos
Autores principales: Naeem, Bilqis, Moorani, Khemchand N, Anjum, Misbah, Imam, Uzma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659073/
https://www.ncbi.nlm.nih.gov/pubmed/31372114
http://dx.doi.org/10.12669/pjms.35.4.715
_version_ 1783439064814321664
author Naeem, Bilqis
Moorani, Khemchand N
Anjum, Misbah
Imam, Uzma
author_facet Naeem, Bilqis
Moorani, Khemchand N
Anjum, Misbah
Imam, Uzma
author_sort Naeem, Bilqis
collection PubMed
description OBJECTIVES: Tumor lysis syndrome (TLS) is common complication of acute lymphoblastic leukemia (ALL). It is characterized by presence of two or more of hyperkalemia, hyperuricemia, hyperphosphatemia and hypocalcemia. TLS may cause acute kidney injury (AKI), arrhythmias and seizures. Our objective was to determine the frequency of TLS and its biochemical abnormalities in children with ALL. METHODS: A retrospective study on 91 children, aged 2-13 years with ALL was carried out in Nephrology and Oncology departments of National Institute of Child Health, Karachi from January 2016 to December 2017. Patients already received chemotherapy were excluded. Data including risk categories, immunophenotyping, laboratory parameters like complete blood picture, serum creatinine (SCr), potassium(K), calcium (Ca), phosphorus(P) and uric acid (UA) on day 0,3 and 7 after chemotherapy were collected. Data analyzed on SPSS using descriptive statistics. Independent t- test was applied to compare means and P- value<0.05 was taken as significant. RESULTS: Ninety-one children with mean age of 6.39±3.08 years were studied. Male were 57% and 43% female. High risk ALL were 61.5%. Pre –BALL were 82.4% and 17.5% had T-cell ALL. All patients had anemia (hemoglobin7.69±2.66 g/dl) and thrombocytopenia (43.61± 18.6 x10(9)) where as hyperleukocytosis and blast cells were observed in 20.87% and 73.6% respectively. Comparing the biochemical parameters of ALL, the difference in SCr from D0 vs D3 (0.46±0.16 vs0.54± 0.35 and D7, 0.44±0.22) was significant (p=0.001). Similarly, difference in UA (D0, 4.12±2.40 vs D3, 3.82±1.73 and D7, 3.56±1.42), SP (D0, 4.24±1.34 vs D3, 4.61±1.76 and D7,4.13±1.07mg/dl)and for K (p=0.038) was significant. There was no difference in Ca from D0 vs D3 (0.092) and D7 (0.277). TLS was found in 62.6% children, it was chemotherapy induced in 72% and spontaneous in 28%. Clinical-TLS was observed in 14% and all CTLS had AKI. Hyperuricemia and hyperphosphatemia were the most common biochemical abnormalities in laboratory-TLS and CTLS. CONCLUSION: TLS was found in 62.6% despite preventive measures. Early recognition and treatment is essential to avoid morbidity and mortality.
format Online
Article
Text
id pubmed-6659073
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Professional Medical Publications
record_format MEDLINE/PubMed
spelling pubmed-66590732019-08-01 Tumor lysis syndrome in pediatric acute lymphoblastic leukemia at tertiary care center Naeem, Bilqis Moorani, Khemchand N Anjum, Misbah Imam, Uzma Pak J Med Sci Original Article OBJECTIVES: Tumor lysis syndrome (TLS) is common complication of acute lymphoblastic leukemia (ALL). It is characterized by presence of two or more of hyperkalemia, hyperuricemia, hyperphosphatemia and hypocalcemia. TLS may cause acute kidney injury (AKI), arrhythmias and seizures. Our objective was to determine the frequency of TLS and its biochemical abnormalities in children with ALL. METHODS: A retrospective study on 91 children, aged 2-13 years with ALL was carried out in Nephrology and Oncology departments of National Institute of Child Health, Karachi from January 2016 to December 2017. Patients already received chemotherapy were excluded. Data including risk categories, immunophenotyping, laboratory parameters like complete blood picture, serum creatinine (SCr), potassium(K), calcium (Ca), phosphorus(P) and uric acid (UA) on day 0,3 and 7 after chemotherapy were collected. Data analyzed on SPSS using descriptive statistics. Independent t- test was applied to compare means and P- value<0.05 was taken as significant. RESULTS: Ninety-one children with mean age of 6.39±3.08 years were studied. Male were 57% and 43% female. High risk ALL were 61.5%. Pre –BALL were 82.4% and 17.5% had T-cell ALL. All patients had anemia (hemoglobin7.69±2.66 g/dl) and thrombocytopenia (43.61± 18.6 x10(9)) where as hyperleukocytosis and blast cells were observed in 20.87% and 73.6% respectively. Comparing the biochemical parameters of ALL, the difference in SCr from D0 vs D3 (0.46±0.16 vs0.54± 0.35 and D7, 0.44±0.22) was significant (p=0.001). Similarly, difference in UA (D0, 4.12±2.40 vs D3, 3.82±1.73 and D7, 3.56±1.42), SP (D0, 4.24±1.34 vs D3, 4.61±1.76 and D7,4.13±1.07mg/dl)and for K (p=0.038) was significant. There was no difference in Ca from D0 vs D3 (0.092) and D7 (0.277). TLS was found in 62.6% children, it was chemotherapy induced in 72% and spontaneous in 28%. Clinical-TLS was observed in 14% and all CTLS had AKI. Hyperuricemia and hyperphosphatemia were the most common biochemical abnormalities in laboratory-TLS and CTLS. CONCLUSION: TLS was found in 62.6% despite preventive measures. Early recognition and treatment is essential to avoid morbidity and mortality. Professional Medical Publications 2019 /pmc/articles/PMC6659073/ /pubmed/31372114 http://dx.doi.org/10.12669/pjms.35.4.715 Text en Copyright: © Pakistan Journal of Medical Sciences http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Naeem, Bilqis
Moorani, Khemchand N
Anjum, Misbah
Imam, Uzma
Tumor lysis syndrome in pediatric acute lymphoblastic leukemia at tertiary care center
title Tumor lysis syndrome in pediatric acute lymphoblastic leukemia at tertiary care center
title_full Tumor lysis syndrome in pediatric acute lymphoblastic leukemia at tertiary care center
title_fullStr Tumor lysis syndrome in pediatric acute lymphoblastic leukemia at tertiary care center
title_full_unstemmed Tumor lysis syndrome in pediatric acute lymphoblastic leukemia at tertiary care center
title_short Tumor lysis syndrome in pediatric acute lymphoblastic leukemia at tertiary care center
title_sort tumor lysis syndrome in pediatric acute lymphoblastic leukemia at tertiary care center
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659073/
https://www.ncbi.nlm.nih.gov/pubmed/31372114
http://dx.doi.org/10.12669/pjms.35.4.715
work_keys_str_mv AT naeembilqis tumorlysissyndromeinpediatricacutelymphoblasticleukemiaattertiarycarecenter
AT mooranikhemchandn tumorlysissyndromeinpediatricacutelymphoblasticleukemiaattertiarycarecenter
AT anjummisbah tumorlysissyndromeinpediatricacutelymphoblasticleukemiaattertiarycarecenter
AT imamuzma tumorlysissyndromeinpediatricacutelymphoblasticleukemiaattertiarycarecenter