Acute sickle cell syndromes in Nigerian adults
Summary The pattern of acute illness was determined in 102 adolescents and adults with sickle cell anaemia who presented to the emergency unit of a Lagos hospital. The patients had a mean age of 20.5 years ( sd 13.1) and a male–female ratio of 1.5. The symptoms included fever (72%), fatigue and weak...
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Published in | Clinical and laboratory haematology Vol. 22; no. 3; pp. 151 - 155 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Science Ltd
01.06.2000
Blackwell Science |
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Abstract | Summary
The pattern of acute illness was determined in 102 adolescents and adults with sickle cell anaemia who presented to the emergency unit of a Lagos hospital. The patients had a mean age of 20.5 years ( sd 13.1) and a male–female ratio of 1.5. The symptoms included fever (72%), fatigue and weakness (59%), anorexia (59%) and pain (57.5%) while major clinical signs were pallor (100%), jaundice (71%) and hepatomegaly (68%). Sixty‐eight per cent of patients had sickle cell crises, including one with hemiplegic stroke, 10% with combined anaemia and pain crises, 33% with anaemia crises only and 23.5% with pain crises only. Sixty‐three per cent had infection which was malaria in 24.5%, bacterial in 17% and viral in 6%. Of 16 patients with pyrexia of unknown origin, seven responded to treatment with chloroquine and eight to antibiotics. Infection was detected in 50% of the patients with sickle cell crises. The association between anaemia crises and malaria was significant (P < 0.05). Of the eight deaths, seven (88%) had anaemia crises. In contrast to studies conducted two decades ago in the same hospital, the prevalence of anaemia crises now exceeds that of pain crises and malaria now exceeds that of bacterial infection. Severe symptomatic anaemia (anaemia crisis) was more frequently associated with infection (mostly malaria) than was bone pain crisis. The Girdle pain crisis more frequently resulted in a fatal outcome than the uncomplicated bone pain crisis. |
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AbstractList | Summary
The pattern of acute illness was determined in 102 adolescents and adults with sickle cell anaemia who presented to the emergency unit of a Lagos hospital. The patients had a mean age of 20.5 years ( sd 13.1) and a male–female ratio of 1.5. The symptoms included fever (72%), fatigue and weakness (59%), anorexia (59%) and pain (57.5%) while major clinical signs were pallor (100%), jaundice (71%) and hepatomegaly (68%). Sixty‐eight per cent of patients had sickle cell crises, including one with hemiplegic stroke, 10% with combined anaemia and pain crises, 33% with anaemia crises only and 23.5% with pain crises only. Sixty‐three per cent had infection which was malaria in 24.5%, bacterial in 17% and viral in 6%. Of 16 patients with pyrexia of unknown origin, seven responded to treatment with chloroquine and eight to antibiotics. Infection was detected in 50% of the patients with sickle cell crises. The association between anaemia crises and malaria was significant (P < 0.05). Of the eight deaths, seven (88%) had anaemia crises. In contrast to studies conducted two decades ago in the same hospital, the prevalence of anaemia crises now exceeds that of pain crises and malaria now exceeds that of bacterial infection. Severe symptomatic anaemia (anaemia crisis) was more frequently associated with infection (mostly malaria) than was bone pain crisis. The Girdle pain crisis more frequently resulted in a fatal outcome than the uncomplicated bone pain crisis. The pattern of acute illness was determined in 102 adolescents and adults with sickle cell anaemia who presented to the emergency unit of a Lagos hospital. The patients had a mean age of 20.5 years (SD 13.1) and a male-female ratio of 1.5. The symptoms included fever (72%), fatigue and weakness (59%), anorexia (59%) and pain (57.5%) while major clinical signs were pallor (100%), jaundice (71%) and hepatomegaly (68%). Sixty-eight per cent of patients had sickle cell crises, including one with hemiplegic stroke, 10% with combined anaemia and pain crises, 33% with anaemia crises only and 23.5% with pain crises only. Sixty-three per cent had infection which was malaria in 24.5%, bacterial in 17% and viral in 6%. Of 16 patients with pyrexia of unknown origin, seven responded to treatment with chloroquine and eight to antibiotics. Infection was detected in 50% of the patients with sickle cell crises. The association between anaemia crises and malaria was significant (P < 0.05). Of the eight deaths, seven (88%) had anaemia crises. In contrast to studies conducted two decades ago in the same hospital, the prevalence of anaemia crises now exceeds that of pain crises and malaria now exceeds that of bacterial infection. Severe symptomatic anaemia (anaemia crisis) was more frequently associated with infection (mostly malaria) than was bone pain crisis. The Girdle pain crisis more frequently resulted in a fatal outcome than the uncomplicated bone pain crisis. The pattern of acute illness was determined in 102 adolescents and adults with sickle cell anaemia who presented to the emergency unit of a Lagos hospital. The patients had a mean age of 20.5 years (SD 13.1) and a male-female ratio of 1.5. The symptoms included fever (72%), fatigue and weakness (59%), anorexia (59%) and pain (57.5%) while major clinical signs were pallor (100%), jaundice (71%) and hepatomegaly (68%). Sixty-eight per cent of patients had sickle cell crises, including one with hemiplegic stroke, 10% with combined anaemia and pain crises, 33% with anaemia crises only and 23.5% with pain crises only. Sixty-three per cent had infection which was malaria in 24.5%, bacterial in 17% and viral in 6%. Of 16 patients with pyrexia of unknown origin, seven responded to treatment with chloroquine and eight to antibiotics. Infection was detected in 50% of the patients with sickle cell crises. The association between anaemia crises and malaria was significant (P < 0.05). Of the eight deaths, seven (88%) had anaemia crises. In contrast to studies conducted two decades ago in the same hospital, the prevalence of anaemia crises now exceeds that of pain crises and malaria now exceeds that of bacterial infection. Severe symptomatic anaemia (anaemia crisis) was more frequently associated with infection (mostly malaria) than was bone pain crisis. The Girdle pain crisis more frequently resulted in a fatal outcome than the uncomplicated bone pain crisis. |
Author | Ibidapo, M.O. Akinyanju, O.O. |
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References | Walters J.H. & Lehmann H. (1956) Distribution of the S and C haemoglobin variants in two Nigerian communities. Transactions of the Royal Society for Tropical Medicine and Hygiene 50, 204 208. Barrett-Connor E. (1971) Bacterial infections and sickle cell anemia. An analysis of 250 infections in 166 patients and a review of the literature. Medicine 50, 97 112. Akinyanju O. (1973) Osteomyelitis in sickle cell disease in Lagos. West African Medical Journal 22, S7. Jellife D.B. & Humphreys J. (1952) The sickle cell trait in western Nigeria. British Medical Journal 1, 405 406. Fleming A.F., Storey J., Molineaux L., Iroko F.A., Attai E.D. (1979) Abnormal haemoglobins in the Sudan savannah of Nigeria. I. Prevalence of haemoglobins and relationships between sickle cell trait, malaria and survival. Annals of Tropical Medicine and Parasitology 73, 161 172. Wong W.Y., Overturf G.D., Powars D.R. (1992) Infection caused by Streptococcus pneumoniae in children with sickle cell disease: epidemiology, immunologic mechanisms, prophylaxis and vaccination. Clinical Infectious Disease 14, 1124 1136. Hendrickse R.G. & Collard P. (1960) Salmonella osteitis in Nigerian children. Lancet 1, 80 82. Akinyanju O. (1989) A profile of sickle cell disease in Nigeria. Annals of the New York Academy of Sciences 565, 126 156. Elesha S.O., Adepoju F.B., Banjo A.A.F. (1993) Rising incidence of cerebral malaria in Lagos, Nigeria: a post mortem study. East African Journal of Medicine 70, 302 305. Brozovic M., Davies S.C., Brownwell A.I. (1987) Acute admissions of patients with sickle cell disease in Britain. British Medical Journal 294, 1206 1208. Dacie J.V. & Lewis S.M. (1984) Practical Haematology. 6th edn. Churchill Livingston, London. Karayalcin C., Rosner F., Kim K., Chandra P., Aballi A. (1975) Sickle cell anemia. Clinical manifestations in 100 patients and review of the literature. American Journal of Medical Sciences 269, 51 68. Kaine W.N. (1983) Morbidity of homozygous sickle cell anaemia in Nigerian children. Journal of Tropical Paediatrics 29, 104 111. Akinyanju O. & Johnson A.O. (1987) Acute illnesses in Nigerian children with sickle cell anaemia. Annals of Tropical Paediatrics 7, 181 186. Mallouh A.A. & Salamah M.M. (1985) Pattern of bacteria infections in homozygous sickle cell disease. A report from Saudi Arabia. American Journal of Diseases of Children 139, 820 822. 1987; 294 1971; 50 1973; 22 1956; 50 1989; 565 1993; 70 1987; 7 1960; 1 1984 1985; 139 1992; 14 1975; 269 1983; 29 1989 1979; 73 1952; 1 Hendrickse (10.1046/j.1365-2257.2000.00292.x-BIB10|cit10) 1960; 1 Brozovic (10.1046/j.1365-2257.2000.00292.x-BIB4|cit5) 1987; 294 Akinyanju (10.1046/j.1365-2257.2000.00292.x-BIB11|cit1) 1973; 22 Elesha (10.1046/j.1365-2257.2000.00292.x-BIB14|cit8) 1993; 70 Karayalcin (10.1046/j.1365-2257.2000.00292.x-BIB9|cit13) 1975; 269 Kaine (10.1046/j.1365-2257.2000.00292.x-BIB6|cit12) 1983; 29 Akinyanju (10.1046/j.1365-2257.2000.00292.x-BIB15|cit2) 1989; 565 Fleming (10.1046/j.1365-2257.2000.00292.x-BIB17|cit9) 1979; 73 Mallouh (10.1046/j.1365-2257.2000.00292.x-BIB12|cit14) 1985; 139 Dacie (10.1046/j.1365-2257.2000.00292.x-BIB8|cit7) 1984 Jellife (10.1046/j.1365-2257.2000.00292.x-BIB1|cit11) 1952; 1 Walters (10.1046/j.1365-2257.2000.00292.x-BIB2|cit15) 1956; 50 Akinyanju (10.1046/j.1365-2257.2000.00292.x-BIB7|cit3) 1987; 7 Brozovic (10.1046/j.1365-2257.2000.00292.x-BIB16|cit6) 1989 Barrett-Connor (10.1046/j.1365-2257.2000.00292.x-BIB5|cit4) 1971; 50 Wong (10.1046/j.1365-2257.2000.00292.x-BIB13|cit16) 1992; 14 |
References_xml | – volume: 73 start-page: 161 year: 1979 end-page: 172 article-title: Abnormal haemoglobins in the Sudan savannah of Nigeria. I. Prevalence of haemoglobins and relationships between sickle cell trait, malaria and survival publication-title: Annals of Tropical Medicine and Parasitology – volume: 22 start-page: S7 year: 1973 article-title: Osteomyelitis in sickle cell disease in Lagos publication-title: West African Medical Journal – year: 1984 – start-page: 103 year: 1989 end-page: 113 – volume: 269 start-page: 51 year: 1975 end-page: 68 article-title: Sickle cell anemia. Clinical manifestations in 100 patients and review of the literature publication-title: American Journal of Medical Sciences – volume: 29 start-page: 104 year: 1983 end-page: 111 article-title: Morbidity of homozygous sickle cell anaemia in Nigerian children publication-title: Journal of Tropical Paediatrics – volume: 139 start-page: 820 year: 1985 end-page: 822 article-title: Pattern of bacteria infections in homozygous sickle cell disease. A report from Saudi Arabia publication-title: American Journal of Diseases of Children – volume: 7 start-page: 181 year: 1987 end-page: 186 article-title: Acute illnesses in Nigerian children with sickle cell anaemia publication-title: Annals of Tropical Paediatrics – volume: 1 start-page: 405 year: 1952 end-page: 406 article-title: The sickle cell trait in western Nigeria publication-title: British Medical Journal – volume: 294 start-page: 1206 year: 1987 end-page: 1208 article-title: Acute admissions of patients with sickle cell disease in Britain publication-title: British Medical Journal – volume: 565 start-page: 126 year: 1989 end-page: 156 article-title: A profile of sickle cell disease in Nigeria publication-title: Annals of the New York Academy of Sciences – volume: 50 start-page: 204 year: 1956 end-page: 208 article-title: Distribution of the S and C haemoglobin variants in two Nigerian communities publication-title: Transactions of the Royal Society for Tropical Medicine and Hygiene – volume: 70 start-page: 302 year: 1993 end-page: 305 article-title: Rising incidence of cerebral malaria in Lagos, Nigeria: a study publication-title: East African Journal of Medicine – volume: 50 start-page: 97 year: 1971 end-page: 112 article-title: Bacterial infections and sickle cell anemia. An analysis of 250 infections in 166 patients and a review of the literature publication-title: Medicine – volume: 14 start-page: 1124 year: 1992 end-page: 1136 article-title: Infection caused by in children with sickle cell disease: epidemiology, immunologic mechanisms, prophylaxis and vaccination publication-title: Clinical Infectious Disease – volume: 1 start-page: 80 year: 1960 end-page: 82 article-title: Salmonella osteitis in Nigerian children publication-title: Lancet – volume: 1 start-page: 405 year: 1952 ident: 10.1046/j.1365-2257.2000.00292.x-BIB1|cit11 article-title: The sickle cell trait in western Nigeria publication-title: British Medical Journal doi: 10.1136/bmj.1.4755.405 contributor: fullname: Jellife – volume: 139 start-page: 820 year: 1985 ident: 10.1046/j.1365-2257.2000.00292.x-BIB12|cit14 article-title: Pattern of bacteria infections in homozygous sickle cell disease. A report from Saudi Arabia publication-title: American Journal of Diseases of Children doi: 10.1001/archpedi.1985.02140100082038 contributor: fullname: Mallouh – volume: 1 start-page: 80 year: 1960 ident: 10.1046/j.1365-2257.2000.00292.x-BIB10|cit10 article-title: Salmonella osteitis in Nigerian children publication-title: Lancet doi: 10.1016/S0140-6736(60)92900-7 contributor: fullname: Hendrickse – volume: 29 start-page: 104 year: 1983 ident: 10.1046/j.1365-2257.2000.00292.x-BIB6|cit12 article-title: Morbidity of homozygous sickle cell anaemia in Nigerian children publication-title: Journal of Tropical Paediatrics doi: 10.1093/tropej/29.2.104 contributor: fullname: Kaine – volume: 294 start-page: 1206 year: 1987 ident: 10.1046/j.1365-2257.2000.00292.x-BIB4|cit5 article-title: Acute admissions of patients with sickle cell disease in Britain publication-title: British Medical Journal doi: 10.1136/bmj.294.6581.1206 contributor: fullname: Brozovic – volume: 7 start-page: 181 year: 1987 ident: 10.1046/j.1365-2257.2000.00292.x-BIB7|cit3 article-title: Acute illnesses in Nigerian children with sickle cell anaemia publication-title: Annals of Tropical Paediatrics doi: 10.1080/02724936.1987.11748503 contributor: fullname: Akinyanju – volume-title: Practical Haematology. year: 1984 ident: 10.1046/j.1365-2257.2000.00292.x-BIB8|cit7 contributor: fullname: Dacie – volume: 70 start-page: 302 year: 1993 ident: 10.1046/j.1365-2257.2000.00292.x-BIB14|cit8 article-title: Rising incidence of cerebral malaria in Lagos, Nigeria: a post mortem study publication-title: East African Journal of Medicine contributor: fullname: Elesha – volume: 73 start-page: 161 year: 1979 ident: 10.1046/j.1365-2257.2000.00292.x-BIB17|cit9 article-title: Abnormal haemoglobins in the Sudan savannah of Nigeria. I. Prevalence of haemoglobins and relationships between sickle cell trait, malaria and survival publication-title: Annals of Tropical Medicine and Parasitology doi: 10.1080/00034983.1979.11687243 contributor: fullname: Fleming – volume: 269 start-page: 51 year: 1975 ident: 10.1046/j.1365-2257.2000.00292.x-BIB9|cit13 article-title: Sickle cell anemia. Clinical manifestations in 100 patients and review of the literature publication-title: American Journal of Medical Sciences doi: 10.1097/00000441-197501000-00007 contributor: fullname: Karayalcin – volume: 50 start-page: 204 year: 1956 ident: 10.1046/j.1365-2257.2000.00292.x-BIB2|cit15 article-title: Distribution of the S and C haemoglobin variants in two Nigerian communities publication-title: Transactions of the Royal Society for Tropical Medicine and Hygiene doi: 10.1016/0035-9203(56)90024-4 contributor: fullname: Walters – volume: 50 start-page: 97 year: 1971 ident: 10.1046/j.1365-2257.2000.00292.x-BIB5|cit4 article-title: Bacterial infections and sickle cell anemia. An analysis of 250 infections in 166 patients and a review of the literature publication-title: Medicine doi: 10.1097/00005792-197103000-00002 contributor: fullname: Barrett-Connor – volume: 22 start-page: S7 year: 1973 ident: 10.1046/j.1365-2257.2000.00292.x-BIB11|cit1 article-title: Osteomyelitis in sickle cell disease in Lagos publication-title: West African Medical Journal contributor: fullname: Akinyanju – volume: 565 start-page: 126 year: 1989 ident: 10.1046/j.1365-2257.2000.00292.x-BIB15|cit2 article-title: A profile of sickle cell disease in Nigeria publication-title: Annals of the New York Academy of Sciences doi: 10.1111/j.1749-6632.1989.tb24159.x contributor: fullname: Akinyanju – volume: 14 start-page: 1124 year: 1992 ident: 10.1046/j.1365-2257.2000.00292.x-BIB13|cit16 article-title: Infection caused by Streptococcus pneumoniae in children with sickle cell disease: epidemiology, immunologic mechanisms, prophylaxis and vaccination publication-title: Clinical Infectious Disease doi: 10.1093/clinids/14.5.1124 contributor: fullname: Wong – start-page: 103 volume-title: Ethnic Factors in Health and Disease. year: 1989 ident: 10.1046/j.1365-2257.2000.00292.x-BIB16|cit6 doi: 10.1016/B978-0-7236-0916-2.50018-6 contributor: fullname: Brozovic |
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The pattern of acute illness was determined in 102 adolescents and adults with sickle cell anaemia who presented to the emergency unit of a Lagos... The pattern of acute illness was determined in 102 adolescents and adults with sickle cell anaemia who presented to the emergency unit of a Lagos hospital. The... |
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SubjectTerms | Acute Disease Acute illness Adolescent Adult anaemia Anemia - etiology Anemia, Sickle Cell - complications Anemia, Sickle Cell - epidemiology Anemia, Sickle Cell - etiology Anemias. Hemoglobinopathies Bacterial Infections - diagnosis Biological and medical sciences Diseases of red blood cells Female Hematologic and hematopoietic diseases Humans infection Malaria - diagnosis Malaria - drug therapy Male Medical sciences Nigeria - epidemiology pain Pain - etiology Respiration Disorders - etiology sickle cell crises |
Title | Acute sickle cell syndromes in Nigerian adults |
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