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Anaesthesia in sickle cell states

1973; Wiley; Volume: 28; Issue: 1 Linguagem: Inglês

10.1111/j.1365-2044.1973.tb00284.x

1365-2044

J.F. Searle,

Neonatal Health and Biochemistry

AnaesthesiaVolume 28, Issue 1 p. 48-58 Free Access Anaesthesia in sickle cell states A review J. F. SEARLE, J. F. SEARLE MB, BS, FFARCS, Senior Registrar, Department of Anaesthetics, Guy's Hospital London SE1 9RT, and lately of University of Ghana Medical School, Korle Bu Teaching Hospital, Accra, Ghana.Search for more papers by this author J. F. SEARLE, J. F. SEARLE MB, BS, FFARCS, Senior Registrar, Department of Anaesthetics, Guy's Hospital London SE1 9RT, and lately of University of Ghana Medical School, Korle Bu Teaching Hospital, Accra, Ghana.Search for more papers by this author First published: January 1973 https://doi.org/10.1111/j.1365-2044.1973.tb00284.xCitations: 30AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References 1 Lehmann, H. & Huntsman, R.G. (1966) Man's Haemoglobins; including the haemoglobino-pathtes and their investigation. Lippincott , Philadelphia . Google Scholar 2 Herrick, J.B. (1910) Peculiar elongated and sickle-shaped red blood corpuscles in a case of severe anemia. Archives of Internal Medicine, 6, 517. 10.1001/archinte.1910.00050330050003 Google Scholar 3 Emmel, V.E. (1917) A study of the erythrocytes in a case of severe anemia with elongated and sickle-shaped red blood corpuscles. Archives of Internal Medicine, 20, 586. 10.1001/archinte.1917.00090040108005 Web of Science®Google Scholar 4 Hahn, E.V. & Gillespie, E.B. (1927) Sickle cell anaemia–report of a case greatly improved by splenectomy. Experimental study of sickle cell formation. Archives of Internal Medicine, 39, 233. 10.1001/archinte.1927.00130020072006 Web of Science®Google Scholar 5 Pauling, L., Itano, N.A., Singer, S.J. & Wells, I.C. (1949) Sickle cell anaemia, a molecular disease. Science, 110, 543. 10.1126/science.110.2865.543 CASPubMedWeb of Science®Google Scholar 6 Ingram, V.M. (1958) Abnormal human haemoglobins. 1. The comparison of normal human and sickle-cell haemoglobins by 'fingerprinting. Biochimica et Biophysica Acta, 28, 539. 10.1016/0006-3002(58)90516-X CASPubMedWeb of Science®Google Scholar 7 Murayama, M. (1966) Molecular mechanisms of red cell sickling. Science, 153, 145. 10.1126/science.153.3732.145 CASPubMedWeb of Science®Google Scholar 8 Perutz, M.F. (1970) Stereochemistry of cooperative effects in haemoglobin. Nature, 228, 726. 10.1038/228726a0 CASPubMedWeb of Science®Google Scholar 9 Stetson, C.A. Jr, (1966) The state of hemoglobin in sickled erythrocytes. Journal of Experimental Medicine, 123, 341. PubMedWeb of Science®Google Scholar 10 Jensen, W.N., Rucknagel, D.L. & Taylor, W.J. (1960) In vivo study of the sickle cell phenomenon. Journal of Laboratory and Clinical Medicine, 56, 854. CASPubMedWeb of Science®Google Scholar 11 Oduntan, S.A. (1969) Blood gas studies in some abnormal haemoglobin syndromes. British Journal of Haematology, 17, 535. 10.1111/j.1365-2141.1969.tb01404.x PubMedWeb of Science®Google Scholar 12 Cawein, M.J., O'Neill, R.P., Danzer, L.A., Lappoat, E.J. & Roach, T. (1969) A study of the sickling phenomenon and oxygen dissociation curve in patients with haemoglobins SS, SD, SF and SC. Blood, 34, 682. CASPubMedWeb of Science®Google Scholar 13 Sluijter, M.E. (1970) In: Recent Advances in Aerospace Medicine (Ed. by D. E. Busby). Reidel , Dordrecht . Google Scholar 14 Green, R.L., Huntsman, R.G. & Serjeant, G.R. (1971) The sickle-cell and altitude. British Medical Journal, iv, 593. 10.1136/bmj.4.5787.593 CASWeb of Science®Google Scholar 15 Lange, R.D., Minnich, V. & Moore, C.V. (1951) Effect of oxygen tension and of pH on the sickling and mechanical fragility of erythrocytes from patients with sickle cell anemia and sickle cell trait. Journal of Laboratory and Clinical Medicine, 37, 789. CASPubMedWeb of Science®Google Scholar 16 Djabanor, F.E.T. (1972) The sickling of erythrocytes–a study of the effect of adrenaline and hydrocortisone on the sickling phenomenon. Ghana Medical Journal, 11, 29. Google Scholar 17 Editorial (1972) The treatment of sickle-cell disease. Lancet, i, 671. Google Scholar 18 NWOKOLO, C. (1960) The diagnosis and management of sickle cell anaemia. West African Medical Journal, 9, 194. CASPubMedGoogle Scholar 19 Konotey-Ahulu, F.I.D. (1969) Patterns of clinical haemoglobinopathy. East African Medical Journal, 46, 149. PubMedGoogle Scholar 20 Oduru, K.A. & Searle, J.F. (1972) Anaesthesia in sickle-cell states–a plea for simplicity. British Medical Journal, (in press). 10.1136/bmj.4.5840.596 Web of Science®Google Scholar 21 Itano, H.A. (1951) A third abnormal hemoglobin associated with hereditary hemolytic anemia. Proceedings of the National Academy of Sciences of the United States of America, 37, 775. 10.1073/pnas.37.12.775 CASPubMedWeb of Science®Google Scholar 22 Marengo-Rowe, A.J. (1971) The anaemias–haemoglobinopathies. British Journal of Hospital Medicine, 6, 617. Google Scholar 23 Loh, Wei-Ping (1971) Evaluation of a rapid test tube turbidity test for the detection of sickle cell haemoglobin. American Journal of Clinical Pathology, 55, 55. PubMedWeb of Science®Google Scholar 24 Huntsman, R.G., Barclay, G.P.T., Canning, D.M. & Yawson, G.I. (1970) A rapid whole blood solubility test to differentiate the sickle-cell trait from sickle-cell anaemia. Journal of Clinical Pathology, 23, 781. 10.1136/jcp.23.9.781 CASPubMedWeb of Science®Google Scholar 25 Konotey-Ahulu, F.I.D. (1969) Anaesthetic deaths and the sickle-cell trait. Lancet, i, 267. 10.1016/S0140-6736(69)91287-2 Google Scholar 26 Oduro, K.A. (1969) Anaesthesia in Ghana. Anaesthesia, 24, 307. 10.1111/j.1365-2044.1969.tb02869.x PubMedWeb of Science®Google Scholar 27 Schenk, E.A. (1964) Sickle cell trait and superior longitudinal sinus thrombosis. Annals of Internal Medicine, 60, 465. 10.7326/0003-4819-60-3-465 CASPubMedWeb of Science®Google Scholar 28 Oduntan, S.A. & Isaacs, W.A. (1971) Anaesthesia in patients with abnormal haemoglobin syndromes: A preliminary report. British Journal of Anaesthesia, 43, 1159. 10.1093/bja/43.12.1159 CASPubMedWeb of Science®Google Scholar 29 Holzmann, L., Finn, H., Lichtman, H.C. & Harmel, M.H. (1969) Anaesthesia in patients with sickle cell disease. Anaesthesia and Analgesia: Current Researches, 48, 566. 10.1213/00000539-196907000-00013 CASPubMedWeb of Science®Google Scholar 30 May, A., Bellingham, A.J., Huehns, E.R. & Beavan, G.H. (1972) Effect of cyanate on sickling. Lancet, i, 658. 10.1016/S0140-6736(72)90462-X CASGoogle Scholar 31 Green, R.L., Huntsman, R.G. & Serjeant, G.R. (1972) Sickle-cell and altitude. British Medical Journal, i, 803. 10.1136/bmj.1.5803.803-d Web of Science®Google Scholar 32 Crawford, J.S. (1971) Anaesthesia for obstetricemergencies. British Journal of Anaesthesia, 43, 864. PubMedGoogle Scholar 33 Shapiro, N.D. & Poe, M.F. (1955) Sickle-cell disease: an anaesthesiological problem. Anesthesiology, 16, 771. 10.1097/00000542-195509000-00017 CASPubMedWeb of Science®Google Scholar 34 Gilbertson, A.A. (1965) Anaesthesia in West African patients with sickle-cell anaemia, haemoglobin SC disease and sickle-cell trait. British Journal of Anaesthesia, 37, 614. 10.1093/bja/37.8.614 CASPubMedWeb of Science®Google Scholar 35 Rosenbaum, J.M. (1965) Fatal haemoglobin S-C disease crises following tonsillectomy. Archives of Otolaryngology, 82, 307. 10.1001/archotol.1965.00760010309019 CASPubMedWeb of Science®Google Scholar 36 Gilbertson, A.A. (1972) Anaesthesia in patients with abnormal haemoglobin syndromes: A preliminary report. British Journal of Anaesthesia, 44, 233. 10.1093/bja/44.2.233-b PubMedWeb of Science®Google Scholar 37 Browne, R. A. (1965) Anaesthesia in patients with sickle-cell anaemia. British Journal of Anaesthesia, 37, 181. 10.1093/bja/37.3.181 PubMedWeb of Science®Google Scholar 38 Gilbertson, A.A. (1967) The management of anaesthesia in sickle cell states. Proceedings of the Royal Society of Medicine, 60, 631. CASPubMedWeb of Science®Google Scholar 39 Macleod, J.A.J. (1969) Exchange transfusion in a 7 year old girl with sickle cell anaemia as a preparation for adenoidectomy. Proceedings of the Royal Society of Medicine, 62, 1095. PubMedWeb of Science®Google Scholar 40 Editorial (1971) Treatment and prevention of sickle-cell crisis. Lancet, ii, 1069. Google Scholar 41 Hugh-Jones, K., Lehmann, H. & McAlister, J.M. (1964) Some experiences in managing sickle-cell anaemia in children and young adults, using alkalis and magnesium. British Medical Journal, ii, 226. 10.1136/bmj.2.5403.226 CASWeb of Science®Google Scholar 42 Ho Ping Kong, H.. & Alleyne, G.A.O. (1969) Acid-base status of adults with sickle-cell anaemia. British Medical Journal, iii, 271. 10.1136/bmj.3.5665.271 Google Scholar 43 Konotey-Ahulu, F.I.D. Personal communication. Google Scholar 44 Konotey-Ahulu, F.I.D. (1971) Computer assisted analysis of data on 1697 patients attending the sickle cell/haemoglobinopathy clinic of Korle Bu Teaching Hospital, Accra, Ghana. Clinical features: 1. Sex, genotype, age, rheumatism and dactylitis frequencies. Ghana Medical Journal, 10, 241. Google Scholar 45 Barnes, P.M., Hendrickse, R.G. & Watson-Williams, E.J. (1965) Low-molecular-weight dextran in treatment of bone-pain crises in sickle-cell disease. A double-blind trial. Lancet, ii, 1271. 10.1016/S0140-6736(65)92284-1 Google Scholar 46 Oski, F.A., Viner, E.D., Purugganam, H. & McElfresh, A.E. (1965) Low molecular weight dextran in sickle-cell crisis. Journal of the American Medical Association, 191, 43. 10.1001/jama.1965.03080010049014 PubMedWeb of Science®Google Scholar 47 McCurdy, P.R. & Mahmood, L. (1971) Intravenous urea treatment of the painful crisis of sickle-cell disease. New England Journal of Medicine, 285, 992. 10.1056/NEJM197110282851803 CASPubMedWeb of Science®Google Scholar 48 Nalbandian, R.M., Schultz, G., Lusher, J.M., Anderson, J.W. & Henry, R.L. (1971) Sickle cell crisis terminated by intravenous urea in sugar solutions–a preliminary report. American Journal of the Medical Sciences, 261, 309. 10.1097/00000441-197106000-00002 CASPubMedWeb of Science®Google Scholar 49 Desforges, J.F. (1971) Treatment of sickle crisis. New England Journal of Medicine, 284, 913. 10.1056/NEJM197104222841612 PubMedWeb of Science®Google Scholar 50 Konotey-Ahulu, F.I.D. (1971) Treatment and prevention of sickle-cell crisis. Lancet, ii, 1255. 10.1016/S0140-6736(71)90563-0 Google Scholar 51 Nalbandian, R.M. (1971) Urea for sickle-cell crisis. New England Journal of Medicine, 284, 1381. 10.1056/NEJM197106172842415 PubMedWeb of Science®Google Scholar 52 Howells, T.H., Huntsman, R.G., Boys, J.E. & Mahmood, A. (1972) Anaesthesia and sickle-cell haemoglobin. British Journal of Anaesthesia, 44, 975. 10.1093/bja/44.9.975 CASPubMedWeb of Science®Google Scholar 53 Vale, R.J. & Lunn, H.F. (1969) Heat balance in anaesthetised surgical patients. Proceedings of the Royal Society of Medicine, 62, 1017. PubMedWeb of Science®Google Scholar 54 DYDE, J.A. & LUNN, H.F. (1970) Heat loss during thoracotomy. Thorax, 25, 355. 10.1136/thx.25.3.355 CASPubMedWeb of Science®Google Scholar 55 Searle, J.F. Unpublished observations. Google Scholar Citing Literature Volume28, Issue1January 1973Pages 48-58 ReferencesRelatedInformation