{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,1]],"date-time":"2026-11-01T01:55:38Z","timestamp":1793498138205,"version":"4.5.0"},"reference-count":81,"publisher":"Oxford University Press (OUP)","issue":"2","license":[{"start":{"date-parts":[[2013,1,1]],"date-time":"2013-01-01T00:00:00Z","timestamp":1356998400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/open_access\/funder_policies\/chorus\/standard_publication_model"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2013,1,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Phaeochromocytoma in pregnancy is a rare and potentially dangerous situation for mother and fetus. This review aimed to assess current mortality rates and how medical and surgical management affect these.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>Articles in English published between 2000 and 2011 were obtained from a MEDLINE search. Eligible publications presented women diagnosed with phaeochromocytoma in the antenatal or immediate postnatal period, and reported management and outcomes.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>A total of 135 reports were identified. After applying inclusion criteria, 77 pregnancies involving 78 fetuses were analysed. Fetal and maternal mortality rates were 17 per cent (13 of 78) and 8 per cent (6 of 77) respectively. Better outcomes were achieved when the diagnosis of phaeochromocytoma was made in the antenatal period than when it was made during labour or immediately postpartum (survival of both mother and fetus(es) in 48 of 56 versus 12 of 21 respectively; P = 0\u00b7012). When the diagnosis was made before 23 weeks' gestation, there was no difference in outcomes when phaeochromocytoma surgery was carried out in the second trimester, compared with when it was postponed to the third trimester or after delivery (fetal death 2 of 18 versus 2 of 8 respectively; P = 0\u00b7563).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>This review, although limited by the rarity of the condition and level of available evidence, demonstrated that survival rates are improved if the diagnosis of phaeochromocytoma can be established antenatally. With diagnosis before 23 weeks' gestation, no definite advantage of proceeding with tumour removal during the second trimester could be demonstrated.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/bjs.8976","type":"journal-article","created":{"date-parts":[[2012,11,23]],"date-time":"2012-11-23T10:46:17Z","timestamp":1353667577000},"page":"182-190","source":"Crossref","is-referenced-by-count":101,"title":["Systematic review of phaeochromocytoma in pregnancy"],"prefix":"10.1093","volume":"100","author":[{"given":"M A","family":"Biggar","sequence":"first","affiliation":[{"name":"Department of Endocrine Surgery, Royal Victoria Infirmary , Newcastle upon Tyne,","place":["UK"]},{"name":"Department of Surgery, Middlemore Hospital, Counties Manukau District Health Board , Otahuhu, Auckland,","place":["New Zealand"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T W J","family":"Lennard","sequence":"additional","affiliation":[{"name":"Department of Endocrine Surgery, Royal Victoria Infirmary , Newcastle upon Tyne,","place":["UK"]},{"name":"Faculty of Medical Sciences, Newcastle University , Newcastle upon Tyne,","place":["UK"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","published-online":{"date-parts":[[2013,1,1]]},"reference":[{"key":"2024092904522400400_bib1","doi-asserted-by":"crossref","first-page":"182","DOI":"10.1007\/PL00013159","article-title":"Adrenal tumors and pregnancy","volume":"23","author":"Harrington","year":"1999","journal-title":"World J Surg"},{"key":"2024092904522400400_bib2","doi-asserted-by":"crossref","first-page":"217","DOI":"10.1530\/eje.0.1300217","article-title":"Low cord blood levels of catecholamine from a newborn of a pheochromocytoma patient","volume":"130","author":"Dahia","year":"1994","journal-title":"Eur J Endocrinol"},{"key":"2024092904522400400_bib3","doi-asserted-by":"crossref","first-page":"472","DOI":"10.1111\/j.1479-828X.1996.tb02196.x","article-title":"Phaeochromocytoma in pregnancy","volume":"36","author":"Lau","year":"1996","journal-title":"Aust N Z J Obstet Gynaecol"},{"key":"2024092904522400400_bib4","doi-asserted-by":"crossref","first-page":"481","DOI":"10.1046\/j.1365-2168.2001.01752.x","article-title":"Phaeochromocytoma in pregnancy","volume":"88","author":"Brunt","year":"2001","journal-title":"Br J Surg"},{"key":"2024092904522400400_bib5","doi-asserted-by":"crossref","first-page":"729","DOI":"10.1080\/01443610701667049","article-title":"Difficult alpha-adrenergic blockade of a phaeochromocytoma in a twin pregnancy","volume":"27","author":"Kennelly","year":"2007","journal-title":"J Obstet Gynaecol"},{"key":"2024092904522400400_bib6","first-page":"266","article-title":"Alpha blockade and surgical intervention of pheochromocytoma in pregnancy","volume":"53","author":"Burgess","year":"1979","journal-title":"Obstet Gynecol"},{"key":"2024092904522400400_bib7","doi-asserted-by":"crossref","first-page":"739","DOI":"10.1097\/00006254-197111000-00001","article-title":"Pheochromocytoma and pregnancy. 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