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1.
Artigo em Inglês | MEDLINE | ID: mdl-35753928

RESUMO

Familial hypokalaemic periodic paralysis (FHPP) is an uncommon genetic disease characterized by muscle weakness associated with hypokalaemia. Episodes are precipitated by drugs, stress, metabolic diseases, hypothermia or infection. We report the case of a 38-year-old pregnant women with FHPP who underwent epidural analgesia for labour. Pregnant women with FHPP require multidisciplinary management involving an anaesthesiologist, a gynaecologist and a paediatrician. It is important to maintain normothermia, prevent hyperventilation, monitor electrolytes, avoid glucose infusions and medications that cause hypokalaemia, and administer potassium supplements when required. Locoregional techniques should be preferred over general anaesthesia. Early epidural analgesia reduces the risk of pain that could trigger an episode of FHPP. In the case of general anaesthesia, drugs that can cause malignant hyperthermia should be avoided, and short-acting non-depolarizing neuromuscular blockers with blockade-depth monitoring should be used.


Assuntos
Analgesia Epidural , Hipopotassemia , Paralisia Periódica Hipopotassêmica , Adulto , Parto Obstétrico , Feminino , Humanos , Hipopotassemia/complicações , Paralisia Periódica Hipopotassêmica/complicações , Paralisia Periódica Hipopotassêmica/genética , Gravidez , Gestantes
2.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-34544596

RESUMO

Familial hypokalaemic periodic paralysis (FHPP) is an uncommon genetic disease characterized by muscle weakness associated with hypokalaemia. Episodes are precipitated by drugs, stress, metabolic diseases, hypothermia or infection. We report the case of a 38-year-old pregnant women with FHPP who underwent epidural analgesia for labour. Pregnant women with FHPP require multidisciplinary management involving an anaesthesiologist, a gynaecologist and a paediatrician. It is important to maintain normothermia, prevent hyperventilation, monitor electrolytes, avoid glucose infusions and medications that cause hypokalaemia, and administer potassium supplements when required. Locoregional techniques should be preferred over general anaesthesia. Early epidural analgesia reduces the risk of pain that could trigger an episode of FHPP. In the case of general anaesthesia, drugs that can cause malignant hyperthermia should be avoided, and short-acting non-depolarizing neuromuscular blockers with blockade-depth monitoring should be used.

3.
Rev Esp Anestesiol Reanim (Engl Ed) ; 68(4): 232-234, 2021 Apr.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-33160688

RESUMO

Kearns-Sayre syndrome is a mitochondrial myopathy characterized by ophthalmoplegia, pigmentary retinopathy and cardiac conduction abnormalities. This article describes the clinical management of a 50-year-old patient with Kearns-Sayre syndrome who underwent subarachnoid anesthesia for a traumatic femoral fracture surgery.


Assuntos
Anestesia , Anestésicos , Síndrome de Kearns-Sayre , Miopatias Mitocondriais , Oftalmoplegia , Humanos , Pessoa de Meia-Idade
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