Acromegaly - NYSORA

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Acromegaly

Learning objectives

  • Describe acromegaly
  • Recognize signs and symptoms of acromegaly
  • Anesthetic management of a patient with acromegaly

Definition and mechanisms

  • Acromegaly is a chronic, progressive, hormone hypersecretion syndrome caused by an excess of growth hormone (GH) after the growth plates have closed (i.e., puberty)
  • The hypersecretion of GH is the result of oversecretion of growth hormone-releasing hormone (GHRH) from the hypothalamus or oversecretion of the hormone itself from a pituitary adenoma

Signs and symptoms

Affected areaSigns and symptoms
FaceIncrease in size of skull and supraorbital ridges; enlarged lower jaw; increase in spacing between teeth/malocclusion
Hands and feetSpade-shaped; carpal tunnel syndrome
Mouth/tongueMacroglossia; thickened pharyngeal and laryngeal soft tissues; thickened vocal cords; reduction in the size of the laryngeal aperture; obstructive sleep apnea
Soft tissueThick skin; doughlike feel to palm
SkeletonVertebral enlargement; osteoporosis; kyphosis
CardiovascularHypertension; cardiomegaly; impaired left ventricular function
EndocrineImpaired glucose tolerance; diabetes
OtherArthropathy; proximal myopathy

Complications

Treatment

  • Surgery: Preferred treatment; to remove the pituitary tumor
  • Drugs: 
    • Somatostatin analogs: Drugs that reduce GH production
    • Dopamine agonists: Drugs to lower hormone levels
    • GH receptor antagonists: Drugs to block the action of GH
  • Radiation therapy: Both used alone or in combination with surgery or drugs

Management

Four grades of airway involvement have been described in acromegaly:

GradeAirway involvement
1No significant involvement
2Nasal and pharyngeal mucosa hypertrophy but normal cords and glottis
3Glottic involvement including glottic stenosis or vocal cord paresis
4Combination of grades 2 and 3: Glottic and soft tissue abnormalities
  • Ventilation with a bag and mask is straightforward in acromegalic patients but an oral airway may be required
  • Laryngoscopy and tracheal intubation prove more difficulty due to a combination of macrognathia, macroglossia, and expansion of the upper airway soft tissues
  • Tracheostomy is recommended for grades 3 and 4, however, fiberoptic laryngoscopy is a safe alternative
  • Tracheal intubation is feasible with standard techniques (i.e., external laryngeal pressure and the use of a gum elastic bougie or airway exchange catheter)
  • Awake fiberoptic intubation is the technique of choice in case of anticipated difficult intubation in these patients
  • Preoperative transthoracic echocardiography is useful to assess left ventricular size and performance, and to estimate pulmonary pressures due to associated cardiopulmonary complications

Keep in mind

  • About one-quarter of acromegalic patients have an enlarged thyroid, which may compress the trachea
  • Preoperative assessments help the anesthesiologist to understand the possibility of difficulties with airway management and tracheal intubation
  • Difficult airway
    • Macroglossia and enlarged epiglottis: Difficult bag-mask ventilation and direct laryngoscopy
    • Recurrent laryngeal nerve palsy, narrow glottic opening, subglottic narrowing (stridor)
    • Nasal turbinate enlargement: Caution with nasal intubation and consider a smaller endotracheal tube

Suggested reading

  • Menon R, Murphy PG, Lindley AM. Anaesthesia and pituitary disease. Continuing Education in Anaesthesia Critical Care & Pain. 2011;11(4):133-137.
  • Smith M, Hirsch NP. Pituitary disease and anaesthesia. Br J Anaesth. 2000;85(1):3-14.
  • Seidman PA, Kofke WA, Policare R, Young M. Anaesthetic complications of acromegaly. Br J Anaesth. 2000;84(2):179-182.

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