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PARATHYROID SURGERY
Inferior parathyroids can be found near or within the thyrothymic tract, which
extends from the lower pole of the thyroid gland into the superior mediastinum. e intersection of the inferior thyroid artery and the recurrent laryngeal nerve is a
useful anatomical landmark.
Most parathyroid glands will lie within a 2.5-cm area either above or below this
point.
Other locations are seen, with the inferior parathyroids having a wider distribution
due to their longer descent. ese anatomical locations are discussed in detail below.
Bilateral Neck Exploration
With the introduction of imaging in parathyroid disease, there has been a shi towards more minimally invasive approaches, but subsets of patients still require BNE, including those with:
Suspected multigland disease
Parathyroid cancer
Failed pre-operative localisation
Failed MIP
Current guidelines from the National Institute for Health and Care Excellence (NICE) on the management of primary hyperparathyroidism (NG132) recommend that patients with nega­tive or equivocal imaging (ultrasound and sestamibi scan—up to 20% of patients) should be oered four-gland exploration and referral to a surgeon with expertise in BNE.
A failed minimally invasive approach will oen require a second operation for suspected multigland disease or a double adenoma. Suspected multigland disease may occur in patients with hyperplasia (up to 15% of patients with PHPT), double adenomas (4% of patients with PHPT), or familial hyperparathyroidism, as in multiple endocrine neoplasia (MEN 1, MEN 2A), familial isolated HPTH, and hyperparathyroidism-jaw tumour syndrome.
Technique
Ideally, patients give informed consent before the day of surgery. e procedure is nor­mally performed under general anaesthesia. e patient is placed in a supine position with 30 degrees of head elevation. e neck is extended using a sandbag placed under the shoul­ders, with the head stabilised on a head ring. Local anaesthetic with or without epinephrine may be inltrated as a supercial cervical block or directly into the site of the incision. A 5-cm curvilinear incision is placed 1–2 cm above the sternal notch. A subplatysmal ap is raised superiorly to a point just above the cricoid cartilage. e strap muscles are then sepa­rated in the bloodless midline plane. Haemostasis is important, because blood in the surgical eld can make visualisation of the parathyroid glands dicult.
e le or right side of the neck is opened by raising the strap muscles o the thyroid, with lateral retraction of the carotid sheath and medial retraction of the thyroid. is manoeuvre ensures that the area directly surrounding the dorsal thyroid and tracheo-oesophageal gut­ter may be explored.
e thyroid lobe is rotated medially into the wound to allow inspection of the posterior aspect (Figure 89.1).
e search should proceed in a methodical way. Ideally, no gland should be removed until all have been visualised.
Superior glands are more constant in position and generally lie on the posterior surface of the thyroid gland, within 1 cm of the cricothyroid joint, posterior to the recurrent laryngeal nerve.
Enlarged superior glands oen migrate downward and inferiorly into a retropharyn-
geal/retro-oesophageal position by the combined eects of gravity and swallowing. Superior glands can be found by identifying the inferior thyroid artery laterally and
the recurrent laryngeal nerve inferomedially and by entering the retropharyngeal space by delicate dissection.
448 Head and Neck Endocrine Surgery
PARATHYROID SURGERY
Figure 89.1 The inverted relationship between the left superior parathyroid (PA) and the left
recurrent laryngeal nerve (RLN) when the left thyroid lobe is retracted onto the trachea.
e inferior thyroid gland is found near or within the thyrothymic tract, which extends from the inferior pole of the thyroid gland into the superior mediastinum, usually anterior to the recurrent laryngeal nerve.
Dissection into the thyrothymic tract will usually identify the gland.
An inferior parathyroid gland can sometimes lie within the thymus and its delivery
should only be performed if an adenoma is not found on either side of the neck, to avoid devascularising a normal but suppressed gland. ymic delivery is facilitated by dissection inferiorly, anterior to the carotid artery but
medial to the recurrent nerve and lateral to the trachea at the level of the clavicle. e thymus continues as an extension of the thyrothymic tract, and progressive traction on its capsule will aid delivery from the chest (Figu re 89.2).
If a superior parathyroid gland is not found, exploration of the retropharyngeal/retro­oesophageal compartment and posteromedial surface of the superior thyroid pole is
Figure 89.2 Left thymic remnant being delivered from the mediastinum and containing an
ectopic inferior parathyroid adenoma.
Head and Neck Endocrine Surgery 449
PARATHYROID SURGERY
BOX 89.1 CONTRAINDICATIONS TO MIP
• Negative imaging
• Multigland disease
• Family history of MEN or familial hyperparathyroidism
• Chronic renal insufciency
• Hyperparathyroidism from lithium therapy
• Suspected parathyroid cancer
warranted; then, inspection behind the hyoid and larynx and within the carotid sheath at the level of the inferior thyroid artery is performed.
If an inferior parathyroid is not identied, the carotid sheath is explored from the level of the superior thyroid artery down to the sternoclavicular joint.
One should remember the law of symmetry in parathyroid surgery:
In 80% of cases, a parathyroid gland located on one side of the neck will have a cor­responding gland in the same location on the other side.
If, aer a meticulous search, no abnormal parathyroid glands are identied, then one should reconsider the diagnosis and carefully document the location of identied glands. If abnor­mal or suspect parathyroid glands are identied, then frozen section and ioPTH are useful adjuncts to decision-making.
Minimally Invasive Parathyroidectomy
e MIP approach to the parathyroid glands is facilitated by accurate pre-operative localisa­tion via scans. See Endocrine imaging (Chapter 79). Contraindications to MIP are listed in
Box 89.1.
Technique
e patient is positioned similarly to positioning for BNE. e procedure can be performed under local or general anaesthesia. e initial incision can be either a medial or a focused lateral approach.
Lateral Approach
Incision is made in the medial border of the sternocleidomastoid muscle (SCM) over
the pre-localised adenoma. e incision is deepened and a subplatysmal plane is developed.
e medial border of the SCM is identied and a plane is developed.
Lateral retraction of the SCM and jugular vein with medial traction on the strap mus-
cles allows the thyroid gland to be identied. ese simple manoeuvres allow most pre-localised parathyroid adenomas to be
identied.
Medial Approach is Like the Approach for BNE
is approach also allows identication of the other parathyroid gland to ensure they
both are normal.
Wounds are closed with absorbable sutures in the strap muscles/platysma and Monocryl sutures for the skin.
Complications
Complications are rare following parathyroid surgery and are listed below in Box 89.2.
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MEDICOLEGAL ASPECTS OF THYROID AND PARATHYROID SURGERY
BOX 89.2 COMPLICATIONS OF PARATHYROIDECTOMY
• Bleeding
• Wound infection
• Recurrent laryngeal nerve palsy (<1%)
• Hypoparathyroidism (rare and more common in BNE)
• Failure to cure (2–5%)
KEY POINTS
Surgery provides the only cure for patients with primary hyperparathyroidism (PHPT).
Bilateral neck exploration is reserved for patients with suspected multigland disease,
patients with negative imaging, or those undergoing revision surgery.
Knowledge of embryology and anatomy is important to ensure successful
identication of parathyroid glands.
The intersection of the recurrent laryngeal nerve and inferior thyroid artery is a key
landmark for identifying parathyroid glands.
Enlarged superior parathyroid glands tend to migrate posteriorly and inferiorly while
inferior glands tend to migrate anteriorly.
Intra-operative PTH assay and frozen section are useful adjuncts in parathyroid surgery.
Further Reading
Glaser SM, Mandish SF, Gill BS, Balasubramani GK, Clump DA, Beriwal S. Anaplastic thyroid
cancer: prognostic factors, patterns of care, and overall survival. Head Neck 2016; 38(Suppl 1): E2083–E2090. doi: 10.1002/hed.24384.
National Institute for Health and Care Excellence (NICE). Hyperparathyroidism (primary):
diagnosis, assessment and initial management. NICE guideline NG132, published May 2019.
90. MEDICOLEGAL ASPECTS OF THYROID AND PARATHYROID SURGERY
Introduction
yroid and parathyroid operations oer unique challenges that are reected in the compli­cations and litigation that can arise. Surger y-related lega l claims (see Box 90.1) have decreased since 2011—with ENT representing about 2.5% of claims—and a higher proportion are being defended. irteen to fourteen claims per year pertain to thyroid disease.
44% of claims are resolved without payment.
<5% of all cases are decided in court.
79% of court cases are successfully defended.
Diagnosis
Delayed and incorrect diagnosis cause approximately one third of all thyroid-related claims in the United Kingdom. Internationally, 6–8% of cancer-related claims and 6% of all thyroid­related claims arise from delayed diagnosis, with the requirement for a second operation increasing the chance of a successful claim.
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MEDICOLEGAL ASPECTS OF THYROID AND PARATHYROID SURGERY
BOX 90.1 THE LEGAL DEFINITION OF MEDICAL NEGLIGENCE
A successful claim of medical negligence must prove:
Breach of duty of care: Treatment below the reasonable/accepted standard
Damage: Patient injury or loss
Causation: The injury would not have occurred or would have been less severe with
appropriate treatment
The claim must be brought within a specic period of limitation. Successful damages awards reect two elements:
Pain, suffering and ‘loss of amenity’ (i.e. nonnancial impact)
Financial loss and extra expenses
NHS Resolution (formerly called the NHS Litigation authority) manages NHS-related claims.
False-negative thyroid ne-needle aspiration (FNA) rates are <3–10.2%, and suspicious fea­tures on ultrasound are reported in 90% of patients with false-negative FNA.
Inadequate or incongruous cytology indicates repeat FNA.
Evidence on the eect of delayed thyroid cancer diagnosis is limited. A small Korean study found mortality was lowest for patients who had thyroid surgery 1–4 weeks aer diagnosis but there was no increased risk with longer delays. An older retrospective study found that cancer mortality was 4% in patients who underwent initial therapy within a year, compared to 10% in others who waited longer. e ‘delayed’ group had twice the 30-year cancer mortality (6% vs. 13%). It is dicult to attribute negative outcomes to delayed diagnosis.
Pre-operative thyroid function, calcium levels, and vitamin D status are predictive of post-operative complications. Studies rarely separate these claims. Guidelines recommend pre-operative biochemistry in at-risk patients.
Pre-Operative Consent
Historically, a legal test (Bolam) determined whether the conduct of a doctor could be sup- ported by a responsible body of U.K. medical opinion. e Sidaway judgement that followed required doctors to decide how much risk information to disclose to patients. However, since an early 2015 Supreme Court judgement (Montgomery v. Lanarkshire Health Board), doc­tors must now take ‘reasonable care to ensure that the patient is aware of any material risks involved in any recommended treatment and of any reasonable alternative or variant treat­ments’. A material risk is one to which a reasonable person would be likely to attach signi­cance (i.e. a risk that might alter a decision).
e importance of adequate informed consent cannot be overstated, mainly for best patient care and, secondly, for avoidance of undesired consequences if a claim of negligence is sub­mitted. In the United States, 19% of vocal cord palsy, 7–9% of recurrent laryngeal nerve injury, and 21% of spinal accessory nerve injury claims relate to consent.
Inadequate consent is a recognised major factor in legal claims being upheld.
Unfortunately, patients have poor retention of consent information, and there is a discrepancy between what surgeons and thyroid cancer patients feel is important. In the United Kingdom, providing information whilst checking and facilitating the patient’s understanding are overriding duties dened by the General Medical Council and Royal College of Surgeons. Risk explanation should be tailored to
452 Head and Neck Endocrine Surgery
MEDICOLEGAL ASPECTS OF THYROID AND PARATHYROID SURGERY
patient-specic factors, such as thyrotoxicosis, age, previous surgery, and pre-existing vocal cord palsy.
Patient information leaets (e.g. ENT UK website) are recommended but do not replace
thorough discussion because they do not improve understanding.
Intra-Operative Factors
Experience of the Surgeon
High-volume thyroid surgeons have better outcomes. Despite variability in what constitutes high volume, current evidence suggests that high volume means 35–40 thyroidectomies per surgeon and 90–100 thyroidectomies per centre per year. is exceeds the British Association of Endocrine and yroid Surgeons recommendation of 20 per year. However, it mirrors the gures for paediatrics, where experience is thought particularly important.
Surgeons performing less than 30 relevant operations per year have approximately dou-
ble the endocrine complications.
Recurrent Laryngeal Nerve (RLN) Injury
RLN palsy is the major motivator of surgery-related claims in U.K. thyroid surgery. Risk factors include Graves’ disease, post-operative bleeding, retrosternal, malignant, recurrent benign, malignant goitre and failure to identify the RLN.
Vocal cord movement should be documented pre-operatively.
Due to the extremely high number of cases required to power a denitive study, it remains uncertain whether intra-operative nerve monitoring (IONM) reduces RLN injury rates, although for temporary RLN palsy, evidence seems to be amassing in favour of IONM.
It is imperative that IONM be carried out in the recommended manner, and failure to do
so can expose surgeons to litigation.
Another IONM debate is whether bilateral thyroid surgery should be stopped and staged in the event of loss of signal on the rst side. To settle this, surgeons and patients will need to dene what is safe and acceptable. In the meantime, studies report that a staged approach in the event of rst-side signal loss can eliminate occurrence of bilateral vocal cord palsy. Regardless of approach, the local management algorithm should be pre-operatively dis­cussed with patients.
Parathyroid Preservation
e preservation or removal of the correct parathyroid gland(s) is implicit to diligent surgery. Recent American yroid Association (ATA) guidelines support the use of loupes and the identication of at least two parathyroid glands.
Documentation
Documentation of relevant ndings, including the results of intra-operative investigations that guided decision-making (e.g. parathyroid hormone biochemistry or frozen-section pathology), should be completed.
e location and preservation of the RLN should be clearly documented on a legible
(preferably typed) operation note that would stand up to scrutiny by an expert third party in the event of a claim.
Post-Operative Factors
Post-operative ca re is as important as all other factors. Recent U.K. claim ana lysis showed eight of een claims related to post-operative care were upheld. e issues in these cases included hypocalcaemia management, diagnosis of vocal cord paresis, and haematoma development.
German experience suggests that claims are more likely to be successful if related to
faulty post-operative care.
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MEDICOLEGAL ASPECTS OF THYROID AND PARATHYROID SURGERY
Diagnosis of Vocal Cord Palsy
German and British guidelines recommend all thyroid patients have pre-and post-operative laryngeal examinations. eir timing, although signicant in terms of detecting neuropraxia, is not prescribed.
e failure to recognise a problem motivates 36% of U.S. vocal cord palsy-related claims
(and 20% of spinal accessory-related claims).
Hypocalcaemia
Assessment of parathyroid function aer completion or total thyroidectomy is mandatory. National specialist databases record post-operative hypocalcaemia rates of 21% aer total thyroidectomy for multinodular goitre (MNG) and, in Scandinavia, 6.4% of patients required intravenous calcium aer total thyroidectomy. Serum calcium or parathyroid hormone biochemistry and routine calcium supplementation are all strategies to manage signicant hypocalcaemia. Recommendations dier between North America and Europe regarding the choice and timing of these tests.
ere is consensus that a robust protocol for management of post-operative hypocalcae-
mia be in place.
Duration of Inpatient Stay
A patient’s attorney may question the safety of a <24-hr inpatient stay for a patient who developed neck haematoma aer surgery. Risk factors for post-operative bleeding, which occurs in 0.6–2.1% of cases, include re-operation and bilateral procedures. Although most haemorrhages occur within 6 hours of surgery, 20–37% will occur aer 6–24 hours, and 0–10% aer 24 hours. Notably, the lowest serum calcium level can occur aer the second post-operative day:
If discharged too soon, patients may develop severe, untreated hypocalcaemia.
When Things Go Wrong
Since 2014, the U.K. duty of candour has placed a legal duty on care providers to inform and to apologize to patients or their families regarding mistakes in care that led to death or severe or moderate harm. is adds to a doctor’s ethical duty to disclose when an incident has occurred.
Patients should be informed as soon as possible of any harm, with an apology and rel-
evant reassurance provided.
A Claim Arises
Medical negligence cases that go to court are generally civil prosecutions. e plainti’s/ defendant’s attorneys will instruct an expert witness to provide a report on possible breach of duty and/or condition and prognosis. An expert witness should provide an independent, balanced opinion for the court (not the lawyers) on the facts of a case, an explanation of tech­nical issues, a view on what is considered ‘reasonable’, and matters of causation (symptoms or condition) that have arisen as a result of damage.
Litigation Rates and Costs
ree U.K. analyses including nearly 400 cases between 1971 and 2016 were analysed. Diagnostic delay (40 cases, 51.4% closed claims successful), incorrect diagnosis (22 cases, 85% closed claims successful), and recurrent laryngeal nerve injury (33 claims, 54.5% closed claims successful) robustly emerged as principal factors.
454 Head and Neck Endocrine Surgery
EVALUATION AND INVESTIGATION OF PITUITARY DISEASE
KEY POINTS
Further investigate any discrepancies between ultrasound and cytology whilst aiming
to minimise diagnostic delay.
Ensure that thyroid function and serum calcium are normal before and after surgery.
Keep in mind the Montgomery v. Lanarkshire Health Board ruling when consenting
patients.
Intraoperative nerve monitoring remains the subject of debate.
At the very least, post-operative laryngoscopy should be performed in a patient with
post-operative voice symptoms.
The defense of a medical negligence claim will depend upon your statement of:
What you did—Were you the appropriate surgeon?
Why you did it—What were the indications for surgery?
What your notes say.
How you managed the complication(s).
91. EVALUATION AND INVESTIGATION OF PITUITARY DISEASE
Introduction
e pituitary gland sits within the sella turcica of the sphenoid bone, inferior to the hypo­thalamus and optic chiasm. It is surgically accessible transnasally via the sphenoid sinus. e gland is composed of two lobes. e anterior pituitary (adenohypophysis) secretes luteinising hormone (LH), follicle-stimulating hormone (FSH), growth hormone (GH), adrenocortico­tropic hormone (ACTH), thyroid-stimulating hormone (TSH), and prolactin. e posterior pituitary (neurohypophysis) is not a gland in itself, but a projection of the hypothalamus, and it releases antidiuretic hormone (ADH) and oxytocin. It is connected to the hypothalamus above by the pituitary stalk (infundibulum), which passes through the diaphragm that forms the roof of the sella. e function of the anterior pituitary is controlled chiey by hypotha­lamic hormonal control; the hypothalamic-pituitary-peripheral axis is regulated by multiple feedback loops.
Clinical Features of Pituitary Disease
Pituitary disease may manifest clinically due to:
Hormone hyposecretion
Hormone hypersecretion
Mass eect
Pituitary apoplexy
A combination of the above
Not all functionally signicant pituitary tumours are visible radiologically; conversely, inci­dental pituitary lesions are common.
Hormone Hyposecretion
One or multiple hormones may be reduced, leading to the clinical syndrome of hypopituitarism. Deciency of GH is most common, leading to lethargy, decreased muscle mass, central adiposity, and reduced bone density. LH and FSH hyposecretion results in reproductive dy sfunction (low l ibido, infertil ity, erectile dysf unction in men, oli gomenorrho ea
Head and Neck Endocrine Surgery 455
EVALUATION AND INVESTIGATION OF PITUITARY DISEASE
in women, and delayed puberty in adolescents). ACTH hyposecretion leads to failure to pro­duce an appropriate level of cortisol. is leads to lethargy, postural hypotension, and hypo­natraemia when the person is under physiological stress (Addisonian crisis). Hypothyroidism is less common but may manifest with typical symptoms of lethargy, dry skin, constipation, etc. Hyposecretion of ADH from the posterior pituitary is rare, but it may lead to diabetes insipidus (polyuria and polydipsia with hypernatraemia).
Hormone Hypersecretion
Hormone hypersecretion occurs due to the proliferation of secretory cells within an ade­noma. e most common functioning pituitary adenoma is a prolactinoma, leading to low libido, infertility, galactorrhoea in women, and gynaecomastia in men. Hypersecretion of GH leads to acromegaly, with an insidious onset of tiredness, sweating, and bony and so-tissue overgrowth. Hypersecretion of ACTH, and thus cortisol, leads to Cushing’s disease, which includes central obesity, striae, diabetes, hypertension, cardiovascular dis­ease, hirsutism, bruising, and proximal myopathy. Hypersecretion of TSH, FSH, or LH is very rare.
Mass Effect
A pituitary macroadenoma may exert mass eect on surrounding structures. Pressure on the optic chiasm due to suprasellar extension of the tumour initially leads to a bitempo­ral superior quadrantanopia, followed by bitemporal hemianopia. e visual eld defect may be asymmetrical. e patient may be unaware of the visual eld defect or may com­plain of nonspecic symptoms, such as clumsiness. Less commonly, lateral expansion into the cavernous sinus may lead to diplopia and ophthalmoplegia. Large pituitary adenomas may cause headaches and rarely hydrocephalus due to obstruction of the third ventricle. Headache is a common presenting symptom in pituitary disease but cannot always be attributed to the tumour.
Pituitary Apoplexy
In a minority of patients, pituitary apoplexy can be the rst presentation of a pituitary ade­noma. e classical presentation is severe, sudden headache and acute visual eld decit. e patient may present with a triphasic abnormality of ADH secretion: initially, diabetes insipi­dus, followed by a period of a syndrome of inappropriate ADH secretion (SIADH), followed by a return of diabetes insipidus.
Anterior Pituitary Function Testing
e presenting symptoms of a patient with a known sellar mass may guide the endocrine investigations. Symptoms in many cases are nonspecic or non-existent. In such cases, the laboratory tests are conducted to screen for either pituitary hormone hypersecretion or hypopituitarism (Table 91.1).
Testing for Hypersecretion
Hyperprolactinemia is diagnosed with ba sal morning prolactin levels. Repeated tests or serial cannulated prolactin levels are necessary to make the diagnosis condently, as levels can be falsely elevated due to a stress response. Prolactin levels can be increased in hypothyroidism,
Table 91.1 Tests for pituitary hormone hypersecretion
Hormone Initial test(s) Conrmatory test(s)
Prolactin Morning serum prolactin level – GH IGF-1 level Oral glucose suppression test ACTH 24-hr urinary cortisol High-dose dexamethasone suppression test TSH Serum free T4 and TSH Alpha-subunit levels ADH Urine/serum Na & osmolalities
456 Head and Neck Endocrine Surger y
EVALUATION AND INVESTIGATION OF PITUITARY DISEASE
in polycystic ovarian syndrome, with the use of some medications (e.g. metoclopramide and some antidepressants), and with some nonfunctioning macroadenomas, due to stalk compression.
Acromegaly (GH hypersecretion) is screened for by checking levels of insulin-like growth factor (IGF-1), a downstream product of GH. e diagnosis is conrmed by a 75-g oral glucose load that fails to suppress the GH level to <1 during the test.
Cushing’s disease (Cushing’s syndrome due to pituitary ACTH hypersecretion) can be chal­lenging to diagnose, as many ACTH-secreting tumours are not visible on MRI. A detailed endocrine workup is essential. Excess cortisol (hypercortisolism) must be demonstrated rst, and subsequently, an adrenal or ectopic source of ACTH must be ruled out to conrm a pituitary cause. As a screening test for hypercortisolism, 24-hour urinary cortisol is mea­sured rst. Obesity, pregnancy, alcohol dependency, and poorly controlled diabetes should be ruled out as potential physiological causes of high cortisol. Cushing’s disease is then con­rmed by:
Dexamethasone suppression and measurement of serum ACTH. Failure of cortisol
suppression to <50% aer dexamethasone suppression suggests Cushing’s. Plasma ACTH levels will be elevated with a pituitary cause of Cushing’s but suppressed with adrenal ACTH hypersecretion. A reduction in serum cortisol aer high-dose dexamethasone administration favours
a pituitary source over an ectopic one. Salivary cortisol can be measured instead of serum cortisol. Inferior petrosal sinus (IPS) sampling is used to conrm the source and lateralisation
of excessive ACTH in pituitary Cushing’s. If the ACTH source is a pituitary adenoma, samples from the IPS will demonstrate high ACTH levels, a dierential between IPS and peripheral blood levels, and an exaggerated spike in ACTH levels following the administration of corticotropin-releasing factor (CRF).
Elevated free T4 and TSH levels suggest the rare diagnosis of a TSH-secreting adenoma. High alpha-subunit levels can be used to distinguish this from thyroid hormone resistance.
Testing for Hypopituitarism
Hypopituitarism is suggested where both the target hormone (e.g. T4) and the tropic hor­mone (e.g. TSH) are low. In most cases, dynamic testing is also required to prove that pitu­itary reserve is aected. Multiple dynamic tests can be performed simultaneously.
GH deciency and ACTH hyposecretion can be demonstrated by an inadequate response to the insulin tolerance test or glucagon stimulation test. e glucagon stimulation test can be performed when insulin is contraindicated (adrenal insuciency, coronary artery disease, or seizure disorders). Basal LH, FSH, and sex hormone levels can be measured and are suf­cient to establish the diagnosis of hypogonadism. e GnRH stimulation test is now rarely used. yroid function tests (TSH, T4, T3) can conrm secondary hypothyroidism, and the TRH test is generally not required.
Posterior Pituitary Function Testing
SIADH
Hyponatraemia has numerous causes and SIADH is an important one. SIADH is a diagnosis of exclusion. SIADH can be conrmed with paired urine and serum sodium osmolalities. Hyponatraemia demonstrated by reduced serum osmolality and associated with inappropri­ately high urinary sodium and osmolality conrms the diagnosis.
ADH Deciency—Diabetes Insipidus
ADH deciency leads to the production of large volumes of inappropriately dilute urine. is results in compensatory polydipsia, urinary frequency, nocturia, and enuresis. A 24-hr
Head and Neck Endocrine Surgery 457