Osmometer

Specimen Requirements and Procedure

Specimen requirements vary between the various commercially available osmometers and are included in the respective machine's instruction manual and laboratory protocols for specimen preparation. Acceptable specimens, in general, include serum, heparinized plasma, tears, sweat, and urine.[1][12] Some osmometers allow for the use of gel tubes to hold samples. In general, urine does not require the addition of preservatives during collection. Specimens should undergo centrifugation before analysis to eliminate any particulate matter. While dilution is unnecessary for many machines, it may be required for certain types of samples.[13][14]

The stability of different samples varies, with some general guidelines as follows:

• Unspun serum/plasma (room temperature or refrigerated at 2 to 8 °C): 3 hours
• Separated serum/plasma (room temperature or refrigerated at 2 to 8 °C): 48 hours
• Urine (room temperature): 24 hours
• Urine (refrigerated or frozen): 7 days

The general procedure for osmometry begins by employing a properly calibrated osmometer. A full calibration of osmometers is required at least every 6 months. Calibration may also be necessary following a part replacement or service of the instrument or if the quality control (QC) reading is repeatedly out of range. For QC purposes, laboratories are typically mandated to conduct 2 controls at 2 different concentrations daily or with each batch of samples. Acceptable controls are generally within ±2 SD from the mean. The institution's QC policy, protocol, and instrument user manual should be followed to ensure accurate sample analysis.

Testing Procedures

General Osmometry Procedure

The testing procedure for specific osmometers varies and is detailed in the user manual for each device. However, a general procedure outline is as follows:

• Enter or scan the sample ID.

• Load the sample to be tested into the osmometer. For freezing point depression osmometers, a small sample amount is drawn in a sampler with a plunger. The sampler tip is inserted into the instrument's sample port, and the analysis begins. Loading the sample into the osmometer may start the analysis automatically. Other systems may require the lab technologist to initiate the process by pressing a button.

• Record the osmolality of the sample.

• Once the test is completed, remove the sampler from the osmometer and discard the sampler tip. Ensure that both the sampler and sample chamber are thoroughly cleaned.

Interfering Factors

Freezing point depression osmometers have a few limitations. Particulate matter can cause premature crystallization of samples, which can be avoided by centrifuging blood and urine samples or filtering urine samples. The presence of air bubbles in a sample may also result in the inadequate freezing of samples. Test samples allowed to evaporate, non-aqueous, or highly viscous may not freeze well and yield an inaccurate result. High concentrations of substances, including ethanol, methanol, acetone, paraldehyde, trichloroethane, or propylene glycol, may not freeze reliably, leading to inaccurate results.

Finally, failure to clean the sample container after sample analysis can lead to the subsequent osmometer measurement being skewed by the previous sample. Vapor pressure osmometers are limited by a lack of precision compared to freezing point depression osmometers. Vapor pressure osmometers cannot be used to measure the osmolality of solutions containing volatile solutes.[1]

Results, Reporting, and Critical Findings

Certain sample types are more prone to inter-sample variability and may require 2 or more replicates. For instance, volatile samples may need to be analyzed in duplicate and the results should agree within a certain range of mOsm. The osmometer's specific protocol and user manual should be followed. The measurement range of osmometers varies depending on the instrument and sample being used. However, a common reportable range for freezing point depression osmometers is 0 to 2000 mOsm/kg. The normal reference range for serum is 275 to 295 mOsm/kg, and urine is 300 to 750 mOsm/kg, although these ranges may vary.[15][16]

Clinical Significance

Serum Osmolality

Changes in serum osmolality can be useful in differentiating the underlying causes of various electrolyte and acid-base balance disorders.[1][3] Serum osmolality is an important initial test employed in investigating hyponatremia. Hyponatremia in the context of normal serum osmolality is termed pseudohyponatremia. This condition is caused by the electrolyte exclusion effect when sodium is measured by the indirect ion-selective electrode method in patients with increased levels of lipids (hypertriglyceridemia) or total protein. Hyponatremia in the context of elevated serum osmolality (>295 mOsm/kg) is most commonly caused by elevated levels of serum glucose, or it may also occur when osmotically active substances such as mannitol, radiographic contrast agents, and glycine (surgical irrigant solutions) are administered. Serum osmolality can be directly measured using osmometers, and it can also be calculated by the measurements of osmotically active substances in the serum. Many formulas for calculating osmolality exist, among which the Smithline-Gardner formula stands out as one of the most commonly employed and straightforward.

Osmolality (mOsm/kg) = 2×Na (mmol/L) + glucose (mg/dL)/18 + urea (mg/dL)/2.8 [3][17] 

The difference between the calculated and measured osmolality is known as the osmol gap, also known as the osmolal or osmolar gap. A normal osmol gap is 2 or less, although according to some sources, it is greater than 10 mOsm/kg in the clinical environment.[1][18]

An elevated serum osmol gap can be found in the following clinical scenarios or disease states:

• Pseudohyponatremia: This condition occurs when a low reported serum sodium concentration (<135 mEq/L) is observed in the presence of normally measured serum osmolality. This discrepancy can be caused by hyperlipidemia or hyperproteinemia, where these molecules comprise an increased portion of the serum sample, resulting in a falsely decreased sodium reading. Based on the aforementioned Smithline-Gardner formula, the falsely decreased sodium concentration decreases the calculated serum osmolality, resulting in an elevated osmol gap compared to the normal range measured osmolality.[1][19]

• Exogenous substances: Ingestion of toxic alcohols such as ethanol, methanol, propylene glycol, and acetone can cause elevated osmol gap. The presence of an elevated osmol gap and suspicion of volatile alcohol poisoning often prompt further investigation by a volatile screen.[20] In addition, osmotically active medications such as mannitol or glycerol are sometimes used to manipulate the osmol gap to drive fluid shifts within the body. For instance, mannitol shifts fluid from the brain into the blood to relieve increased intracranial pressure. The increased solute in the blood after mannitol ingestion results in an osmotic gradient moving fluid across the blood-brain barrier.[21] An important but often overlooked cause of exogenous substances elevating a patient's osmol gap is ingesting propylene glycol from medications using this molecule as a vehicle, such as nitroglycerin, lorazepam, or etomidate.[18]

• Endogenous substances: Metabolic states such as diabetic ketoacidosis or alcoholic ketoacidosis increase the concentration of ketones in the bloodstream, increasing the osmolality within the blood and creating an osmol gap. Lactic acidosis can result in moderate lactic acidosis due to the accumulation of products from the breakdown of glycogen.[18] A hyperglycemic hyperosmolar state can also drive an increased osmol gap secondary to hyperglycemia.[22] In addition, diseases causing the retention of small molecules, such as renal failure, can also produce a similar effect.[15] Finally, shock can result in the accumulation of cationic or neutral amino acids, increasing the osmol gap.[18]

The value of change in the osmol gap can also give some insight into the cause of the elevation. For instance, renal failure and ketoacidosis often present with an osmol gap equal to or less than 15 to 20 mOsm/kg, whereas an osmol gap greater than 20 mOsm/kg indicates alcohol or acetone accumulation. Lactic acidosis often produces an average osmol gap of approximately 11 mOsm/kg.[18]

Urine Osmolality

Urine osmolality is useful for investigating electrolyte disturbances, particularly in hypo- or hypernatremia.[23][24] Hypernatremia and hyperosmolar plasma in the context of hypoosmolar urine (<300 mOsm/kg) are suggestive of diabetes insipidus. In this disease, a large volume of urine is excreted due to the failure to produce antidiuretic hormone by the hypothalamus (central diabetes insipidus) or lack of response to antidiuretic hormone by the kidney (nephrogenic diabetes insipidus). Hypernatremia in the presence of hyperosmolar urine (>600 mOsm/kg) is suggestive of extrarenal water loss, such as diarrhea, burn, or fever, or sodium overload resulting from the administration of hypertonic saline or salt poisoning.[24]

In patients with low serum osmolality and a clinically normal extracellular fluid volume, urine osmolality can aid in distinguishing between various etiologies. In these cases, a urine osmolality >100 mOsm/kg is indicative of the syndrome of inappropriate antidiuretic hormone, hypothyroidism, or glucocorticoid deficiency. On the other hand, a urine osmolality <100 mOsm/kg is observed in patients with primary polydipsia or beer potomania.[23]

Stool Osmolality

Measuring stool osmolality can help evaluate patients with diarrhea to differentiate osmotic diarrhea from secretory diarrhea. The stool osmotic gap is defined as the difference between the measured osmolality and a calculated osmolality (2*([fecal Na+] + [fecal K+]).[25] A stool osmotic gap <50 mOsm/kg implies that the diarrhea is secretory. In patients with osmotic diarrhea, the stool osmotic gap is typically >75 mOsm/kg. The osmolality should be measured within 30 minutes of stool sample collection, or the sample should be refrigerated until analysis because bacterial metabolism produces osmotically active substances that can alter the reading.[26] A stool osmolality <290 mOsm/kg may result from the intentional addition of water to a stool sample. In contrast, a stool osmolality >330 mOsm/kg without an elevated serum osmolality can suggest improper storage of the sample or contamination with concentrated urine.[27]

Quality Control and Lab Safety

Accurate osmolality testing is crucial for patient care. Daily analysis of commercially prepared control solutions with known low, normal, and high osmolality values is vital. Measured control values must fall within pre-defined limits, with deviations triggering corrective and preventive action.[17]

Maintaining instrument accuracy extends beyond regular control checks. Regular calibration employing manufacturer-supplied solutions with known osmolality values is vital. The calibration frequency may vary based on the specific instrument model, laboratory workload, and manufacturer recommendations. Furthermore, adhering to the manufacturer's guidelines for preventive maintenance, which encompasses cleaning, part replacement, and verification of proper component function, is essential.[28]

Participation in external proficiency testing programs offered by external organizations is highly recommended to ensure consistent quality and minimize inter-laboratory variability. These programs involve analyzing blinded samples with known osmolality and comparing the results to those of other laboratories. This collaborative approach facilitates identifying and rectifying any systematic biases that might be present within the testing procedures.[29] The documentation of all QC procedures is paramount for establishing a robust and reliable osmolality testing process within the laboratory. This documentation should include control results, calibration records, and any corrective actions taken. In addition, it is crucial to provide comprehensive training for personnel on instrument operation, QC procedures, and troubleshooting protocols.[30]

A robust safety program safeguarding patients and staff is paramount for any clinical laboratory. This program proactively identifies and manages potential hazards inherent to laboratory operations. Stringent protocols, including consistent use of barrier protection and frequent hand washing, minimize exposure risks. All specimens are treated as potentially infectious, and proper disposal procedures for sharps and infected materials are followed.[31] The Occupational Safety and Health Administration mandates hepatitis B vaccination for at-risk personnel, whereas the International Organization for Standardization 15190 standard ensures safety excellence through defined roles, fire and radiation safety measures, and continuous improvement initiatives.[31][32]

Enhancing Healthcare Team Outcomes

Determining serum and urine osmolality and assessing the difference between the calculated and measured osmolality (measurement of osmolar gap) are crucial for diagnosing and treating patients in various clinical scenarios. Modern osmometers in clinical laboratories are simple to operate and produce rapid and accurate results using a small specimen volume. Performing osmolality measurements is recommended for better accuracy and minimum errors.

Effective communication among all members of a patient's interprofessional care team, including laboratory technologists, clinicians, pharmacists, and other healthcare professionals, is essential for ensuring patients receive appropriate and timely medical care. A systematic process for immediate osmolality measurement is beneficial, as is a properly equipped and calibrated osmometer and fully qualified and trained laboratory technologists to run this instrument.[33][34]