Lower than normal levels of potassium in the circulating blood. ICD-10-CM E87.6 is grouped within Diagnostic Related Group (s) (MS-DRG v38.0): 640 Miscellaneous disorders of nutrition, metabolism, fluids and electrolytes with mcc 641 Miscellaneous disorders of nutrition, metabolism, fluids and electrolytes without mcc
E56.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM E56.1 became effective on October 1, 2021. This is the American ICD-10-CM version of E56.1 - other international versions of ICD-10 E56.1 may differ. A type 1 excludes note is a pure excludes.
Abnormal results of kidney function studies. The 2019 edition of ICD-10-CM R94.4 became effective on October 1, 2018. This is the American ICD-10-CM version of R94.4 - other international versions of ICD-10 R94.4 may differ.
Condition due to a deficiency of vitamin k. Deficiency of vitamin k. It may lead to bleeding, manifested with ecchymoses, petechiae, and hematomas. In infants it may cause hemorrhagic disease of newborn with intracranial and retroperitoneal bleeding. ICD-10-CM E56.1 is grouped within Diagnostic Related Group(s) (MS-DRG v 38.0):
ICD-10 | Hyperkalemia (E87. 5)
ICD-10-CM Code for Hyperkalemia E87. 5.
001180: Potassium | Labcorp.
Hypokalemia is a metabolic imbalance characterized by extremely low potassium levels in the blood. It is a symptom of another disease or condition, or a side effect of diuretic drugs.
Hyperkalemia is the medical term that describes a potassium level in your blood that's higher than normal. Potassium is a chemical that is critical to the function of nerve and muscle cells, including those in your heart. Your blood potassium level is normally 3.6 to 5.2 millimoles per liter (mmol/L).
ICD-Code I10 is a billable ICD-10 code used for healthcare diagnosis reimbursement of Essential (Primary) Hypertension.
A potassium blood test is often included in a series of routine blood tests called an electrolyte panel. The test may also be used to monitor or diagnose conditions related to abnormal potassium levels. These conditions include kidney disease, high blood pressure, and heart disease.
More severe cases of low potassium may cause signs and symptoms such as:Muscle twitches.Muscle cramps.Severe muscle weakness, leading to paralysis.Low blood pressure (hypotension).Lightheadedness or faintness.Abnormal heart rhythms (arrhythmias).Excessive urination (polyuria).Excessive thirst (polydipsia).
A potassium blood test is used to detect abnormal potassium levels, including high potassium (hyperkalemia) and low potassium (hypokalemia). It is often used as part of an electrolyte panel or basic metabolic panel for a routine health exam.
In hypokalemia, the level of potassium in blood is too low.A low potassium level has many causes but usually results from vomiting, diarrhea, adrenal gland disorders, or use of diuretics.A low potassium level can make muscles feel weak, cramp, twitch, or even become paralyzed, and abnormal heart rhythms may develop.More items...
Hypokalemia is an electrolyte characterized by low serum potassium concentrations (normal range: 3.5–5.0 mEq/L). Severe and life-threatening hypokalemia is defined when potassium levels are <2.5 mEq/L.
A type 1 excludes note is a pure excludes. It means "not coded here". A type 1 excludes note indicates that the code excluded should never be used at the same time as E56.1. A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
Condition due to a deficiency of vitamin k. Deficiency of vitamin k. It may lead to bleeding, manifested with ecchymoses, petechiae, and hematomas. In infants it may cause hemorrhagic disease of newborn with intracranial and retroperitoneal bleeding.
Gitelman syndrome is an autosomal recessive kidney disorder characterized by hypokalemic metabolic alkalosis with hypocalciuria, and hypomagnesemia. It is caused by loss of function mutations of the thiazide sensitive sodium-chloride symporter (also known as NCC, NCCT, or TSC) located in the distal convoluted tubule.
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive.
DRG Group #640-641 - Misc disorders of nutrition, metabolism, fluids or electrolytes with MCC.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E87.6. Click on any term below to browse the alphabetical index.
This is the official exact match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that in all cases where the ICD9 code 276.8 was previously used, E87.6 is the appropriate modern ICD10 code.
BILLABLE K71.6 Toxic liver disease with hepatitis, not elsewhere classified. BILLABLE K71.7 Toxic liver disease with fibrosis and cirrhosis of liver. BILLABLE K71.8 Toxic liver disease with other disorders of liver. BILLABLE K71.9 Toxic liver disease, unspecified.
Type-2 Excludes means the excluded conditions are different, although they may appear similar. A patient may have both conditions, but one does not include the other. Excludes 2 means "not coded here.". Certain conditions originating in the perinatal period - instead, use Section P04-P96.