Metabolic alkalosis differential diagnosis: Difference between revisions

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==References==
==References==
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{{reflist|2}}
[[Category:Medicine]]
[[Category:Medicine]]
[[Category:Nephrology]]
[[Category:Nephrology]]
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[[Category:Primary care]]

Latest revision as of 22:43, 29 July 2020

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sadaf Sharfaei M.D.[2]

Overview

Metabolic alkalosis might be consequence of several conditions such as exogenous HCO3 loads, medications and poisoning, gastrointestinal, renal, endocrine, and systemic diseases.

Metabolic Alkalosis

Differential diagnosis of metabolic alkalosis is as follow:

Category Disease Mechanism Clinical Paraclinical Gold standard diagnosis Other findings
Symptoms Signs Lab data
ABG Chemistry Enzyme Renal function
Hydrogen loss Accumulation of base Chloride depletion Mineralocorticoid excess Fever Dyspnea Edema Toxic/ill BP Dehydration HCO3 paCO2 O2 Cl K+ Na+ Ca+ Mg+ Renin Bun Cr Urine Cl
Exogenous HCO3 loads Acute alkali administration[1] + + + Nl Nl Nl Clinical manifestations
Milk−alkali syndrome[2] + + + + + Nl Clinical manifestationsk + exclusion of other causes of hypercalcemia
Transfusion[3] + ± ± + ↓/↑ Nl to ↑ Nl to ↑ Nl History of administration of large quantities of blood products that contain sodium citrate
Drugs/Medication Chloruretic diuretics[4] + + + + Nl Nl Nl Nl to ↑ Nl to ↑ History of diuretic use
Penicillin[5] + Nl Nl Nl Nl Nl Nl History of penicillin use
  • Not applicable
Licorice[6][7] + + + Nl to ↑ Nl Nl Nl Nl to ↑ Nl to ↑ Nl Clinical manifestations
Laxative abuse[8] + + ± + + Nl Nl Nl to ↑ Nl High level of suspicion
Antacids[9][10]
  • Aluminum hydroxide
  • Sodium polystyrene sulfonate  
+ + Nl Nl Nl Nl Nl to ↑ Nl to ↑ Nl Clinical manifestations
  • Not applicable
Category Disease Hydrogen loss Accumulation of base Chloride depletion Mineralocorticoid excess Fever Dyspnea Edema Toxic/ill BP Dehydration HCO3 paCO2 O2 Cl K+ Na+ Ca+ Mg+ Renin Bun Cr Urine Cl Gold standard diagnosis Other findings
Gastrointestinal origin Vomiting[11] + + ± + + Nl Nl Nl Nl to ↑ Nl Clinical manifestations
  • Not applicable
Nasogastric tube suction[12] + + + + Nl Nl Nl Nl to ↑ Nl Clinical manifestations
Zollinger−Ellison syndrome[13] + + + + Nl Nl Nl Nl to ↑ Nl Serum gastrin concentration + secretin stimulation test 
Bulimia nervosa[14] + + ± + + Nl Nl Nl to ↑ Nl High level of suspicion
Congenital chloridorrhea[15] + + ± + + Nl Nl to ↑ Nl to ↑ Nl to ↑ Clinical manifestations+ lab findings
Pyloric stenosis[16] + + + + Nl ↓ ↑ Nl Nl Nl to ↑ Nl Physical exam + imaging
  • Palpation of the “olive”
Villous adenoma[17] + + + + Nl Nl to ↑ Nl Colonoscopy
Gastrocystoplasty[18] + + Nl Nl Nl Nl Nl Nl Nl to ↑ Nl to ↑ Nl History of operation
Category Disease Hydrogen loss Accumulation of base Chloride depletion Mineralocorticoid excess Fever Dyspnea Edema Toxic/ill BP Dehydration HCO3 paCO2 O2 Cl K+ Na+ Ca+ Mg+ Renin Bun Cr Urine Cl Gold standard diagnosis Other findings
Renal origin Posthypercapnic state[19] + + ± Nl ↑↑ Nl Nl Nl Nl Nl Lab findings
Hypomagnesemia[20] + Nl Nl Nl Nl Nl Nl Nl Lab findings
  • Not applicable
Hypokalemia[21] + Nl Nl Nl Nl Nl Nl Nl Lab findings
  • Not applicable
Bartter's syndrome[22] + + Nl + Nl ↓↓ Nl Nl to ↑ Nl to ↑ Nl Genetic testing
Gitelman’s syndrome[23][24] + + + Nl ↓↓ Nl Nl Nl Nl Genetic testing
Renal artery stenosis[25] + + + + + + Nl Nl Clinical manifestations+ imaging
Liddle syndrome[26] + + + Nl ↓↓ Nl Nl Nl Nl Genetic testing
  • Not applicable
Renal tumors[27] + + + + + + Nl Nl Biopsy
  • Not applicable
Endocrine Cushing's syndrome[28] + + + + Nl Nl Nl 24−hour urinary cortisol excretion + low−dose dexamethasone suppression test
Hyperaldosteronism Primary[29] + + + + Nl Nl to ↓ Nl Nl Lab findings
Secondary[30] + + + + + + Nl Nl Nl Lab findings
Congenital adrenal hyperplasia 11β−Hydroxylase deficiency[31] + + + Nl Nl Nl Nl Nl Genetic testing
17α−Hydroxylase deficiency[32] + + + Nl Nl Nl Nl Nl Genetic testing
Systemic Cystic fibrosis[33] + + + + + Nl Nl Nl Nl Nl to ↑ Nl Genetic testing
Category Disease Hydrogen loss Accumulation of base Chloride depletion Mineralocorticoid excess Fever Dyspnea Edema Toxic/ill BP Dehydration HCO3 paCO2 O2 Cl K+ Na+ Ca+ Mg+ Renin Bun Cr Urine Cl Gold standard diagnosis Other findings

References

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  5. Zaki, SyedAhmed; Lad, Vijay (2011). "Piperacillin-tazobactam-induced hypokalemia and metabolic alkalosis". Indian Journal of Pharmacology. 43 (5): 609. doi:10.4103/0253-7613.84986. ISSN 0253-7613.
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  12. Gilbertson, Heather Ruth; Rogers, Elizabeth Jessie; Ukoumunne, Obioha Chukwunyere (2011). "Determination of a Practical pH Cutoff Level for Reliable Confirmation of Nasogastric Tube Placement". Journal of Parenteral and Enteral Nutrition. 35 (4): 540–544. doi:10.1177/0148607110383285. ISSN 0148-6071.
  13. Hung, Patrick D.; Schubert, Mitchell L.; Mihas, Anastasios A. (2003). "Zollinger-Ellison syndrome". Current Treatment Options in Gastroenterology. 6 (2): 163–170. doi:10.1007/s11938-003-0017-6. ISSN 1092-8472.
  14. Shapiro, Jennifer R.; Berkman, Nancy D.; Brownley, Kimberly A.; Sedway, Jan A.; Lohr, Kathleen N.; Bulik, Cynthia M. (2007). "Bulimia nervosa treatment: A systematic review of randomized controlled trials". International Journal of Eating Disorders. 40 (4): 321–336. doi:10.1002/eat.20372. ISSN 0276-3478.
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  16. Bakal, Unal; Sarac, Mehmet; Aydin, Mustafa; Tartar, Tugay; Kazez, Ahmet (2016). "Recent changes in the features of hypertrophic pyloric stenosis". Pediatrics International. 58 (5): 369–371. doi:10.1111/ped.12860. ISSN 1328-8067.
  17. Gennari, F. J.; Weise, W. J. (2008). "Acid-Base Disturbances in Gastrointestinal Disease". Clinical Journal of the American Society of Nephrology. 3 (6): 1861–1868. doi:10.2215/CJN.02450508. ISSN 1555-9041.
  18. Kurzrock, Eric A.; Baskin, Laurence S.; Kogan, Barry A. (1998). "GASTROCYSTOPLASTY: LONG-TERM FOLLOWUP". The Journal of Urology. 160 (6): 2182–2186. doi:10.1016/S0022-5347(01)62289-4. ISSN 0022-5347.
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  20. Elisaf M, Milionis H, Siamopoulos KC (1997). "Hypomagnesemic hypokalemia and hypocalcemia: clinical and laboratory characteristics". Miner Electrolyte Metab. 23 (2): 105–12. PMID 9252977.
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  22. Simon, David B.; Karet, Fiona E.; Hamdan, Jahed M.; Pietro, Antonio Di; Sanjad, Sami A.; Lifton, Richard P. (1996). "Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na–K–2CI cotransporter NKCC2". Nature Genetics. 13 (2): 183–188. doi:10.1038/ng0696-183. ISSN 1061-4036.
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