Management of acute ge
"acute gastroenteritis" AND management
acute gastroenteritis management algorithm oral rehydration dehydration

This clinical photograph displays a young child exhibiting classic signs of severe dehydration, likely secondary to acute watery diarrhea. The primary visual finding is the presence of deeply sunken eyes (enophthalmos), a critical physical marker of significant fluid volume deficit. The child demonstrates a depressed level of consciousness, appearing obtunded or lethargic with eyes closed and a lack of responsiveness to the surrounding environment. The facial features appear pinched, and there is a suggestion of reduced tissue turgor. This image serves as an educational tool for identifying the clinical 'danger signs' of dehydration in pediatric patients, emphasizing the need for urgent fluid resuscitation, such as intravenous therapy or intensive oral rehydration salts (ORS) protocols. The context suggests a global health setting where monitoring and managing electrolyte balance is vital for survival in cases of severe diarrheal illness.

This medical infographic presents three clinical algorithms (A, B, and C) for managing massive bleeding in acute settings. Algorithm A details a ROTEM-guided approach for uncoagulated patients, using viscoelastic parameters (EXTEM, FIBTEM, APTEM) to differentiate and treat hyperfibrinolysis (tranexamic acid), hypofibrinogenemia (fibrinogen concentrate), thrombin deficiency (prothrombin complex), and thrombocytopenia. Algorithm B outlines management for uncoagulated patients when ROTEM is unavailable, focusing on monitoring for the 'lethal triad' (acidosis, hypothermia, coagulopathy), lab values like hemoglobin and base excess, and the administration of blood products or PCC. Algorithm C addresses oral anticoagulant overdose, branching by agent type: Vitamin K Antagonists (VKA) or Direct Oral Anticoagulants (DOACs). It provides decision nodes based on INR levels and hemorrhage severity, recommending reversal agents such as Vitamin K, prothrombin complex (PCC), or Idarucizumab for dabigatran. The diagrams use standardized medical terminology and dosage guidelines suitable for emergency medicine, hematology, and trauma surgery education.

This medical illustration depicts the effects of acute plasma osmolality shifts on the brain in a coronal cross-section. The diagram is divided into three panels: a central 'Normal Brain' (normal osmolarity), a 'Hypo-osmotic State' (left), and a 'Hyper-osmotic State' (right). The hypo-osmotic panel illustrates cerebral swelling typically caused by SIADH, rapid rehydration, or dialysis disequilibrium. Key findings include brainstem downward displacement (indicated by blue arrows) and contusions (red X/XX) from contact with the meninges and foramen magnum. The hyper-osmotic panel illustrates water loss and brain shrinkage due to dehydration, renal insufficiency, or rapid mannitol therapy. Significant markers include the brain 'sinking' (magenta arrows), stretching of cortical vessels (indicated by 'O'), and pontine white matter demyelination ('XXX'). A horizontal axis at the bottom highlights the risks of 'Too rapid dehydration' and 'Too rapid rehydration' as iatrogenic drivers of these transitions. The illustration serves as a clinical guide for understanding the Monro-Kellie doctrine and the mechanical consequences of osmotic brain injury, specifically focusing on herniation and vascular damage.
| Score | Appearance | Eyes | Oral Mucosa | Tears | Interpretation |
|---|---|---|---|---|---|
| 0 | Normal | Normal | Moist | Normal | No dehydration |
| 1 | Thirsty/restless | Mildly sunken | Sticky | Decreased | Some dehydration |
| 2 | Drowsy/limp/cold/diaphoretic | Very sunken | Dry | None | Severe dehydration |
| Solution | Na⁺ (mmol/L) | Glucose (mmol/L) | Osmolarity |
|---|---|---|---|
| WHO reduced-osmolarity (2002) | 75 | 75 | 245 mOsm/L |
| Pedialyte | 45 | 139 | ~250 mOsm/L |
| Sports drinks / juices | Very low | Very high | NOT suitable |
| Pathogen | Recommendation |
|---|---|
| Shigella | Treat all cases - azithromycin (first-line); ceftriaxone for parenteral therapy. Ampicillin/TMP-SMX only if susceptible. |
| Salmonella (non-typhoidal) | Do NOT treat routine cases - a Cochrane review (12 trials, 767 patients) showed no benefit and more adverse events with antibiotics. Treat only high-risk patients: <3 months, immunocompromised, sickle cell disease, IBD. |
| Campylobacter | Treat if started within 3 days of onset; azithromycin preferred (high fluoroquinolone resistance). |
| E. coli O157:H7 / STEC | Contraindicated - antibiotics significantly increase the risk of hemolytic-uremic syndrome (HUS). |
| Cholera (V. cholerae) | Doxycycline, azithromycin, or TMP-SMX. |
| Yersinia | Treat only if severe disease, bacteremia, or extraintestinal infection - TMP-SMX, aminoglycosides, fluoroquinolones, doxycycline. |
| C. difficile | Stop offending antibiotic if possible; treat with oral vancomycin or fidaxomicin. |
| Severity | Management |
|---|---|
| None / Minimal | Early refeeding, replace ongoing losses with ORS, discharge with education |
| Mild-Moderate | ORT (50-100 mL/kg over 2-4 hours), reassess, resume diet after rehydration |
| Severe | IV rehydration (20 mL/kg boluses), correct electrolyte abnormalities, admit |