Friday, August 29, 2025

Hoover’s sign (Neurological)

1. Core Concept

Hoover's sign is a physical exam maneuver used to help differentiate organic leg weakness from functional (non-organic) leg weakness , often seen in Functional Neurological Disorder (FND) or conversion disorder.

2. The Principle

The test is based on a normal, involuntary synergistic movement: when a supine patient flexes one hip (by trying to raise that leg), they automatically and involuntarily extend (push down) the contralateral hip to brace themselves. This is known as a "associated movement."

  • Organic Paralysis: This associated movement is absent. The patient cannot voluntarily lift the "good" leg, and the "bad" leg does not push down.
  • Functional Paralysis: This associated movement is preserved but disconnected from voluntary effort. The patient doesn't voluntarily push down with the "bad" leg when asked to lift the "good" one, but the automatic movement occurs.

3. Indications for Use

  • A patient presenting with unilateral leg weakness or paralysis.
  • When the clinical picture is inconsistent or there are positive signs of a functional disorder (e.g., give-way weakness, bizarre gait).
  • To provide objective evidence for a functional component to the weakness.

4. How to Perform the Test (Step-by-Step)

Position: Patient lies supine on an examination table.

Part A: Testing the "Bad" (Weak) Leg

  1. Place your hand under the heel of the patient's "good" (strong) leg. This is your sensing hand.
  2. Ask the patient to press down with their "bad" (weak) leg ("Press your weak leg down into the bed as hard as you can").
  3. Normal/Organic Finding: You will feel firm downward pressure in your sensing hand under the good heel (the associated movement of hip extension).
  4. Functional Finding: You will feel little or no pressure in your sensing hand, indicating a lack of genuine effort from the "bad" leg.

Part B: Testing the "Good" (Strong) Leg

  1. Keep your sensing hand under the heel of the "bad" (weak) leg.
  2. Ask the patient to lift their "good" (strong) leg ("Lift your good leg up off the bed, keeping your knee straight").
  3. Normal/Organic Finding: You will feel firm downward pressure in your sensing hand under the weak heel (the involuntary associated movement).
  4. Functional Finding: You will feel little or no pressure under the "bad" heel. The patient may even flex the "bad" hip (a true paradox), demonstrating that the motor pathways are intact but not being used voluntarily.

5. Interpretation of Results

Test Component

Normal / Organic Weakness

Functional Weakness

Press down with BAD leg

Positive reinforcement: Strong downward pressure felt under the GOOD heel.

Negative: No pressure felt under the good heel.

Lift up with GOOD leg

Positive reinforcement: Strong downward pressure felt under the BAD heel.

Negative: No pressure (or paradoxical flexion) felt under the bad heel.

A "Positive Hoover's Sign" for functional weakness is when the test is negative—i.e., the expected associated movement is absent.

6. Key Advantages

  • Objective: Provides a physical sign, not just a subjective report.
  • Reliable: Has good inter-rater reliability when performed correctly.
  • Bedside: Requires no special equipment.
  • Diagnostically powerful: A clear positive sign is strongly suggestive of a functional etiology.

7. Important Caveats & Pitfalls

  • False Positives: Can occur with pain (e.g., severe back or hip pain), apraxia, profound weakness (e.g., complete spinal cord injury), or lack of patient understanding.
  • False Negatives: A savvy patient may learn to fake the sign.
  • Not a Standalone Test: Must be used in the context of a full neurological exam and history. It is one of several "positive signs of functional weakness."
  • Communication is Key: Deliver instructions clearly and neutrally. Avoid implying you are testing for "faking."

8. Classic Phrasing for Note

"Hoover's test was positive for functional weakness: absence of expected hip extension in the right leg when flexing the contralateral hip."

ACOG 2025 RECOMMENDATION on Delayed Cord Clamping

The American College of Obstetricians and Gynecologists (ACOG) has issued new guidelines on deferred umbilical cord clamping in preterm babies, based on evidence showing that such delays save lives.
  • Defer umbilical cord clamping for at least 60 seconds in preterm neonates born before 37 weeks of gestation who do not require immediate resuscitation.
  • In neonates born between 28 0/7 and 36 6/7 weeks of gestation, when deferred clamping is not performed, umbilical cord milking is a reasonable alternative to immediate clamping to improve hematologic outcomes. 

 

 

Comparison of Early vs. Delayed Cord Clamping           

 

Parameter

Early Cord Clamping (ECC)

Delayed Cord Clamping (DCC)

Timing

Within 15–30 seconds after birth

≥30 seconds to ≥120 seconds (often 60–180 sec)

Placental transfusion

Limited

Enhanced (20–40 mL/kg additional blood volume)

Hemoglobin & Hematocrit levels

Lower

Higher

Iron stores

Reduced

Improved (lower risk of iron-deficiency anemia)

Need for RBC transfusion

Higher, especially in preterm infants

Lower, particularly <32 weeks gestation

Neonatal jaundice risk

Lower

Slightly increased (due to higher blood volume)

Polycythemia & blood viscosity

Less frequent

Slightly increased risk

Intraventricular hemorrhage (IVH)

No reduction

Reduced incidence in preterm neonates

Necrotizing enterocolitis (NEC)

No protective effect

Lower incidence in preterm infants

Cardiovascular stability

Less optimal

Improved BP regulation and perfusion

Maternal outcomes

Historically preferred for rapid resuscitation

No adverse impact; safe with proper monitoring

Clinical recommendation

Outdated standard

Recommended by WHO, ACOG, and other bodie

 📌 Note: While DCC offers substantial neonatal benefits, especially in preterm births, it requires readiness for jaundice monitoring and institutional protocols to support safe implementation.

     







































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Thursday, August 28, 2025

Abdominojugular Reflux Test

 A man with heart failure presented with 2 weeks of shortness of breath. The jugular venous pressure was seen at the angle of the jaw and increased for more than 10 seconds when pressure was applied to the abdomen 

 NEJM Evidence

Thursday, August 21, 2025

IV Drip Rate: Formula.

What is IV drip rate? 

IV drip rate describes the rate at which an intravenous infusion is administered in drops per minute.

Use of an IV pump to automatically control the rate of infusion is now common in most medical settings in the United States; however, an IV pump may not be available in some settings/emergencies. In these situations, it is important that nurses know how to calculate the IV drip rate and set the rate of infusion using the IV tubing roller clamp.

How to select the correct tubing type

Factors such as client age and size will guide selection of IV tubing. Different tubing types deliver a larger or smaller number of drops per milliliter. Pediatric clients are very sensitive to fluid volume, so microdrip tubing is used to tightly control fluid volume administration (60 gtt(mL). Macrodrip tubing (10, 15, or 20 gtt/mL) is typically used for adult clients.

What is the drop factor? 

The drop factor (or drip factor) refers to the number of drops (gtts) that make up one milliliter of fluid. Specific to the type of IV tubing being used (typically indicated on the packaging), it is used to calculate the flow rate for manual IV infusions. 

Example order for IV infusion

Typically, the order will include the volume of medication or fluid to be infused and either a rate per hour or the overall duration of the infusion.

It is your job as the nurse to use this information to determine the IV drip rate in gtt/min.

How to calculate IV flow rate: Drops per minute 

We are using the example order of 0.9% normal saline, 1000 mL IV over 8 hr for the calculation. The drop factor is 10 gtts/mL.

Step 1: Convert time units to get the total infusion time in minutes 

Total infusion time in minutes: The order states 8 hours, which is calculated by multiplying 60 minutes x 8 hours, equaling 480 minutes overall. 

Step 2: Calculate gtt per minute with the IV drip rate formula

Formula:

  • The total volume is given in the doctor's order. 
  • The drop factor is determined by the use of the correct tubing, which is required for the calculation.
  • The time is the overall infusion time in minutes. 

 

Since you can't actually administer a fraction of a drop, if you get a fraction as a result, round to the nearest whole number. 

How to set the drip rate

To set the IV drip rate, count the drops as fluid enters the drip chamber. Adjust the roller clamp until you count the correct number of drops entering the chamber per minute (21 for our example above). For safety, label IV bag with the ordered rate and time the hourly markings for infusion.


Saturday, August 9, 2025

SOP for Antenatal Ultrasound Services – PCPNDT Compliance (Odisha)

📝 Standard Operating Procedure (SOP)

For Antenatal Ultrasound Services – PCPNDT Compliance (Odisha)

1. Objective

To ensure ethical, legal, and standardized practice of antenatal ultrasound in compliance with the PCPNDT Act and Odisha Health Department guidelines.

2. Scope

Applicable to all registered ultrasound centers, radiologists, sonologists, and support staff involved in antenatal USG services.

3. Pre-USG Protocol

  • Verification of Pregnancy
    • Confirmed by prescription from a registered medical practitioner (RMP)
    • Must include gestational age and indication for USG
  • Photo ID Proof Collection
    • Acceptable IDs: Aadhaar, Voter ID, PAN card, Driving License, or Government-issued ID
    • Photocopy to be attached with Form F
    • ID number to be recorded in Form F
  • Form F Completion
    • Must be filled before the ultrasound
    • Signed by both the pregnant woman and the radiologist
    • Ensure all fields are complete, especially:
      • Address
      • Age
      • Gravida/Para
      • Indication for USG
      • Declaration of non-disclosure of sex

4. During USG

  • Only medically indicated scans to be performed
  • No disclosure or suggestion of fetal sex
  • Maintain professional and ethical conduct

5. Post-USG Documentation

  • Form F to be filed and stored securely
  • Daily record register to be updated
  • Monthly reports to be submitted to the District Appropriate Authority

6. Audit & Compliance

  • Internal audit every 3 months
  • Random verification of Form F and ID proof
  • Staff sensitization on PCPNDT provisions

✅ Antenatal USG Compliance Checklist

Step

Requirement

Status

1

Prescription from RMP

2

Photo ID proof collected

3

Form F filled before USG

4

Form F signed by patient & radiologist

5

No sex disclosure

6

Daily register updated

7

Monthly report submitted

8

ID proof attached to Form F

 


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